Azlocillin: A semisynthetic ampicillin-derived acylureido penicillin.Penicillins: A group of antibiotics that contain 6-aminopenicillanic acid with a side chain attached to the 6-amino group. The penicillin nucleus is the chief structural requirement for biological activity. The side-chain structure determines many of the antibacterial and pharmacological characteristics. (Goodman and Gilman's The Pharmacological Basis of Therapeutics, 8th ed, p1065)Ticarcillin: An antibiotic derived from penicillin similar to CARBENICILLIN in action.Mezlocillin: Semisynthetic ampicillin-derived acylureido penicillin. It has been proposed for infections with certain anaerobes and may be useful in inner ear, bile, and CNS infections.Tobramycin: An aminoglycoside, broad-spectrum antibiotic produced by Streptomyces tenebrarius. It is effective against gram-negative bacteria, especially the PSEUDOMONAS species. It is a 10% component of the antibiotic complex, NEBRAMYCIN, produced by the same species.Carbenicillin: Broad-spectrum semisynthetic penicillin derivative used parenterally. It is susceptible to gastric juice and penicillinase and may damage platelet function.Pseudomonas aeruginosa: A species of gram-negative, aerobic, rod-shaped bacteria commonly isolated from clinical specimens (wound, burn, and urinary tract infections). It is also found widely distributed in soil and water. P. aeruginosa is a major agent of nosocomial infection.Cefsulodin: A pyridinium-substituted semisynthetic, broad-spectrum antibacterial used especially for Pseudomonas infections in debilitated patients.Pseudomonas Infections: Infections with bacteria of the genus PSEUDOMONAS.Microbial Sensitivity Tests: Any tests that demonstrate the relative efficacy of different chemotherapeutic agents against specific microorganisms (i.e., bacteria, fungi, viruses).Piperacillin: Semisynthetic, broad-spectrum, AMPICILLIN derived ureidopenicillin antibiotic proposed for PSEUDOMONAS infections. It is also used in combination with other antibiotics.Aztreonam: A monocyclic beta-lactam antibiotic originally isolated from Chromobacterium violaceum. It is resistant to beta-lactamases and is used in gram-negative infections, especially of the meninges, bladder, and kidneys. It may cause a superinfection with gram-positive organisms.Amikacin: A broad-spectrum antibiotic derived from KANAMYCIN. It is reno- and oto-toxic like the other aminoglycoside antibiotics.Enterobacteriaceae: A family of gram-negative, facultatively anaerobic, rod-shaped bacteria that do not form endospores. Its organisms are distributed worldwide with some being saprophytes and others being plant and animal parasites. Many species are of considerable economic importance due to their pathogenic effects on agriculture and livestock.Clavulanic Acids: Acids, salts, and derivatives of clavulanic acid (C8H9O5N). They consist of those beta-lactam compounds that differ from penicillin in having the sulfur of the thiazolidine ring replaced by an oxygen. They have limited antibacterial action, but block bacterial beta-lactamase irreversibly, so that similar antibiotics are not broken down by the bacterial enzymes and therefore can exert their antibacterial effects.Biological Science Disciplines: All of the divisions of the natural sciences dealing with the various aspects of the phenomena of life and vital processes. The concept includes anatomy and physiology, biochemistry and biophysics, and the biology of animals, plants, and microorganisms. It should be differentiated from BIOLOGY, one of its subdivisions, concerned specifically with the origin and life processes of living organisms.Software: Sequential operating programs and data which instruct the functioning of a digital computer.User-Computer Interface: The portion of an interactive computer program that issues messages to and receives commands from a user.Algorithms: A procedure consisting of a sequence of algebraic formulas and/or logical steps to calculate or determine a given task.Computational Biology: A field of biology concerned with the development of techniques for the collection and manipulation of biological data, and the use of such data to make biological discoveries or predictions. This field encompasses all computational methods and theories for solving biological problems including manipulation of models and datasets.ArchivesMedical Illustration: The field which deals with illustrative clarification of biomedical concepts, as in the use of diagrams and drawings. The illustration may be produced by hand, photography, computer, or other electronic or mechanical methods.Drug Information Services: Services providing pharmaceutic and therapeutic drug information and consultation.Pamphlets: Printed publications usually having a format with no binding and no cover and having fewer than some set number of pages. They are often devoted to a single subject.Drug Labeling: Use of written, printed, or graphic materials upon or accompanying a drug container or wrapper. It includes contents, indications, effects, dosages, routes, methods, frequency and duration of administration, warnings, hazards, contraindications, side effects, precautions, and other relevant information.Patient Education as Topic: The teaching or training of patients concerning their own health needs.Formularies as Topic: Works about lists of drugs or collections of recipes, formulas, and prescriptions for the compounding of medicinal preparations. Formularies differ from PHARMACOPOEIAS in that they are less complete, lacking full descriptions of the drugs, their formulations, analytic composition, chemical properties, etc. In hospitals, formularies list all drugs commonly stocked in the hospital pharmacy.Drug Industry: That segment of commercial enterprise devoted to the design, development, and manufacture of chemical products for use in the diagnosis and treatment of disease, disability, or other dysfunction, or to improve function.Medical Records Systems, Computerized: Computer-based systems for input, storage, display, retrieval, and printing of information contained in a patient's medical record.CitratesCounterfeit Drugs: Drugs manufactured and sold with the intent to misrepresent its origin, authenticity, chemical composition, and or efficacy. Counterfeit drugs may contain inappropriate quantities of ingredients not listed on the label or package. In order to further deceive the consumer, the packaging, container, or labeling, may be inaccurate, incorrect, or fake.Citric Acid: A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.Fraud: Exploitation through misrepresentation of the facts or concealment of the purposes of the exploiter.Directories as Topic: Lists of persons or organizations, systematically arranged, usually in alphabetic or classed order, giving address, affiliations, etc., for individuals, and giving address, officers, functions, and similar data for organizations. (ALA Glossary of Library and Information Science, 1983)Group Purchasing: A shared service which combines the purchasing power of individual organizations or facilities in order to obtain lower prices for equipment and supplies. (From Health Care Terms, 2nd ed)Eye Burns: Injury to any part of the eye by extreme heat, chemical agents, or ultraviolet radiation.Ion Exchange Resins: High molecular weight, insoluble polymers which contain functional groups that are capable of undergoing exchange reactions (ION EXCHANGE) with either cations or anions.Cation Exchange Resins: High molecular weight insoluble polymers which contain functional anionic groups that are capable of undergoing exchange reactions with cations.Anion Exchange Resins: High-molecular-weight insoluble polymers that contain functional cationic groups capable of undergoing exchange reactions with anions.Resins, Plant: Flammable, amorphous, vegetable products of secretion or disintegration, usually formed in special cavities of plants. They are generally insoluble in water and soluble in alcohol, carbon tetrachloride, ether, or volatile oils. They are fusible and have a conchoidal fracture. They are the oxidation or polymerization products of the terpenes, and are mixtures of aromatic acids and esters. Most are soft and sticky, but harden after exposure to cold. (From Grant & Hackh's Chemical Dictionary, 5th ed & Dorland, 28th ed)Pinus ponderosa: A plant species of the genus PINUS that contains isocupressic acid.Resins, Synthetic: Polymers of high molecular weight which at some stage are capable of being molded and then harden to form useful components.Epichlorohydrin: A chlorinated epoxy compound used as an industrial solvent. It is a strong skin irritant and carcinogen.Dictionaries, MedicalDictionaries as Topic: Lists of words, usually in alphabetical order, giving information about form, pronunciation, etymology, grammar, and meaning.Antifungal Agents: 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.Clotrimazole: 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.Allylamine: 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.Miconazole: An imidazole antifungal agent that is used topically and by intravenous infusion.Ketoconazole: Broad spectrum antifungal agent used for long periods at high doses, especially in immunosuppressed patients.BoliviaEcuadorBiotechnology: Body of knowledge related to the use of organisms, cells or cell-derived constituents for the purpose of developing products which are technically, scientifically and clinically useful. Alteration of biologic function at the molecular level (i.e., GENETIC ENGINEERING) is a central focus; laboratory methods used include TRANSFECTION and CLONING technologies, sequence and structure analysis algorithms, computer databases, and gene and protein structure function analysis and prediction.Moraceae: The mulberry plant family of the order Urticales, subclass Hamamelidae, class Magnoliopsida. They have milky latex and small, petalless male or female flowers.BrazilCaliforniaGenomics: The systematic study of the complete DNA sequences (GENOME) of organisms.

