Substances that destroy fungi by suppressing their ability to grow or reproduce. They differ from FUNGICIDES, INDUSTRIAL because they defend against fungi present in human or animal tissues.
A genus of yeast-like mitosporic Saccharomycetales fungi characterized by producing yeast cells, mycelia, pseudomycelia, and blastophores. It is commonly part of the normal flora of the skin, mouth, intestinal tract, and vagina, but can cause a variety of infections, including CANDIDIASIS; ONYCHOMYCOSIS; vulvovaginal candidiasis (CANDIDIASIS, VULVOVAGINAL), and thrush (see CANDIDIASIS, ORAL). (From Dorland, 28th ed)
Macrolide antifungal antibiotic produced by Streptomyces nodosus obtained from soil of the Orinoco river region of Venezuela.
Cyclic hexapeptides of proline-ornithine-threonine-proline-threonine-serine. The cyclization with a single non-peptide bond can lead them to be incorrectly called DEPSIPEPTIDES, but the echinocandins lack ester links. Antifungal activity is via inhibition of 1,3-beta-glucan synthase production of BETA-GLUCANS.
A unicellular budding fungus which is the principal pathogenic species causing CANDIDIASIS (moniliasis).
Triazoles are a class of antifungal drugs that contain a triazole ring in their chemical structure and work by inhibiting the synthesis of ergosterol, an essential component of fungal cell membranes, thereby disrupting the integrity and function of the membrane.
Triazole antifungal agent that is used to treat oropharyngeal CANDIDIASIS and cryptococcal MENINGITIS in AIDS.
An imidazole antifungal agent that is used topically and by intravenous infusion.
A triazole antifungal agent that inhibits cytochrome P-450-dependent enzymes required for ERGOSTEROL synthesis.
Five membered rings containing a NITROGEN atom.
Broad spectrum antifungal agent used for long periods at high doses, especially in immunosuppressed patients.
Mycoses are a group of diseases caused by fungal pathogens that can infect various tissues and organs, potentially leading to localized or systemic symptoms, depending on the immune status of the host.
A fluorinated cytosine analog that is used as an antifungal agent.
Infection with a fungus of the genus CANDIDA. It is usually a superficial infection of the moist areas of the body and is generally caused by CANDIDA ALBICANS. (Dorland, 27th ed)
Any tests that demonstrate the relative efficacy of different chemotherapeutic agents against specific microorganisms (i.e., bacteria, fungi, viruses).
The ability of fungi to resist or to become tolerant to chemotherapeutic agents, antifungal agents, or antibiotics. This resistance may be acquired through gene mutation.
A kingdom of eukaryotic, heterotrophic organisms that live parasitically as saprobes, including MUSHROOMS; YEASTS; smuts, molds, etc. They reproduce either sexually or asexually, and have life cycles that range from simple to complex. Filamentous fungi, commonly known as molds, refer to those that grow as multicellular colonies.
Peptides whose amino and carboxy ends are linked together with a peptide bond forming a circular chain. Some of them are ANTI-INFECTIVE AGENTS. Some of them are biosynthesized non-ribosomally (PEPTIDE BIOSYNTHESIS, NON-RIBOSOMAL).
Compounds consisting of a short peptide chain conjugated with an acyl chain.
Infections with fungi of the genus ASPERGILLUS.
A species of imperfect fungi from which the antibiotic fumigatin is obtained. Its spores may cause respiratory infection in birds and mammals.
A steroid of interest both because its biosynthesis in FUNGI is a target of ANTIFUNGAL AGENTS, notably AZOLES, and because when it is present in SKIN of animals, ULTRAVIOLET RAYS break a bond to result in ERGOCALCIFEROL.
A genus of mitosporic fungi containing about 100 species and eleven different teleomorphs in the family Trichocomaceae.
Macrolide antifungal antibiotic complex produced by Streptomyces noursei, S. aureus, and other Streptomyces species. The biologically active components of the complex are nystatin A1, A2, and A3.
An imidazole derivative that is commonly used as a topical antifungal agent.
An imidazole derivative with a broad spectrum of antimycotic activity. It inhibits biosynthesis of the sterol ergostol, an important component of fungal CELL MEMBRANES. Its action leads to increased membrane permeability and apparent disruption of enzyme systems bound to the membrane.
The ability of fungi to resist or to become tolerant to several structurally and functionally distinct drugs simultaneously. This resistance phenotype may be attributed to multiple gene mutations.
A species of MITOSPORIC FUNGI commonly found on the body surface. It causes opportunistic infections especially in immunocompromised patients.
A species of the fungus CRYPTOCOCCUS. Its teleomorph is Filobasidiella neoformans.
A synthetic antifungal agent.
A mitosporic fungal genus and an anamorphic form of Arthroderma. Various species attack the skin, nails, and hair.
A family of 6-membered heterocyclic compounds occurring in nature in a wide variety of forms. They include several nucleic acid constituents (CYTOSINE; THYMINE; and URACIL) and form the basic structure of the barbiturates.
A form of invasive candidiasis where species of CANDIDA are present in the blood.
A mitosporic fungal genus previously called Monosporium. Teleomorphs include PSEUDALLESCHERIA.
A family of ascomycetous fungi, order Onygenales, characterized by smooth ascospores. Genera in the family include Arthroderma, Keratinomyces, and Ctenomyces. Several well-known anamorphic forms are parasitic upon the skin.
Superficial infections of the skin or its appendages by any of various fungi.
Amphoteric macrolide antifungal antibiotic from Streptomyces natalensis or S. chattanoogensis. It is used for a variety of fungal infections, mainly topically.
Ascomycetous fungi, family Microascaceae, order Microascales, commonly found in the soil. They are causative agents of mycetoma, maduromycosis, and other infections in humans.
The presence of fungi circulating in the blood. Opportunistic fungal sepsis is seen most often in immunosuppressed patients with severe neutropenia or in postoperative patients with intravenous catheters and usually follows prolonged antibiotic therapy.
Infection of the mucous membranes of the mouth by a fungus of the genus CANDIDA. (Dorland, 27th ed)
An NADPH-dependent P450 enzyme that plays an essential role in the sterol biosynthetic pathway by catalyzing the demethylation of 14-methyl sterols such as lanosterol. The enzyme acts via the repeated hydroxylation of the 14-methyl group, resulting in its stepwise conversion into an alcohol, an aldehyde and then a carboxylate, which is removed as formic acid. Sterol 14-demethylase is an unusual cytochrome P450 enzyme in that it is found in a broad variety of organisms including ANIMALS; PLANTS; FUNGI; and protozoa.
Hydrocarbons with more than one double bond. They are a reduced form of POLYYNES.
Infection with a fungus of the species CRYPTOCOCCUS NEOFORMANS.
A large and heterogenous group of fungi whose common characteristic is the absence of a sexual state. Many of the pathogenic fungi in humans belong to this group.
Infection of the VULVA and VAGINA with a fungus of the genus CANDIDA.
A general term for single-celled rounded fungi that reproduce by budding. Brewers' and bakers' yeasts are SACCHAROMYCES CEREVISIAE; therapeutic dried yeast is YEAST, DRIED.
Pulmonary diseases caused by fungal infections, usually through hematogenous spread.
A human or animal whose immunologic mechanism is deficient because of an immunodeficiency disorder or other disease or as the result of the administration of immunosuppressive drugs or radiation.
A species of imperfect fungi which grows on peanuts and other plants and produces the carcinogenic substance aflatoxin. It is also used in the production of the antibiotic flavicin.
A species of MITOSPORIC FUNGI that is a major cause of SEPTICEMIA and disseminated CANDIDIASIS, especially in patients with LYMPHOMA; LEUKEMIA; and DIABETES MELLITUS. It is also found as part of the normal human mucocutaneous flora.
A fungal infection of the nail, usually caused by DERMATOPHYTES; YEASTS; or nondermatophyte MOLDS.
A chronic progressive subcutaneous infection caused by species of fungi (eumycetoma), or actinomycetes (actinomycetoma). It is characterized by tumefaction, abscesses, and tumor-like granules representing microcolonies of pathogens, such as MADURELLA fungi and bacteria ACTINOMYCETES, with different grain colors.
A mitosporic Tremellales fungal genus whose species usually have a capsule and do not form pseudomycellium. Teleomorphs include Filobasidiella and Fidobasidium.
A mitosporic Hypocreales fungal genus, various species of which are important parasitic pathogens of plants and a variety of vertebrates. Teleomorphs include GIBBERELLA.
Two-ring crystalline hydrocarbons isolated from coal tar. They are used as intermediates in chemical synthesis, as insect repellents, fungicides, lubricants, preservatives, and, formerly, as topical antiseptics.
An important nosocomial fungal infection with species of the genus CANDIDA, most frequently CANDIDA ALBICANS. Invasive candidiasis occurs when candidiasis goes beyond a superficial infection and manifests as CANDIDEMIA, deep tissue infection, or disseminated disease with deep organ involvement.
Fungal infection of keratinized tissues such as hair, skin and nails. The main causative fungi include MICROSPORUM; TRICHOPHYTON; and EPIDERMOPHYTON.
A mitosporic fungal genus that causes MYCETOMA in humans. Madurella grisea and M. mycetomatis are the etiological agents.
Infection by a variety of fungi, usually through four possible mechanisms: superficial infection producing conjunctivitis, keratitis, or lacrimal obstruction; extension of infection from neighboring structures - skin, paranasal sinuses, nasopharynx; direct introduction during surgery or accidental penetrating trauma; or via the blood or lymphatic routes in patients with underlying mycoses.
An order of ascomycetous FUNGI which includes many economically important plant parasites as well as saprophytes.
Encrustations, formed from microbes (bacteria, algae, fungi, plankton, or protozoa) embedding in extracellular polymers, that adhere to surfaces such as teeth (DENTAL DEPOSITS); PROSTHESES AND IMPLANTS; and catheters. Biofilms are prevented from forming by treating surfaces with DENTIFRICES; DISINFECTANTS; ANTI-INFECTIVE AGENTS; and antifouling agents.
Proteins found in any species of fungus.
Any liquid or solid preparation made specifically for the growth, storage, or transport of microorganisms or other types of cells. The variety of media that exist allow for the culturing of specific microorganisms and cell types, such as differential media, selective media, test media, and defined media. Solid media consist of liquid media that have been solidified with an agent such as AGAR or GELATIN.
An antifungal agent used in the treatment of TINEA infections.
Please note that 'Lacquer' is not a term typically used in medical definitions; it is more commonly found in the context of materials science, where it refers to a hard, clear coating or finish. If you're referring to a medical term related to lacquer, I would need more information to provide an accurate definition.
The ability of microorganisms, especially bacteria, to resist or to become tolerant to chemotherapeutic agents, antimicrobial agents, or antibiotics. This resistance may be acquired through gene mutation or foreign DNA in transmissible plasmids (R FACTORS).
A fungal infection that may appear in two forms: 1, a primary lesion characterized by the formation of a small cutaneous nodule and small nodules along the lymphatics that may heal within several months; and 2, chronic granulomatous lesions characterized by thick crusts, warty growths, and unusual vascularity and infection in the middle or upper lobes of the lung.
Chemicals that kill or inhibit the growth of fungi in agricultural applications, on wood, plastics, or other materials, in swimming pools, etc.
Microscopic threadlike filaments in FUNGI that are filled with a layer of protoplasm. Collectively, the hyphae make up the MYCELIUM.
A mitosporic fungal genus occasionally causing human diseases such as pulmonary infections, mycotic keratitis, endocarditis, and opportunistic infections. Its teleomorph is BYSSOCHLAMYS.
A group of small, histidine-rich, cationic peptides in human SALIVA which are antibacterial and antifungal.
An infection caused by an organism which becomes pathogenic under certain conditions, e.g., during immunosuppression.
The study of the structure, growth, function, genetics, and reproduction of fungi, and MYCOSES.
A genus of zygomycetous fungi of the family Mucoraceae, order MUCORALES, a common saprophyte and facultative parasite of mature fruits and vegetables. It may cause cerebral mycoses in diabetes and cutaneous infection in severely burned patients.
Cholestadiene derivatives containing a hydroxy group anywhere in the molecule.
The commonest and least serious of the deep mycoses, characterized by nodular lesions of the cutaneous and subcutaneous tissues. It is caused by inhalation of contaminated dust or by infection of a wound.
A mitosporic Oxygenales fungal genus causing various diseases of the skin and hair. The species Microsporum canis produces TINEA CAPITIS and tinea corporis, which usually are acquired from domestic cats and dogs. Teleomorphs includes Arthroderma (Nannizzia). (Alexopoulos et al., Introductory Mycology, 4th edition, p305)
A mitosporic Trichocomaceae fungal genus that develops fruiting organs resembling a broom. When identified, teleomorphs include EUPENICILLIUM and TALAROMYCES. Several species (but especially PENICILLIUM CHRYSOGENUM) are sources of the antibiotic penicillin.
A mitosporic fungal genus causing opportunistic infections, endocarditis, fungemia, a hypersensitivity pneumonitis (see TRICHOSPORONOSIS) and white PIEDRA.
Procedures for identifying types and strains of fungi.
The action of a drug in promoting or enhancing the effectiveness of another drug.
Infection in humans and animals caused by any fungus in the order Mucorales (e.g., Absidia, Mucor, Rhizopus etc.) There are many clinical types associated with infection of the central nervous system, lung, gastrointestinal tract, skin, orbit and paranasal sinuses. In humans, it usually occurs as an opportunistic infection in patients with a chronic debilitating disease, particularly uncontrolled diabetes, or who are receiving immunosuppressive agents. (From Dorland, 28th ed)
Anaerobic degradation of GLUCOSE or other organic nutrients to gain energy in the form of ATP. End products vary depending on organisms, substrates, and enzymatic pathways. Common fermentation products include ETHANOL and LACTIC ACID.
OPPORTUNISTIC INFECTIONS with the soil fungus FUSARIUM. Typically the infection is limited to the nail plate (ONYCHOMYCOSIS). The infection can however become systemic especially in an IMMUNOCOMPROMISED HOST (e.g., NEUTROPENIA) and results in cutaneous and subcutaneous lesions, fever, KERATITIS, and pulmonary infections.
Substances that reduce the growth or reproduction of BACTERIA.
A phylum of fungi which have cross-walls or septa in the mycelium. The perfect state is characterized by the formation of a saclike cell (ascus) containing ascospores. Most pathogenic fungi with a known perfect state belong to this phylum.
A family of fused-ring hydrocarbons isolated from coal tar that act as intermediates in various chemical reactions and are used in the production of coumarone-indene resins.
Deoxyribonucleic acid that makes up the genetic material of fungi.
A mitosporic fungal genus that causes a variety of skin disorders. Malassezia furfur (Pityrosporum orbiculare) causes TINEA VERSICOLOR.
Colored azo compounds formed by the reduction of tetrazolium salts. Employing this reaction, oxidoreductase activity can be determined quantitatively in tissue sections by allowing the enzymes to act on their specific substrates in the presence of tetrazolium salts.
The location of the atoms, groups or ions relative to one another in a molecule, as well as the number, type and location of covalent bonds.
Fungal infections caused by TRICHOSPORON that may become systemic especially in an IMMUNOCOMPROMISED HOST. Clinical manifestations range from superficial cutaneous infections to systemic lesions in multiple organs.
Any technique by which an unknown color is evaluated in terms of standard colors. The technique may be visual, photoelectric, or indirect by means of spectrophotometry. It is used in chemistry and physics. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
A mitosporic Ophiostomataceae fungal genus, whose species Sporothrix schenckii is a well-known animal pathogen. The conidia of this soil fungus may be inhaled causing a primary lung infection, or may infect independently via skin punctures.
Preclinical testing of drugs in experimental animals or in vitro for their biological and toxic effects and potential clinical applications.
Dermatological pruritic lesion in the feet, caused by Trichophyton rubrum, T. mentagrophytes, or Epidermophyton floccosum.
Steroids with a hydroxyl group at C-3 and most of the skeleton of cholestane. Additional carbon atoms may be present in the side chain. (IUPAC Steroid Nomenclature, 1987)
Enumeration by direct count of viable, isolated bacterial, archaeal, or fungal CELLS or SPORES capable of growth on solid CULTURE MEDIA. The method is used routinely by environmental microbiologists for quantifying organisms in AIR; FOOD; and WATER; by clinicians for measuring patients' microbial load; and in antimicrobial drug testing.
'Pyrans' are heterocyclic organic compounds containing a six-membered ring with one oxygen atom and five carbon atoms, which can be found in various natural substances and synthesized compounds, and may have potential applications in medicinal chemistry.
Possesses an unusual and selective cytotoxicity for VASCULAR SMOOTH MUSCLE cells in dogs and rats. Useful for experiments dealing with arterial injury, myocardial fibrosis or cardiac decompensation.
Oils which evaporate readily. The volatile oils occur in aromatic plants, to which they give odor and other characteristics. Most volatile oils consist of a mixture of two or more TERPENES or of a mixture of an eleoptene (the more volatile constituent of a volatile oil) with a stearopten (the more solid constituent). The synonym essential oils refers to the essence of a plant, as its perfume or scent, and not to its indispensability.
An enzyme that converts UDP glucosamine into chitin and UDP. EC 2.4.1.16.
Techniques used in microbiology.
Inflammation of the cornea.
Meningitis caused by fungal agents which may occur as OPPORTUNISTIC INFECTIONS or arise in immunocompetent hosts.
A decrease in the number of NEUTROPHILS found in the blood.
An enzyme that catalyzes the synthesis of fructose-6-phosphate plus GLUTAMINE from GLUTAMATE plus glucosamine-6-phosphate.
An imperfect fungus causing smut or black mold of several fruits, vegetables, etc.
Reproductive bodies produced by fungi.
A cinnamate derivative of the shikamate pathway found in CLOVE OIL and other PLANTS.
Hypersensitivity reaction (ALLERGIC REACTION) to fungus ASPERGILLUS in an individual with long-standing BRONCHIAL ASTHMA. It is characterized by pulmonary infiltrates, EOSINOPHILIA, elevated serum IMMUNOGLOBULIN E, and skin reactivity to Aspergillus antigen.
Infections of the respiratory tract with fungi of the genus ASPERGILLUS. Infections may result in allergic reaction (ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS), colonization in pulmonary cavities as fungus balls (MYCETOMA), or lead to invasion of the lung parenchyma (INVASIVE PULMONARY ASPERGILLOSIS).
Ability of a microbe to survive under given conditions. This can also be related to a colony's ability to replicate.
A species of the genus SACCHAROMYCES, family Saccharomycetaceae, order Saccharomycetales, known as "baker's" or "brewer's" yeast. The dried form is used as a dietary supplement.
Glucose polymers consisting of a backbone of beta(1->3)-linked beta-D-glucopyranosyl units with beta(1->6) linked side chains of various lengths. They are a major component of the CELL WALL of organisms and of soluble DIETARY FIBER.
Members of the class of compounds composed of AMINO ACIDS joined together by peptide bonds between adjacent amino acids into linear, branched or cyclical structures. OLIGOPEPTIDES are composed of approximately 2-12 amino acids. Polypeptides are composed of approximately 13 or more amino acids. PROTEINS are linear polypeptides that are normally synthesized on RIBOSOMES.
Inflammation of the OUTER EAR including the external EAR CANAL, cartilages of the auricle (EAR CARTILAGE), and the TYMPANIC MEMBRANE.
Infection in humans and animals caused by fungi in the class Zygomycetes. It includes MUCORMYCOSIS and entomophthoramycosis. The latter is a tropical infection of subcutaneous tissue or paranasal sinuses caused by fungi in the order Entomophthorales. Phycomycosis, closely related to zygomycosis, describes infection with members of Phycomycetes, an obsolete classification.
Cell wall components constituting a polysaccharide core found in fungi. They may act as antigens or structural substrates.
The action of a drug that may affect the activity, metabolism, or toxicity of another drug.
A normally saprophytic mitosporic Chaetothyriales fungal genus. Infections in humans include PHAEOHYPHOMYCOSIS; and PERITONITIS.. Exophiala jeanselmei (previously Phialophora jeanselmei) is an etiological agent of MYCETOMA.
Thiazoles are heterocyclic organic compounds containing a sulfur atom and a nitrogen atom, which are bound by two carbon atoms to form a five-membered ring, and are widely found in various natural and synthetic substances, including some pharmaceuticals and vitamins.
Opportunistic infections found in patients who test positive for human immunodeficiency virus (HIV). The most common include PNEUMOCYSTIS PNEUMONIA, Kaposi's sarcoma, cryptosporidiosis, herpes simplex, toxoplasmosis, cryptococcosis, and infections with Mycobacterium avium complex, Microsporidium, and Cytomegalovirus.
An order of zygomycetous fungi, usually saprophytic, causing damage to food in storage, but which may cause respiratory infection or MUCORMYCOSIS in persons suffering from other debilitating diseases.
Quaternary salts derived from tetrazoles. They are used in tests to distinguish between reducing sugars and simple aldehydes, for detection of dehydrogenase in tissues, cells, and bacteria, for determination of corticosteroids, and in color photography. (From Mall's Dictionary of Chemistry, 5th ed, p455)
Pyridine derivatives with one or more keto groups on the ring.
Single preparations containing two or more active agents, for the purpose of their concurrent administration as a fixed dose mixture.
Any of the processes by which nuclear, cytoplasmic, or intercellular factors influence the differential control of gene action in fungi.
Spectroscopic method of measuring the magnetic moment of elementary particles such as atomic nuclei, protons or electrons. It is employed in clinical applications such as NMR Tomography (MAGNETIC RESONANCE IMAGING).
Phenomena and pharmaceutics of compounds that inhibit the function of agonists (DRUG AGONISM) and inverse agonists (DRUG INVERSE AGONISM) for a specific receptor. On their own, antagonists produce no effect by themselves to a receptor, and are said to have neither intrinsic activity nor efficacy.
Infection with a fungus of the genus COCCIDIOIDES, endemic to the SOUTHWESTERN UNITED STATES. It is sometimes called valley fever but should not be confused with RIFT VALLEY FEVER. Infection is caused by inhalation of airborne, fungal particles known as arthroconidia, a form of FUNGAL SPORES. A primary form is an acute, benign, self-limited respiratory infection. A secondary form is a virulent, severe, chronic, progressive granulomatous disease with systemic involvement. It can be detected by use of COCCIDIOIDIN.
Concentrated pharmaceutical preparations of plants obtained by removing active constituents with a suitable solvent, which is evaporated away, and adjusting the residue to a prescribed standard.
Inbred ICR mice are a strain of albino laboratory mice that have been selectively bred for consistent genetic makeup and high reproductive performance, making them widely used in biomedical research for studies involving reproduction, toxicology, pharmacology, and carcinogenesis.
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
A bile acid formed by bacterial action from cholate. It is usually conjugated with glycine or taurine. Deoxycholic acid acts as a detergent to solubilize fats for intestinal absorption, is reabsorbed itself, and is used as a choleretic and detergent.
A method where a culturing surface inoculated with microbe is exposed to small disks containing known amounts of a chemical agent resulting in a zone of inhibition (usually in millimeters) of growth of the microbe corresponding to the susceptibility of the strain to the agent.
Therapy with two or more separate preparations given for a combined effect.
Compounds with a core of 10 carbons generally formed via the mevalonate pathway from the combination of 3,3-dimethylallyl pyrophosphate and isopentenyl pyrophosphate. They are cyclized and oxidized in a variety of ways. Due to the low molecular weight many of them exist in the form of essential oils (OILS, VOLATILE).
The application of drug preparations to the surfaces of the body, especially the skin (ADMINISTRATION, CUTANEOUS) or mucous membranes. This method of treatment is used to avoid systemic side effects when high doses are required at a localized area or as an alternative systemic administration route, to avoid hepatic processing for example.
A colorless liquid extracted from oils of plants such as citronella, neroli, cyclamen, and tuberose. It is an intermediate step in the biological synthesis of cholesterol from mevalonic acid in vertebrates. It has a delicate odor and is used in perfumery. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed)
A genus of bacteria that form a nonfragmented aerial mycelium. Many species have been identified with some being pathogenic. This genus is responsible for producing a majority of the ANTI-BACTERIAL AGENTS of practical value.
The outermost layer of a cell in most PLANTS; BACTERIA; FUNGI; and ALGAE. The cell wall is usually a rigid structure that lies external to the CELL MEMBRANE, and provides a protective barrier against physical or chemical agents.
The functional hereditary units of FUNGI.
The relationship between the dose of an administered drug and the response of the organism to the drug.
Lipid-protein complexes involved in the transportation and metabolism of lipids in the body. They are spherical particles consisting of a hydrophobic core of TRIGLYCERIDES and CHOLESTEROL ESTERS surrounded by a layer of hydrophilic free CHOLESTEROL; PHOSPHOLIPIDS; and APOLIPOPROTEINS. Lipoproteins are classified by their varying buoyant density and sizes.
Cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure. Large cyclic lactones of over a dozen atoms are MACROLIDES.
Enzymes that catalyze the transfer of glucose from a nucleoside diphosphate glucose to an acceptor molecule which is frequently another carbohydrate. EC 2.4.1.-.
Liquid chromatographic techniques which feature high inlet pressures, high sensitivity, and high speed.
Family of antimicrobial peptides that have been identified in humans, animals, and plants. They are thought to play a role in host defenses against infections, inflammation, wound repair, and acquired immunity.
The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups.
A mitosporic Ceratobasidiaceae fungal genus that is an important plant pathogen affecting potatoes and other plants. There are numerous teleomorphs.
Compounds containing 1,3-diazole, a five membered aromatic ring containing two nitrogen atoms separated by one of the carbons. Chemically reduced ones include IMIDAZOLINES and IMIDAZOLIDINES. Distinguish from 1,2-diazole (PYRAZOLES).
The middle portion of the pharynx that lies posterior to the mouth, inferior to the SOFT PALATE, and superior to the base of the tongue and EPIGLOTTIS. It has a digestive function as food passes from the mouth into the oropharynx before entering ESOPHAGUS.
Microscopy in which the object is examined directly by an electron beam scanning the specimen point-by-point. The image is constructed by detecting the products of specimen interactions that are projected above the plane of the sample, such as backscattered electrons. Although SCANNING TRANSMISSION ELECTRON MICROSCOPY also scans the specimen point by point with the electron beam, the image is constructed by detecting the electrons, or their interaction products that are transmitted through the sample plane, so that is a form of TRANSMISSION ELECTRON MICROSCOPY.
The complete gene complement contained in a set of chromosomes in a fungus.