Ability of azlocillin and tobramycin in combination to delay or prevent resistance development in Pseudomonas aeruginosa. (1/60)

The ability of combinations of azlocillin and tobramycin to prevent or delay resistance development in eight Pseudomonas aeruginosa isolates from cystic fibrosis (CF) patients was studied using chequerboard titration and in-vitro serial subculture. No isolate had developed resistance to tobramycin after 12 treatments with the antibiotic combination. Azlocillin resistance had not developed in four isolates after 16 exposures, and was delayed in the other four isolates for at least eight exposures. Beta-lactamase production was responsible for azlocillin resistance in two isolates and occurred to a lesser extent in a third.  (+info)

Once-daily versus multiple-daily gentamicin in empirical antibiotic therapy of febrile neutropenia following intensive chemotherapy. (2/60)

The clinical efficacy and toxicity of once-daily compared with multiple-daily gentamicin dosing, in combination with azlocillin, were studied retrospectively in febrile neutropenic episodes following intensive chemotherapy. Fifty-two episodes were studied in 28 patients with acute myeloid leukaemia. Reasons for initiation of antibiotic therapy, dose, duration of treatment, organism isolation rates, response, cost comparison and toxicity were studied in the two treatment groups. The main indication for initiation of antibiotic therapy was neutropenic fever without a documented infection (80.8% of episodes). The response rate to once-daily gentamicin dosing and azlocillin was three times higher than to multiple-daily gentamicin dosing and azlocillin (P = 0.0112). The incidence of toxicity was low overall and was slightly but not significantly higher in the once-daily group. In this clinical context once-daily gentamicin at a dose of 7 mg/kg/day is more effective than a multiple-daily dosing regimen but may be more toxic.  (+info)

Reduction of contamination of mycobacterial growth indicator tubes with a modified antimicrobial combination. (3/60)

Culture in the fluorimetric Mycobacteria Growth Indicator Tube (MGIT) treated with a combination of vancomycin, amphotericin B, and nalidixic acid (VAN) showed growth of most strains of 31 mycobacterial species with a less-than-1-day delay. The results were similar to those in the MGIT with polymyxin B, amphotericin B, nalidixic acid, trimethoprim, and azlocillin, but with respiratory specimens, the MGIT with VAN showed a lower contamination rate with no change in the detection rate or time.  (+info)

A murein hydrolase is the specific target of bulgecin in Escherichia coli. (4/60)

A deletion in the structural gene for the soluble lytic transglycosylase, the predominant murein hydrolase in the soluble fraction of Escherichia coli, has been constructed. The mutant grows normally but exhibits increased sensitivity toward mecillinam, a beta-lactam specific for penicillin-binding protein 2. In the presence of furazlocillin or other beta-lactams with a specificity for penicillin-binding protein 3 which normally cause filamentation, bulges were formed prior to rapid bacteriolysis. Similar morphological alterations are known to develop in wild type E. coli cells when furazlocillin is combined with bulgecin, an antibiotic of unusual glucosaminyl structure. It turned out that bulgecin specifically inhibits the Sl-transglycosylase in a noncompetitive manner. Since bulgecin shows some structural analogy to the murein subunits we postulate that the soluble lytic transglycosylase, in addition to its active site, has a recognition site for specific murein structures. The possibility of an allosteric modulation of the activity of the enzyme by changes in the structure of the murein sacculus is discussed.  (+info)

Structure-activity relationships of different beta-lactam antibiotics against a soluble form of Enterococcus faecium PBP5, a type II bacterial transpeptidase. (5/60)

Penicillin-binding proteins (PBPs) catalyze the essential reactions in the biosynthesis of cell wall peptidoglycan from glycopeptide precursors. beta-Lactam antibiotics normally interfere with this process by reacting covalently with the active site serine to form a stable acyl-enzyme. The design of novel beta-lactams active against penicillin-susceptible and penicillin-resistant organisms will require a better understanding of the molecular details of this reaction. To that end, we compared the affinities of different beta-lactam antibiotics to a modified soluble form of a resistant Enterococcus faecium PBP5 (Delta1-36 rPBP5). The soluble protein, Delta1-36 rPBP5, was expressed in Escherichia coli and purified, and the NH(2)-terminal protein sequence was verified by amino acid sequencing. Using beta-lactams with different R1 side chains, we show that azlocillin has greater affinity for Delta1-36 rPBP5 than piperacillin and ampicillin (apparent K(i) = 7 +/- 0.3 microM, compared to 36 +/- 3 and 51 +/- 10 microM, respectively). Azlocillin also exhibits the most rapid acylation rate (apparent k(2) = 15 +/- 4 M(-1) s(-1)). Meropenem demonstrates an affinity for Delta1-36 rPBP5 comparable to that of ampicillin (apparent K(i) = 51 +/- 15 microM) but is slower at acylating (apparent k(2) = 0.14 +/- 0.02 M(-1) s(-1)). This characterization defines important structure-activity relationships for this clinically relevant type II transpeptidase, shows that the rate of formation of the acyl-enzyme is an essential factor determining the efficacy of a beta-lactam, and suggests that the specific side chain interactions of beta-lactams could be modified to improve inactivation of resistant PBPs.  (+info)

Invalidity for Pseudomonas aeruginosa of an accepted model of bacterial permeability to beta-lactam antibiotics. (6/60)

The accepted model for the penetration of beta-lactam antibiotics into gram-negative bacteria is that proposed by Zimmermann and Rosselet (Antimicrob. Agents Chemother. 12:368-372, 1977). The model assumes (i) that diffusion of the antibiotic molecules across the outer membrane obeys Fick's law and can be characterized by a permeability constant for any given combination of organism and drug, (ii) that drug hydrolysis within the periplasm obeys Michaelis-Menten kinetics, and (iii) that a steady state is rapidly attained between drug uptake and hydrolysis. The model has allowed accurate prediction of antibiotic MICs for Escherichia coli strains from a knowledge of their beta-lactamase production and permeability characteristics. It has been suggested that the model is inappropriate for Pseudomonas aeruginosa, but attempts to confirm this have been bedevilled by experimental difficulties in estimating permeability coefficients for this species. In the present study, we tested a prediction of the model that the overall resistance of P. aeruginosa transconjugants containing a plasmid-encoded beta-lactamase should continue to depend partly on permeability. Transconjugants with PSE-4 beta-lactamase were constructed in host strains with widely different levels of intrinsic, presumably impermeability-determined resistance. Contrary to the prediction of the model, all the transconjugants developed identical overall levels of resistance to substrate beta-lactams, such as azlocillin and cefoperazone, irrespective of the initial levels of intrinsic resistance of the recipient strains. We conclude that the model is inappropriate for P. aeruginosa, and possible explanations for the organism's behavior are discussed.  (+info)

Partitioning of a mini-F plasmid into anucleate cells of the mukB null mutant. (7/60)

The partition-proficient mini-F plasmid pXX325 was stably maintained in the mukB null mutant, which is defective in chromosome partitioning into the two daughter cells. In the null mutant, the plasmid was partitioned into both nucleate and anucleate daughter cells, independently of host chromosomes.  (+info)

Contrasting patterns of phylogeographic relationships in sympatric sister species of ironclad beetles (Zopheridae: Phloeodes spp.) in California's Transverse Ranges. (8/60)

 (+info)

*Azlocillin

... is considered a broad spectrum antibiotic and can be used against a number of Gram positive and Gram negative ... Azlocillin is an acylampicillin antibiotic with an extended spectrum of activity and greater in vitro potency than the carboxy ... Azlocillin is similar to mezlocillin and piperacillin. It demonstrates antibacterial activity against a broad spectrum of ... 0.03 μg/mL - 2 μg/mL Pseudomonas aeruginosa 4 μg/mL - 6.25 μg/mL An interesting alternative synthesis of azlocillin involves ...

*Difloxacin

Azlocillin, cimetidine and probenecid increase blood levels of difloxacin. Compounds (i.e. sucralfate, antacids, multivitamins ...

*Imidazolidinone

Drugs featuring this ring system include emicerfont, imidapril, and azlocillin. Dimethylol ethylene urea is the reagent used in ...

*Mezlocillin

The closely related analogue azlocillin is made in essentially the same manner as mezlocillin. but with omission of the ...

*List of MeSH codes (D03)

... azlocillin MeSH D03.438.260.825.750.050.500 --- mezlocillin MeSH D03.438.260.825.750.050.650 --- piperacillin MeSH D03.438. ... azlocillin MeSH D03.605.084.737.750.050.500 --- mezlocillin MeSH D03.605.084.737.750.050.650 --- piperacillin MeSH D03.605. ...

*Pseudomonas aeruginosa

... azlocillin, and piperacillin). P. aeruginosa is intrinsically resistant to all other penicillins. carbapenems (meropenem, ...

*Ureidopenicillin

There are three ureidopenicillins in clinical use: Azlocillin Piperacillin Mezlocillin They are mostly ampicillin derivatives ...

*List of β-lactam antibiotics

Azlocillin Mezlocillin Piperacillin Cefazolin Cephalexin Cephalosporin C Cephalothin Cefaclor Cefamandole Cefuroxime Cefotetan ...

*List of MeSH codes (D02)

... azlocillin MeSH D02.065.589.099.750.750.050.500 --- mezlocillin MeSH D02.065.589.099.750.750.050.650 --- piperacillin MeSH ...

*Extended-spectrum penicillin

Ureidopenicillins Azlocillin Mezlocillin Piperacillin Carboxypenicillins Ticarcillin (generally in the combination ticarcillin/ ...

*Ampicillin

Amoxycillin (p-hydroxy metabolite of ampicillin) Pivampicillin (special pro-drug of ampicillin) Azlocillin and pirbenicillin ( ...

*List of drugs: As-Az

Azlin azlocillin (INN) Azmacort Azo Gantanol Azo Gantrisin Azolid azolimine (INN) Azopt azosemide (INN) azotomycin (INN) ...

*ATC code J01

J01CA04 Amoxicillin J01CA05 Carindacillin J01CA06 Bacampicillin J01CA07 Epicillin J01CA08 Pivmecillinam J01CA09 Azlocillin ...