Microbial and chemical transformations of some 12,13-epoxytrichothec-9,10-enes. (1/8644)

Resting cells of Streptomyces griseus, Mucor mucedo, and a growing culture of Acinetobacter calcoaceticus when mixed with compounds related to 12,13-epoxytrichothec-9-ene-4beta,15-diacetoxy-3alpha-ol(anguidine) produced a series of derivatives that were either partially hydrolyzed or selectively acylated. These derivatives showed marked differences in activities as assayed by antifungal and tissue culture cytotoxicity tests.  (+info)

Early mycological treatment failure in AIDS-associated cryptococcal meningitis. (2/8644)

Cryptococcal meningitis causes significant morbidity and mortality in persons with AIDS. Of 236 AIDS patients treated with amphotericin B plus flucytosine, 29 (12%) died within 2 weeks and 62 (26%) died before 10 weeks. Just 129 (55%) of 236 patients were alive with negative cerebrospinal fluid (CSF) cultures at 10 weeks. Multivariate analyses identified that titer of cryptococcal antigen in CSF, serum albumin level, and CD4 cell count, together with dose of amphotericin B, had the strongest joint association with failure to achieve negative CSF cultures by day 14. Among patients with similar CSF cryptococcal antigen titers, CD4 cell counts, and serum albumin levels, the odds of failure at week 10 for those without negative CSF cultures by day 14 was five times that for those with negative CSF cultures by day 14 (odds ratio, 5.0; 95% confidence interval, 2.2-10.9). Prognosis is dismal for patients with AIDS-related cryptococcal meningitis. Multivariate analyses identified three components that, along with initial treatment, have the strongest joint association with early outcome. Clearly, more effective initial therapy and patient management strategies that address immune function and nutritional status are needed to improve outcomes of this disease.  (+info)

Infectious complications in 126 patients treated with high-dose chemotherapy and autologous peripheral blood stem cell transplantation. (3/8644)

The effect of an extensive prophylactic antimicrobial regimen was prospectively assessed in 126 patients after high-dose chemotherapy and autologous PBSC. They received ciprofloxacin (500 mg/12 h), acyclovir (200 mg/6 h), and itraconazole (200 mg/12 h) orally until neutrophil recovery. Febrile patients received i.v. imipenem (500 mg/6 h) to which vancomycin and amikacin were added if fever persisted for 2-3 and 5 days, respectively. Amphotericin B lipid complex was further given on day 7 or 8 of fever. Median times for a neutrophil count of >0.5 x 10(9)/l and a platelet count of >20 x 10(9)/l were 9 and 11 days. Severe neutropenia (<0.1 x 10(9)/l) lasted for a median of 5 days in which 72% of febrile episodes and 50% of cases of bacteremia occurred. Gram-positive bacteria were isolated in 30 of 40 episodes of bacteremia, 25 of which were caused by Staphylococcus epidermidis. Clinical foci were the intravascular catheter in 35 cases, respiratory infection in 11, cellulitis in two, anal abscess in one, and neutropenic enterocolitis in one. The high incidence of febrile episodes (94%) and bacteremias (31%) may be due to the lack of efficacy of antimicrobial prophylaxis and the persistence of a 5-day period of severe neutropenia.  (+info)

Systemic candidiasis with candida vasculitis due to Candida kruzei in a patient with acute myeloid leukaemia. (4/8644)

Candida kruzei-related systemic infections are increasing in frequency, particularly in patients receiving prophylaxis with antifungal triazoles. A Caucasian male with newly diagnosed acute myeloid leukaemia (AML M1) developed severe and persistent fever associated with a micropustular eruption scattered over the trunk and limbs during induction chemotherapy. Blood cultures grew Candida kruzei, and biopsies of the skin lesions revealed a candida vasculitis. He responded to high doses of liposomal amphotericin B and was discharged well from hospital.  (+info)

Structure of the complex between the antibiotic cerulenin and its target, beta-ketoacyl-acyl carrier protein synthase. (5/8644)

In the biosynthesis of fatty acids, the beta-ketoacyl-acyl carrier protein (ACP) synthases catalyze chain elongation by the addition of two-carbon units derived from malonyl-ACP to an acyl group bound to either ACP or CoA. The enzyme is a possible drug target for treatment of certain cancers and for tuberculosis. The crystal structure of the complex of the enzyme from Escherichia coli, and the fungal mycotoxin cerulenin reveals that the inhibitor is bound in a hydrophobic pocket formed at the dimer interface. Cerulenin is covalently attached to the active site cysteine through its C2 carbon atom. The fit of the inhibitor to the active site is not optimal, and there is thus room for improvement through structure based design.  (+info)

BE-31405, a new antifungal antibiotic produced by Penicillium minioluteum. I. Description of producing organism, fermentation, isolation, physico-chemical and biological properties. (6/8644)

A new antifungal antibiotic, BE-31405, was isolated from the culture broth of a fungal strain, Penicillium minioluteum F31405. BE-31405 was isolated by adsorption on high porous polymer resin (Diaion HP-20), followed by solvent extraction, precipitation and crystallization. BE-31405 showed potent growth inhibitory activity against pathogenic fungal strains such as Candida albicans, Candida glabrata and Cryptococcus neoformans, but did not show cytotoxic activity against mammalian cells such as P388 mouse leukemia. The mechanism studies indicated that BE-31405 inhibited the protein synthesis of C. albicans but not of mammalian cells.  (+info)

In vitro and in vivo activities of NS-718, a new lipid nanosphere incorporating amphotericin B, against Aspergillus fumigatus. (7/8644)

We evaluated the in vitro and in vivo potencies of a new lipid nanosphere that incorporates amphotericin B (AmB), NS-718, against Aspergillus fumigatus. The in vitro activity of NS-718 (the MIC at which 90% of strains are inhibited [MIC90], 0.25 microgram/ml) against 18 isolates of A. fumigatus was similar to that of deoxycholate AmB (D-AmB; Fungizone; MIC90, 0.25 microgram/ml), but NS-718 was more potent than liposomal AmB (L-AmB; AmBi-some; MIC90, 1.0 microgram/ml). The in vivo efficacy of NS-718 in a rat model of invasive pulmonary aspergillosis was compared with those of D-AmB and L-AmB. A low dose (1 mg/kg of body weight) of L-AmB was ineffective (survival rate, 0%), although equivalent doses of D-AmB and NS-718 were more effective (survival rate, 17%). However, a higher dose of NS-718 (3 mg/kg) was more effective (survival rate, 100%) than equivalent doses of D-AmB and L-AmB (survival rate, 0%). To explain these differences, pharmacokinetic studies showed higher concentrations of AmB in the plasma of rats treated with NS-718 than in the plasma of those treated with D-AmB. Our results suggest that NS-718, a new preparation of AmB, is a promising antifungal agent with activity against pulmonary aspergillosis.  (+info)

Effect of fasting on temporal variation in the nephrotoxicity of amphotericin B in rats. (8/8644)

Evidence for temporal variation in the nephrotoxicity of amphotericin B was recently reported in experimental animals. The role of food in these variations was determined by studying the effect of a short fasting period on the temporal variation in the renal toxicity of amphotericin B. Twenty-eight normally fed and 28 fasted female Sprague-Dawley rats were used. Food was available ad libitum to the fed rats, while the fasted animals were fasted 12 h before and 24 h after amphotericin B injection to minimize stress for the animals. Water was available ad libitum to both groups of rats, which were maintained on a 14-h light, 10-h dark regimen (light on at 0600 h). Renal toxicity was determined by comparing the levels of excretion of renal enzyme and the serum creatinine and blood urea nitrogen (BUN) levels at the time of the maximal (0700 h) or the minimal (1900 h) nephrotoxicity after the intraperitoneal administration of a single dose of dextrose (5%; control group) or amphotericin B (50 mg/kg of body weight; treated group) to the rats. The nephrotoxicities obtained after amphotericin B administration at both times of day were compared to the nephrotoxicities observed for time-matched controls. In fed animals, the 24-h urinary excretion of N-acetyl-beta-D-glucosaminidase and beta-galactosidase was significantly higher when amphotericin B was injected at 0700 and 1900 h. The excretion of these two enzymes was reduced significantly (P < 0.05) in fasting rats, and this effect was larger at 0700 h (P < 0.05) than at 1900 h. The serum creatinine level was also significantly higher (P < 0.05) in fed animals treated at 0700 h than in fed animals treated at 1900 h. Fasting reduced significantly (P < 0.05) the increase in the serum creatinine level, and this effect was larger in the animals treated at 0700 h. Similar data were obtained for BUN levels. Amphotericin B accumulation was significantly higher (P < 0.05) in the renal cortexes of fed rats than in those of fasted animals, but there was no difference according to the time of injection. These results demonstrated that fasting reduces the nephrotoxicity of amphotericin B and that food availability is of crucial importance in the temporal variation in the renal toxicity of amphotericin B in rats.  (+info)

Antifungal agents are a type of medication used to treat and prevent fungal infections. These agents work by targeting and disrupting the growth of fungi, which include yeasts, molds, and other types of fungi that can cause illness in humans.

There are several different classes of antifungal agents, including:

1. Azoles: These agents work by inhibiting the synthesis of ergosterol, a key component of fungal cell membranes. Examples of azole antifungals include fluconazole, itraconazole, and voriconazole.
2. Echinocandins: These agents target the fungal cell wall, disrupting its synthesis and leading to fungal cell death. Examples of echinocandins include caspofungin, micafungin, and anidulafungin.
3. Polyenes: These agents bind to ergosterol in the fungal cell membrane, creating pores that lead to fungal cell death. Examples of polyene antifungals include amphotericin B and nystatin.
4. Allylamines: These agents inhibit squalene epoxidase, a key enzyme in ergosterol synthesis. Examples of allylamine antifungals include terbinafine and naftifine.
5. Griseofulvin: This agent disrupts fungal cell division by binding to tubulin, a protein involved in fungal cell mitosis.

Antifungal agents can be administered topically, orally, or intravenously, depending on the severity and location of the infection. It is important to use antifungal agents only as directed by a healthcare professional, as misuse or overuse can lead to resistance and make treatment more difficult.

'Candida' is a type of fungus (a form of yeast) that is commonly found on the skin and inside the body, including in the mouth, throat, gut, and vagina, in small amounts. It is a part of the normal microbiota and usually does not cause any problems. However, an overgrowth of Candida can lead to infections known as candidiasis or thrush. Common sites for these infections include the skin, mouth, throat, and genital areas. Some factors that can contribute to Candida overgrowth are a weakened immune system, certain medications (such as antibiotics and corticosteroids), diabetes, pregnancy, poor oral hygiene, and wearing damp or tight-fitting clothing. Common symptoms of candidiasis include itching, redness, pain, and discharge. Treatment typically involves antifungal medication, either topical or oral, depending on the site and severity of the infection.

Amphotericin B is an antifungal medication used to treat serious and often life-threatening fungal infections. It works by binding to the ergosterol in the fungal cell membrane, creating pores that lead to the loss of essential cell components and ultimately cell death.

The medical definition of Amphotericin B is:

A polyene antifungal agent derived from Streptomyces nodosus, with a broad spectrum of activity against various fungi, including Candida, Aspergillus, Cryptococcus, and Histoplasma capsulatum. Amphotericin B is used to treat systemic fungal infections, such as histoplasmosis, cryptococcosis, candidiasis, and aspergillosis, among others. It may be administered intravenously or topically, depending on the formulation and the site of infection.

Adverse effects associated with Amphotericin B include infusion-related reactions (such as fever, chills, and hypotension), nephrotoxicity, electrolyte imbalances, and anemia. These side effects are often dose-dependent and may be managed through careful monitoring and adjustment of the dosing regimen.

Echinocandins are a class of antifungal medications that inhibit the synthesis of 1,3-β-D-glucan, a key component of the fungal cell wall. This results in osmotic instability and ultimately leads to fungal cell death. Echinocandins are commonly used to treat invasive fungal infections caused by Candida species and Aspergillus species. The three drugs in this class that are approved for use in humans are caspofungin, micafungin, and anidulafungin.

Here's a brief overview of each drug:

1. Caspofungin (Cancidas, Cancidas-W): This is the first echinocandin to be approved for use in humans. It is indicated for the treatment of invasive candidiasis, including candidemia, acute disseminated candidiasis, and other forms of Candida infections. Caspofungin is also approved for the prevention of Candida infections in patients undergoing hematopoietic stem cell transplantation.
2. Micafungin (Mycamine): This echinocandin is approved for the treatment of candidemia, esophageal candidiasis, and other forms of Candida infections. It is also used for the prevention of Candida infections in patients undergoing hematopoietic stem cell transplantation.
3. Anidulafungin (Eraxis): This echinocandin is approved for the treatment of esophageal candidiasis and candidemia, as well as other forms of Candida infections. It is also used for the prevention of Candida infections in patients undergoing hematopoietic stem cell transplantation.

Echinocandins have a broad spectrum of activity against many fungal species, including those that are resistant to other classes of antifungal medications. They are generally well-tolerated and have a low incidence of drug interactions. However, they should be used with caution in patients with hepatic impairment, as their metabolism may be affected by liver dysfunction.

'Candida albicans' is a species of yeast that is commonly found in the human body, particularly in warm and moist areas such as the mouth, gut, and genital region. It is a part of the normal microbiota and usually does not cause any harm. However, under certain conditions like a weakened immune system, prolonged use of antibiotics or steroids, poor oral hygiene, or diabetes, it can overgrow and cause infections known as candidiasis. These infections can affect various parts of the body including the skin, nails, mouth (thrush), and genital area (yeast infection).

The medical definition of 'Candida albicans' is:

A species of yeast belonging to the genus Candida, which is commonly found as a commensal organism in humans. It can cause opportunistic infections when there is a disruption in the normal microbiota or when the immune system is compromised. The overgrowth of C. albicans can lead to various forms of candidiasis, such as oral thrush, vaginal yeast infection, and invasive candidiasis.

Triazoles are a class of antifungal medications that have broad-spectrum activity against various fungi, including yeasts, molds, and dermatophytes. They work by inhibiting the synthesis of ergosterol, an essential component of fungal cell membranes, leading to increased permeability and disruption of fungal growth. Triazoles are commonly used in both systemic and topical formulations for the treatment of various fungal infections, such as candidiasis, aspergillosis, cryptococcosis, and dermatophytoses. Some examples of triazole antifungals include fluconazole, itraconazole, voriconazole, and posaconazole.

Fluconazole is an antifungal medication used to treat and prevent various fungal infections, such as candidiasis (yeast infections), cryptococcal meningitis, and other fungal infections that affect the mouth, throat, blood, lungs, genital area, and other parts of the body. It works by inhibiting the growth of fungi that cause these infections. Fluconazole is available in various forms, including tablets, capsules, and intravenous (IV) solutions, and is typically prescribed to be taken once daily.

The medical definition of Fluconazole can be found in pharmacological or medical dictionaries, which describe it as a triazole antifungal agent that inhibits fungal cytochrome P450-dependent synthesis of ergosterol, a key component of the fungal cell membrane. This results in increased permeability and leakage of cellular contents, ultimately leading to fungal death. Fluconazole has a broad spectrum of activity against various fungi, including Candida, Cryptococcus, Aspergillus, and others.

It is important to note that while Fluconazole is an effective antifungal medication, it may have side effects and interactions with other medications. Therefore, it should only be used under the guidance of a healthcare professional.

Miconazole is an antifungal medication used to treat various fungal infections, including those affecting the skin, mouth, and vagina. According to the Medical Subject Headings (MeSH) database maintained by the National Library of Medicine, miconazole is classified as an imidazole antifungal agent that works by inhibiting the synthesis of ergosterol, a key component of fungal cell membranes. By disrupting the structure and function of the fungal cell membrane, miconazole can help to kill or suppress the growth of fungi, providing therapeutic benefits in patients with fungal infections.

Miconazole is available in various formulations, including creams, ointments, powders, tablets, and vaginal suppositories, and is typically applied or administered topically or vaginally, depending on the site of infection. In some cases, miconazole may also be given intravenously for the treatment of severe systemic fungal infections.

As with any medication, miconazole can have side effects and potential drug interactions, so it is important to use it under the guidance of a healthcare professional. Common side effects of miconazole include skin irritation, redness, and itching at the application site, while more serious side effects may include allergic reactions, liver damage, or changes in heart rhythm. Patients should be sure to inform their healthcare provider of any other medications they are taking, as well as any medical conditions they have, before using miconazole.

Itraconazole is an antifungal medication used to treat various fungal infections, including blastomycosis, histoplasmosis, aspergillosis, and candidiasis. It works by inhibiting the synthesis of ergosterol, a vital component of fungal cell membranes, thereby disrupting the integrity and function of these membranes. Itraconazole is available in oral and intravenous forms for systemic use and as a topical solution or cream for localized fungal infections.

Medical Definition:
Itraconazole (i-tra-KON-a-zole): A synthetic triazole antifungal agent used to treat various fungal infections, such as blastomycosis, histoplasmosis, aspergillosis, and candidiasis. It inhibits the synthesis of ergosterol, a critical component of fungal cell membranes, leading to disruption of their integrity and function. Itraconazole is available in oral (capsule and solution) and intravenous forms for systemic use and as a topical solution or cream for localized fungal infections.

"Azoles" is a class of antifungal medications that have a similar chemical structure, specifically a five-membered ring containing nitrogen and two carbon atoms (a "azole ring"). The most common azoles used in medicine include:

1. Imidazoles: These include drugs such as clotrimazole, miconazole, and ketoconazole. They are used to treat a variety of fungal infections, including vaginal yeast infections, thrush, and skin infections.
2. Triazoles: These include drugs such as fluconazole, itraconazole, and voriconazole. They are also used to treat fungal infections, but have a broader spectrum of activity than imidazoles and are often used for more serious or systemic infections.

Azoles work by inhibiting the synthesis of ergosterol, an essential component of fungal cell membranes. This leads to increased permeability of the cell membrane, which ultimately results in fungal cell death.

While azoles are generally well-tolerated, they can cause side effects such as nausea, vomiting, and abdominal pain. In addition, some azoles can interact with other medications and affect liver function, so it's important to inform your healthcare provider of all medications you are taking before starting an azole regimen.

Ketoconazole is an antifungal medication that is primarily used to treat various fungal infections, including those caused by dermatophytes, Candida, and pityrosporum. It works by inhibiting the synthesis of ergosterol, a crucial component of fungal cell membranes, which leads to increased permeability and ultimately results in fungal cell death.

Ketoconazole is available as an oral tablet for systemic use and as a topical cream or shampoo for localized applications. The oral formulation is used to treat severe or invasive fungal infections, while the topical preparations are primarily indicated for skin and scalp infections, such as athlete's foot, ringworm, jock itch, candidiasis, and seborrheic dermatitis.

Common side effects of oral ketoconazole include nausea, vomiting, headache, and altered liver function tests. Rare but serious adverse reactions may include hepatotoxicity, adrenal insufficiency, and interactions with other medications that can affect the metabolism and elimination of drugs. Topical ketoconazole is generally well-tolerated, with local irritation being the most common side effect.

It's important to note that due to its potential for serious liver toxicity and drug-drug interactions, oral ketoconazole has been largely replaced by other antifungal agents, such as fluconazole and itraconazole, which have more favorable safety profiles. Topical ketoconazole remains a valuable option for treating localized fungal infections due to its effectiveness and lower risk of systemic side effects.

Mycoses are a group of diseases caused by fungal infections. These infections can affect various parts of the body, including the skin, nails, hair, lungs, and internal organs. The severity of mycoses can range from superficial, mild infections to systemic, life-threatening conditions, depending on the type of fungus and the immune status of the infected individual. Some common types of mycoses include candidiasis, dermatophytosis, histoplasmosis, coccidioidomycosis, and aspergillosis. Treatment typically involves antifungal medications, which can be topical or systemic, depending on the location and severity of the infection.

Flucytosine is an antifungal medication used to treat serious and life-threatening fungal infections, such as cryptococcal meningitis and candidiasis. It works by interfering with the production of DNA and RNA in the fungal cells, which inhibits their growth and reproduction.

The medical definition of Flucytosine is:

A synthetic fluorinated pyrimidine nucleoside analogue that is converted to fluorouracil after uptake into susceptible fungal cells. It is used as an antifungal agent in the treatment of serious systemic fungal infections, particularly those caused by Candida and Cryptococcus neoformans. Flucytosine has both fungistatic and fungicidal activity, depending on the concentration achieved at the site of infection and the susceptibility of the organism.

Flucytosine is available in oral form and is often used in combination with other antifungal agents to increase its effectiveness and prevent the development of resistance. Common side effects include nausea, vomiting, diarrhea, and bone marrow suppression. Regular monitoring of blood counts and liver function tests is necessary during treatment to detect any potential toxicity.

Candidiasis is a fungal infection caused by Candida species, most commonly Candida albicans. It can affect various parts of the body, including the skin, mucous membranes (such as the mouth and vagina), and internal organs (like the esophagus, lungs, or blood).

The symptoms of candidiasis depend on the location of the infection:

1. Oral thrush: White patches on the tongue, inner cheeks, gums, or roof of the mouth. These patches may be painful and can bleed slightly when scraped.
2. Vaginal yeast infection: Itching, burning, redness, and swelling of the vagina and vulva; thick, white, odorless discharge from the vagina.
3. Esophageal candidiasis: Difficulty swallowing, pain when swallowing, or feeling like food is "stuck" in the throat.
4. Invasive candidiasis: Fever, chills, and other signs of infection; multiple organ involvement may lead to various symptoms depending on the affected organs.

Risk factors for developing candidiasis include diabetes, HIV/AIDS, use of antibiotics or corticosteroids, pregnancy, poor oral hygiene, and wearing tight-fitting clothing that traps moisture. Treatment typically involves antifungal medications, such as fluconazole, nystatin, or clotrimazole, depending on the severity and location of the infection.

Microbial sensitivity tests, also known as antibiotic susceptibility tests (ASTs) or bacterial susceptibility tests, are laboratory procedures used to determine the effectiveness of various antimicrobial agents against specific microorganisms isolated from a patient's infection. These tests help healthcare providers identify which antibiotics will be most effective in treating an infection and which ones should be avoided due to resistance. The results of these tests can guide appropriate antibiotic therapy, minimize the potential for antibiotic resistance, improve clinical outcomes, and reduce unnecessary side effects or toxicity from ineffective antimicrobials.

There are several methods for performing microbial sensitivity tests, including:

1. Disk diffusion method (Kirby-Bauer test): A standardized paper disk containing a predetermined amount of an antibiotic is placed on an agar plate that has been inoculated with the isolated microorganism. After incubation, the zone of inhibition around the disk is measured to determine the susceptibility or resistance of the organism to that particular antibiotic.
2. Broth dilution method: A series of tubes or wells containing decreasing concentrations of an antimicrobial agent are inoculated with a standardized microbial suspension. After incubation, the minimum inhibitory concentration (MIC) is determined by observing the lowest concentration of the antibiotic that prevents visible growth of the organism.
3. Automated systems: These use sophisticated technology to perform both disk diffusion and broth dilution methods automatically, providing rapid and accurate results for a wide range of microorganisms and antimicrobial agents.

The interpretation of microbial sensitivity test results should be done cautiously, considering factors such as the site of infection, pharmacokinetics and pharmacodynamics of the antibiotic, potential toxicity, and local resistance patterns. Regular monitoring of susceptibility patterns and ongoing antimicrobial stewardship programs are essential to ensure optimal use of these tests and to minimize the development of antibiotic resistance.

Fungal drug resistance is a condition where fungi are no longer susceptible to the antifungal drugs that were previously used to treat infections they caused. This can occur due to genetic changes in the fungi that make them less sensitive to the drug's effects, or due to environmental factors that allow the fungi to survive and multiply despite the presence of the drug.