*Timeline of antibiotics

... azlocillin 1977 - cefadroxil 1977 - cefamandole 1977 - cefoxitin 1977 - cefuroxime 1977 - mezlocillin 1977 - pivmecillinam 1979 ...
The in vitro activity of cefepime was compared to that of ceftazidime, ceftriaxone, and cefotaxime in a multicenter study involving 10 clinical microbiology laboratories and clinical isolates from 18 Brazilian hospitals from 7 cities (4 states). A total of 982 isolates consecutively collected between December 1995 and March 1996 were susceptibility tested by using Etest and following the NCCLS procedures for agar diffusion tests. The cefepime spectrum was broader than that of the other broad-spectrum cephalosporins against both Gram-negative rods and Gram-positive cocci. Cefepime tons particularly move active against Enterobacter sp. (MIC90, 2 mu g/ml), Serratia sp. (MIC90, 2 mu g/ml) and oxacillin-susceptible Staphylococcus aureus (MIC90, 3 mu g/ml). Against Pseudomonas aeruginosa, cefepime (MIC90 16 mu g/ml) was slightly more active than ceftazidime (MIC90 32 mu g/ml) and 8- to 16-fold more active than ceftriaxone or cefotaxime (MIC90 ,256 mu g/ml). Our results show that nosocomial bacteria, ...
This study examined the effects of fasting in patients with acute heart failure (AHF) using data from a large multi-center heart failure registry. Effect of dietary tadalafil prix en pharmacie fat in isocaloric rations on the nitrogen content of milk from Holstein cows. Changing epidemiology of pediatric Staphylococcus aureus bacteremia in Denmark from 1971 through 2000. The isolated and hydrogen bonded groups are the most important as these readily exchange with D(2)O and thus are exposed to reactant molecules.. In the other 3 patients azlocillin levels of 23 and 39 micrograms/ml and moderate bactericidal activity against P. The plasma membrane of eukaryotic cells tadalafila is the limit to interact with the environment. Primary bladder stone is a common pediatric surgical problem in developing countries.. Dentists reflected that their VIG session had been insightful and considered the review process as beneficial to communication skills training in dentistry. The objective of this study was to ...
The design and implementation of a new input switching capacitive microaccelerometer interface circuit with /spl mu/g resolution is presented. The accelero
Two different strains of Escherichia coli exhibiting unusual patterns of resistance to beta-lactam antibiotics were isolated from patients at Cochin Hospital. Both isolates showed a low level of resistance to amoxycillin, ticarcillin and ureidopenicillins but were susceptible to cephalosporins, aztreonam and imipenem; beta-lactamase inhibitors potentiated the activities of the beta-lactams to only a limited extent. All resistance characteristics of the strains were transferable by conjugation to E. coli K12. Resistance was shown to be due to beta-lactamases of pI 5.20 and relative molecular masses of 24,000. The hydrolytic and inhibition profiles of these enzymes were similar to each other but differed from those of broad-spectrum beta-lactamases (TEM-1). The rates of hydrolysis (Vmax) of amoxycillin (c. 200%) were higher than that for TEM-1 (84%). Ticarcillin, ureidopenicillins and cephaloridine were hydrolyzed slowly. However, as for TEM-1, no hydrolysis was observed with cefoxitin, third generation
beipackzettel ciprofloxacin prednisolone 20 mg zentiva betamethasone cialis yellow pills remedio original. online blood in urine accutane is it allowed.European Scientific Journal November 2015 edition vol.11 CHRONIC URINARY TRACT INFECTION: ETIOLOGICAL AGENTS AND SUSCEPTIBILITY TESTING Dr. Nawal S. Faris 0 0.Ciprofloxacin; Amikacin; Aminoglycosides; Azlocillin; Aztreonam; Anti-Infective Agents; Phenazines; Cephalosporins; Polymyxins; Piperacillin; Siderophores; Hydrogen.Ciprofloxacine; Norfloxacine; Ofloxacine; Macrolides: azithromycine; Rifamycine; Antiglaucomateux. Voie générale. Inhibiteur de lanhydrase carbonique.toutou ÉnergisÉ tout tout guÉrit ♥ ♥ angel mascotte ♥ ♥ du. les animaux sont de petits anges envoyÉs sur la terre pour aider les humains qui souffrent.Looking for a cefixime? Not a problem! Guaranteed Worldwide Shipping Discreet Package Low Prices 24/7/365 Customer Support 100% Satisfaction Guaranteed. Visit This ...
Thin Al foils of 50 mu g/cm/sup 2/ thickness were implanted with /sup 4/He ions with fluences ranging between 10/sup 17/ and 10/sup 18/ atoms/cm/sup 2/. The bulk He contents was measured by the Rutherford backscattering method. The He implantation profile versus depth was obtained by elastic recoil detection analysis. He-implanted targets will be used to measure ( alpha , gamma ) reactions of astrophysical interest, in inverse kinematics. ...
Read "Conserved genomes of ΦKMV-like bacteriophages (T7 supergroup) active on Pseudomonas aeruginosa, Russian Journal of Genetics" on DeepDyve, the largest online rental service for scholarly research with thousands of academic publications available at your fingertips.
Objectives: Exposure to fine particles in urban air has been associated with a number of negative health effects. High levels of fine particles have been detected at underground stations in big cities. We investigated the exposure conditions in four occupational groups in the Stockholm underground train system to identify high-exposed groups and study variations in exposure.. Methods: PM1 and PM2.5 were measured during three full work shifts on 44 underground workers. Fluctuations in exposure were monitored by a real-time particle monitoring instrument, pDR, DataRAM. Qualitative analysis of particle content was performed using inductively coupled plasma mass spectrometry. Nitrogen dioxide was measured using passive monitors.. Results: For all underground workers, the geometric mean (GM) of PM1 was 18 mu g/m(3) and of PM2.5 was 37 mu g/m(3). The particle exposure was highest for cleaners/platform workers, and the GM of PM1 was 31.6 mu g/m(3) [geometric standard deviation (GSD), 1.6] and of PM2.5 ...
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PubMed comprises more than 30 million citations for biomedical literature from MEDLINE, life science journals, and online books. Citations may include links to full-text content from PubMed Central and publisher web sites.
to produce (somebody) appear absurd or stupid. He produced an actual idiot of her by promising to marry her and afterwards leaving her when he had expended all her income. iemand belaglik maak; iemand vir die gek hou يَجْعَلُه أضْحوكَةً правя на глупак fazer de tolo dělat si blázny z jemanden zum Narren halten gøre en til grin; gøre nar af en γελοιοποιώ poner en ridículo narriks tegema احمق جلوه دادن saattaa jk naurunalaiseksi rendre ridicule לְשָׁטוֹת किसी को बेवकूफ बनाना praviti budalu od nekoga bolonddá tesz vkit mengejek, memperolok-olokkan, mengelabui gera að fileífli farsi gioco di ばかにする 바보 취급하다 pastatyti į kvailio padėtį apmuļķot; nostādīt kādu muļķīgā stāvoklī memperbodoh-bodohkan voor gek zetten latterliggjøre robić durnia z, wystrychnąć na dudka احمقی fazer de parvo a-şi bate joc de одурачить robiť si blázna z osmešiti ...
BioAssay record AID 165188 submitted by ChEMBL: In vitro antibacterial activity of compound was measured on Pseudomonas aeruginosa IAM 1095.
Groups of four adult male rats [ZUR:SIV -Z] were pretreated with corn oil (control; 2 ml/kg/day i. p. for 3 days), trans-stilbene-oxide (SO; 200 mg/kg/day i. p. for 2 days), 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD; 10 \(\mu\)g/kg i. p. once, 4 days before killing), phenobarbital (PB; 1 gjliter in the drinking water for 8 days), and dieldrin (20 mg/kg/day i. p. for 3 or 9 days). They received an injection of [G-\(^3\)H]benzo(a)pyrene (BaP, 31 \(\mu\)g/kg, 7.4. 10\(^9\) dpm/kg; i. v.) 16 h before killing. In the liver of each rat, five enzymatic activities and the covalent binding of BaP to DNA have been determined. The rnicrosomal aryl hydrocarbon monooxygenase activity (AHM) ranged frorn 75% of control (SO) to 356% (TCDD), the nuclear AHM from 63% (SO) to 333% (TCDD). Microsomal epoxide hydrolase activity (EH) was induced up to 238% (PB), nuclear EH ranged from 86% (TCDD) to 218% (PB). A different extent of induction was observed in the two compartments. Highest induction of glutathione ...
In this work, we have investigated theoretically the structure/hyperpolarizability correlations of push-pull molecules sing a two-form two-state model. For this, we have defined a parameter MIX characterizing the mixing between the two-limiting resonance forms and thus ruling the molecular structure and polarization. Also, we have analyzed the solvent effect on the structure and on the polarizabilities of push-pull molecules using the Onsager reaction field theory. We have shown that the dependences of the linear and nonlinear polarizabilities on the solvent dielectric constant look similar to the structure/(hyper)polarizability correlations. Finally, we have investigated experimentally the solvent effect on a series of push-pull polyenes of increasing length. In particular, we have determined the scalar (mu) g(Beta) (0) product (where (mu) g is the ground-state dipole and (Beta) (0) the vector part of static quadratic hyperpolarizability tensor) in different solvents using the ...
Takei Y, however, is often short meidcation so take into account side-effects such as proximal myopathy and poor wound healing. Opal SM, Jhung JW, Keith JC Jr, et al Recombinant human interleukin-11 in experimental Pseudomonas aeruginosa sepsis in immunocompromised animals. The size of the system and the amount of in-house (vs.
Looking for online definition of mezlocillin in the Medical Dictionary? mezlocillin explanation free. What is mezlocillin? Meaning of mezlocillin medical term. What does mezlocillin mean?
The main focus of this study is to mechanistically introduce a new qualitative and quantitative technique for mapping the lipid profile of a sectional brain via non-catalytic transesterification reaction (i.e., pseudo catalytic reaction in the presence of porous materials). One of the biggest technical advances achieved in this study is the qualitative and quantitative analysis of lipid from bovine brain in trace quantities in the magnitude of mu g via the non-catalytic pathway. Moreover, newly introduced derivatization in this work showed high tolerance against impurities (i.e., water and extractives ...
PubMed comprises more than 30 million citations for biomedical literature from MEDLINE, life science journals, and online books. Citations may include links to full-text content from PubMed Central and publisher web sites.
Increasing the stability and lifetime of the electrodes is one of the most important factors in order to realise a large scale use of polymer electrolyte membrane fuel cells (PEMFC). By using well-defined thin-film model electrodes, the stability of Pt and Pt on Ir were examined as cathode catalysts in a single cell PEMFC setup. The electrodes were fabricated by evaporating thin layers of Pt and Pt on Ir onto the microporous layer of a gas diffusion layer. The amount of Pt deposited was equivalent to 3 nm (about 6.3 mu g cm(-2)) and the amount of Ir was varied between 1.5 nm and 20 nm (between 3.4 mu g cm(-2) and 45.3 mu g cm(-2)). All samples with Ir showed an increased stability over samples with sole Pt during cyclic corrosion test between 0.6V and 1.2V vs. the reversible hydrogen electrode. For thin layers of Ir, the initial activity for the oxygen reduction reaction was equal to or superior to that of sole Pt but for thicker Ir films it was somewhat lower. Hydrogen underpotential deposition ...
Objective: The paper describes the results of a polycentric study for the assessment of reference values of urinary chromium (U-Cr) in the Italian population. Method: A total of 890 subjects (58.3% males and 41.7% females) were selected on the basis of standardized criteria in eight different areas of Italy. Urinary chromium was determined on morning spot samples collected using standardized procedures. The U-Cr was determined independently by three laboratories using an Electrothermic atomization-Atomic Absorption Spectrometry (ETA-AAS) method with a detection limit of 0.05 mu g/l, adopting - for the statistical analysis - the median value of the results of the three laboratories. The between-laboratories within-subjects standard deviation was 0.049 mu g/l. Due to the high proportion (approx. 28%) of undetectable chromium levels, the geometric mean (GM) and geometric standard deviation (GSD) were estimated using a procedure of linear interpolation. The analysis of the effects of some variables ...
Fourteen people graded their aches and pains and general health for 28 days. They then took either up to 500 mu g of molybdenum as amino acid chelate per day, or placebo for the next 28 days, while they continued their records. The groups were crossed over for a third 28-day period. Their aches and pains improved on molybdenum (significant at the 0.05 level). Their general health also improved on molybdenum (significant at the 0.025 level). Suggestions are made for categories of people who may benefit from molybdenum supplementation, and for areas of further research.. ...
Fourteen people graded their aches and pains and general health for 28 days. They then took either up to 500 mu g of molybdenum as amino acid chelate per day, or placebo for the next 28 days, while they continued their records. The groups were crossed over for a third 28-day period. Their aches and pains improved on molybdenum (significant at the 0.05 level). Their general health also improved on molybdenum (significant at the 0.025 level). Suggestions are made for categories of people who may benefit from molybdenum supplementation, and for areas of further research.. ...
Multidrug-resistant tuberculosis (TB) threatens TB control worldwide. The microscopic observation drug susceptibility (MODS) assay is a low-cost, high-performance TB diagnostic tool for rapid liquid culture and direct isoniazid and rifampicin drug susceptibility testing (DST). The objective of this study was to explore the potential for extending the MODS assay to rapid second-line DST and to identify critical concentrations of candidate drugs for prospective testing. Sputum samples from 94 TB culture-positive patients receiving second-line TB agents were cultured following standardised MODS protocols, with a range of titrations of antimicrobial drugs added. Critical concentrations were determined using a modified Kaplan-Meier survival curve analysis. Candidate critical concentrations were determined for capreomycin (10 mu g.mL(-1)), ciprofloxacin (1.25 mu g.mL(-1)), cycloserine (40 mu g.mL(-1)), ethambutol (10 mu g.mL(-1)), ethionamide (5 mu g.mL(-1)), kanamycin (5 mu g.mL(-1)) ...
TY - JOUR. T1 - High-pressure liquid chromatographic assay of cefotaxime and desacetylcefotaxime in human myometrium. AU - Bawdon, R. E.. AU - Novick, W. J.. AU - Hemsell, D. L.. AU - Welch, W. D.. PY - 1984. Y1 - 1984. N2 - An analytic high-pressure liquid chromatographic (HPLC) procedure for the assay of desacetylcefotaxime and cefotaxime in gynecologic tissue was developed. Normal individuals undergoing elective hysterectomy were subjects in this study. Blood and myometrium were removed up to four hours after a l-g intramuscular dose of cefotaxime. Since cefotaxime is unstable in homogenized tissue at room temperature, the specimens must be maintained at 4 degree C during homogenization and extraction. Mean serum desacetylcefotaxime and cefotaxime levels were 3. 2 plus or minus 2. 0 mu g/ml and 6. 8 plus or minus 4. 4 mu g/ml, respectively. The mean myometrium concentrations of desacetylcefotaxime and cefotaxime were 8. 4 plus or minus 10. 0 mu g/g and 6. 3 plus or minus 8. 9 mu g/g, ...
The present study was undertaken to investigate the antioxidative and anti-inflammatory activities of the extract of the flower of Campsis grandiflora (Thunb.) K. Schum. Exposure of human dermal fibroblasts to 50% EtOH extract of Campsis grandiflora flower (ECG) at 10 and 100 mu g/ml showed significant protective effect against hydrogen peroxide (300 mu M). ECG not only protected cell survival from H2O2-induced toxicity, but also inhibited the H2O2-induced leakage of lactate dehydrogenase (LDH) enzyme release and DNA fragmentation significantly. It was also found that ECG showed scavenging activities of radicals and reactive oxygen species with IC50 values of 20 mu g/ml against 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical and 52 mu g/ml against superoxide radicals in the xanthine/xanthine oxidase system, respectively. Topically applied ECG dose-dependently inhibited arachidonic acid (AA)- and 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced ear edema in mice. Consistent with its antioxidative ...
phospho-N-acetylmuramoyl pentapeptide transferase: enzyme important in murein synthesis which transfers the N-acetylmuramoylpentapeptide to a membrane-bound carrier that is a C-55 terpene alcohol phosphate; minor descriptor (75-84); on-line & Index Medicus search PHOSPHOTRANSFERASES (75-84)
Penicillin Penicillin is a group of antibiotic Benzylpenicillin penicillin G Benzylpenicilloyl-polylysine (BPP) Phenoxymethyl penicillin s penicillin V Semi-synthetic Penicillins Methicillin Nafcillin Cloxacillin Dicloxacillin Ampicillin Amoxicillin Bacampicillin Pivampicillin Carbenicillin Ticarcillin Azlocillin Mezlocillin Piperacillin Hetacillin Penicillins approved for veterinary use
The objective of this study was to evaluate the sub-lethal toxicity of hexabromocyclododecane (HBCDD) in fish. Adult Chinese rare minnows as in vivo models were exposed to waterborne HBCDD from 1 to 500 mu g/l for 14, 28 and 42 days. Hepatic CYP1A1 (ethoxyresorufin-O-deethylase, EROD) and CYP2B1 (pentaoxyresorufin-O-depentylase, PROD) activities were measured. At the same time, molecular biomarkers of oxidative stress were also assayed in the brain, including reactive oxygen species (ROS), lipid peroxidation products (thiobarbituric acid-reactive substances, TBARS), DNA damage and protein carbonyl, as well as superoxide dismutase (SOD) activity and glutathione (GSH) content. DNA damage was evaluated using the Comet assay on erythrocytes. Besides, the content of HBCDD in whole fish was determined after 42 days exposure. The results show that HBCDD could induce EROD and PROD at 500 mu g/l after 28 days exposure, and at 100 to 500 mu g/l after 42 days exposure (P < 0.05), respectively. ROS ...
Biochemical analyses can point to toxicant presence before its effects can be detected at higher organizational levels. We investigated responses of larval mass and alkaline phosphatase (ALP) to different cadmium treatments in 4th instar gypsy moth larvae from 20 full-sib families. Changes in trait values and trait plasticities as well as their variation were monitored after acute and chronic exposure or recovery from two cadmium concentrations (Cd(1) = 10 mu g and Cd(2) = 30 mu g Cd/g dry food). Larval mass only decreased, without returning to the control level at recovery stage following chronic cadmium challenge. Acute stress did not change trait value but increased genetic variance of larval mass. Significant ALP activity changes, sensitivity of isozyme patterns (Mr of 60, 64, and 85 kDa) and increased variation in ALP plasticity during acute exposure to cadmium point to its possible aplication as an exposure biomarker. (C) 2008 Elsevier Inc. All rights reserved ...
September 2016 - BronchUK team publish on Pseudomonas and microbial cross infection and evolution in bronchiectasis in the European respiratory ...
The galactose specific lectin LecA partly mediates the formation of antibiotic resistant biofilms by Pseudomonas aeruginosa, an opportunistic pathogen causing lethal airways infections in immunocompromised and cystic fibrosis patients, suggesting that preventing LecA binding to natural saccharides might prov Multivalent Biomolecular Recognition
In order to optimize culture conditions of bovine pulmonary endothelial cells (CPAE), we have compared different culture media, supports and extracellular matrices. Cell biomass was estimated by protein assay using Lowrys method. Different constituents including albumin, hydrocortisone, insulin, transferrin, triiodotyronine, Epidermal Growth Factor (EGF) and Fibroblast Growth Factor were separately added to Basal Defined Medium (BDM). Among them, BDM supplemented with EGF (1 ng/ml), hydrocortisone (100 nM), insulin (1 mu g/ml), triiodotyronine (2 nM) and linoleic acid complexed to albumin (10 mu g/ml) also named synthetic BDM appeared to be the best serum-free nutritive medium and showed similar results as compared to DMEM supplemented with 10% Fetal Bovine Serum (FBS). Several supports have then been tested including tissue culture polystyrene (as a reference), teflon, polycarbonate or poly(ethylene terephthalate) track-etched membranes. Among them, cells cultivated on surface treated ...
Purpose: To define a mitotane dose for pediatric patients with adrenocortical cancer (ACC) that maintains therapeutic plasma levels (TL) between 14 and 20 mu g/mL and to verify its antitumor efficacy in association with 8 cycles of cisplatin, etoposide, and doxorubicin (CED). Methods: Powdered mitotane was dissolved in a medium chain triglyceride oil and administered to 11 children with ACC (2.4 to 15.4 y of age); an initial low dose was increased to 4 g/m(2)/d. Ten of the 11 children had a germline TP53 R337H mutation. Mitotane plasma levels were determined using high-performance liquid chromatography. Results: The mitotane dose to maintain TL in 7 patients ranged from 1.0 to 5.3 g/m(2)/d. Six children reached mitotane levels of 10 mu g/mL in 3.6 months (1.5 to 5.0mo), whereas 5 children took 8 months (6.5 to 12.5 mo). Minor to partial tumor remission was found in 5 patients (, 1 y) and complete remission was found in 2 patients. Of the 3 patients who are alive at the time of report, 1 patient ...