There are several mechanisms by which fungi can develop drug resistance, including:

1. Mutations in genes that encode drug targets: Fungi can acquire mutations in the genes that encode for the proteins or enzymes that the antifungal drugs target. These mutations can alter the structure or function of these targets, making them less susceptible to the drug's effects.
2. Overexpression of efflux pumps: Fungi can increase the expression of genes that encode for efflux pumps, which are proteins that help fungi expel drugs from their cells. This can reduce the intracellular concentration of the drug and make it less effective.
3. Changes in membrane composition: Fungi can alter the composition of their cell membranes to make them less permeable to antifungal drugs, making it more difficult for the drugs to enter the fungal cells and exert their effects.
4. Biofilm formation: Fungi can form biofilms, which are complex communities of microorganisms that adhere to surfaces and are protected by a matrix of extracellular material. Biofilms can make fungi more resistant to antifungal drugs by limiting drug penetration and creating an environment that promotes the development of resistance.

Fungal drug resistance is a significant clinical problem, particularly in patients with weakened immune systems, such as those with HIV/AIDS or cancer. It can lead to treatment failures, increased morbidity and mortality, and higher healthcare costs. To address this issue, there is a need for new antifungal drugs, as well as strategies to prevent and manage drug resistance.

Fungi, in the context of medical definitions, are a group of eukaryotic organisms that include microorganisms such as yeasts and molds, as well as the more familiar mushrooms. The study of fungi is known as mycology.

Fungi can exist as unicellular organisms or as multicellular filamentous structures called hyphae. They are heterotrophs, which means they obtain their nutrients by decomposing organic matter or by living as parasites on other organisms. Some fungi can cause various diseases in humans, animals, and plants, known as mycoses. These infections range from superficial, localized skin infections to systemic, life-threatening invasive diseases.

Examples of fungal infections include athlete's foot (tinea pedis), ringworm (dermatophytosis), candidiasis (yeast infection), histoplasmosis, coccidioidomycosis, and aspergillosis. Fungal infections can be challenging to treat due to the limited number of antifungal drugs available and the potential for drug resistance.

Cyclic peptides are a type of peptides in which the N-terminus and C-terminus of the peptide chain are linked to form a circular structure. This is in contrast to linear peptides, which have a straight peptide backbone with a free N-terminus and C-terminus. The cyclization of peptides can occur through various mechanisms, including the formation of an amide bond between the N-terminal amino group and the C-terminal carboxylic acid group (head-to-tail cyclization), or through the formation of a bond between side chain functional groups.

Cyclic peptides have unique structural and chemical properties that make them valuable in medical and therapeutic applications. For example, they are more resistant to degradation by enzymes compared to linear peptides, which can increase their stability and half-life in the body. Additionally, the cyclic structure allows for greater conformational rigidity, which can enhance their binding affinity and specificity to target molecules.

Cyclic peptides have been explored as potential therapeutics for a variety of diseases, including cancer, infectious diseases, and neurological disorders. They have also been used as tools in basic research to study protein-protein interactions and cell signaling pathways.

Lipopeptides are a type of molecule that consists of a lipid (fatty acid) tail attached to a small peptide (short chain of amino acids). They are produced naturally by various organisms, including bacteria, and play important roles in cell-to-cell communication, signaling, and as components of bacterial membranes. Some lipopeptides have also been found to have antimicrobial properties and are being studied for their potential use as therapeutic agents.

Aspergillosis is a medical condition that is caused by the infection of the Aspergillus fungi. This fungus is commonly found in decaying organic matter, such as leaf litter and compost piles, and can also be found in some indoor environments like air conditioning systems and old buildings with water damage.

There are several types of aspergillosis, including:

1. Allergic bronchopulmonary aspergillosis (ABPA): This type of aspergillosis occurs when a person's immune system overreacts to the Aspergillus fungi, causing inflammation in the airways and lungs. ABPA is often seen in people with asthma or cystic fibrosis.
2. Invasive aspergillosis: This is a serious and potentially life-threatening condition that occurs when the Aspergillus fungi invade the bloodstream and spread to other organs, such as the brain, heart, or kidneys. Invasive aspergillosis typically affects people with weakened immune systems, such as those undergoing chemotherapy or organ transplantation.
3. Aspergilloma: Also known as a "fungus ball," an aspergilloma is a growth of the Aspergillus fungi that forms in a preexisting lung cavity, such as one caused by previous lung disease or injury. While an aspergilloma itself is not typically harmful, it can cause symptoms like coughing up blood or chest pain if it grows too large or becomes infected.

Symptoms of aspergillosis can vary depending on the type and severity of the infection. Treatment may include antifungal medications, surgery to remove the fungal growth, or management of underlying conditions that increase the risk of infection.

'Aspergillus fumigatus' is a species of fungi that belongs to the genus Aspergillus. It is a ubiquitous mold that is commonly found in decaying organic matter, such as leaf litter, compost, and rotting vegetation. This fungus is also known to be present in indoor environments, including air conditioning systems, dust, and water-damaged buildings.

Aspergillus fumigatus is an opportunistic pathogen, which means that it can cause infections in people with weakened immune systems. It can lead to a range of conditions known as aspergillosis, including allergic reactions, lung infections, and invasive infections that can spread to other parts of the body.

The fungus produces small, airborne spores that can be inhaled into the lungs, where they can cause infection. In healthy individuals, the immune system is usually able to eliminate the spores before they can cause harm. However, in people with weakened immune systems, such as those undergoing chemotherapy or organ transplantation, or those with certain underlying medical conditions like asthma or cystic fibrosis, the fungus can establish an infection.

Infections caused by Aspergillus fumigatus can be difficult to treat, and treatment options may include antifungal medications, surgery, or a combination of both. Prompt diagnosis and treatment are essential for improving outcomes in people with aspergillosis.

Ergosterol is a steroid found in the cell membranes of fungi, which is similar to cholesterol in animals. It plays an important role in maintaining the fluidity and permeability of fungal cell membranes. Ergosterol is also the target of many antifungal medications, which work by disrupting the synthesis of ergosterol or binding to it, leading to increased permeability and eventual death of the fungal cells.

"Aspergillus" is a genus of filamentous fungi (molds) that are widely distributed in the environment. These molds are commonly found in decaying organic matter such as leaf litter, compost piles, and rotting vegetation. They can also be found in indoor environments like air conditioning systems, dust, and building materials.

The medical relevance of Aspergillus comes from the fact that some species can cause a range of diseases in humans, particularly in individuals with weakened immune systems or underlying lung conditions. The most common disease caused by Aspergillus is called aspergillosis, which can manifest as allergic reactions, lung infections (like pneumonia), and invasive infections that can spread to other parts of the body.

Aspergillus species produce small, airborne spores called conidia, which can be inhaled into the lungs and cause infection. The severity of aspergillosis depends on various factors, including the individual's immune status, the specific Aspergillus species involved, and the extent of fungal invasion in the body.

Common Aspergillus species that can cause human disease include A. fumigatus, A. flavus, A. niger, and A. terreus. Preventing exposure to Aspergillus spores and maintaining a healthy immune system are crucial steps in minimizing the risk of aspergillosis.

Nystatin is an antifungal medication used to treat various fungal infections such as candidiasis, which can affect the skin, mouth, throat, and vagina. It works by binding to ergosterol, a component of fungal cell membranes, creating pores that increase permeability and ultimately lead to fungal cell death.

The medical definition of Nystatin is:

A polyene antifungal agent derived from Streptomyces noursei, used primarily for topical treatment of mucocutaneous candidiasis. It has little systemic absorption and is therefore not useful for treating systemic fungal infections. Common side effects include local irritation and burning sensations at the application site.

Econazole is an antifungal medication used to treat various fungal infections of the skin, nails, and mucous membranes. It works by inhibiting the synthesis of ergosterol, a key component of fungal cell membranes, thereby weakening the cell membrane and increasing permeability, ultimately leading to fungal cell death.

Econazole is available in various formulations, including creams, lotions, powders, and tablets. It is commonly used to treat conditions such as athlete's foot, jock itch, ringworm, candidiasis (yeast infection), and other fungal skin infections.

It is important to follow the instructions of a healthcare provider when using econazole or any medication, and to report any side effects or concerns promptly.

Clotrimazole is an antifungal medication used to treat various fungal infections such as athlete's foot, jock itch, ringworm, candidiasis (yeast infection), and oral thrush. It works by inhibiting the growth of fungi that cause these infections. Clotrimazole is available in several forms, including creams, lotions, powders, tablets, and lozenges.

The medical definition of Clotrimazole is:

A synthetic antifungal agent belonging to the imidazole class, used topically to treat various fungal infections such as candidiasis, tinea pedis, tinea cruris, and tinea versicolor. It works by inhibiting the biosynthesis of ergosterol, a key component of fungal cell membranes, leading to increased permeability and death of fungal cells.

Multiple drug resistance in fungi refers to the ability of certain fungal strains or species to resist the effects of multiple antifungal agents. This occurs when these organisms develop mechanisms that prevent the drugs from interfering with their growth and survival. As a result, the drugs become less effective or even completely ineffective at treating fungal infections caused by these resistant strains or species.

Multiple drug resistance in fungi can arise due to various factors, including genetic mutations, overuse or misuse of antifungal agents, and the ability of fungi to exchange genetic material with other fungi. This makes treatment of fungal infections more challenging, as doctors may need to use higher doses of drugs or try alternative therapies that may have more side effects or be less effective.

Multiple drug resistance in fungi is a significant concern in healthcare settings, particularly for patients who are immunocompromised or have underlying medical conditions that make them more susceptible to fungal infections. It is essential to take measures to prevent the development and spread of multiple drug-resistant fungi, such as using antifungal agents appropriately, practicing good infection control practices, and conducting surveillance for resistant strains.

'Candida glabrata' is a species of yeast that is commonly found on the skin and mucous membranes of humans. It is a member of the genus Candida, which includes several species of fungi that can cause infections in humans. C. glabrata is one of the more common causes of candidiasis, or yeast infections, particularly in the mouth (oral thrush) and genital area. It can also cause invasive candidiasis, a serious systemic infection that can affect various organs and tissues in the body. C. glabrata is often resistant to some of the antifungal drugs commonly used to treat Candida infections, making it more difficult to treat.

'Cryptococcus neoformans' is a species of encapsulated, budding yeast that is an important cause of fungal infections in humans and animals. The capsule surrounding the cell wall is composed of polysaccharides and is a key virulence factor, allowing the organism to evade host immune responses. C. neoformans is found worldwide in soil, particularly in association with bird droppings, and can be inhaled, leading to pulmonary infection. In people with weakened immune systems, such as those with HIV/AIDS, hematological malignancies, or organ transplants, C. neoformans can disseminate from the lungs to other sites, most commonly the central nervous system (CNS), causing meningitis. The infection can also affect other organs, including the skin, bones, and eyes.

The diagnosis of cryptococcosis typically involves microscopic examination and culture of clinical specimens, such as sputum, blood, or cerebrospinal fluid (CSF), followed by biochemical and molecular identification of the organism. Treatment usually consists of a combination of antifungal medications, such as amphotericin B and fluconazole, along with management of any underlying immunodeficiency. The prognosis of cryptococcosis depends on various factors, including the patient's immune status, the extent and severity of infection, and the timeliness and adequacy of treatment.

Tolnaftate is an antifungal medication used to treat various fungal infections such as athlete's foot, jock itch, and ringworm. It works by preventing the growth of fungus. According to the medical definition, Tolnaftate is a synthetic thiocarbamate derivative with antifungal properties. It is available as a cream, powder, spray, or solution for topical application.

It's important to note that Tolnaftate should be used only on the skin and not on mucous membranes or inside the mouth or nose, unless directed by a healthcare professional. Additionally, it may take several days to weeks of using Tolnaftate before symptoms start to improve, and it is important to continue using the medication as directed even after symptoms have improved to ensure that the infection is fully treated.

Trichophyton is a genus of fungi that are primarily responsible for causing various superficial and cutaneous infections in humans and animals. These infections, known as dermatophytoses or ringworm, typically involve the skin, hair, and nails. Some common examples of diseases caused by Trichophyton species include athlete's foot (T. rubrum), jock itch (T. mentagrophytes), and scalp ringworm (T. tonsurans).

The fungi in the Trichophyton genus are called keratinophilic, meaning they have a preference for keratin, a protein found in high concentrations in skin, hair, and nails. This characteristic allows them to thrive in these environments and cause infection. The specific species of Trichophyton involved in an infection will determine the clinical presentation and severity of the disease.

In summary, Trichophyton is a medical term referring to a group of fungi that can cause various skin, hair, and nail infections in humans and animals.

Pyrimidines are heterocyclic aromatic organic compounds similar to benzene and pyridine, containing two nitrogen atoms at positions 1 and 3 of the six-member ring. They are one of the two types of nucleobases found in nucleic acids, the other being purines. The pyrimidine bases include cytosine (C) and thymine (T) in DNA, and uracil (U) in RNA, which pair with guanine (G) and adenine (A), respectively, through hydrogen bonding to form the double helix structure of nucleic acids. Pyrimidines are also found in many other biomolecules and have various roles in cellular metabolism and genetic regulation.

Candidemia is a medical condition defined as the presence of the fungus Candida in the bloodstream. It is a type of invasive candidiasis, which occurs when Candida invades normally sterile areas of the body such as the blood, heart, brain, eyes, or bones. Candidemia is usually acquired in healthcare settings and can cause serious illness, especially in people with weakened immune systems. Symptoms may include fever, chills, hypotension, and organ dysfunction. Treatment typically involves antifungal medications.

"Scedosporium" is a genus of filamentous fungi (molds) that can be found in various environments such as soil, water, and decaying organic matter. It includes several species, with Scedosporium apiospermum and Scedosporium boydii being the most common ones. These fungi can cause a range of infections in humans, ranging from superficial skin and nail infections to more serious invasive diseases affecting the lungs, brain, or other organs. Invasive scedosporiosis often occurs in immunocompromised individuals, such as those with HIV/AIDS, cancer, or organ transplant recipients. The infection can be difficult to treat due to its resistance to many antifungal agents.

Arthrodermataceae is a family of fungi that includes several medically important dermatophytes, which are fungi that can cause skin and nail infections known as tinea. Some notable genera within this family include:

1. Trichophyton: This genus contains several species that can cause various types of tinea infections, such as athlete's foot (tinea pedis), ringworm (tinea corporis), and jock itch (tinea cruris). Some species can also cause nail infections (tinea unguium or onychomycosis).
2. Microsporum: This genus includes some of the less common causes of tinea infections, such as tinea capitis (scalp ringworm) and tinea corporis.
3. Epidermophyton: This genus contains species that can cause tinea infections of the feet, hands, and nails.

These fungi primarily feed on keratin, a protein found in skin, hair, and nails, and typically invade dead or damaged tissue. Infections caused by Arthrodermataceae are usually treatable with antifungal medications, either topical or oral, depending on the severity and location of the infection.

Dermatomycoses are a group of fungal infections that affect the skin, hair, and nails. These infections are caused by various types of fungi, including dermatophytes, yeasts, and molds. Dermatophyte infections, also known as tinea, are the most common type of dermatomycoses and can affect different areas of the body, such as the scalp (tinea capitis), beard (tinea barbae), body (tinea corporis), feet (tinea pedis or athlete's foot), hands (tinea manuum), and nails (tinea unguium or onychomycosis). Yeast infections, such as those caused by Candida albicans, can lead to conditions like candidal intertrigo, vulvovaginitis, and balanitis. Mold infections are less common but can cause skin disorders like scalded skin syndrome and phaeohyphomycosis. Dermatomycoses are typically treated with topical or oral antifungal medications.

Natamycin is an antifungal medication used to treat and prevent fungal infections. It is a polyene macrolide antibiotic produced by the bacterium Streptomyces natalensis. In medical contexts, it is often used as a topical treatment for eye, skin, and mucous membrane infections caused by susceptible fungi. Natamycin works by binding to ergosterol, a component of fungal cell membranes, which disrupts the membrane's structure and function, ultimately leading to fungal cell death.

In addition to its medical uses, natamycin is also used as a food preservative to prevent mold growth in certain dairy products, such as cheese, and in some countries, it is approved for use in the production of certain types of sausages and fermented meat products.

Pseudallescheria is a medical term that refers to a fungal infection caused by the organism Pseudallescheria boydii (also known as Scedosporium apiospermum). This fungus is commonly found in soil and water, and can cause various types of infections in humans, ranging from superficial skin infections to serious invasive diseases affecting the lungs, brain, or other organs. The infection can be particularly difficult to treat due to its resistance to many antifungal agents.

The term "Pseudallescheria" is used less frequently than "Scedosporium," but it refers to the same organism and the same type of infection. In medical literature, you may also encounter the term "Pseudallescheriasis" to describe the disease caused by this fungus.

Fungemia is the presence of fungi (fungal organisms) in the blood. It's a type of bloodstream infection, which can be serious and life-threatening, particularly for people with weakened immune systems. The fungi that cause fungemia often enter the bloodstream through medical devices like catheters or from a fungal infection somewhere else in the body.

Fungemia is often associated with conditions like candidemia (caused by Candida species) and aspergillemia (caused by Aspergillus species). Symptoms can vary widely but often include fever, chills, and other signs of infection. It's important to diagnose and treat fungemia promptly to prevent serious complications like sepsis.

Oral candidiasis is a medical condition characterized by an infection of the oral mucous membranes caused by the Candida fungus species, most commonly Candida albicans. It is also known as thrush or oral thrush. The infection typically appears as white, creamy, or yellowish patches or plaques on the tongue, inner cheeks, roof of the mouth, gums, and sometimes on the tonsils or back of the throat. These lesions can be painful, causing soreness, burning sensations, and difficulty swallowing. Oral candidiasis can affect people of all ages; however, it is more commonly seen in infants, elderly individuals, and those with weakened immune systems due to illness or medication use. Various factors such as poor oral hygiene, dentures, smoking, dry mouth, and certain medical conditions like diabetes or HIV/AIDS can increase the risk of developing oral candidiasis. Treatment usually involves antifungal medications in the form of topical creams, lozenges, or oral solutions, depending on the severity and underlying cause of the infection.

Sterol 14-demethylase is an enzyme that plays a crucial role in the biosynthesis of sterols, particularly ergosterol in fungi and cholesterol in animals. This enzyme is classified as a cytochrome P450 (CYP) enzyme and is located in the endoplasmic reticulum.

The function of sterol 14-demethylase is to remove methyl groups from the sterol molecule at the 14th position, which is a necessary step in the biosynthesis of ergosterol or cholesterol. Inhibition of this enzyme can disrupt the normal functioning of cell membranes and lead to various physiological changes, including impaired growth and development.

Sterol 14-demethylase inhibitors (SDIs) are a class of antifungal drugs that target this enzyme and are used to treat fungal infections. Examples of SDIs include fluconazole, itraconazole, and ketoconazole. These drugs work by binding to the heme group of the enzyme and inhibiting its activity, leading to the accumulation of toxic sterol intermediates and disruption of fungal cell membranes.

Polyenes are a group of antibiotics that contain a long, unsaturated hydrocarbon chain with alternating double and single bonds. They are characterized by their ability to bind to ergosterol, a steroid found in fungal cell membranes, forming pores that increase the permeability of the membrane and lead to fungal cell death.

The most well-known polyene antibiotic is amphotericin B, which is used to treat serious systemic fungal infections such as candidiasis, aspergillosis, and cryptococcosis. Other polyenes include nystatin and natamycin, which are primarily used to treat topical fungal infections of the skin or mucous membranes.

While polyenes are effective antifungal agents, they can also cause significant side effects, particularly when used systemically. These may include kidney damage, infusion reactions, and electrolyte imbalances. Therefore, their use is typically reserved for severe fungal infections that are unresponsive to other treatments.

Cryptococcosis is a fungal infection caused by the yeast-like fungus Cryptococcus neoformans or Cryptococcus gattii. It can affect people with weakened immune systems, such as those with HIV/AIDS, cancer, organ transplants, or long-term steroid use. The infection typically starts in the lungs and can spread to other parts of the body, including the brain (meningitis), causing various symptoms like cough, fever, chest pain, headache, confusion, and vision problems. Treatment usually involves antifungal medications, and the prognosis depends on the patient's immune status and the severity of the infection.

Mitosporic fungi, also known as asexual fungi or anamorphic fungi, are a group of fungi that produce mitospores (also called conidia) during their asexual reproduction. Mitospores are produced from the tip of specialized hyphae called conidiophores and are used for dispersal and survival of the fungi in various environments. These fungi do not have a sexual reproductive stage or it has not been observed, making their taxonomic classification challenging. They are commonly found in soil, decaying organic matter, and water, and some of them can cause diseases in humans, animals, and plants. Examples of mitosporic fungi include Aspergillus, Penicillium, and Fusarium species.

Vulvovaginal candidiasis is a medical condition that refers to an infection in the vagina and vulva caused by Candida fungus, most commonly Candida albicans. This type of infection is also commonly known as a yeast infection. The symptoms of vulvovaginal candidiasis can include itching, redness, swelling, pain, and soreness in the affected area, as well as thick, white vaginal discharge that may resemble cottage cheese. In some cases, there may also be burning during urination or sexual intercourse. Vulvovaginal candidiasis is a common condition that affects many women at some point in their lives, and it can be treated with antifungal medications.

Yeasts are single-celled microorganisms that belong to the fungus kingdom. They are characterized by their ability to reproduce asexually through budding or fission, and they obtain nutrients by fermenting sugars and other organic compounds. Some species of yeast can cause infections in humans, known as candidiasis or "yeast infections." These infections can occur in various parts of the body, including the skin, mouth, genitals, and internal organs. Common symptoms of a yeast infection may include itching, redness, irritation, and discharge. Yeast infections are typically treated with antifungal medications.

Fungal lung diseases, also known as fungal pneumonia or mycoses, refer to a group of respiratory disorders caused by the infection of fungi in the lungs. These fungi are commonly found in the environment, such as soil, decaying organic matter, and contaminated materials. People can develop lung diseases from fungi after inhaling spores or particles that contain fungi.

There are several types of fungal lung diseases, including:

1. Aspergillosis: This is caused by the Aspergillus fungus and can affect people with weakened immune systems. It can cause allergic reactions, lung infections, or invasive aspergillosis, which can spread to other organs.
2. Cryptococcosis: This is caused by the Cryptococcus fungus and is usually found in soil contaminated with bird droppings. It can cause pneumonia, meningitis, or skin lesions.
3. Histoplasmosis: This is caused by the Histoplasma capsulatum fungus and is commonly found in the Ohio and Mississippi River valleys. It can cause flu-like symptoms, lung infections, or disseminated histoplasmosis, which can spread to other organs.
4. Blastomycosis: This is caused by the Blastomyces dermatitidis fungus and is commonly found in the southeastern and south-central United States. It can cause pneumonia, skin lesions, or disseminated blastomycosis, which can spread to other organs.
5. Coccidioidomycosis: This is caused by the Coccidioides immitis fungus and is commonly found in the southwestern United States. It can cause flu-like symptoms, lung infections, or disseminated coccidioidomycosis, which can spread to other organs.

Fungal lung diseases can range from mild to severe, depending on the type of fungus and the person's immune system. Treatment may include antifungal medications, surgery, or supportive care. Prevention measures include avoiding exposure to contaminated soil or dust, wearing protective masks in high-risk areas, and promptly seeking medical attention if symptoms develop.

An immunocompromised host refers to an individual who has a weakened or impaired immune system, making them more susceptible to infections and decreased ability to fight off pathogens. This condition can be congenital (present at birth) or acquired (developed during one's lifetime).

Acquired immunocompromised states may result from various factors such as medical treatments (e.g., chemotherapy, radiation therapy, immunosuppressive drugs), infections (e.g., HIV/AIDS), chronic diseases (e.g., diabetes, malnutrition, liver disease), or aging.

Immunocompromised hosts are at a higher risk for developing severe and life-threatening infections due to their reduced immune response. Therefore, they require special consideration when it comes to prevention, diagnosis, and treatment of infectious diseases.

'Aspergillus flavus' is a species of fungi that belongs to the genus Aspergillus. It is commonly found in soil, decaying vegetation, and other organic matter. This fungus is known for its ability to produce aflatoxins, which are highly toxic compounds that can contaminate food crops such as corn, peanuts, and cottonseed.

Aflatoxins produced by A. flavus are among the most potent carcinogens known to humans and can cause liver damage and cancer with prolonged exposure. The fungus can also cause invasive aspergillosis, a serious infection that primarily affects people with weakened immune systems, such as those undergoing chemotherapy or organ transplantation.

In addition to its medical importance, A. flavus is also used in biotechnology for the production of industrial enzymes and other products.

'Candida tropicalis' is a species of yeast that can be found normally in certain environments, including the human body (such as the skin, mouth, and digestive system). However, it can also cause infections in people with weakened immune systems or underlying medical conditions. These infections can occur in various parts of the body, including the bloodstream, urinary tract, and skin.

Like other Candida species, C. tropicalis is a type of fungus that reproduces by budding, forming oval-shaped cells. It is often resistant to certain antifungal medications, which can make infections more difficult to treat. Proper diagnosis and treatment, usually with antifungal drugs, are essential for managing C. tropicalis infections.

Onychomycosis is a medical term that refers to a fungal infection in the nails (both fingernails and toenails). This condition occurs when fungi, usually dermatophytes, invade the nail bed and cause damage to the nail plate. It can lead to symptoms such as discoloration, thickening, crumbling, and separation of the nail from the nail bed. Onychomycosis can be challenging to treat and may require long-term antifungal therapy, either topical or oral, or even removal of the infected nail in severe cases.