Patent US8883213 - Ion exchange resin treated to control swelling - Google PatentsPatent US8883213 - Ion exchange resin treated to control swelling - Google Patents

... azlocillin, bacampicillin, cefamandole, cefonicid, cefotaxime, cefotetan, cefoxitin, ceftriaxone, mezlocillin and piperacillin ... azlocillin, bacampicillin, cefamandole, cefonicid, cefotaxime, cefotetan, cefoxitin, ceftriaxone, mezlocillin, piperacillin, ... azlocillin, bacampicillin, cefamandole, cefonicid, cefotaxime, cefotetan, cefoxitin, ceftriaxone, mezlocillin, piperacillin, ... azlocillin, bacampicillin, cefamandole, cefonicid, cefotaxime, cefotetan, cefoxitin, ceftriaxone, mezlocillin, piperacillin, ...
more infohttp://www.google.com.au/patents/US8883213

Azlocillin - WikipediaAzlocillin - Wikipedia

Azlocillin is considered a broad spectrum antibiotic and can be used against a number of Gram positive and Gram negative ... Azlocillin is an acylampicillin antibiotic with an extended spectrum of activity and greater in vitro potency than the carboxy ... Azlocillin is similar to mezlocillin and piperacillin. It demonstrates antibacterial activity against a broad spectrum of ... 0.03 μg/mL - 2 μg/mL Pseudomonas aeruginosa 4 μg/mL - 6.25 μg/mL An interesting alternative synthesis of azlocillin involves ...
more infohttps://en.wikipedia.org/wiki/Azlocillin

Azlocillin - Substance Information - ECHAAzlocillin - Substance Information - ECHA

Here you can find all of the regulations and regulatory lists in which this substance appears, according to the data available to ECHA. This substance has been found in the following regulatory activities (directly, or inheriting the regulatory context of a parent substance):. ...
more infohttps://echa.europa.eu/substance-information/-/substanceinfo/100.048.483

Azlocillin sodium | definition of azlocillin sodium by Medical dictionaryAzlocillin sodium | definition of azlocillin sodium by Medical dictionary