Mycetoma is a chronic granulomatous infection of the skin and subcutaneous tissues, often characterized by tumefaction, sinus formation, and grains. It's typically caused by certain species of fungi (eumycetoma) or bacteria (actinomycetoma). The infection usually enters the body through traumatic inoculation of the organism into the skin or underlying tissue, often in the foot or hand. The disease is most commonly found in tropical and subtropical regions, particularly in Africa, Latin America, and Asia.

'Cryptococcus' is a genus of encapsulated, budding yeast that are found in the environment, particularly in soil and bird droppings. The most common species that causes infection in humans is Cryptococcus neoformans, followed by Cryptococcus gattii.

Infection with Cryptococcus can occur when a person inhales the microscopic yeast cells, which can then lead to lung infections (pneumonia) or disseminated disease, particularly in people with weakened immune systems. The most common form of disseminated cryptococcal infection is meningitis, an inflammation of the membranes surrounding the brain and spinal cord.

Cryptococcal infections can be serious and even life-threatening, especially in individuals with HIV/AIDS or other conditions that weaken the immune system. Treatment typically involves antifungal medications, such as amphotericin B and fluconazole.

"Fusarium" is a genus of fungi that are widely distributed in the environment, particularly in soil, water, and on plants. They are known to cause a variety of diseases in animals, including humans, as well as in plants. In humans, Fusarium species can cause localized and systemic infections, particularly in immunocompromised individuals. These infections often manifest as keratitis (eye infection), onychomycosis (nail infection), and invasive fusariosis, which can affect various organs such as the lungs, brain, and bloodstream. Fusarium species produce a variety of toxins that can contaminate crops and pose a threat to food safety and human health.

Naphthalene is not typically referred to as a medical term, but it is a chemical compound with the formula C10H8. It is a white crystalline solid that is aromatic and volatile, and it is known for its distinctive mothball smell. In a medical context, naphthalene is primarily relevant as a potential toxin or irritant.

Naphthalene can be found in some chemical products, such as mothballs and toilet deodorant blocks. Exposure to high levels of naphthalene can cause symptoms such as nausea, vomiting, diarrhea, and headaches. Long-term exposure has been linked to anemia and damage to the liver and nervous system.

In addition, naphthalene is a known environmental pollutant that can be found in air, water, and soil. It is produced by the combustion of fossil fuels and is also released from some industrial processes. Naphthalene has been shown to have toxic effects on aquatic life and may pose a risk to human health if exposure levels are high enough.

Invasive candidiasis is a serious and potentially life-threatening fungal infection caused by the Candida species, most commonly Candida albicans. It occurs when the fungus invades normally sterile areas of the body, such as the bloodstream, heart, brain, or eyes. Invasive candidiasis can cause a variety of symptoms depending on the site of infection, and may include fever, chills, hypotension, sepsis, organ dysfunction, and skin lesions.

Risk factors for invasive candidiasis include prolonged use of broad-spectrum antibiotics, immunosuppression, indwelling catheters, recent surgery, critical illness, and underlying medical conditions such as diabetes or cancer. Diagnosis typically involves blood cultures and sometimes tissue biopsy, and treatment usually requires intravenous antifungal medications such as echinocandins, fluconazole, or amphotericin B. Prompt diagnosis and treatment are essential to prevent serious complications and improve outcomes.

Tinea is a common fungal infection of the skin, also known as ringworm. It's called ringworm because of its characteristic red, circular, and often scaly rash with raised edges that can resemble a worm's shape. However, it has nothing to do with any kind of actual worm.

The fungi responsible for tinea infections belong to the genus Trichophyton, Microsporum, or Epidermophyton. These fungi thrive in warm, damp environments and can be contracted from infected people, animals, or contaminated soil. Common types of tinea infections include athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm of the scalp (tinea capitis).

Treatment for tinea typically involves antifungal medications, either topical or oral, depending on the location and severity of the infection. Proper hygiene and avoiding sharing personal items can help prevent the spread of this contagious condition.

"Madurella" is not a medical term itself, but it is the name of a genus of fungi that can cause certain types of infections in humans. This genus is part of the family "Bipolarisaceae" and order "Chaetothyriales." The most common species that affects humans is "Madurella mycetomatis," which is known to cause a chronic subcutaneous infection called mycetoma. Mycetoma is a slowly progressive, granulomatous disease characterized by the formation of multiple sinuses and grains in the affected tissues. It primarily affects the feet but can also involve other parts of the body. The fungus enters the body through traumatic implantation, usually from contaminated soil or thorn pricks.

In summary, "Madurella" is a genus of fungi that includes species capable of causing mycetoma, a chronic subcutaneous infection in humans.

Fungal eye infections, also known as fungal keratitis or ocular fungal infections, are caused by the invasion of fungi into the eye. The most common types of fungi that cause these infections include Fusarium, Aspergillus, and Candida. These infections can affect any part of the eye, including the cornea, conjunctiva, sclera, and vitreous humor.

Fungal eye infections often present with symptoms such as redness, pain, sensitivity to light, tearing, blurred vision, and discharge. In severe cases, they can lead to corneal ulcers, perforation of the eye, and even blindness if left untreated. Risk factors for fungal eye infections include trauma to the eye, contact lens wear, immunosuppression, and pre-existing eye conditions such as dry eye or previous eye surgery.

Diagnosis of fungal eye infections typically involves a thorough eye examination, including visual acuity testing, slit lamp examination, and sometimes corneal scrapings for microbiological culture and sensitivity testing. Treatment usually involves topical antifungal medications, such as natamycin or amphotericin B, and in some cases may require oral or intravenous antifungal therapy. In severe cases, surgical intervention may be necessary to remove infected tissue or repair any damage caused by the infection.

Xylariales is an order of fungi in the class Sordariomycetes, which are primarily wood-inhabiting species. This group includes both saprobic and pathogenic fungi, with some members known to cause various plant diseases. The order contains several families, including Xylariaceae, Amphisphaeriaceae, and Graphostromataceae, among others. Many species in Xylariales produce dark-colored, melanized structures called pycnidia or stromata, which contain the reproductive structures of the fungi. Some members of this order also have potential industrial applications, such as the production of enzymes and bioactive compounds.

Biofilms are defined as complex communities of microorganisms, such as bacteria and fungi, that adhere to surfaces and are enclosed in a matrix made up of extracellular polymeric substances (EPS). The EPS matrix is composed of polysaccharides, proteins, DNA, and other molecules that provide structural support and protection to the microorganisms within.

Biofilms can form on both living and non-living surfaces, including medical devices, implants, and biological tissues. They are resistant to antibiotics, disinfectants, and host immune responses, making them difficult to eradicate and a significant cause of persistent infections. Biofilms have been implicated in a wide range of medical conditions, including chronic wounds, urinary tract infections, middle ear infections, and device-related infections.

The formation of biofilms typically involves several stages, including initial attachment, microcolony formation, maturation, and dispersion. Understanding the mechanisms underlying biofilm formation and development is crucial for developing effective strategies to prevent and treat biofilm-associated infections.

Fungal proteins are a type of protein that is specifically produced and present in fungi, which are a group of eukaryotic organisms that include microorganisms such as yeasts and molds. These proteins play various roles in the growth, development, and survival of fungi. They can be involved in the structure and function of fungal cells, metabolism, pathogenesis, and other cellular processes. Some fungal proteins can also have important implications for human health, both in terms of their potential use as therapeutic targets and as allergens or toxins that can cause disease.

Fungal proteins can be classified into different categories based on their functions, such as enzymes, structural proteins, signaling proteins, and toxins. Enzymes are proteins that catalyze chemical reactions in fungal cells, while structural proteins provide support and protection for the cell. Signaling proteins are involved in communication between cells and regulation of various cellular processes, and toxins are proteins that can cause harm to other organisms, including humans.

Understanding the structure and function of fungal proteins is important for developing new treatments for fungal infections, as well as for understanding the basic biology of fungi. Research on fungal proteins has led to the development of several antifungal drugs that target specific fungal enzymes or other proteins, providing effective treatment options for a range of fungal diseases. Additionally, further study of fungal proteins may reveal new targets for drug development and help improve our ability to diagnose and treat fungal infections.

Culture media is a substance that is used to support the growth of microorganisms or cells in an artificial environment, such as a petri dish or test tube. It typically contains nutrients and other factors that are necessary for the growth and survival of the organisms being cultured. There are many different types of culture media, each with its own specific formulation and intended use. Some common examples include blood agar, which is used to culture bacteria; Sabouraud dextrose agar, which is used to culture fungi; and Eagle's minimum essential medium, which is used to culture animal cells.

Griseofulvin is an antifungal medication used to treat various fungal infections, including those affecting the skin, hair, and nails. It works by inhibiting the growth of fungi, particularly dermatophytes, which cause these infections. Griseofulvin can be obtained through a prescription and is available in oral (by mouth) and topical (on the skin) forms.

The primary mechanism of action for griseofulvin involves binding to tubulin, a protein necessary for fungal cell division. This interaction disrupts the formation of microtubules, which are crucial for the fungal cell's structural integrity and growth. As a result, the fungi cannot grow and multiply, allowing the infected tissue to heal and the infection to resolve.

Common side effects associated with griseofulvin use include gastrointestinal symptoms (e.g., nausea, vomiting, diarrhea), headache, dizziness, and skin rashes. It is essential to follow the prescribing physician's instructions carefully when taking griseofulvin, as improper usage may lead to reduced effectiveness or increased risk of side effects.

It is important to note that griseofulvin has limited use in modern medicine due to the development of newer and more effective antifungal agents. However, it remains a valuable option for specific fungal infections, particularly those resistant to other treatments.

I must clarify that "lacquer" does not have a specific medical definition. The term "lacquer" is commonly used in dermatology to describe a type of scale found on the skin, but it is not a formal medical term with a widely accepted definition. It's essential to provide more context or specify the field when seeking definitions to ensure accurate and helpful information.

Microbial drug resistance is a significant medical issue that refers to the ability of microorganisms (such as bacteria, viruses, fungi, or parasites) to withstand or survive exposure to drugs or medications designed to kill them or limit their growth. This phenomenon has become a major global health concern, particularly in the context of bacterial infections, where it is also known as antibiotic resistance.

Drug resistance arises due to genetic changes in microorganisms that enable them to modify or bypass the effects of antimicrobial agents. These genetic alterations can be caused by mutations or the acquisition of resistance genes through horizontal gene transfer. The resistant microbes then replicate and multiply, forming populations that are increasingly difficult to eradicate with conventional treatments.

The consequences of drug-resistant infections include increased morbidity, mortality, healthcare costs, and the potential for widespread outbreaks. Factors contributing to the emergence and spread of microbial drug resistance include the overuse or misuse of antimicrobials, poor infection control practices, and inadequate surveillance systems.

To address this challenge, it is crucial to promote prudent antibiotic use, strengthen infection prevention and control measures, develop new antimicrobial agents, and invest in research to better understand the mechanisms underlying drug resistance.

Blastomycosis is a fungal infection caused by the inhalation of spores of the fungus Blastomyces dermatitidis. It primarily affects the lungs but can also spread to other parts of the body, such as the skin, bones, and central nervous system. The initial symptoms of blastomycosis may include cough, fever, chest pain, and difficulty breathing. If left untreated, the infection can become severe and potentially life-threatening. Treatment typically involves antifungal medications, such as itraconazole or amphotericin B.

Industrial fungicides are antimicrobial agents used to prevent, destroy, or inhibit the growth of fungi and their spores in industrial settings. These can include uses in manufacturing processes, packaging materials, textiles, paints, and other industrial products. They work by interfering with the cellular structure or metabolic processes of fungi, thereby preventing their growth or reproduction. Examples of industrial fungicides include:

* Sodium hypochlorite (bleach)
* Formaldehyde
* Glutaraldehyde
* Quaternary ammonium compounds
* Peracetic acid
* Chlorhexidine
* Iodophors

It's important to note that some of these fungicides can be harmful or toxic to humans and other organisms, so they must be used with caution and in accordance with safety guidelines.

Hyphae (singular: hypha) are the long, branching filamentous structures of fungi that make up the mycelium. They are composed of an inner layer of cell wall materials and an outer layer of proteinaceous fibrils. Hyphae can be divided into several types based on their structure and function, including septate (with cross-walls) and coenocytic (without cross-walls) hyphae, as well as vegetative and reproductive hyphae. The ability of fungi to grow as hyphal networks allows them to explore and exploit their environment for resources, making hyphae critical to the ecology and survival of these organisms.

"Paecilomyces" is a genus of filamentous fungi that belongs to the family Aspergillaceae. These fungi are widely distributed in the environment and can be found in various habitats such as soil, decaying vegetation, and insects. Some species of Paecilomyces are known to produce secondary metabolites with potential medicinal applications, while others have been identified as opportunistic pathogens that can cause invasive infections in immunocompromised individuals.

In medical contexts, "Paecilomyces" typically refers to the species P. lilacinus and P. variotii, which are the most commonly encountered human pathogens. These fungi can cause a range of infections, including mycetoma, endocarditis, pneumonia, and disseminated infections. The diagnosis of Paecilomyces infections typically involves microscopic examination of clinical specimens and culture-based methods, while treatment usually requires the use of antifungal agents such as amphotericin B or voriconazole.

It's worth noting that "Paecilomyces" is a complex genus with many species, some of which have been reclassified or renamed in recent years. Therefore, it's important to consult up-to-date taxonomic resources when working with this group of fungi.

Histatins are a group of histidine-rich proteins that are produced by the salivary glands in humans and other mammals. They have various functions, including antibacterial, antifungal, and wound healing properties. Histatins are composed of 21-24 amino acids and are named based on their molecular weight. The most well-studied histatins are Histatin 1, Histatin 3, and Histatin 5. They play a crucial role in maintaining oral health by helping to prevent dental caries and oral candidiasis.

Opportunistic infections (OIs) are infections that occur more frequently or are more severe in individuals with weakened immune systems, often due to a underlying condition such as HIV/AIDS, cancer, or organ transplantation. These infections are caused by microorganisms that do not normally cause disease in people with healthy immune function, but can take advantage of an opportunity to infect and cause damage when the body's defense mechanisms are compromised. Examples of opportunistic infections include Pneumocystis pneumonia, tuberculosis, candidiasis (thrush), and cytomegalovirus infection. Preventive measures, such as antimicrobial medications and vaccinations, play a crucial role in reducing the risk of opportunistic infections in individuals with weakened immune systems.

Mycology is the branch of biology that deals with the study of fungi, including their genetic and biochemical properties, their taxonomy and classification, their role in diseases and decomposition processes, and their potential uses in industry, agriculture, and medicine. It involves the examination and identification of various types of fungi, such as yeasts, molds, and mushrooms, and the investigation of their ecological relationships with other organisms and their environments. Mycologists may also study the medical and veterinary importance of fungi, including the diagnosis and treatment of fungal infections, as well as the development of antifungal drugs and vaccines.

Rhizopus is a genus of saprophytic fungi that belong to the family Mucoraceae. These fungi are commonly found in soil, decaying vegetation, and fruits. They are characterized by the presence of rhizoids, which are multicellular filaments that anchor the fungus to its substrate.

Rhizopus species are known to produce spores in large numbers, which can be dispersed through the air and cause infections in humans, particularly in individuals with weakened immune systems. One of the most common diseases caused by Rhizopus is mucormycosis, a serious and often life-threatening fungal infection that can affect various organs, including the sinuses, lungs, brain, and skin.

It's worth noting that while Rhizopus species are important pathogens in certain populations, they also have beneficial uses. For example, some species of Rhizopus are used in the production of tempeh, a traditional Indonesian food made from fermented soybeans.

Cholestadienols are a type of steroid alcohol that contain a double bond in the side chain. They are precursors to the synthesis of cholesterol, which is an essential component of cell membranes and a precursor to various hormones and vitamins. Cholestadienols can be found in some foods, such as fish liver oil, and are also produced endogenously in the body. They are not typically used in medical treatments, but understanding their role in cholesterol synthesis is important for developing therapies to treat conditions related to cholesterol metabolism, such as high cholesterol and certain inherited disorders of cholesterol biosynthesis.

Sporotrichosis is a fungal infection caused by the dimorphic fungus Sporothrix schenckii. It primarily affects the skin and subcutaneous tissues, although it can rarely disseminate to other organs in immunocompromised individuals. The infection often occurs after traumatic inoculation of the fungus through cuts or abrasions in the skin, particularly in people who work with plant materials like sphagnum moss, rose bushes, or hay.

The disease presents in three main clinical forms: cutaneous, lymphocutaneous, and disseminated. The cutaneous form involves a single ulcerating or verrucous lesion at the site of inoculation. The lymphocutaneous form is characterized by the spread of the infection along the lymphatic channels, resulting in a chain of nodular or ulcerative lesions. Disseminated sporotrichosis occurs when the infection spreads hematogenously to various organs, primarily affecting immunocompromised individuals and causing severe, life-threatening manifestations.

Diagnosis typically involves direct examination and culture of clinical specimens, as well as serological tests and molecular techniques like PCR. Treatment usually consists of systemic antifungal therapy with itraconazole or posaconazole, although amphotericin B may be required in severe cases or for disseminated infection.

Microsporum is a genus of fungi belonging to the family Arthrodermataceae. These fungi are known to cause various types of tinea (ringworm) infections in humans and animals. They are characterized by their ability to produce large, thick-walled macroconidia that are typically round to oval in shape.

The most common species of Microsporum that infect humans include M. canis, M. audouinii, and M. gypsum. These fungi are often found in soil and on the skin or fur of animals such as cats, dogs, and cattle. They can cause a variety of skin infections, including tinea capitis (scalp ringworm), tinea corporis (body ringworm), and tinea unguium (nail ringworm).

Microsporum infections are typically treated with topical or oral antifungal medications. Prevention measures include good personal hygiene, avoiding contact with infected animals, and prompt treatment of any fungal infections.

"Penicillium" is not a medical term per se, but it is a genus of mold that is widely used in the field of medicine, specifically in the production of antibiotics. Here's a scientific definition:

Penicillium is a genus of ascomycete fungi that are commonly found in the environment, particularly in soil, decaying vegetation, and food. Many species of Penicillium produce penicillin, a group of antibiotics with activity against gram-positive bacteria. The discovery and isolation of penicillin from Penicillium notatum by Alexander Fleming in 1928 revolutionized the field of medicine and led to the development of modern antibiotic therapy. Since then, various species of Penicillium have been used in the industrial production of penicillin and other antibiotics, as well as in the production of enzymes, organic acids, and other industrial products.

Trichosporon is a genus of fungi that are commonly found in the environment, particularly in soil, water, and air. They are also part of the normal flora of the human skin and mucous membranes. Some species of Trichosporon can cause various types of infections, mainly in people with weakened immune systems. These infections can range from superficial (e.g., skin and nail) to systemic and invasive, affecting internal organs. The most common Trichosporon-related infection is white piedra, a superficial mycosis that affects the hair shafts.

In a medical context, Trichosporon refers specifically to these fungi with potential pathogenic properties. It's essential to distinguish between the general term "trichosporon" (referring to the genus) and "Trichosporon" as a medically relevant entity causing infections.

Mycological typing techniques are methods used to identify and classify fungi at the species or strain level, based on their unique biological characteristics. These techniques are often used in clinical laboratories to help diagnose fungal infections and determine the most effective treatment approaches.

There are several different mycological typing techniques that may be used, depending on the specific type of fungus being identified and the resources available in the laboratory. Some common methods include:

1. Phenotypic methods: These methods involve observing and measuring the physical characteristics of fungi, such as their growth patterns, colonial morphology, and microscopic features. Examples include macroscopic and microscopic examination, as well as biochemical tests to identify specific metabolic properties.

2. Genotypic methods: These methods involve analyzing the DNA or RNA of fungi to identify unique genetic sequences that can be used to distinguish between different species or strains. Examples include PCR-based methods, such as restriction fragment length polymorphism (RFLP) analysis and amplified fragment length polymorphism (AFLP) analysis, as well as sequencing-based methods, such as internal transcribed spacer (ITS) sequencing and multilocus sequence typing (MLST).

3. Proteotypic methods: These methods involve analyzing the proteins expressed by fungi to identify unique protein profiles that can be used to distinguish between different species or strains. Examples include matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) and liquid chromatography-mass spectrometry (LC-MS).

Mycological typing techniques are important tools for understanding the epidemiology of fungal infections, tracking outbreaks, and developing effective treatment strategies. By accurately identifying the specific fungi causing an infection, healthcare providers can tailor their treatments to target the most vulnerable aspects of the pathogen, improving patient outcomes and reducing the risk of drug resistance.

Drug synergism is a pharmacological concept that refers to the interaction between two or more drugs, where the combined effect of the drugs is greater than the sum of their individual effects. This means that when these drugs are administered together, they produce an enhanced therapeutic response compared to when they are given separately.

Drug synergism can occur through various mechanisms, such as:

1. Pharmacodynamic synergism - When two or more drugs interact with the same target site in the body and enhance each other's effects.
2. Pharmacokinetic synergism - When one drug affects the metabolism, absorption, distribution, or excretion of another drug, leading to an increased concentration of the second drug in the body and enhanced therapeutic effect.
3. Physiochemical synergism - When two drugs interact physically, such as when one drug enhances the solubility or permeability of another drug, leading to improved absorption and bioavailability.

It is important to note that while drug synergism can result in enhanced therapeutic effects, it can also increase the risk of adverse reactions and toxicity. Therefore, healthcare providers must carefully consider the potential benefits and risks when prescribing combinations of drugs with known or potential synergistic effects.

Mucormycosis is a serious and often life-threatening invasive fungal infection caused by the Mucorales family of fungi. It primarily affects people with weakened immune systems, such as those with uncontrolled diabetes, cancer, organ transplant recipients, or those who have been treated with high doses of corticosteroids.

The infection typically begins in the respiratory tract after inhaling spores from the environment, but it can also occur through skin wounds or gastrointestinal exposure to the fungi. The infection can quickly spread to other parts of the body, including the sinuses, brain, and lungs, causing tissue damage and necrosis.

Symptoms of mucormycosis depend on the site of infection but may include fever, cough, shortness of breath, chest pain, headache, sinus congestion, facial swelling, and blackened areas of skin or tissue. Treatment typically involves a combination of antifungal medications, surgical debridement of infected tissue, and management of underlying medical conditions that increase the risk of infection.

Fermentation is a metabolic process in which an organism converts carbohydrates into alcohol or organic acids using enzymes. In the absence of oxygen, certain bacteria, yeasts, and fungi convert sugars into carbon dioxide, hydrogen, and various end products, such as alcohol, lactic acid, or acetic acid. This process is commonly used in food production, such as in making bread, wine, and beer, as well as in industrial applications for the production of biofuels and chemicals.

Fusariosis is a rare but serious invasive fungal infection caused by the Fusarium species, a type of filamentous fungi that are commonly found in the environment, particularly in soil and plants. The infection can affect various organs and tissues, including the lungs, sinuses, skin, nails, and internal organs such as the brain, heart, and kidneys.

Fusariosis is often difficult to diagnose due to its nonspecific symptoms and the challenges of detecting the fungus in clinical samples. The infection can occur in people with weakened immune systems, such as those undergoing chemotherapy, organ transplantation, or treatment with immunosuppressive drugs.

The severity of fusariosis varies depending on the site of infection and the patient's underlying health status. In some cases, it can cause severe illness and even death, especially in patients with prolonged neutropenia (low white blood cell count) or other serious medical conditions. Treatment typically involves antifungal medications, such as voriconazole or amphotericin B, and sometimes surgical debridement of infected tissues.

Anti-bacterial agents, also known as antibiotics, are a type of medication used to treat infections caused by bacteria. These agents work by either killing the bacteria or inhibiting their growth and reproduction. There are several different classes of anti-bacterial agents, including penicillins, cephalosporins, fluoroquinolones, macrolides, and tetracyclines, among others. Each class of antibiotic has a specific mechanism of action and is used to treat certain types of bacterial infections. It's important to note that anti-bacterial agents are not effective against viral infections, such as the common cold or flu. Misuse and overuse of antibiotics can lead to antibiotic resistance, which is a significant global health concern.

Ascomycota is a phylum in the kingdom Fungi, also known as sac fungi. This group includes both unicellular and multicellular organisms, such as yeasts, mold species, and morel mushrooms. Ascomycetes are characterized by their reproductive structures called ascus, which contain typically eight haploid spores produced sexually through a process called ascogony. Some members of this phylum have significant ecological and economic importance, as they can be decomposers, mutualistic symbionts, or plant pathogens causing various diseases. Examples include the baker's yeast Saccharomyces cerevisiae, ergot fungus Claviceps purpurea, and morel mushroom Morchella esculenta.

I'm sorry for any confusion, but "Indenes" is not a recognized medical term or concept in the field of medicine or healthcare. It may be that there is a spelling mistake or typo in your question. If you are referring to "Indenes" as a chemical compound, it is a polycyclic aromatic hydrocarbon (PAH) with the molecular formula C9H8. However, I would recommend consulting a chemistry or toxicology resource for information on its non-medical uses and properties.

Fungal DNA refers to the genetic material present in fungi, which are a group of eukaryotic organisms that include microorganisms such as yeasts and molds, as well as larger organisms like mushrooms. The DNA of fungi, like that of all living organisms, is made up of nucleotides that are arranged in a double helix structure.

Fungal DNA contains the genetic information necessary for the growth, development, and reproduction of fungi. This includes the instructions for making proteins, which are essential for the structure and function of cells, as well as other important molecules such as enzymes and nucleic acids.

Studying fungal DNA can provide valuable insights into the biology and evolution of fungi, as well as their potential uses in medicine, agriculture, and industry. For example, researchers have used genetic engineering techniques to modify the DNA of fungi to produce drugs, biofuels, and other useful products. Additionally, understanding the genetic makeup of pathogenic fungi can help scientists develop new strategies for preventing and treating fungal infections.

Malassezia is a genus of fungi (specifically, yeasts) that are commonly found on the skin surfaces of humans and other animals. They are part of the normal flora of the skin, but under certain conditions, they can cause various skin disorders such as dandruff, seborrheic dermatitis, pityriasis versicolor, and atopic dermatitis.

Malassezia species require lipids for growth, and they are able to break down the lipids present in human sebum into fatty acids, which can cause irritation and inflammation of the skin. Malassezia is also associated with fungal infections in people with weakened immune systems.

The genus Malassezia includes several species, such as M. furfur, M. globosa, M. restricta, M. sympodialis, and others. These species can be identified using various laboratory methods, including microscopy, culture, and molecular techniques.

Formazans are colored compounds produced during certain chemical reactions, such as the reduction of tetrazolium salts. These compounds have a characteristic deep red or purple color and are often used as an indicator of metabolic activity in biological systems, including cells and microorganisms. In medical research and diagnostics, formazans are sometimes used to measure cell viability, enzyme activity, and other physiological processes. However, it's important to note that 'formazans' is not a medical term per se, but rather a chemical term with applications in the medical field.

Molecular structure, in the context of biochemistry and molecular biology, refers to the arrangement and organization of atoms and chemical bonds within a molecule. It describes the three-dimensional layout of the constituent elements, including their spatial relationships, bond lengths, and angles. Understanding molecular structure is crucial for elucidating the functions and reactivities of biological macromolecules such as proteins, nucleic acids, lipids, and carbohydrates. Various experimental techniques, like X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy, and cryo-electron microscopy (cryo-EM), are employed to determine molecular structures at atomic resolution, providing valuable insights into their biological roles and potential therapeutic targets.

Trichosporonosis is a fungal infection caused by the organism Trichosporon spp., which are commonly found in the environment, particularly in soil and water. This infection primarily affects the skin and nails but can also cause invasive systemic disease, especially in immunocompromised individuals. The symptoms of trichosporonosis vary depending on the location and severity of the infection. Superficial infections may present as white plaques or pustules on the mucous membranes, while invasive infections can cause fever, chills, and organ dysfunction. Treatment typically involves antifungal medications, with the choice of drug depending on the severity and location of the infection.

Colorimetry is the scientific measurement and quantification of color, typically using a colorimeter or spectrophotometer. In the medical field, colorimetry may be used in various applications such as:

1. Diagnosis and monitoring of skin conditions: Colorimeters can measure changes in skin color to help diagnose or monitor conditions like jaundice, cyanosis, or vitiligo. They can also assess the effectiveness of treatments for these conditions.
2. Vision assessment: Colorimetry is used in vision testing to determine the presence and severity of visual impairments such as color blindness or deficiencies. Special tests called anomaloscopes or color vision charts are used to measure an individual's ability to distinguish between different colors.
3. Environmental monitoring: In healthcare settings, colorimetry can be employed to monitor the cleanliness and sterility of surfaces or equipment by measuring the amount of contamination present. This is often done using ATP (adenosine triphosphate) bioluminescence assays, which emit light when they come into contact with microorganisms.
4. Medical research: Colorimetry has applications in medical research, such as studying the optical properties of tissues or developing new diagnostic tools and techniques based on color measurements.

In summary, colorimetry is a valuable tool in various medical fields for diagnosis, monitoring, and research purposes. It allows healthcare professionals to make more informed decisions about patient care and treatment plans.

"Sporothrix" is a genus of fungi that includes several species, the most well-known of which is "Sporothrix schenckii." This particular species is an environmental saprophyte, commonly found in soil, plant matter, and decaying organic material. It can cause a disease in humans and animals known as sporotrichosis, which is a subcutaneous infection that typically affects the skin and underlying tissue. The infection usually occurs after traumatic inoculation of the fungus through the skin, often from activities such as gardening or handling contaminated plant material.

The infection initially presents as a painless, nodular lesion at the site of inoculation, which can later ulcerate and spread to other parts of the body through lymphatic channels. Disseminated sporotrichosis is rare but can occur in immunocompromised individuals, affecting various organs such as the lungs, bones, and central nervous system.

Proper diagnosis of sporotrichosis involves direct examination and culture of clinical specimens, as well as serological tests and molecular techniques. Treatment typically includes oral antifungal medications such as itraconazole or posaconazole, although amphotericin B may be required in severe cases or in patients with compromised immune systems.

Preclinical drug evaluation refers to a series of laboratory tests and studies conducted to determine the safety and effectiveness of a new drug before it is tested in humans. These studies typically involve experiments on cells and animals to evaluate the pharmacological properties, toxicity, and potential interactions with other substances. The goal of preclinical evaluation is to establish a reasonable level of safety and understanding of how the drug works, which helps inform the design and conduct of subsequent clinical trials in humans. It's important to note that while preclinical studies provide valuable information, they may not always predict how a drug will behave in human subjects.

Tinea Pedis, also known as athlete's foot, is a fungal infection that affects the skin on the feet, particularly between the toes. The causative agents are dermatophytes, which thrive in warm and damp environments. Common symptoms include itching, burning, cracked, blistered, or scaly skin, and sometimes painful peeling or cracking of the skin. It is contagious and can spread to other parts of the body or to other people through direct contact or via contaminated surfaces. Proper hygiene, keeping the feet dry, and using antifungal medications are common methods of preventing and treating this condition.

Sterols are a type of organic compound that is derived from steroids and found in the cell membranes of organisms. In animals, including humans, cholesterol is the most well-known sterol. Sterols help to maintain the structural integrity and fluidity of cell membranes, and they also play important roles as precursors for the synthesis of various hormones and other signaling molecules. Phytosterols are plant sterols that have been shown to have cholesterol-lowering effects in humans when consumed in sufficient amounts.

A "colony count" is a method used to estimate the number of viable microorganisms, such as bacteria or fungi, in a sample. In this technique, a known volume of the sample is spread onto the surface of a solid nutrient medium in a petri dish and then incubated under conditions that allow the microorganisms to grow and form visible colonies. Each colony that grows on the plate represents an individual cell (or small cluster of cells) from the original sample that was able to divide and grow under the given conditions. By counting the number of colonies that form, researchers can make a rough estimate of the concentration of microorganisms in the original sample.

The term "microbial" simply refers to microscopic organisms, such as bacteria, fungi, or viruses. Therefore, a "colony count, microbial" is a general term that encompasses the use of colony counting techniques to estimate the number of any type of microorganism in a sample.

Colony counts are used in various fields, including medical research, food safety testing, and environmental monitoring, to assess the levels of contamination or the effectiveness of disinfection procedures. However, it is important to note that colony counts may not always provide an accurate measure of the total number of microorganisms present in a sample, as some cells may be injured or unable to grow under the conditions used for counting. Additionally, some microorganisms may form clusters or chains that can appear as single colonies, leading to an overestimation of the true cell count.

"Pyrans" is not a term commonly used in medical definitions. It is a chemical term that refers to a class of heterocyclic compounds containing a six-membered ring with one oxygen atom and five carbon atoms. The name "pyran" comes from the fact that it contains a pyroline unit (two double-bonded carbons) and a ketone group (a carbon double-bonded to an oxygen).

While pyrans are not directly related to medical definitions, some of their derivatives have been studied for potential medicinal applications. For example, certain pyran derivatives have shown anti-inflammatory, antiviral, and anticancer activities in laboratory experiments. However, more research is needed before these compounds can be considered as potential therapeutic agents.

Allylamine is an organic compound with the formula CH2=CH-CH2-NH2. It is a colorless liquid that is soluble in water and polar organic solvents. Allylamine is used as a building block in the synthesis of various chemical compounds, including pharmaceuticals, agrochemicals, and polymers.

In the medical field, allylamine derivatives are used as antifungal agents. These drugs work by inhibiting the enzyme squalene epoxidase, which is necessary for the synthesis of ergosterol, a key component of fungal cell membranes. By blocking the production of ergosterol, allylamine derivatives disrupt the integrity of fungal cell membranes and prevent the growth of fungi. Examples of allylamine antifungal drugs include terbinafine and naftifine.

Volatile oils, also known as essential oils, are a type of organic compound that are naturally produced in plants. They are called "volatile" because they evaporate quickly at room temperature due to their high vapor pressure. These oils are composed of complex mixtures of various compounds, including terpenes, terpenoids, aldehydes, ketones, esters, and alcohols. They are responsible for the characteristic aroma and flavor of many plants and are often used in perfumes, flavors, and aromatherapy. In a medical context, volatile oils may have therapeutic properties and be used in certain medications or treatments, but it's important to note that they can also cause adverse reactions if not used properly.

Chitin synthase is an enzyme that is responsible for the biosynthesis of chitin, which is a long-chain polymer of N-acetylglucosamine. Chitin is a structural component in the exoskeletons of arthropods, such as insects and crustaceans, as well as in the cell walls of fungi.

Chitin synthase catalyzes the transfer of N-acetylglucosamine from UDP-N-acetylglucosamine to a growing chitin chain. There are several different isoforms of chitin synthase, which are classified based on their sequence similarity and biochemical properties. These isoforms play distinct roles in the biosynthesis of chitin in different organisms.

Inhibitors of chitin synthase have been developed as potential therapeutic agents for the control of insect pests and fungal pathogens.

Microbiological techniques refer to the various methods and procedures used in the laboratory for the cultivation, identification, and analysis of microorganisms such as bacteria, fungi, viruses, and parasites. These techniques are essential in fields like medical microbiology, food microbiology, environmental microbiology, and industrial microbiology.

Some common microbiological techniques include:

1. Microbial culturing: This involves growing microorganisms on nutrient-rich media in Petri dishes or test tubes to allow them to multiply. Different types of media are used to culture different types of microorganisms.
2. Staining and microscopy: Various staining techniques, such as Gram stain, acid-fast stain, and methylene blue stain, are used to visualize and identify microorganisms under a microscope.
3. Biochemical testing: These tests involve the use of specific biochemical reactions to identify microorganisms based on their metabolic characteristics. Examples include the catalase test, oxidase test, and sugar fermentation tests.
4. Molecular techniques: These methods are used to identify microorganisms based on their genetic material. Examples include polymerase chain reaction (PCR), DNA sequencing, and gene probes.
5. Serological testing: This involves the use of antibodies or antigens to detect the presence of specific microorganisms in a sample. Examples include enzyme-linked immunosorbent assay (ELISA) and Western blotting.
6. Immunofluorescence: This technique uses fluorescent dyes to label antibodies or antigens, allowing for the visualization of microorganisms under a fluorescence microscope.
7. Electron microscopy: This method uses high-powered electron beams to produce detailed images of microorganisms, allowing for the identification and analysis of their structures.

These techniques are critical in diagnosing infectious diseases, monitoring food safety, assessing environmental quality, and developing new drugs and vaccines.

Keratitis is a medical condition that refers to inflammation of the cornea, which is the clear, dome-shaped surface at the front of the eye. The cornea plays an essential role in focusing vision, and any damage or infection can cause significant visual impairment. Keratitis can result from various causes, including bacterial, viral, fungal, or parasitic infections, as well as trauma, allergies, or underlying medical conditions such as dry eye syndrome. Symptoms of keratitis may include redness, pain, tearing, sensitivity to light, blurred vision, and a feeling of something foreign in the eye. Treatment for keratitis depends on the underlying cause but typically includes antibiotics, antivirals, or anti-fungal medications, as well as measures to alleviate symptoms and promote healing.

Fungal meningitis is a form of meningitis, which is an inflammation of the membranes (meninges) surrounding the brain and spinal cord. It is specifically caused by the invasion of the meninges by fungi. The most common causative agents are Cryptococcus neoformans and Histoplasma capsulatum.

Fungal meningitis typically occurs in individuals with weakened immune systems, such as those with HIV/AIDS, cancer, or organ transplant recipients. It begins gradually, often with symptoms including headache, fever, stiff neck, and sensitivity to light. Other possible symptoms can include confusion, nausea, vomiting, and altered mental status.

Diagnosis of fungal meningitis typically involves a combination of clinical examination, imaging studies (such as CT or MRI scans), and laboratory tests (such as cerebrospinal fluid analysis). Treatment usually requires long-term antifungal therapy, often administered intravenously in a hospital setting. The prognosis for fungal meningitis depends on several factors, including the underlying immune status of the patient, the specific causative agent, and the timeliness and adequacy of treatment.

Neutropenia is a condition characterized by an abnormally low concentration (less than 1500 cells/mm3) of neutrophils, a type of white blood cell that plays a crucial role in fighting off bacterial and fungal infections. Neutrophils are essential components of the innate immune system, and their main function is to engulf and destroy microorganisms that can cause harm to the body.

Neutropenia can be classified as mild, moderate, or severe based on the severity of the neutrophil count reduction:

* Mild neutropenia: Neutrophil count between 1000-1500 cells/mm3
* Moderate neutropenia: Neutrophil count between 500-1000 cells/mm3
* Severe neutropenia: Neutrophil count below 500 cells/mm3

Severe neutropenia significantly increases the risk of developing infections, as the body's ability to fight off microorganisms is severely compromised. Common causes of neutropenia include viral infections, certain medications (such as chemotherapy or antibiotics), autoimmune disorders, and congenital conditions affecting bone marrow function. Treatment for neutropenia typically involves addressing the underlying cause, administering granulocyte-colony stimulating factors to boost neutrophil production, and providing appropriate antimicrobial therapy to prevent or treat infections.

'Aspergillus niger' is a species of fungi that belongs to the genus Aspergillus. It is a ubiquitous microorganism that can be found in various environments, including soil, decaying vegetation, and indoor air. 'Aspergillus niger' is a black-colored mold that produces spores that are easily dispersed in the air.

This fungus is well known for its ability to produce a variety of enzymes and metabolites, some of which have industrial applications. For example, it is used in the production of citric acid, which is widely used as a food additive and preservative.

However, 'Aspergillus niger' can also cause health problems in humans, particularly in individuals with weakened immune systems or underlying lung conditions. It can cause allergic reactions, respiratory symptoms, and invasive aspergillosis, a serious infection that can spread to other organs in the body.

In addition, 'Aspergillus niger' can produce mycotoxins, which are toxic compounds that can contaminate food and feed and cause various health effects in humans and animals. Therefore, it is important to prevent the growth and proliferation of this fungus in indoor environments and food production facilities.

Fungal spores are defined as the reproductive units of fungi that are produced by specialized structures called hyphae. These spores are typically single-celled and can exist in various shapes such as round, oval, or ellipsoidal. They are highly resistant to extreme environmental conditions like heat, cold, and dryness, which allows them to survive for long periods until they find a suitable environment to germinate and grow into a new fungal organism. Fungal spores can be found in the air, water, soil, and on various surfaces, making them easily dispersible and capable of causing infections in humans, animals, and plants.

Eugenol is defined in medical terms as a phenolic compound that is the main active component of oil of cloves, which is derived from the clove tree (Syzygium aromaticum). It has been used in dentistry for its analgesic and antibacterial properties. In addition, eugenol is used in perfumes, flavorings, and as a local antiseptic and anesthetic in medical applications. It's also used in some mouthwashes and toothpastes. However, it can cause allergic reactions in some people, so its use should be monitored carefully.

Allergic bronchopulmonary aspergillosis (ABPA) is a medical condition characterized by an hypersensitivity reaction to the fungus Aspergillus species, most commonly A. fumigatus. It primarily affects the airways and lung tissue. The immune system overreacts to the presence of the fungus, leading to inflammation and damage in the lungs.

The main symptoms of ABPA include wheezing, coughing, production of thick mucus, shortness of breath, and chest tightness. These symptoms are similar to those seen in asthma and other respiratory conditions. Some people with ABPA may also experience fever, weight loss, and fatigue.

Diagnosis of ABPA typically involves a combination of clinical evaluation, imaging studies (such as chest X-rays or CT scans), and laboratory tests (such as blood tests or sputum cultures) to detect the presence of Aspergillus species and elevated levels of certain antibodies.

Treatment for ABPA usually involves a combination of corticosteroids to reduce inflammation and antifungal medications to eradicate the Aspergillus infection. In some cases, immunomodulatory therapies may also be used to help regulate the immune system's response to the fungus.

It is important to note that ABPA can lead to serious complications if left untreated, including bronchiectasis (permanent enlargement of the airways), pulmonary fibrosis (scarring of the lung tissue), and respiratory failure. Therefore, prompt diagnosis and treatment are essential for managing this condition.

Pulmonary aspergillosis is a respiratory infection caused by the fungus Aspergillus. It mainly affects the lungs, but it can also spread to other parts of the body. There are several forms of pulmonary aspergillosis, including:

1. Allergic bronchopulmonary aspergillosis (ABPA): This form occurs in people with asthma or cystic fibrosis. The immune system overreacts to the presence of Aspergillus, causing inflammation and damage to the airways.
2. Aspergilloma: Also known as a fungus ball, this is a growth of Aspergillus that develops in a preexisting lung cavity, usually caused by old tuberculosis or scarring from previous lung infections.
3. Invasive pulmonary aspergillosis (IPA): This is the most severe form and occurs when the fungus invades the lung tissue, blood vessels, and other organs. It primarily affects people with weakened immune systems due to conditions like cancer, HIV/AIDS, organ transplants, or long-term use of corticosteroids.

Symptoms of pulmonary aspergillosis can vary depending on the form and severity of the infection. They may include cough, chest pain, shortness of breath, fever, fatigue, weight loss, and bloody sputum. Diagnosis typically involves imaging tests like chest X-rays or CT scans, along with laboratory tests to detect Aspergillus antigens or DNA in blood or respiratory samples. Treatment options include antifungal medications, surgery to remove fungal growths, and management of underlying conditions that weaken the immune system.

Microbial viability is the ability of a microorganism to grow, reproduce and maintain its essential life functions. It can be determined through various methods such as cell growth in culture media, staining techniques that detect metabolic activity, or direct observation of active movement. In contrast, non-viable microorganisms are those that have been killed or inactivated and cannot replicate or cause further harm. The measurement of microbial viability is important in various fields such as medicine, food safety, water quality, and environmental monitoring to assess the effectiveness of disinfection and sterilization procedures, and to determine the presence and concentration of harmful bacteria in different environments.

"Saccharomyces cerevisiae" is not typically considered a medical term, but it is a scientific name used in the field of microbiology. It refers to a species of yeast that is commonly used in various industrial processes, such as baking and brewing. It's also widely used in scientific research due to its genetic tractability and eukaryotic cellular organization.

However, it does have some relevance to medical fields like medicine and nutrition. For example, certain strains of S. cerevisiae are used as probiotics, which can provide health benefits when consumed. They may help support gut health, enhance the immune system, and even assist in the digestion of certain nutrients.

In summary, "Saccharomyces cerevisiae" is a species of yeast with various industrial and potential medical applications.

Beta-glucans are a type of complex carbohydrate known as polysaccharides, which are found in the cell walls of certain cereals, bacteria, and fungi, including baker's yeast, mushrooms, and algae. They consist of long chains of glucose molecules linked together by beta-glycosidic bonds.

Beta-glucans have been studied for their potential health benefits, such as boosting the immune system, reducing cholesterol levels, and improving gut health. They are believed to work by interacting with immune cells, such as macrophages and neutrophils, and enhancing their ability to recognize and destroy foreign invaders like bacteria, viruses, and tumor cells.

Beta-glucans are available in supplement form and are also found in various functional foods and beverages, such as baked goods, cereals, and sports drinks. However, it is important to note that the effectiveness of beta-glucans for these health benefits may vary depending on the source, dose, and individual's health status. Therefore, it is recommended to consult with a healthcare professional before taking any dietary supplements or making significant changes to your diet.

Peptides are short chains of amino acid residues linked by covalent bonds, known as peptide bonds. They are formed when two or more amino acids are joined together through a condensation reaction, which results in the elimination of a water molecule and the formation of an amide bond between the carboxyl group of one amino acid and the amino group of another.

Peptides can vary in length from two to about fifty amino acids, and they are often classified based on their size. For example, dipeptides contain two amino acids, tripeptides contain three, and so on. Oligopeptides typically contain up to ten amino acids, while polypeptides can contain dozens or even hundreds of amino acids.

Peptides play many important roles in the body, including serving as hormones, neurotransmitters, enzymes, and antibiotics. They are also used in medical research and therapeutic applications, such as drug delivery and tissue engineering.

Otitis externa, also known as swimmer's ear, is a medical condition characterized by inflammation or infection of the external auditory canal (the outermost part of the ear canal leading to the eardrum). It often occurs when water stays in the ear after swimming, creating a moist environment that promotes bacterial growth.

The symptoms of otitis externa may include:
- Redness and swelling of the ear canal
- Pain or discomfort in the ear, especially when moving the jaw or chewing
- Itching in the ear
- Discharge from the ear (pus or clear fluid)
- Hearing loss or difficulty hearing

Otitis externa is typically treated with antibiotic eardrops and sometimes oral antibiotics. Keeping the ear dry during treatment is important to prevent further irritation and promote healing. In severe cases, a healthcare provider may need to clean the ear canal before administering medication.

Zygomycosis is a rare, but serious fungal infection caused by filamentous fungi of the class Zygomycetes. These fungi are commonly found in the environment, particularly in soil and decaying organic matter. The infection primarily affects individuals with weakened immune systems, such as those with uncontrolled diabetes, HIV/AIDS, or those receiving immunosuppressive therapy.

Zygomycosis can manifest in various forms depending on the site of infection. The two main types are rhinocerebral zygomycosis (affecting the sinuses and brain) and pulmonary zygomycosis (affecting the lungs). Other forms include cutaneous (skin), gastrointestinal, and disseminated zygomycosis. Symptoms can range from mild to severe and may include fever, cough, shortness of breath, sinus pain or congestion, skin lesions, and neurological symptoms like headache, altered mental status, or vision changes.

Early diagnosis and prompt treatment with antifungal medications and surgical debridement are crucial for managing zygomycosis. The prognosis depends on the patient's underlying health condition and the extent of infection at the time of diagnosis.

Fungal polysaccharides refer to complex carbohydrates that are produced and found in fungi, including yeasts, molds, and mushrooms. These polysaccharides are made up of long chains of sugar molecules that are linked together by glycosidic bonds.

Fungal polysaccharides have various structures and functions depending on the specific fungal species they come from. Some fungal polysaccharides, such as beta-glucans, have been shown to have immunomodulatory effects and are used in some medical treatments. Beta-glucans, for example, can stimulate the immune system's response to infections and cancer.

Other fungal polysaccharides, such as chitin, are structural components of fungal cell walls. Chitin is a polysaccharide made up of N-acetylglucosamine units and is also found in the exoskeletons of insects and crustaceans.

Fungal polysaccharides have been studied for their potential therapeutic uses, including as antimicrobial, antitumor, and immunomodulatory agents. However, more research is needed to fully understand their mechanisms of action and potential benefits and risks.

A drug interaction is the effect of combining two or more drugs, or a drug and another substance (such as food or alcohol), which can alter the effectiveness or side effects of one or both of the substances. These interactions can be categorized as follows:

1. Pharmacodynamic interactions: These occur when two or more drugs act on the same target organ or receptor, leading to an additive, synergistic, or antagonistic effect. For example, taking a sedative and an antihistamine together can result in increased drowsiness due to their combined depressant effects on the central nervous system.
2. Pharmacokinetic interactions: These occur when one drug affects the absorption, distribution, metabolism, or excretion of another drug. For example, taking certain antibiotics with grapefruit juice can increase the concentration of the antibiotic in the bloodstream, leading to potential toxicity.
3. Food-drug interactions: Some drugs may interact with specific foods, affecting their absorption, metabolism, or excretion. An example is the interaction between warfarin (a blood thinner) and green leafy vegetables, which can increase the risk of bleeding due to enhanced vitamin K absorption from the vegetables.
4. Drug-herb interactions: Some herbal supplements may interact with medications, leading to altered drug levels or increased side effects. For instance, St. John's Wort can decrease the effectiveness of certain antidepressants and oral contraceptives by inducing their metabolism.
5. Drug-alcohol interactions: Alcohol can interact with various medications, causing additive sedative effects, impaired judgment, or increased risk of liver damage. For example, combining alcohol with benzodiazepines or opioids can lead to dangerous levels of sedation and respiratory depression.

It is essential for healthcare providers and patients to be aware of potential drug interactions to minimize adverse effects and optimize treatment outcomes.