... azlocillin sodium explanation free. What is azlocillin sodium? Meaning of azlocillin sodium medical term. What does azlocillin ... Looking for online definition of azlocillin sodium in the Medical Dictionary? ... azlocillin sodium. azlocillin sodium. [az′lōsil′in] a semisynthetic penicillin antibiotic. indications It is prescribed for ... Azlocillin sodium , definition of azlocillin sodium by Medical dictionary https://medical-dictionary.thefreedictionary.com/ ...
more infohttp://medical-dictionary.thefreedictionary.com/azlocillin+sodium

Azlocillin and Mezlocillin: New Ureido Penicillins | Antimicrobial Agents and ChemotherapyAzlocillin and Mezlocillin: New Ureido Penicillins | Antimicrobial Agents and Chemotherapy

Azlocillin and Mezlocillin: New Ureido Penicillins Message Subject (Your Name) has forwarded a page to you from Antimicrobial ... Azlocillin and mezlocillin were less active than cefazolin against β-lactamase-producing E. coli and Klebsiella strains but ... Azlocillin and Mezlocillin: New Ureido Penicillins. Kwung P. Fu, Harold C. Neu ... The activity of azlocillin and mezlocillin, new semisynthetic ureido penicillins, was investigated and compared with that of ...
more infohttps://aac.asm.org/content/13/6/930.short

Antifection<...Antifection<...

Azlocillin sodium salt Catalog No. A16422. Quick View .category-products .products-list .btn-quickcart { background: white; ... Azlocillin is an acylampicillin with a broad spectrum against bacteria. Learn More ...
more infohttps://www.adooq.com/antifection.html

Bupropion (Oral Route) Side Effects - Mayo ClinicBupropion (Oral Route) Side Effects - Mayo Clinic

Check with your doctor before using this medicine with alcohol or other medicines that affect the central nervous system (CNS). The use of alcohol or other medicines that affect the CNS with bupropion may worsen the side effects of this medicine, such as dizziness, poor concentration, drowsiness, unusual dreams, and trouble with sleeping. Some examples of medicines that affect the CNS are antihistamines or medicine for allergies or colds, sedatives, tranquilizers, or sleeping medicines, medicine for depression, medicine for anxiety, prescription pain medicine or narcotics, medicine for attention deficit and hyperactivity disorder, medicine for seizures or barbiturates, muscle relaxants, or anesthetics, including some dental anesthetics. Bupropion may cause some people to be agitated, irritable, or display other abnormal behaviors. It may also cause some people to have suicidal thoughts and tendencies, or to become more depressed. Make sure the doctor knows if you have trouble sleeping, get upset ...
more infohttps://www.mayoclinic.org/drugs-supplements/bupropion-oral-route/side-effects/drg-20062478?p=1

Aplenzin Advanced Patient Information - Drugs.comAplenzin Advanced Patient Information - Drugs.com

Detailed drug Information for Aplenzin. Includes common brand names, drug descriptions, warnings, side effects and dosing information.
more infohttps://www.drugs.com/cons/aplenzin.html

Bupropion (Oral Route) Before Using - Mayo ClinicBupropion (Oral Route) Before Using - Mayo Clinic

Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.. Using this medicine with any of the following medicines is not recommended. Your doctor may decide not to treat you with this medication or change some of the other medicines you take.. ...
more infohttps://www.mayoclinic.org/es-es/drugs-supplements/bupropion-oral-route/before-using/drg-20062478

Aricept Advanced Patient Information - Drugs.comAricept Advanced Patient Information - Drugs.com

Detailed drug Information for Aricept. Includes common brand names, drug descriptions, warnings, side effects and dosing information.
more infohttps://www.drugs.com/cons/aricept.html

Culture media for clinical diagnosis (2)Culture media for clinical diagnosis (2)

Condalab offers a wide range of culture media for routine clinical diagnosis, CE marked for IVD, as well as a wide range of chromogenic media for quick and easy bacterial identification, or the reagents needed to perform antibiograms and specific culture media for the detection of bacterial resistance to antibiotics. Our products can be found in both forms: Dehydrated powder and ready to use. Their packaging guarantees their innocuousness, so important in the diagnosis of infectious diseases. Their easy use combined with an optimal recovery and differentiation of pathogens make our culture media and reagents the best ally for daily clinical practice.
more infohttps://www.condalab.com/int/en/4101-culture-media-for-clinical-diagnosis?page=2

ID - ABx Flashcards by Michael Salgado | BrainscapeID - ABx Flashcards by Michael Salgado | Brainscape

Use Pipercillin, ticarcillin, azlocillin mezlocillin for? Gram negatives, enterobacteria, pseudomonads #Cholecystitis, ...
more infohttps://www.brainscape.com/flashcards/id-abx-2837877/packs/1779975

Sodium Citrate Factory - Sodium Citrate Factory Suppliers, Buyers, Wholesalers and Manufacturers - ecplaza.netSodium Citrate Factory - Sodium Citrate Factory Suppliers, Buyers, Wholesalers and Manufacturers - ecplaza.net

Factory Supply High Quality Antibiotic AZLOCILLIN SODIUM CAS:37091-65-9 Basic Info. Name:AZLOCILLIN SODIUM Synonym:Azlocillin; ... Factory Supply High Quality Antibiotic AZLOCILLIN SODIUM CAS:37091-65-9. ...
more infohttps://www.ecplaza.net/sodium-citrate-factory--everything

Difloxacin - WikipediaDifloxacin - Wikipedia

Azlocillin, cimetidine and probenecid increase blood levels of difloxacin. Compounds (i.e. sucralfate, antacids, multivitamins ...
more infohttps://en.wikipedia.org/wiki/Difloxacin

Abbreviations and Conventions | Journal of Clinical MicrobiologyAbbreviations and Conventions | Journal of Clinical Microbiology

Statistical analysis of data is a crucial component of scientific publication. Authors who are unsure of proper statistical analysis should have their manuscripts checked by a qualified statistician.. The following is a list of important items that must be considered before manuscript submission. Deficiencies in any of these areas may delay review and/or publication.. (i) The same reference (gold) standard should be used for all samples for a given analyte. That reference standard might include more than one test, but it should be used and interpreted consistently for all samples. The reference standard should not include results from the test that is under study.. (ii) Do not use sensitivity or specificity to describe results which compare a new test to a non-reference standard. Use the terms positive percent agreement and negative percent agreement for these results, as recommended by the FDA guidance document Statistical Guidance on Reporting Results from Studies Evaluating ...
more infohttps://jcm.asm.org/content/abbreviations-and-conventions

Exam 4 Flashcards by Michael Renecle | BrainscapeExam 4 Flashcards by Michael Renecle | Brainscape

Broad: ampicillin, amoxicillin, piperacillin, ticarcillin and azlocillin. - All beta-lactamase sensitive except for methicillin ...
more infohttps://www.brainscape.com/flashcards/exam-4-4316967/packs/6040369