"Exophiala" is a genus of fungi that belongs to the family Herpotrichiellaceae. These fungi are also known as black yeasts because they can form pigmented, thick-walled cells that resemble yeast. They are widely distributed in the environment and have been found in various habitats such as soil, water, and air. Some species of Exophiala are known to cause human diseases, particularly in individuals with weakened immune systems. These infections can affect various organs, including the skin, lungs, and brain. It is important to note that while some species of Exophiala can be pathogenic, many others are not harmful to humans.

Thiazoles are organic compounds that contain a heterocyclic ring consisting of a nitrogen atom and a sulfur atom, along with two carbon atoms and two hydrogen atoms. They have the chemical formula C3H4NS. Thiazoles are present in various natural and synthetic substances, including some vitamins, drugs, and dyes. In the context of medicine, thiazole derivatives have been developed as pharmaceuticals for their diverse biological activities, such as anti-inflammatory, antifungal, antibacterial, and antihypertensive properties. Some well-known examples include thiazide diuretics (e.g., hydrochlorothiazide) used to treat high blood pressure and edema, and the antidiabetic drug pioglitazone.

AIDS-related opportunistic infections (AROIs) are infections that occur more frequently or are more severe in people with weakened immune systems, such as those with advanced HIV infection or AIDS. These infections take advantage of a weakened immune system and can affect various organs and systems in the body.

Common examples of AROIs include:

1. Pneumocystis pneumonia (PCP), caused by the fungus Pneumocystis jirovecii
2. Mycobacterium avium complex (MAC) infection, caused by a type of bacteria called mycobacteria
3. Candidiasis, a fungal infection that can affect various parts of the body, including the mouth, esophagus, and genitals
4. Toxoplasmosis, caused by the parasite Toxoplasma gondii
5. Cryptococcosis, a fungal infection that affects the lungs and central nervous system
6. Cytomegalovirus (CMV) infection, caused by a type of herpes virus
7. Tuberculosis (TB), caused by the bacterium Mycobacterium tuberculosis
8. Cryptosporidiosis, a parasitic infection that affects the intestines
9. Progressive multifocal leukoencephalopathy (PML), a viral infection that affects the brain

Preventing and treating AROIs is an important part of managing HIV/AIDS, as they can cause significant illness and even death in people with weakened immune systems. Antiretroviral therapy (ART) is used to treat HIV infection and prevent the progression of HIV to AIDS, which can help reduce the risk of opportunistic infections. In addition, medications to prevent specific opportunistic infections may be prescribed for people with advanced HIV or AIDS.

Mucorales is a order of fungi that includes several genera of mold-like fungi, such as Mucor, Rhizopus, and Absidia. These fungi are commonly found in soil, decaying vegetation, and animal manure. Some species can cause mucormycosis, a serious and often life-threatening invasive fungal infection that primarily affects people with weakened immune systems, such as those with uncontrolled diabetes, cancer, or organ transplants. The infection typically begins in the respiratory tract, but it can spread to other parts of the body, including the sinuses, brain, and lungs. Mucormycosis is difficult to diagnose and treat, and it has a high mortality rate.

Tetrazolium salts are a group of compounds that are commonly used as indicators of cell viability and metabolic activity. These salts are reduced by the action of dehydrogenase enzymes in living cells, resulting in the formation of formazan dyes, which are colored and can be measured spectrophotometrically.

The most commonly used tetrazolium salt is 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), which is reduced to a purple formazan product by mitochondrial dehydrogenases in viable cells. Other tetrazolium salts include 2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT), which is reduced to a water-soluble formazan product, and 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS), which is reduced to a water-soluble formazan product by NAD(P)H-dependent dehydrogenases.

Tetrazolium salts are widely used in cell culture studies, toxicity testing, and drug development to assess cell viability, proliferation, and cytotoxicity. However, it is important to note that tetrazolium salt reduction can also occur in some non-viable cells or under certain experimental conditions, which may lead to false positive results. Therefore, these assays should be used with caution and validated for specific applications.

Pyridones are a class of organic compounds that contain a pyridone ring, which is a heterocyclic ring consisting of a six-membered ring with five carbon atoms and one nitrogen atom, with one oxygen atom attached to the nitrogen atom by a double bond. Pyridones can be found in various natural sources, including plants and microorganisms, and they also have important applications in the pharmaceutical industry as building blocks for drug design and synthesis. Some drugs that contain pyridone rings include antihistamines, anti-inflammatory agents, and antiviral agents.

A drug combination refers to the use of two or more drugs in combination for the treatment of a single medical condition or disease. The rationale behind using drug combinations is to achieve a therapeutic effect that is superior to that obtained with any single agent alone, through various mechanisms such as:

* Complementary modes of action: When different drugs target different aspects of the disease process, their combined effects may be greater than either drug used alone.
* Synergistic interactions: In some cases, the combination of two or more drugs can result in a greater-than-additive effect, where the total response is greater than the sum of the individual responses to each drug.
* Antagonism of adverse effects: Sometimes, the use of one drug can mitigate the side effects of another, allowing for higher doses or longer durations of therapy.

Examples of drug combinations include:

* Highly active antiretroviral therapy (HAART) for HIV infection, which typically involves a combination of three or more antiretroviral drugs to suppress viral replication and prevent the development of drug resistance.
* Chemotherapy regimens for cancer treatment, where combinations of cytotoxic agents are used to target different stages of the cell cycle and increase the likelihood of tumor cell death.
* Fixed-dose combination products, such as those used in the treatment of hypertension or type 2 diabetes, which combine two or more active ingredients into a single formulation for ease of administration and improved adherence to therapy.

However, it's important to note that drug combinations can also increase the risk of adverse effects, drug-drug interactions, and medication errors. Therefore, careful consideration should be given to the selection of appropriate drugs, dosing regimens, and monitoring parameters when using drug combinations in clinical practice.

Gene expression regulation in fungi refers to the complex cellular processes that control the production of proteins and other functional gene products in response to various internal and external stimuli. This regulation is crucial for normal growth, development, and adaptation of fungal cells to changing environmental conditions.

In fungi, gene expression is regulated at multiple levels, including transcriptional, post-transcriptional, translational, and post-translational modifications. Key regulatory mechanisms include:

1. Transcription factors (TFs): These proteins bind to specific DNA sequences in the promoter regions of target genes and either activate or repress their transcription. Fungi have a diverse array of TFs that respond to various signals, such as nutrient availability, stress, developmental cues, and quorum sensing.
2. Chromatin remodeling: The organization and compaction of DNA into chromatin can influence gene expression. Fungi utilize ATP-dependent chromatin remodeling complexes and histone modifying enzymes to alter chromatin structure, thereby facilitating or inhibiting the access of transcriptional machinery to genes.
3. Non-coding RNAs: Small non-coding RNAs (sncRNAs) play a role in post-transcriptional regulation of gene expression in fungi. These sncRNAs can guide RNA-induced transcriptional silencing (RITS) complexes to specific target loci, leading to the repression of gene expression through histone modifications and DNA methylation.
4. Alternative splicing: Fungi employ alternative splicing mechanisms to generate multiple mRNA isoforms from a single gene, thereby increasing proteome diversity. This process can be regulated by RNA-binding proteins that recognize specific sequence motifs in pre-mRNAs and promote or inhibit splicing events.
5. Protein stability and activity: Post-translational modifications (PTMs) of proteins, such as phosphorylation, ubiquitination, and sumoylation, can influence their stability, localization, and activity. These PTMs play a crucial role in regulating various cellular processes, including signal transduction, stress response, and cell cycle progression.

Understanding the complex interplay between these regulatory mechanisms is essential for elucidating the molecular basis of fungal development, pathogenesis, and drug resistance. This knowledge can be harnessed to develop novel strategies for combating fungal infections and improving agricultural productivity.

Magnetic Resonance Spectroscopy (MRS) is a non-invasive diagnostic technique that provides information about the biochemical composition of tissues, including their metabolic state. It is often used in conjunction with Magnetic Resonance Imaging (MRI) to analyze various metabolites within body tissues, such as the brain, heart, liver, and muscles.

During MRS, a strong magnetic field, radio waves, and a computer are used to produce detailed images and data about the concentration of specific metabolites in the targeted tissue or organ. This technique can help detect abnormalities related to energy metabolism, neurotransmitter levels, pH balance, and other biochemical processes, which can be useful for diagnosing and monitoring various medical conditions, including cancer, neurological disorders, and metabolic diseases.

There are different types of MRS, such as Proton (^1^H) MRS, Phosphorus-31 (^31^P) MRS, and Carbon-13 (^13^C) MRS, each focusing on specific elements or metabolites within the body. The choice of MRS technique depends on the clinical question being addressed and the type of information needed for diagnosis or monitoring purposes.

Drug antagonism is a type of interaction between two or more drugs, where one drug (known as the antagonist) reduces or blocks the effects of another drug (known as the agonist). This can occur through various mechanisms, such as binding to the same receptor site as the agonist and preventing it from activating the receptor, or by increasing the metabolism or excretion of the agonist.

Drug antagonism is often used in medical treatment to counteract the negative effects of certain drugs. For example, naloxone is an opioid antagonist that can be used to reverse the respiratory depression caused by opioid overdose. Similarly, flumazenil is a benzodiazepine antagonist that can be used to reverse the sedative effects of benzodiazepines in cases of overdose or adverse reactions.

However, drug antagonism can also lead to unintended consequences, such as when one medication reduces the effectiveness of another medication that a patient is taking for a different condition. Therefore, it is important for healthcare providers to be aware of potential drug interactions and to carefully monitor their patients' responses to medications.

Coccidioidomycosis is a fungal infection caused by the inhalation of spores of the Coccidioides species, mainly C. immitis and C. posadasii. These fungi are commonly found in the soil of dry regions such as the southwestern United States, Mexico, and Central and South America.

The infection often begins when a person inhales the microscopic spores, which can lead to respiratory symptoms resembling a common cold or pneumonia. Some people may develop more severe symptoms, especially those with weakened immune systems. The infection can disseminate to other parts of the body, causing skin lesions, bone and joint inflammation, meningitis, or other complications in rare cases.

Diagnosis typically involves a combination of clinical evaluation, imaging studies, and laboratory tests such as fungal cultures, histopathological examination, or serological tests to detect antibodies against Coccidioides antigens. Treatment depends on the severity of the infection and the patient's immune status. Antifungal medications like fluconazole, itraconazole, or amphotericin B are commonly used for treating coccidioidomycosis. Preventive measures include avoiding inhaling dust in endemic areas, especially during excavation or construction activities.

A plant extract is a preparation containing chemical constituents that have been extracted from a plant using a solvent. The resulting extract may contain a single compound or a mixture of several compounds, depending on the extraction process and the specific plant material used. These extracts are often used in various industries including pharmaceuticals, nutraceuticals, cosmetics, and food and beverage, due to their potential therapeutic or beneficial properties. The composition of plant extracts can vary widely, and it is important to ensure their quality, safety, and efficacy before use in any application.

ICR (Institute of Cancer Research) is a strain of albino Swiss mice that are widely used in scientific research. They are an outbred strain, which means that they have been bred to maintain maximum genetic heterogeneity. However, it is also possible to find inbred strains of ICR mice, which are genetically identical individuals produced by many generations of brother-sister mating.

Inbred ICR mice are a specific type of ICR mouse that has been inbred for at least 20 generations. This means that they have a high degree of genetic uniformity and are essentially genetically identical to one another. Inbred strains of mice are often used in research because their genetic consistency makes them more reliable models for studying biological phenomena and testing new therapies or treatments.

It is important to note that while inbred ICR mice may be useful for certain types of research, they do not necessarily represent the genetic diversity found in human populations. Therefore, it is important to consider the limitations of using any animal model when interpreting research findings and applying them to human health.

Molecular sequence data refers to the specific arrangement of molecules, most commonly nucleotides in DNA or RNA, or amino acids in proteins, that make up a biological macromolecule. This data is generated through laboratory techniques such as sequencing, and provides information about the exact order of the constituent molecules. This data is crucial in various fields of biology, including genetics, evolution, and molecular biology, allowing for comparisons between different organisms, identification of genetic variations, and studies of gene function and regulation.

Deoxycholic acid is a bile acid, which is a natural molecule produced in the liver and released into the intestine to aid in the digestion of fats. It is also a secondary bile acid, meaning that it is formed from the metabolism of primary bile acids by bacteria in the gut.

Deoxycholic acid has a chemical formula of C~24~H~39~NO~4~ and a molecular weight of 391.57 g/mol. It is a white crystalline powder that is soluble in water and alcohol. In the body, deoxycholic acid acts as a detergent to help break down dietary fats into smaller droplets, which can then be absorbed by the intestines.

In addition to its role in digestion, deoxycholic acid has been investigated for its potential therapeutic uses. For example, it is approved by the US Food and Drug Administration (FDA) as an injectable treatment for reducing fat in the submental area (the region below the chin), under the brand name Kybella. When injected into this area, deoxycholic acid causes the destruction of fat cells, which are then naturally eliminated from the body over time.

It's important to note that while deoxycholic acid is a natural component of the human body, its therapeutic use can have potential side effects and risks, so it should only be used under the supervision of a qualified healthcare professional.

Disk diffusion antimicrobial susceptibility tests, also known as Kirby-Bauer tests, are laboratory methods used to determine the effectiveness of antibiotics against a specific bacterial strain. This test provides a simple and standardized way to estimate the susceptibility or resistance of a microorganism to various antibiotics.

In this method, a standardized inoculum of the bacterial suspension is spread evenly on the surface of an agar plate. Antibiotic-impregnated paper disks are then placed on the agar surface, allowing the diffusion of the antibiotic into the agar. After incubation, the zone of inhibition surrounding each disk is measured. The size of the zone of inhibition correlates with the susceptibility or resistance of the bacterial strain to that specific antibiotic.

The results are interpreted based on predefined criteria established by organizations such as the Clinical and Laboratory Standards Institute (CLSI) or the European Committee on Antimicrobial Susceptibility Testing (EUCAST). These interpretive criteria help categorize the susceptibility of the bacterial strain into one of three categories: susceptible, intermediate, or resistant.

It is important to note that disk diffusion tests have limitations and may not always accurately predict clinical outcomes. However, they remain a valuable tool in guiding empirical antibiotic therapy and monitoring antimicrobial resistance trends.

Combination drug therapy is a treatment approach that involves the use of multiple medications with different mechanisms of action to achieve better therapeutic outcomes. This approach is often used in the management of complex medical conditions such as cancer, HIV/AIDS, and cardiovascular diseases. The goal of combination drug therapy is to improve efficacy, reduce the risk of drug resistance, decrease the likelihood of adverse effects, and enhance the overall quality of life for patients.

In combining drugs, healthcare providers aim to target various pathways involved in the disease process, which may help to:

1. Increase the effectiveness of treatment by attacking the disease from multiple angles.
2. Decrease the dosage of individual medications, reducing the risk and severity of side effects.
3. Slow down or prevent the development of drug resistance, a common problem in chronic diseases like HIV/AIDS and cancer.
4. Improve patient compliance by simplifying dosing schedules and reducing pill burden.

Examples of combination drug therapy include:

1. Antiretroviral therapy (ART) for HIV treatment, which typically involves three or more drugs from different classes to suppress viral replication and prevent the development of drug resistance.
2. Chemotherapy regimens for cancer treatment, where multiple cytotoxic agents are used to target various stages of the cell cycle and reduce the likelihood of tumor cells developing resistance.
3. Cardiovascular disease management, which may involve combining medications such as angiotensin-converting enzyme (ACE) inhibitors, beta-blockers, diuretics, and statins to control blood pressure, heart rate, fluid balance, and cholesterol levels.
4. Treatment of tuberculosis, which often involves a combination of several antibiotics to target different aspects of the bacterial life cycle and prevent the development of drug-resistant strains.

When prescribing combination drug therapy, healthcare providers must carefully consider factors such as potential drug interactions, dosing schedules, adverse effects, and contraindications to ensure safe and effective treatment. Regular monitoring of patients is essential to assess treatment response, manage side effects, and adjust the treatment plan as needed.

Monoterpenes are a class of terpenes that consist of two isoprene units and have the molecular formula C10H16. They are major components of many essential oils found in plants, giving them their characteristic fragrances and flavors. Monoterpenes can be further classified into various subgroups based on their structural features, such as acyclic (e.g., myrcene), monocyclic (e.g., limonene), and bicyclic (e.g., pinene) compounds. In the medical field, monoterpenes have been studied for their potential therapeutic properties, including anti-inflammatory, antimicrobial, and anticancer activities. However, more research is needed to fully understand their mechanisms of action and clinical applications.

Topical administration refers to a route of administering a medication or treatment directly to a specific area of the body, such as the skin, mucous membranes, or eyes. This method allows the drug to be applied directly to the site where it is needed, which can increase its effectiveness and reduce potential side effects compared to systemic administration (taking the medication by mouth or injecting it into a vein or muscle).

Topical medications come in various forms, including creams, ointments, gels, lotions, solutions, sprays, and patches. They may be used to treat localized conditions such as skin infections, rashes, inflammation, or pain, or to deliver medication to the eyes or mucous membranes for local or systemic effects.

When applying topical medications, it is important to follow the instructions carefully to ensure proper absorption and avoid irritation or other adverse reactions. This may include cleaning the area before application, covering the treated area with a dressing, or avoiding exposure to sunlight or water after application, depending on the specific medication and its intended use.

Farnesol is a chemical compound classified as a sesquiterpene alcohol. It is produced by various plants and insects, including certain types of roses and citrus fruits, and plays a role in their natural defense mechanisms. Farnesol has a variety of uses in the perfume industry due to its pleasant, floral scent.

In addition to its natural occurrence, farnesol is also synthetically produced for use in various applications, including as a fragrance ingredient and as an antimicrobial agent in cosmetics and personal care products. It has been shown to have antibacterial and antifungal properties, making it useful for preventing the growth of microorganisms in these products.

Farnesol is not typically used as a medication or therapeutic agent in humans, but it may have potential uses in the treatment of certain medical conditions due to its antimicrobial and anti-inflammatory properties. However, more research is needed to fully understand its effects and safety profile in these contexts.

Streptomyces is a genus of Gram-positive, aerobic, saprophytic bacteria that are widely distributed in soil, water, and decaying organic matter. They are known for their complex morphology, forming branching filaments called hyphae that can differentiate into long chains of spores.

Streptomyces species are particularly notable for their ability to produce a wide variety of bioactive secondary metabolites, including antibiotics, antifungals, and other therapeutic compounds. In fact, many important antibiotics such as streptomycin, neomycin, tetracycline, and erythromycin are derived from Streptomyces species.

Because of their industrial importance in the production of antibiotics and other bioactive compounds, Streptomyces have been extensively studied and are considered model organisms for the study of bacterial genetics, biochemistry, and ecology.

A cell wall is a rigid layer found surrounding the plasma membrane of plant cells, fungi, and many types of bacteria. It provides structural support and protection to the cell, maintains cell shape, and acts as a barrier against external factors such as chemicals and mechanical stress. The composition of the cell wall varies among different species; for example, in plants, it is primarily made up of cellulose, hemicellulose, and pectin, while in bacteria, it is composed of peptidoglycan.

Fungal genes refer to the genetic material present in fungi, which are eukaryotic organisms that include microorganisms such as yeasts and molds, as well as larger organisms like mushrooms. The genetic material of fungi is composed of DNA, just like in other eukaryotes, and is organized into chromosomes located in the nucleus of the cell.

Fungal genes are segments of DNA that contain the information necessary to produce proteins and RNA molecules required for various cellular functions. These genes are transcribed into messenger RNA (mRNA) molecules, which are then translated into proteins by ribosomes in the cytoplasm.

Fungal genomes have been sequenced for many species, revealing a diverse range of genes that encode proteins involved in various cellular processes such as metabolism, signaling, and regulation. Comparative genomic analyses have also provided insights into the evolutionary relationships among different fungal lineages and have helped to identify unique genetic features that distinguish fungi from other eukaryotes.

Understanding fungal genes and their functions is essential for advancing our knowledge of fungal biology, as well as for developing new strategies to control fungal pathogens that can cause diseases in humans, animals, and plants.

A dose-response relationship in the context of drugs refers to the changes in the effects or symptoms that occur as the dose of a drug is increased or decreased. Generally, as the dose of a drug is increased, the severity or intensity of its effects also increases. Conversely, as the dose is decreased, the effects of the drug become less severe or may disappear altogether.

The dose-response relationship is an important concept in pharmacology and toxicology because it helps to establish the safe and effective dosage range for a drug. By understanding how changes in the dose of a drug affect its therapeutic and adverse effects, healthcare providers can optimize treatment plans for their patients while minimizing the risk of harm.

The dose-response relationship is typically depicted as a curve that shows the relationship between the dose of a drug and its effect. The shape of the curve may vary depending on the drug and the specific effect being measured. Some drugs may have a steep dose-response curve, meaning that small changes in the dose can result in large differences in the effect. Other drugs may have a more gradual dose-response curve, where larger changes in the dose are needed to produce significant effects.

In addition to helping establish safe and effective dosages, the dose-response relationship is also used to evaluate the potential therapeutic benefits and risks of new drugs during clinical trials. By systematically testing different doses of a drug in controlled studies, researchers can identify the optimal dosage range for the drug and assess its safety and efficacy.

Lipoproteins are complex particles composed of multiple proteins and lipids (fats) that play a crucial role in the transport and metabolism of fat molecules in the body. They consist of an outer shell of phospholipids, free cholesterols, and apolipoproteins, enclosing a core of triglycerides and cholesteryl esters.

There are several types of lipoproteins, including:

1. Chylomicrons: These are the largest lipoproteins and are responsible for transporting dietary lipids from the intestines to other parts of the body.
2. Very-low-density lipoproteins (VLDL): Produced by the liver, VLDL particles carry triglycerides to peripheral tissues for energy storage or use.
3. Low-density lipoproteins (LDL): Often referred to as "bad cholesterol," LDL particles transport cholesterol from the liver to cells throughout the body. High levels of LDL in the blood can lead to plaque buildup in artery walls and increase the risk of heart disease.
4. High-density lipoproteins (HDL): Known as "good cholesterol," HDL particles help remove excess cholesterol from cells and transport it back to the liver for excretion or recycling. Higher levels of HDL are associated with a lower risk of heart disease.

Understanding lipoproteins and their roles in the body is essential for assessing cardiovascular health and managing risks related to heart disease and stroke.

Lactones are not a medical term per se, but they are important in the field of pharmaceuticals and medicinal chemistry. Lactones are cyclic esters derived from hydroxy acids. They can be found naturally in various plants, fruits, and some insects. In medicine, lactones have been used in the synthesis of drugs, including certain antibiotics and antifungal agents. For instance, the penicillin family of antibiotics contains a beta-lactone ring in their structure, which is essential for their antibacterial activity.

Glucosyltransferases (GTs) are a group of enzymes that catalyze the transfer of a glucose molecule from an activated donor to an acceptor molecule, resulting in the formation of a glycosidic bond. These enzymes play crucial roles in various biological processes, including the biosynthesis of complex carbohydrates, cell wall synthesis, and protein glycosylation. In some cases, GTs can also contribute to bacterial pathogenesis by facilitating the attachment of bacteria to host tissues through the formation of glucans, which are polymers of glucose molecules.

GTs can be classified into several families based on their sequence similarities and catalytic mechanisms. The donor substrates for GTs are typically activated sugars such as UDP-glucose, TDP-glucose, or GDP-glucose, which serve as the source of the glucose moiety that is transferred to the acceptor molecule. The acceptor can be a wide range of molecules, including other sugars, proteins, lipids, or small molecules.

In the context of human health and disease, GTs have been implicated in various pathological conditions, such as cancer, inflammation, and microbial infections. For example, some GTs can modify proteins on the surface of cancer cells, leading to increased cell proliferation, migration, and invasion. Additionally, GTs can contribute to bacterial resistance to antibiotics by modifying the structure of bacterial cell walls or by producing biofilms that protect bacteria from host immune responses and antimicrobial agents.

Overall, Glucosyltransferases are essential enzymes involved in various biological processes, and their dysregulation has been associated with several human diseases. Therefore, understanding the structure, function, and regulation of GTs is crucial for developing novel therapeutic strategies to target these enzymes and treat related pathological conditions.

High-performance liquid chromatography (HPLC) is a type of chromatography that separates and analyzes compounds based on their interactions with a stationary phase and a mobile phase under high pressure. The mobile phase, which can be a gas or liquid, carries the sample mixture through a column containing the stationary phase.

In HPLC, the mobile phase is a liquid, and it is pumped through the column at high pressures (up to several hundred atmospheres) to achieve faster separation times and better resolution than other types of liquid chromatography. The stationary phase can be a solid or a liquid supported on a solid, and it interacts differently with each component in the sample mixture, causing them to separate as they travel through the column.

HPLC is widely used in analytical chemistry, pharmaceuticals, biotechnology, and other fields to separate, identify, and quantify compounds present in complex mixtures. It can be used to analyze a wide range of substances, including drugs, hormones, vitamins, pigments, flavors, and pollutants. HPLC is also used in the preparation of pure samples for further study or use.

Defensins are small, cationic host defense peptides that contribute to the innate immune system's response against microbial pathogens. They are produced by various cell types, including neutrophils, epithelial cells, and some bone marrow-derived cells. Defensins have a broad spectrum of antimicrobial activity against bacteria, fungi, viruses, and enveloped lipid bilayers.

Defensins are classified into two main groups: α-defensins and β-defensins. Human α-defensins include human neutrophil peptides (HNP) 1-4 and human defensin 5, 6 (HD5, HD6). These are primarily produced by neutrophils and Paneth cells in the small intestine. β-defensins, on the other hand, are produced by various epithelial cells throughout the body.

Defensins work by disrupting the microbial membrane's integrity, leading to cell lysis and death. They also have immunomodulatory functions, such as chemotaxis of immune cells, modulation of cytokine production, and enhancement of adaptive immune responses. Dysregulation of defensin expression has been implicated in several diseases, including inflammatory bowel disease, chronic obstructive pulmonary disease, and certain skin disorders.

A Structure-Activity Relationship (SAR) in the context of medicinal chemistry and pharmacology refers to the relationship between the chemical structure of a drug or molecule and its biological activity or effect on a target protein, cell, or organism. SAR studies aim to identify patterns and correlations between structural features of a compound and its ability to interact with a specific biological target, leading to a desired therapeutic response or undesired side effects.

By analyzing the SAR, researchers can optimize the chemical structure of lead compounds to enhance their potency, selectivity, safety, and pharmacokinetic properties, ultimately guiding the design and development of novel drugs with improved efficacy and reduced toxicity.

Rhizoctonia is a genus of saprophytic and facultative parasitic fungi that belong to the order Corticiales. It is widely distributed in soil and on plant debris, and can cause various plant diseases known as "rhizoctonioses." The most common species associated with plant pathogenicity is Rhizoctonia solani. These fungi infect a wide range of plants, including crops, turfgrass, and ornamentals, causing symptoms such as root rot, stem canker, damping-off, and wirestem blight. The fungus can also form sclerotia, which are compact masses of hardened fungal mycelium that can survive in the soil for many years, serving as a source of infection for future plant growth.

Imidazoles are a class of heterocyclic organic compounds that contain a double-bonded nitrogen atom and two additional nitrogen atoms in the ring. They have the chemical formula C3H4N2. In a medical context, imidazoles are commonly used as antifungal agents. Some examples of imidazole-derived antifungals include clotrimazole, miconazole, and ketoconazole. These medications work by inhibiting the synthesis of ergosterol, a key component of fungal cell membranes, leading to increased permeability and death of the fungal cells. Imidazoles may also have anti-inflammatory, antibacterial, and anticancer properties.

The oropharynx is the part of the throat (pharynx) that is located immediately behind the mouth and includes the back one-third of the tongue, the soft palate, the side and back walls of the throat, and the tonsils. It serves as a passageway for both food and air, and is also an important area for the immune system due to the presence of tonsils.

Scanning electron microscopy (SEM) is a type of electron microscopy that uses a focused beam of electrons to scan the surface of a sample and produce a high-resolution image. In SEM, a beam of electrons is scanned across the surface of a specimen, and secondary electrons are emitted from the sample due to interactions between the electrons and the atoms in the sample. These secondary electrons are then detected by a detector and used to create an image of the sample's surface topography. SEM can provide detailed images of the surface of a wide range of materials, including metals, polymers, ceramics, and biological samples. It is commonly used in materials science, biology, and electronics for the examination and analysis of surfaces at the micro- and nanoscale.

A fungal genome refers to the complete set of genetic material or DNA present in the cells of a fungus. It includes all the genes and non-coding regions that are essential for the growth, development, and survival of the organism. The fungal genome is typically haploid, meaning it contains only one set of chromosomes, unlike diploid genomes found in many animals and plants.

Fungal genomes vary widely in size and complexity, ranging from a few megabases to hundreds of megabases. They contain several types of genetic elements such as protein-coding genes, regulatory regions, repetitive elements, and mobile genetic elements like transposons. The study of fungal genomes can provide valuable insights into the evolution, biology, and pathogenicity of fungi, and has important implications for medical research, agriculture, and industrial applications.