Category:Penicillin antibiotics - Wikimedia CommonsCategory:Penicillin antibiotics - Wikimedia Commons

penicilina (es); Penisillín (is); Penisilin (ms); Penicillin (en-gb); پنسلين (ps); Пеницилин (bg); پنسلین (pnb); پنسلین (ur); Benseliin (so); Penicilín (sk); Penicillina (oc); 青黴素 (zh-hant); Penicilino (io); Penicilline (gsw); 페니실린 (ko); পেনিচিলিন (as); penicilino (eo); пеницилин (mk); Penicilin (bs); Penicilina (an); পেনিসিলিন (bn); pénicilline (fr); Penisilin (jv); Penicilin (hr); پینی سیلین (lrc); פעניצילין (yi); पेनिसिलिन (mr); penicillin (vi); Penicilīni (lv); Penisillien (af); пеницилин (sr); penicilin (cs); Penicilina (pt-br); Penicillin (sco); Пенициллин (mn); penicillin (nn); penicillin (nb); Pénisilin (su); πενικιλίνη (el); Penicillin (fo); ಪೆನ್ಸಿಲಿನ್ (kn); پێنیسیلین (ckb); penicillin (en); بنسلين (ar); Penisilin (br); Пенициллин (kk); ပင်နီဆီလင် (my); 盤尼西林 ...
more infohttps://commons.wikimedia.org/wiki/Category:Penicillin_antibiotics

Category:Carboxylic acids - Wikimedia CommonsCategory:Carboxylic acids - Wikimedia Commons

ácido carboxílico (es); Карбон қышқылдары (kk-kz); Asid karboksilik (ms); كاربون قىشقىلدارى (kk-cn); Карбоксилна киселина (bg); کاربوکسلک تیزاب (pnb); 羧酸 (zh-hk); Karboxylová kyselina (sk); карбонові кислоти (uk); 羧酸 (zh-hant); 羧酸 (zh-cn); 카복실산 (ko); Carboxylsýra (fo); karboksilata acido (eo); Карбоксилна киселина (mk); Karboksilne kiseline (bs); কার্বক্সিলিক অ্যাসিড (bn); acide carboxylique (fr); Karboksilne kiseline (hr); axit cacboxylic (vi); كاربون قىشقىلدارى (kk-arab); Karbon qışqıldarı (kk-latn); Karboksielsuur (af); карбоксилна киселина (sr); 羧酸 (zh-sg); Карбон қышқылдары (kk-cyrl); karboksylsyre (nn); karboksylsyre (nb); Asam karboksilat (su); 羧酸 (lzh); ترشی کاربۆکسیلی (ckb); carboxylic acid (en); حمض كربوكسيلي (ar); 羧酸 (yue); ...
more infohttps://commons.wikimedia.org/wiki/Category:Carboxylic_acids?uselang=de

View Mountain Of Black Glass (Otherland, Volume 3) 1999View Mountain Of Black Glass (Otherland, Volume 3) 1999

... create with your azlocillin Retrieved veggies for the several contact! Act! CRM Training is the most important part in CRM ...
more infohttp://actplatinum.com/LivezillaOLD/vcards/library/view-Mountain-of-Black-Glass-%28Otherland%2C-Volume-3%29-1999/

PenicillinPenicillin

Azlocillin Penicillins with beta-lactamase inhibitors. Penicillins may be combined with beta-lactamase inhibitors to increase ... Amoxicillin • Ampicillin • Azlocillin • Carbenicillin • Cloxacillin • Dicloxacillin • Flucloxacillin • Mezlocillin • Nafcillin ...
more infohttps://www.bionity.com/en/encyclopedia/Penicillin.html

ALL PHARM 2 FlashcardsALL PHARM 2 Flashcards

Tetracycline, Demeclocycline. Passive diffusion so broad. ALL bac + protoza. Absorption is prevented by *(Ca, Mg, Fe2+, Al3+)- dairy, antiacids, supplements. Renal and bile clearance. MOA: 30S A site ( inhibits elongation). Doxycycline more lipid soluble so DOC: Vibrio, Spirochete(rickettsia, borrelia) , Mycoplasma, Chlamydiae, Brucella (w/ rifampin). Mino is very water soluble in tears, saliva= asymptomatic meningococcal carriers, Doxy is lipid and not cleared by renal. TCA resistance: pumps increasing efflux, change in ribosome binding site, inactivates enzyme. Adverse: ^^ clostridium, *bone and teeth(enamel hypolasia or permanent tooth discoloration,photosensitivity**, Demeclocycline (ADH receptor blocker used in SIADH, so never used as ATX) ** Quinolones, Sulfonamides (rash due to sun) ...
more infohttps://www.flashcardmachine.com/anti-inflammatorydrugs.html

Antimycotic | definition of antimycotic by Medical dictionaryAntimycotic | definition of antimycotic by Medical dictionary

Systemic ciprofloxacin; ticarcillin + clavulanic acid; azlocillin; piperacillin. Anaerobic infection. Systemic metronidazole ( ...
more infohttps://medical-dictionary.thefreedictionary.com/antimycotic

Penicillin-binding protein 1A - DrugBankPenicillin-binding protein 1A - DrugBank

Azlocillin. approved. yes. inhibitor. Details. DB01066. Cefditoren. approved, investigational. yes. inhibitor. Details. ...
more infohttps://www.drugbank.ca/bio_entities/BE0000576
  • 0.03 μg/mL - 2 μg/mL Pseudomonas aeruginosa 4 μg/mL - 6.25 μg/mL An interesting alternative synthesis of azlocillin involves activation of the substituted phenylglycine analogue 1 with 1,3-dimethyl-2-chloro-1-imidazolinium chloride (2) and then condensation with 6-APA. (wikipedia.org)
  • At a concentration of 25 μg/ml, azlocillin inhibited 74% of Enterobacter , 97% of Proteus mirabilis , 64% of Citrobacter , 91% of Pseudomonas aeruginosa , and 82% of Bacteroides strains tested. (asm.org)
  • These seminal findings strongly suggests that azlocillin can be effective in treating B. burgdorferi sensu stricto JLB31 infection and furthermore in depth research is necessary to evaluate its potential use for Lyme disease therapy. (stanford.edu)
  • A study provides evidence that the drug azlocillin eliminates the bacteria that cause Lyme disease at the onset of infection in lab mice and cultures. (stanford.edu)
  • Azlocillin can be the potential drug candidate against drug-tolerant Borrelia burgdorferi sensu stricto JLB31. (stanford.edu)
  • In order to identify effective drug molecules that kill drug-tolerant borrelia we have tested two antibiotics, azlocillin and cefotaxime that were identified by us earlier. (stanford.edu)
  • The in vitro efficacy studies of azlocillin and cefotaxime on drug-tolerant persisters were done by semisolid plating method. (stanford.edu)
  • Moreover, the combination drug treatment of azlocillin and cefotaxime effectively killed doxycycline-tolerant B. burgdorferi. (stanford.edu)
  • Probenecid and azlocillin increase in the amount of drug in the blood. (helppointhub.com)
  • We find that sulfamethoxypyridazine, azlocillin, hydroflumethiazide, and ifenprodil can be repurposed for the treatment of prostate cancer based on an in silico cell viability assay. (diva-portal.org)
  • Conversely, prior treatment with amdinocillin did not potentiate the efficacy of either azlocillin or cefotaxime in the treatment of mice infected with an Escherichia coli strain that was highly susceptible to all three drugs. (elsevier.com)