There is currently only one ocular antifungal available. This is Natamycin. However, various other antifungal agents could be ... Dixon, Dennis M.; Walsh, Thomas J. (1996), Baron, Samuel (ed.), "Antifungal Agents", Medical Microbiology (4th ed.), Galveston ... Sheehan DJ, Hitchcock CA, Sibley CM (January 1999). "Current and emerging azole antifungal agents". Clinical Microbiology ... Kyriakidis I, Tragiannidis A, Munchen S, Groll AH (February 2017). "Clinical hepatotoxicity associated with antifungal agents ...
Discuss with healthcare professionals before the use of topical antifungal agents. Prior to using topical antifungals, wash the ... The four classes of topical antifungal drugs are azole antifungals, polyene antifungals, allylamine antifungals, and other ... ciclopirox olamine antifungals, thiocarbamate antifungals and undecylenic alkanolamide antifungals. Topical antifungal drugs ... Most antifungal agents treat both dermatophyte and yeast infections. However, some, such as nystatin, are not suitable for ...
"Antifungal Agents". Polyene Antifungal Drugs. ISBN 9780963117212. PMID 21413319. Retrieved 29 January 2010. {{cite book}}: , ... v t e (CS1 errors: periodical ignored, Articles with short description, Short description matches Wikidata, Antifungals, ... Robbins, Nicole; Caplan, Tavia; Cowen, Leah E. (September 8, 2017). "Molecular Evolution of Antifungal Drug Resistance". Annual ... "Solution NMR structure of five representative glycosylated polyene macrolide antibiotics with a sterol-dependent antifungal ...
However, ketoconazole has largely been replaced as a first-line systemic antifungal medication by other azole antifungal agents ... part 4. Synthesis and antifungal activity of ketoconazole, a new potent orally active broad-spectrum antifungal agent". Journal ... Tarbit MH, Robertson WR, Lambert A (1990). "Hepatic and Endocrine Effects of Azole Antifungal Agents". Chemotherapy of Fungal ... As with all azole antifungal agents, ketoconazole works principally by inhibiting the enzyme cytochrome P450 14α-demethylase ( ...
Graininger W, Diab-Elschahawi M, Presterl E (2019). "3. Antifungal agents". In Presterl E (ed.). Clinically Relevant Mycoses: A ... and usually requires topical or systemic antifungal medicines. Pneumocystosis that does not respond to anti-fungals is treated ... Treatment is generally performed using antifungal medicines, usually in the form of a cream or by mouth or injection, depending ... Blyth CC, Hale K, Palasanthiran P, O'Brien T, Bennett MH (February 2010). "Antifungal therapy in infants and children with ...
Baron, S.; Dixon, D. M.; Walsh, T. J. (1996). "Chapter 76:Antifungal Agents". Medical microbiology (4th ed.). Galveston, Tex.: ... It also serves as an anti-fouling agent in paints to cover and protect surfaces against mildew and algae. Clioquinol and PBT2 ... It is also used as a food additive, shelf-life extending agent in food packaging, and wood preservative in timber treatment. ... Some synthetic agents are not macrocyclic, e.g. carbonyl cyanide-p-trifluoromethoxyphenylhydrazone. Even simple organic ...
It contains a water-repellent base (consisting of oils/waxes); protective and emollient agents; antibacterial and antifungal ... agents; and a weak anesthetic. As well as nappy rash, it can also be used to treat eczema, bedsores, minor burns, surface ...
Hiraki, J. (1995). "Basic and applied studies on ε-polylysine". Journal of Antibacterial Antifungal Agents. 23: 349-354. Mazia ... s as delivery agents for antisense oligonucleotides". Pharmaceutical Research. 24 (8): 1581-1589. doi:10.1007/s11095-006-9231-y ... which offers a new way to deliver therapeutic agents specifically to the sites of injury after vascular damage. In 2010, ... which can be used either as surfactants or emulsifiers in the encapsulation of water-insoluble drugs or as antimicrobial agents ...
Odds, Frank C.; Brown, Alistair J.P.; Gow, Neil A.R. (2003). "Antifungal agents: mechanisms of action". Trends in Microbiology ... His studies of how the cell walls of fungal pathogenic species is assembled, responds to antifungal antibiotics and is ... recognised by the human immune system directly impacts on the design and use of antifungal drugs, diagnostics and ...
Editorial: Resistance to antifungal agents. Fungal Genetics and Biology : Fg & B. 47: 190. PMID 20026235DOI: 10.1016/J.Fgb. ... case reports of antifungal agents, and copious international studies. Before his death in 2020, Odds helped establish the ... Antimicrobial Agents and Chemotherapy. 56: 208-17. PMID 21986821DOI: 10.1128/Aac.00683-11 Ostrosky-Zeichner L, Casadevall A, ... An insight into the antifungal pipeline: selected new molecules and beyond. Nature Reviews. Drug Discovery. 9: 719-27. PMID ...
... is an antifungal agent. 2-Aminotetralin () is alkylated with ethylchloroacetate to afford the glycine derivative. ... a novel type of antifungal agents". Journal of Medicinal Chemistry. 10 (6): 1160-1. doi:10.1021/jm00318a039. PMID 6056048. v t ... Antifungals, Ethyl esters, Imidazoles, 1-Aminotetralins, All stub articles, Antiinfective agent stubs). ...
Antibiotics are used to treat bacterial infections; antiviral agents treat viral infections; and antifungal agents treat fungal ... Infectious diseases specialists employ a variety of antimicrobial agents to help treat infections. The type of antimicrobial ...
They usually contain a single use antifungal agent such as clotrimazole. Oral antifungal agents are also available. Pessaries ...
... is a triterpenoid antifungal agent. It acts via inhibition of the enzyme glucan synthase, which is involved in ... It is the first non-azole oral antifungal drug to be approved by the U.S. Food and Drug Administration (FDA) for the treatment ... Azie N, Angulo D, Dehn B, Sobel JD (September 2020). "Oral Ibrexafungerp: an investigational agent for the treatment of ... Ibrexafungerp, sold under the brand name Brexafemme, is an antifungal medication used to treat vulvovaginal candidiasis (VVC) ( ...
Mühlbacher JM (1991). "Naftifine: a topical allylamine antifungal agent". Clinics in Dermatology. 9 (4): 479-85. doi:10.1016/ ... It was the first successful antifungal medication of the allylamine class. Naftifine has triple action: antifungal, ... Naftifine hydrochloride (brand names include Exoderil and Naftin) is an allylamine antifungal drug for the topical treatment of ... It is also effective as an antibacterial agent in treating pyoderma.[citation needed] Naftifine is almost completely ...
Yoshida Y (1988). "Cytochrome P450 of fungi: primary target for azole antifungal agents". Current Topics in Medical Mycology. 2 ... Sheehan DJ, Hitchcock CA, Sibley CM (January 1999). "Current and emerging azole antifungal agents". Clinical Microbiology ... Terconazole is an antifungal drug used to treat vaginal yeast infection. It comes as a lotion or a suppository and disrupts the ... Terconazole is non-reactive except when exposed to strong oxidizing agents or strong bases due to the nitrogen attached to the ...
Van Der Linden, Jan W. M.; Warris, Adilia; Verweij, Paul E. (April 2011). "species intrinsically resistant to antifungal agents ... to the antifungal drug amphotericin B though it is generally thought susceptible to other antifungal drugs such as voriconazole ... Arendrup, M.C. (June 2014). "Update on antifungal resistance in Aspergillus and Candida". Clinical Microbiology and Infection. ... Resistance to Antifungal Drugs". Mycopathologia. 174 (2): 131-141. doi:10.1007/s11046-012-9526-y. PMID 22327841. S2CID 11172300 ...
"Pharmacotherapy Update - New Antifungal Agents: Additions to the Existing Armamentarium (Part 1)". Debono M, Gordee RS (1994 ... Boucher HW, Groll AH, Chiou CC, Walsh TJ (2004). "Newer systemic antifungal agents : pharmacokinetics, safety and efficacy". ... 2006). "Pharmacology of Systemic Antifungal Agents". Clinical Infectious Diseases. 43 (Suppl 1): S28. doi:10.1086/504492. ... All three agents are well-tolerated, with the most common adverse effects being fever, rash, nausea, and phlebitis at the ...
Dharma R (28 August 2023). "Sandoz concludes acquisition of Mycamine antifungal agent". Pharmaceutical Technology. Retrieved 29 ... a novel systemic antifungal agent". Alimentary Pharmacology & Therapeutics. 20 (4): 475-81. doi:10.1111/j.1365-2036.2004.02083. ... Micafungin is a natural antifungal product derived from other fungi as a defense mechanism for competition of nutrients, etc. ... Fujie A (2007). "Discovery of micafungin (FK463): A novel antifungal drug derived from a natural product lead". Pure and ...
"Antifungal agents: chemotherapeutic targets and immunologic strategies". Antimicrobial Agents and Chemotherapy. 40 (2): 279-91 ...
Schiller DS, Fung HB (September 2007). "Posaconazole: an extended-spectrum triazole antifungal agent". Clinical Therapeutics. ... Posaconazole, sold under the brand name Noxafil among others, is a triazole antifungal medication. It was approved for medical ...
2007, 72, 6753-6757 doi:10.1021/jo0707939 Overhand, Mark; Hecht, Sidney M. (1994). "A Concise Synthesis of the Antifungal Agent ...
... was initially developed as an antifungal agent. However, this use was abandoned when it was discovered to have potent ... Rapamycin is used in biology research as an agent for chemically induced dimerization. In this application, rapamycin is added ... Vézina C, Kudelski A, Sehgal SN (October 1975). "Rapamycin (AY-22,989), a new antifungal antibiotic. I. Taxonomy of the ... Due to its immunosuppressant activity, Rapamycin has been assessed as prophylaxis or treatment agent of Graft-versus-host ...
Leyva Salas, M; Mounier, J; Valence, F; Coton, M; Thierry, A; Coton, E (8 July 2017). "Antifungal Microbial Agents for Food ... Another common crisping agent is calcium chloride, which evolved from the practice of using pickling lime. See also firming ... The yeast from the bread, along with other pickling agents and spices fermented under the hot sun, give the cucumbers a unique ... Some pickle cultures are said to contain bacteria producing natural antifungals. Nitrites, responsible for the creation of N- ...
... novel antifungal agents produced by Penicillium restrictum. I. Production, taxonomy of the producing organism and biological ...
Martín, ML; San Román, L; Domínguez, A (1990). "In vitro activity of protoanemonin, an antifungal agent". Planta Medica. 56 (1 ...
ISBN 978-1-284-17132-7. Miceli MH, Kauffman CA (November 2015). "Isavuconazole: A New Broad-Spectrum Triazole Antifungal Agent ... January 2003). "Design, synthesis and antifungal activity of a novel water soluble prodrug of antifungal triazole". Bioorganic ... Voronin AP, Vasilev NA, Surov AO, Churakov AV, Perlovich GL (2021). "Exploring the solid form landscape of the antifungal drug ... Isavuconazonium sulfate, sold under the brand name Cresemba, is a systemic antifungal medication of the triazole class which is ...
Studies have linked the anti-fungal activity of several anti-fungal agents to the inhibition of cystathionine beta-lyase; ... Jastrzębowska K, Gabriel I (February 2015). "Inhibitors of amino acids biosynthesis as antifungal agents". Amino Acids. 47 (2 ... leads for new antimicrobial agents and probes of enzyme structure and function". Journal of Medicinal Chemistry. 50 (4): 755-64 ...
... is resistant to the antifungal agent cycloheximide. However the growth of this species is inhibited by ... Geomyces pannorum has been identified as an agent of disfigurement of pigments used in the 15,000-year-old paintings on the ... Xanthomonas campestris and the causative agent of plant crown gall tumours, Agrobacterium tumefaciens. Fungal 18S rDNA ...
... antifungal agents are used to treat these infections. Amphotericin B deoxycholate is the most common treatment antifungal agent ... Nystatin is a type of antifungal agent used because it is not absorbed by the gastrointestinal tract. These types of agents ... Topical antifungal agents are commonly taken in 3 forms: oral suspension, ointment and powder. Oral suspension is mainly used ... Many conditions that contribute to C. tropicalis survival and colonization are: a) increase the use of antifungal regimen, b) ...
A fungicidal allylamine antifungal agent. Considered a third-line agent against sporotrichosis. Blocks ergosterol synthesis by ... A broad-spectrum azole antifungal agent. Considered a third-line agent for sporotrichosis treatment. Effective for various ... Antifungal agents. Class Summary. The mechanism of action may involve an alteration of RNA and DNA metabolism or an ... Most patients are treated with some form of antifungal therapy. Many agents are reported to be successful. For simple cutaneous ...
Imidazole antifungal agents appear to be the agents of choice. Of the azole group of antifungal agents, ketoconazole appears to ... Antifungal Agents. Class Summary. Reportedly, imidazole antifungal agents are variably effective in the treatment of eumycetoma ... Ketoconazole is a synthetic imidazole antifungal agent. It is a broad-spectrum agent known to be a potent inhibitor of the ... Itraconazole is a triazole antifungal agent known to be a potent inhibitor of the cytochrome P-450-dependent synthesis of ...
The antifungal agents herein described are most often used as monotherapy regimens because there is no uniform consensus on the ... Some agents have displaced conventional amphotericin B for the treatment of specific fungal diseases. For example, voriconazole ... Knowledge of the characteristics of the newer agents is important, given the increasing numbers of patients who are being ... This notwithstanding, conventional amphotericin B remains a useful agent for the treatment of paediatric fungal infections. ...
... by RIKEN In vivo imaging reveals the binding sites of theonellamide (TNM), a novel ... This unique mechanism promises to spur development of innovative antifungal agents. "We believe that TNM is the first compound ... phys.org/news/2010-09-antifungal-agents.html This document is subject to copyright. Apart from any fair dealing for the purpose ... Antifungal drugs are the best means to fight these parasitic species; however, because mammalian and fungal cells share many ...
In search of a natural anti-fungal agent against pathogenic Candida species, the researchers decided to investigate the ... tricolor is a promising natural anti-fungal agent that can be used to treat candidiasis. Sources include: Science.news Botany. ... alternative medicine Antifungal candida Candidiasis Croton tricolor essential oil fungal infection goodhealth goodmedicine ... Tags: alternative medicine, Antifungal, candida, Candidiasis, Croton tricolor, essential oil, fungal infection, goodhealth, ...
Oxygenated monoterpenes-rich volatile oils as potential antifungal agents for dermatophytes. Download Prime PubMed App to ... Oxygenated Monoterpenes-rich Volatile Oils as Potential Antifungal Agents for Dermatophytes. Nat Prod Res. 2017;31(4):460-464. ... Oxygenated monoterpenes-rich volatile oils as potential antifungal agents for dermatophytes. Nat Prod Res. 2017;31(4):460-464. ... Oxygenated monoterpenes-rich volatile oils as potential antifungal agents for dermatophytes.. Nat Prod Res. 2017 Feb; 31(4):460 ...
In addition, silibinin was recently reported to have antifungal effect related to fungal apoptosis against Candida albica … ... Assessment of silibinin as a potential antifungal agent and investigation of its mechanism of action IUBMB Life. 2017 Aug;69(8 ... In this study, we found another mode of antifungal action of silibinin and its antibiofilm activity on C. albicans. To ... In addition, silibinin was recently reported to have antifungal effect related to fungal apoptosis against Candida albicans and ...
While some patients have reported feeling better after taking antifungal agents, interfere with immune function. The ... Antifungal agents such as fluconazole (Diflucan) are sometimes prescribed to treat fungal infections, of which Candida is one ... While some patients have reported feeling better after taking antifungal agents, antifungals interfere with immune function. ... Antifungal agents such as fluconazole (Diflucan) are sometimes prescribed to treat fungal infections, of which Candida is one ...
We aim to develop a new class of antifungal agents that disarm the invasive forms of fungal cells instead of merely eradicating ... The situation illustrates the urgent need for new classes of antifungal agents with high efficacy and low toxicity at the same ... Current fungal therapy is limited, since only a few classes of antifungal agents exist whereby many of those exhibit ... Current antifungal therapy has a limited range of molecular targets and only few companies are engaged in the production of ...
title = "Introduction to the updated Australian and New Zealand consensus guidelines for the use of antifungal agents in the ... T1 - Introduction to the updated Australian and New Zealand consensus guidelines for the use of antifungal agents in the ... Introduction to the updated Australian and New Zealand consensus guidelines for the use of antifungal agents in the haematology ... Introduction to the updated Australian and New Zealand consensus guidelines for the use of antifungal agents in the haematology ...
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After 6 months of antifungal therapy with fluconazole and amphotericin B, the size of the liver mass was decreased, but no ... To control the cryptococcosis, a laparoscopic left adrenalectomy was performed, followed by antifungal therapy. After the ... management of cryptococcosis of the bilateral adrenal glands and liver by unilateral adrenalectomy with antifungal agents: a ...
Antifungal agents. Class Summary. These agents are used to treat oral candidiasis in association with hairy tongue. ... It is an imidazole broad-spectrum antifungal agent. It inhibits the synthesis of ergosterol, causing cellular components to ... Clotrimazole is a broad-spectrum antifungal agent that inhibits yeast growth by altering cell membrane permeability, causing ... 18, 19] Keratolytic agents are effective but may be irritating. Although reportedly successful, the agents listed above (with ...
... the search for more effective antifungal drugs becomes a challenge. Part of the preclinical trials of such drugs can be carried ... Antifungal Agents * Thiazolidinediones Grants and funding The ROS electrochemical measurements were carried out within the ... In connection with the emergence of new pathogenic strains of Candida, the search for more effective antifungal drugs becomes a ... Keywords: Candida; HEK239; PC3; ROS level; SICM; anticancer; antifungal; cell stiffness; thiazolidinedione. ...
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We explain why antifungal agents play an important role during the custom product development process for your products to pass ... How Antifungal Agents Fight Against Fungus and Mold In Everyday Products. Everyday products without antifungal additives that ... Adding Antifungal Agents During Your Custom Product Development Process Offering consumers a product that has antifungal ... Perhaps the most noticeable is the aesthetic damage which is caused in products lacking antifungal agents, leaving mold and ...
Which antifungal drug is the most toxic drug and is administered intravenously? a. Fluconazole. b. ... Antifungal and Antiviral Agents MCQs With Answers. 1. Which antifungal drug is the most toxic drug and is administered ... Antifungal and Antiviral Agents MCQs With Answers. by Fenee Patel. October 24, 2021. October 24, 2021. 01414 ... 4. Which antifungal agent is NOT indicated for use in fungal infections of the skin and nails?. a. Tolnaftate.. b. Flucytosine. ...
We compared the antifungal biofilm effects of antifungal agents, a denture cleaning agent and PDT in an in vitro acrylic resin ... However, fluconazole is not commonly used as denture soaking agent. The concept of using an antifungal agent to inhibit Candida ... Antifungal Agent Preparation. Ery solution was prepared by dissolving 19.34 mg of Ery (Sigma-Aldrich, St. Louis, MO, United ... Three milliliters of the antifungal agent sample were pipetted onto resin acrylic plate with biofilms ([Fig. 1]). Ery with nano ...
There is currently only one ocular antifungal available. This is Natamycin. However, various other antifungal agents could be ... Dixon, Dennis M.; Walsh, Thomas J. (1996), Baron, Samuel (ed.), "Antifungal Agents", Medical Microbiology (4th ed.), Galveston ... Sheehan DJ, Hitchcock CA, Sibley CM (January 1999). "Current and emerging azole antifungal agents". Clinical Microbiology ... Kyriakidis I, Tragiannidis A, Munchen S, Groll AH (February 2017). "Clinical hepatotoxicity associated with antifungal agents ...
Amphiphilic tobramycin analogues as antibacterial and antifungal agents. Antimicrobial Agents and Chemotherapy. 2015 Aug 1;59(8 ... Amphiphilic tobramycin analogues as antibacterial and antifungal agents. In: Antimicrobial Agents and Chemotherapy. 2015 ; Vol ... Amphiphilic tobramycin analogues as antibacterial and antifungal agents. Antimicrobial Agents and Chemotherapy, 59(8), 4861- ... Amphiphilic tobramycin analogues as antibacterial and antifungal agents, Antimicrobial Agents and Chemotherapy, vol. 59, no. 8 ...
Antifungal agent. MIC range (μg/mL). MIC50 (μg/mL). MIC90 (μg/mL). MIC geometric mean (μg/mL). ... Antifungal Susceptibilities of Cryptococcus neoformans Lennox K. Archibald*1. , Marion J. Tuohy†, Deborah A. Wilson†, Okey ...
Antifungal chemotherapy / edited by D. C. E. Speller. by Speller, D. C. E. ...
Here, we use a reporter gene-based screen in Saccharomyces cerevisiae for the discovery of antifungal inhibitors of GPI- ... Jawsamycin displays antifungal activity in vitro against several pathogenic fungi including Mucorales, and in vivo in a mouse ... Synthesis and evaluation of novel antifungal agents-quinoline and pyridine amide derivatives. Bioorg. Med. Chem. Lett. 20, 4624 ... Testing the assay with two antifungal agents and one known GPI inhbitor19 revealed an increase of signal in the medium ...
Chapter 29 The Antifungal Agents published on Dec 2022 by ASHP. ... Topical Antifungals. A large variety of antifungal agents are ... The Antifungal Agents. Polyenes. The polyenes are a class of antifungal agents that are fungicidal-they have the ability to ... Despite this challenge, several successful antifungal agents are available. To understand how antifungal agents work, it is ... continued antifungal activity seen even after the antifungal agent has been removed. ...
... and a greater focus on the principles of antifungal stewardship. We also introduce an entirely new chapter dedicated to helping ... healthcare workers convey important concepts related to IFD, infection prevention and antifungal therapy, to patients. ... of the Australian and New Zealand consensus guidelines for the management of invasive fungal disease and use of antifungal ... agents in the haematology/oncology setting. These guidelines are comprised of nine articles as presented in this special issue ...
Introduction to the updated Australian and New Zealand consensus guidelines for the use of antifungal agents in the haematology ... Guidelines for Antifungal Therapy. Expand All. * ASID Australian antifungal guidelines updated 2014. Published in Internal ... The ECIL 1 antifungal guidelines for infections in leukemia, 2007. The ECIL-1 is a common initiative of the following groups or ... Survey of antifungal prophylaxis and fungal diagnostic tests employed in malignant haematology and haemopoietic stem cell ...
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The currently used anti-fungal agent Natamycin has severe disadvantages. It is not active anymore to fungi responsible for ... Based on existing data of Prime chatoyant has anti-fungal properties. These data provide a basis to develop a new generation ... Chitosan: the basis of a new generation of anti-fungal and natural sausage casings and cheese coatings.. ... Goal: Develop a new generation anti-fungal food coatings based on chatoyant, a natural biopolymer manufactured from shrimp ...
Pillar five - antifungal agents. At some point, we need to incorporate antifungals to help kill off the mold spores that are ... Again, antifungal therapy can be done using natural agents and/or pharmaceuticals. ... Oregano, thyme, cinnamon, pau darco, garlic, and grapefruit seed extract are all good anti-fungal agents. ... Jill Crista who uses this with her patients, and I have also found it to open up the sinuses and have a good antifungal effect. ...
Home » Natural antifungal/antitumor agents discovered by Fujisawa. X. Upgrade your daily dose of biopharma and medtech news. ... has investigated their CD206 ligand AUR-300 as a novel therapeutic agent for systemic sclerosis treatment. ...
  • In search of a natural anti-fungal agent against pathogenic Candida species, the researchers decided to investigate the potential of C. tricolor essential oil. (naturalnews.com)
  • Antifungal agents such as fluconazole (Diflucan) are sometimes prescribed to treat fungal infections, of which Candida is one kind. (mpkb.org)
  • If Candida albicans is present, topical antifungal medications can be used when the condition is symptomatic (eg, glossopyrosis). (medscape.com)
  • In connection with the emergence of new pathogenic strains of Candida , the search for more effective antifungal drugs becomes a challenge. (nih.gov)
  • The Antifungal medicines can deal with several treatment conditions such as candida infections, esophageal candidiasis, peritonitis, urinary tract infections, etc. (topmedsexport.com)
  • For example, Candida auris , a pathogen of great clinical significance, causes candidiasis (especially in immunocompromised people) and has become resistant to treatments with several antifungals, including amphotericin B and fluconazole. (asm.org)
  • Isavuconazole, an azole antifungal agent, is currently undergoing international phase III trials with centers in the US, Europe and other regions in patients with invasive fungal infections caused by Aspergillus or other filamentous fungi (mold infections) and Candida fungi (yeast infections). (astellas.com)
  • Although the genus Candida consists of around 200 species, only 20 are reported as etiological agents of IC, being Candida albicans the most frequent causal agent. (intechopen.com)
  • Even when there is a broad range of antifungals drugs for Candida infections, azoles, polyenes, and echinocandins are considered among the most effective treatment. (intechopen.com)
  • However, there is some incidence for antifungal resistance among some Candida strains, limiting treatment options. (intechopen.com)
  • 3 , 4 Echinocandins, polyenes, pyrimidine, allylamine, and azoles are the most common antifungal agents available for the treatment of topical Candida spp. (dovepress.com)
  • ABSTRACT This study was carried out from October 2003 to March 2007 to investigate susceptibility patterns to antifungals of Candida strains isolated from 410 immunocompromised patients in Shiraz, Islamic Republic of Iran. (who.int)
  • infungihavebeenusedinthedevelop- clinicalsamples(blood,urine,oesopha- these recommended end-points for mentofcurrentlyavailableantifungal geal,oropharyngeal,vagina,biopsyand azolesarethelowestdrugconcentra- agents[1].Resistanceamong Candida broncho-alveolarlavage)wereexam- tionwithaprominentdecreaseintur- spp.toantifungaldrugsisanincreas- inedforfungalinfectionusingroutine bidity(inhibitoryconcentrationthat ingprobleminimmunocompromised methods.The Candida speciesisolated gives50%growthreduction),whilefor patients[2]. (who.int)
  • Also in this issue, a novel agent of fungemia, Candida auris , is reported as having been detected in India. (cdc.gov)
  • resistant to the antifungal agent fluconazole, which is concerning because fluconazole is frequently the first-line treatment for invasive Candida species infections in many countries. (cdc.gov)
  • Traditionally, the mainstay of systemic antifungal therapy has been amphotericin B deoxycholate (conventional amphotericin B). Newer agents have been developed to fulfill special niches and to compete with conventional amphotericin B by virtue of having more favourable toxicity profiles. (hindawi.com)
  • Some agents have displaced conventional amphotericin B for the treatment of specific fungal diseases. (hindawi.com)
  • This notwithstanding, conventional amphotericin B remains a useful agent for the treatment of paediatric fungal infections. (hindawi.com)
  • citation needed] Amphotericin B Candicidin Filipin - 35 carbons, binds to cholesterol (toxic) Hamycin Natamycin - 33 carbons, binds well to ergosterol Nystatin Rimocidin Azole antifungals inhibit conversion of lanosterol to ergosterol by inhibition of lanosterol 14α-demethylase. (wikipedia.org)
  • Amphotericin B is an amphoteric, forming soluble salts in both basic and acidic environments, and due to extensive unsaturation, it is unstable, primarily used as antifungal agents. (pharmacy180.com)
  • Prophylactic antifungal therapy, such as amphotericin B nasal spray, may be effective in controlling respiratory and sinus colonization. (medscape.com)
  • With clinically relevant antifungal potency against a broad range of yeasts, dimorphic fungi, and molds, isavuconazole has a spectrum of activity reminiscent of the polyene amphotericin B. Moreover, clinical experience thus far has revealed isavuconazole to be associated with fewer toxicities than voriconazole, even when administered without therapeutic drug monitoring. (wustl.edu)
  • Amphotericin B (AMB) is a polyene antibiotic with broad spectrum antifungal activity, but its clinical toxicities and poor solubility limit the wide application of AMB in clinical practice. (dovepress.com)
  • A broad-spectrum azole antifungal agent. (medscape.com)
  • It is a broad-spectrum agent known to be a potent inhibitor of the cytochrome P-450 3A4 enzyme system in vitro. (medscape.com)
  • Clotrimazole is an orally applicable antifungal substance with broad-spectrum activity. (axonmedchem.com)
  • Clotrimazole is a broad-spectrum antifungal agent that inhibits yeast growth by altering cell membrane permeability, causing death of fungal cells. (medscape.com)
  • It is an imidazole broad-spectrum antifungal agent. (medscape.com)
  • It is a synthetic oral antifungal (broad-spectrum bistriazole) that selectively inhibits fungal cytochrome P-450 and sterol C-14 alpha-demethylation, which prevents conversion of lanosterol to ergosterol, thereby disrupting cellular membranes. (medscape.com)
  • 3. Which antifungal drug is most effective with a broad spectrum? (remixeducation.in)
  • Amphiphilic TOB analogues showed broad-spectrum antifungal activities with minimal mammalian cell cytotoxicity. (uky.edu)
  • Treatment should involve broad-spectrum antifungal medications that have adequate central nervous system penetration. (cdc.gov)
  • We aim to develop a new class of antifungal agents that disarm the invasive forms of fungal cells instead of merely eradicating them. (ubi.se)
  • APT worked with F2G on the preclinical and early phase clinical PK-PD of F901318, which is the lead candidate for a new class of antifungal agents. (liverpool.ac.uk)
  • Current fungal therapy is limited, since only a few classes of antifungal agents exist whereby many of those exhibit considerable toxic side effects. (ubi.se)
  • The situation illustrates the urgent need for new classes of antifungal agents with high efficacy and low toxicity at the same time. (ubi.se)
  • Compare and contrast the mechanisms of action of various classes of antifungal agents. (ashp.org)
  • Of the azole group of antifungal agents, ketoconazole appears to be antifungal agent of choice, although isolated reports of successful treatment with itraconazole exist. (medscape.com)
  • Ketoconazole is a synthetic imidazole antifungal agent. (medscape.com)
  • Like the other antifungals, ketoconazole cream may inhibit bacteria die-off, especially in the skin areas where it has the highest concentration. (mpkb.org)
  • Imidazole antifungal agents appear to be the agents of choice. (medscape.com)
  • Reportedly, imidazole antifungal agents are variably effective in the treatment of eumycetoma when they are used alone or in conjunction with surgical therapy. (medscape.com)
  • The imidazole antifungals contain a 1,3-diazole (imidazole) ring (two nitrogen atoms), whereas the triazole antifungals have a ring with three nitrogen atoms. (wikipedia.org)
  • As the global leader in antimicrobial and antifungal solution technologies, Microban® is working with manufacturers who want their products to fight against the damage that fungus and mold can cause. (microban.com)
  • Antimicrobial Agents and Chemotherapy , 59 (8), 4861-4869. (uky.edu)
  • APT collaborates with multiple companies and academics to develop new antimicrobial agents, especially to address AMR. (liverpool.ac.uk)
  • The AMR centre works globally with companies and research institutions to support the development of new antimicrobial agents from lead optimization through to proof of concept and beyond. (liverpool.ac.uk)
  • Due to their antifungal, antibacterial, antiviral, and antimicrobial properties, silver nanoparticle s (AgNPsare used in consumer products intended for use by children or in the home. (cdc.gov)
  • The use of oral antimicrobial agents may provide a beneficial effect for denture stomatitis patients that are under antifungal therapy and that have poor oral hygiene and unfavorable salivary parameters. (bvsalud.org)
  • Itraconazole is a triazole antifungal agent known to be a potent inhibitor of the cytochrome P-450-dependent synthesis of ergosterol in vitro. (medscape.com)
  • 6. Synthesis and antifungal properties of terconazole, a novel triazole ketal. (nih.gov)
  • Isavuconazole: Pharmacology, Pharmacodynamics, and Current Clinical Experience with a New Triazole Antifungal Agent. (wustl.edu)
  • Although previously available second-generation triazole antifungals have significantly expanded the spectrum of the triazole antifungal class, these agents are laden with shortcomings in their safety profiles as well as formulation and pharmacokinetic challenges. (wustl.edu)
  • Isavuconazole, administered as the prodrug isavuconazonium, is the latest second-generation triazole antifungal to receive U.S. Food and Drug Administration approval. (wustl.edu)
  • These characteristics, in an agent available in both a highly bioavailable oral and a β-cyclodextrin-free intravenous formulation, will likely make isavuconazole a welcome addition to the triazole class of antifungals. (wustl.edu)
  • Because most invasive fungal infections have high mortality rates, reducing the incidence of these diseases often relies on rapid and specific diagnostics, effective antifungal drugs, novel immunotherapeutic strategies, and adherence to infection control and sterility practices. (cdc.gov)
  • most die despite appropriate systemic antifungal therapy. (medscape.com)
  • The evolution of antifungal resistance is a growing threat to health globally. (wikipedia.org)
  • What is driving this increase in antifungal resistance and what can be done to stop it? (asm.org)
  • What is Driving Antifungal Resistance? (asm.org)
  • In addition to changing environmental factors that drive evolution in fungal species (e.g., global warming and climate change have resulted in identification of new fungal pathogens, including new clades of C. auris ), multiple anthropological factors contribute to the development of antifungal resistance. (asm.org)
  • As humans and animals end up consuming antifungals as medicines , they might also inhale/ingest fungal spores from the environment, thus disrupting the microbiome by tampering with the equilibrium and potentially prompting the evolution of resistance. (asm.org)
  • Further, the tendency to not finish the antifungal course and improper disposal of drugs are also key drivers of resistance. (asm.org)
  • Factors that contribute to acquisition of antifungal resistance. (asm.org)
  • Several molecular mechanisms with antifungal agents have been reported for C. albicans where insertions, deletions, and point mutations in genes codifying target proteins are frequently related to the antifungal drug resistance. (intechopen.com)
  • Furthermore, gene overexpression is also frequently associated to antifungal resistance as well as an increase in the activity of proteins that reduce oxidative damage. (intechopen.com)
  • This chapter summarizes the main molecular mechanisms to C. albicans antifungal drug resistance, besides offering an overview of new antifungal agents and new antifungal targets to combat fungal infections. (intechopen.com)
  • Regular investigations into antifungal resistance in medical centres is highly recommended as this will result in more efficient management of invasive candidiasis in immunocompromised patients. (who.int)
  • Essential oils (EOs) extracted from Lavandula luisieri and Cymbopogon citratus were tested for their antifungal activity against ten clinical isolates of dermatophytes isolated from cases of tinea pedis. (unboundmedicine.com)
  • Fifty isolates of Exserohilum rostratum were cultured from patient specimens and tested for their susceptibility to a variety of antifungal drugs. (cdc.gov)
  • Susceptibility of the isolates to antifungal agents was determined using the reference broth microdilution method. (who.int)
  • Antifungal medicines supplied by us are used to treat fungal infections of different types. (topmedsexport.com)
  • Antifungal medicines are known to treat serious fungal as well as yeast infections. (topmedsexport.com)
  • 4. Which antifungal agent is NOT indicated for use in fungal infections of the skin and nails? (remixeducation.in)
  • An antifungal medication, also known as an antimycotic medication, is a pharmaceutical fungicide or fungistatic used to treat and prevent mycosis such as athlete's foot, ringworm, candidiasis (thrush), serious systemic infections such as cryptococcal meningitis, and others. (wikipedia.org)
  • Despite increasing numbers of affected patients with life-threatening infections and the concomitant increased burden on public healthcare systems, there remains only three main classes of established antifungal agents to treat systemic infections. (nature.com)
  • European guidelines for primary antifungal prophylaxis in adult haematology patients: summary of the updated recommendations from the European Conference on Infections in Leukaemia. (edu.au)
  • In addition, the available antifungals with proven efficacy in the treatment of these infections remain severely limited. (wustl.edu)
  • Many of these reports describe infections caused by new agents, as well as by traditional agents with new virulence factors or new mechanisms of infection. (cdc.gov)
  • and immunomodulatory agents for treating underlying diseases from cancer to rheumatoid arthritishas contributed to the increase in fungal infections in immunocompromised hosts. (cdc.gov)
  • Risk factors such as changes in land use, seasonal migration, international travel, extreme weather, and natural disasters, and the use of azole antifungal agents in large-scale agriculture are believed to underlay many of the increases in community-acquired fungal infections. (cdc.gov)
  • TY - JOUR T1 - Oxygenated monoterpenes-rich volatile oils as potential antifungal agents for dermatophytes. (unboundmedicine.com)
  • Inhibition of conidial germination and antifungal drug/EO combination assay were tested on two ATCC reference strains of Trichophyton rubrum and Trichophyton mentagrophytes. (unboundmedicine.com)
  • Strong antifungal activity was observed for the majority of clinical strains, and fungicidal activity was demonstrated. (unboundmedicine.com)
  • Analogues with C 12 and C 14 chains showed promising antifungal activities against tested fungal strains, with MIC values ranging from 1.95 to 62.5 mg/liter and 1.95 to 7.8 mg/liter, respectively. (uky.edu)
  • However, these antifungal drugs have several defects in clinical practice, such as low efficacy and serious adverse drug reactions (ADRs) and even the emergence of resistant strains. (dovepress.com)
  • [3] Treatment is typically with antifungal creams such as clotrimazole or miconazole . (wikipedia.org)
  • To assess the number of Streptococcus mutans in saliva of patients with denture stomatitis before and after antifungal therapy. (bvsalud.org)
  • This study describes the antifungal activity of L. luisieri and C. citratus EOs against dermatophytes, which could be useful in designing new formulations for topical treatments. (unboundmedicine.com)
  • Treatment includes topical antifungal products and mouthwashes. (medicalnewstoday.com)
  • We conclude that topical intra-antral application of anti-fungal agents is effective in patients with recurrent fungal maxillary sinusitis after surgical debulking. (biomedcentral.com)
  • Anti-fungal agents can be used as systemic medications or as topical preparations delivered directly to the sinuses. (biomedcentral.com)
  • Several other coating agents and topical anesthetics can help to soothe inflamed tissue. (medscape.com)
  • Topical agents are listed in Table 1. (medscape.com)
  • Treatment, based on severity, can involve a variety of topical and systemic agents directed at reducing sebum production, comedone formation, inflammation, and bacterial counts and at normalizing keratinization. (msdmanuals.com)
  • Knowledge of the characteristics of the newer agents is important, given the increasing numbers of patients who are being treated with these drugs. (hindawi.com)
  • By increasing levels of 25-D and therefore inhibiting immunopathology, long-term use of antifungal drugs may delay progress on the Marshall Protocol (MP). (mpkb.org)
  • Current antifungal therapy has a limited range of molecular targets and only few companies are engaged in the production of these drugs. (ubi.se)
  • Nevertheless, the global market for antifungal drugs in 2015 was analyzed for 6.82 billion US dollars with an annual increase of 0.1-0.2 billion US dollars. (ubi.se)
  • Conclusively, prices for antifungal drugs are relatively high. (ubi.se)
  • Even when you treat it with antifungal drugs, the infection may take several weeks to disappear and may come back after treatment. (webmd.com)
  • This upward trend is concerning considering the limited number of antifungal drugs available. (dovepress.com)
  • Patients who continue to undergo treatment with oral or intravenous antifungal medications require periodic follow-up care as outpatients. (medscape.com)
  • In this study, we investigated the in vitro antifungal activities, cytotoxicities, and membrane-disruptive actions of amphiphilic tobramycin (TOB) analogues. (uky.edu)
  • The compound targets the catalytic subunit Spt14 (also referred to as Gpi3) of the fungal UDP-glycosyltransferase, the first step in GPI biosynthesis, with good selectivity over the human functional homolog PIG-A. Jawsamycin displays antifungal activity in vitro against several pathogenic fungi including Mucorales, and in vivo in a mouse model of invasive pulmonary mucormycosis due to Rhyzopus delemar infection. (nature.com)
  • This study aimed to develop AMB-loaded PLGA-TPGS nanoparticles (AMB-NPs) and evaluate their antifungal effects in vitro and in vivo. (dovepress.com)
  • Finally, the antifungal activity of AMB-NPs was investigated in vitro and in vivo. (dovepress.com)
  • The researchers' next task-unraveling the complex mechanisms of TNM-induced membrane signaling-may throw light on how to avoid unwanted side-effects in humans during antifungal treatments. (phys.org)
  • The use of itraconazole and voriconazole as prophylactic agents have shown to be beneficial in some studies to protect granulocytopenic patients from invasive aspergillosis. (medscape.com)
  • 6. The antiviral agent, amantadine, inhibits the replication of which strain of virus? (remixeducation.in)
  • however, biofilm-associated C. albicans can be resistant to these agents. (thieme-connect.de)
  • Considered a third-line agent for sporotrichosis treatment. (medscape.com)
  • The use of various antifungal agents in the treatment of eumycetoma has been reported. (medscape.com)
  • Although reportedly successful, the agents listed above (with the exception of treatment of oral candidiasis) are used off label and their application should be limited to selected cases with close monitoring. (medscape.com)
  • 2. Which antifungal drug is available as a troche, for treatment of oral candidiasis? (remixeducation.in)
  • It has been shown that early treatment with effective antifungals reduces patient mortality. (astellas.com)
  • The AMB-PLGA-TPGS NP system significantly improves the AMB bioavailability by improving its antifungal activities and reducing its toxicity, and thus, these NPs may become a good drug carrier for antifungal treatment. (dovepress.com)
  • Treatment is with drying agents and antifungals. (msdmanuals.com)
  • 7. Which anti-herpetic agent is most potent? (remixeducation.in)
  • Fifty percent inhibitory concentrations (IC 50 s) for the most potent TOB analogues (C 12 and C 14 ) against A549 and Beas 2B cells were 4- to 64-fold and 32- to 64-fold higher, respectively, than their antifungal MIC values against various fungi. (uky.edu)
  • Here, we use a reporter gene-based screen in Saccharomyces cerevisiae for the discovery of antifungal inhibitors of GPI-anchoring of proteins, and identify the oligocyclopropyl-containing natural product jawsamycin (FR-900848) as a potent hit. (nature.com)
  • In vivo experiments indicated that AMB-NPs achieved significantly better and prolonged antifungal effects when compared with free AMB. (dovepress.com)
  • A polyene antifungal is a macrocyclic polyene with a heavily hydroxylated region on the ring opposite the conjugated system. (wikipedia.org)
  • if the antifungal has good bioavailability, this is a common route to handle a fungal infection. (wikipedia.org)
  • Introduction to the updated Australian and New Zealand consensus guidelines for the use of antifungal agents in the haematology/oncology setting, 2014. (edu.au)
  • A growing concern about our exposure to fungus and mold, along with a willingness to stop the aesthetic and surface damage it can cause, has led many consumers to invest in products that have built-in antifungal agents. (microban.com)
  • Without antifungal coatings and additives in products, fungus and mold can dirty our bathroom ceramics, stain our windows, clog up our garbage disposal units, and produce unsightly patches in the depths of our basements. (microban.com)
  • More often than not, mold and fungus growth is maximized in areas where there is high humidity, or water damage or dampness, making built-in antifungal agents key for preventing its growth. (microban.com)
  • Everyday products without antifungal additives that are exposed to fungus and mold can be impacted in a variety of ways. (microban.com)
  • Perhaps the most noticeable is the aesthetic damage which is caused in products lacking antifungal agents, leaving mold and fungus to flourish. (microban.com)
  • When the likes of fungus and mold come into contact with the product surface, Microban's antifungal technology penetrates the cell wall of the microbe and disrupts key cell functions so that it cannot function or reproduce. (microban.com)
  • The currently used anti-fungal agent Natamycin has severe disadvantages. (europa.eu)
  • Here, we present a case of utilization of intra-antral application of an anti-fungal agent in the management of recurrent fungal sinusitis in an indigent Nigerian patient. (biomedcentral.com)
  • After intra-nasal antrostomy for debulking with a systemic anti-fungal agent, our patient had a recurrence after four months. (biomedcentral.com)
  • 1. Which antifungal drug is the most toxic drug and is administered intravenously? (remixeducation.in)
  • Describe the drug interaction potential for each class of antifungals. (ashp.org)
  • The antifungal activity of this drug depends, at least, in part, on its binding to a sterol moiety. (pharmacy180.com)
  • However, when it comes to drug discovery, it is important to understand that very few of antifungals actually can be used as therapeutics. (asm.org)
  • However, C 4 , C 6 , and C 8 TOB analogues and TOB itself exhibited little to no antifungal activity. (uky.edu)
  • However, C4, C6, and C8 TOB analogues and TOB itself exhibited little to no antifungal activity. (uky.edu)
  • continued antifungal activity seen even after the antifungal agent has been removed. (ashp.org)
  • technical runs physical to download interactions of yeasts moulds and antifungal agents how, inspection, and recovery as a activity of going 48610002013-01-01T00:00:00Installation history. (sammlerbedarf-rother.de)
  • The current study aimed to synthesize zinc oxide nanoparticles (ZnO-NPs) by chemically or green method and investigate their antifungal activity against A. citri . (ppjonline.org)
  • This unique mechanism promises to spur development of innovative antifungal agents. (phys.org)
  • Kasse Centre is clinical to topics and techniques at the University of Cambridge, and to any logistics with an download interactions of yeasts moulds and antifungal agents how to detect who judge heating Cambridge, for together wide or just a destination. (sammlerbedarf-rother.de)
  • Pharmacodynamics of flubendazole for cryptococcal meningoencephalitis: repurposing and reformulation of an anti-parasitic agent for a neglected fungal disease. (liverpool.ac.uk)
  • http://www.who.int/phi/news/consultation_stewardship-framework/en/ (accessed 6 April 2016). (who.int)
  • This study aimed to compare the anticandidal efficacy of photodynamic therapy by erythrosine with nano-titanium dioxide (nano-TiO 2 ) stimulated by a blue light emitting diode with three standard dental antifungal agents. (thieme-connect.de)
  • During World War I, the AUES was established to investigate testing, production and effects of chemical warfare agents, antidotes and protective equipment. (cdc.gov)
  • Ibrexafungerp Acrisorcin Amorolfine - a morpholine derivative used topically in dermatophytosis Aurones - possess antifungal properties Benzoic acid - has antifungal properties, such as in Whitfield's ointment, Friar's Balsam, and Balsam of Peru Carbol fuchsin (Castellani's paint) Ciclopirox (ciclopirox olamine) - a hydroxypyridone antifungal that interferes with active membrane transport, cell membrane integrity, and fungal respiratory processes. (wikipedia.org)