The application of high intensity ultrasound to liquids.
A subfield of acoustics dealing in the radio frequency range higher than acoustic SOUND waves (approximately above 20 kilohertz). Ultrasonic radiation is used therapeutically (DIATHERMY and ULTRASONIC THERAPY) to generate HEAT and to selectively destroy tissues. It is also used in diagnostics, for example, ULTRASONOGRAPHY; ECHOENCEPHALOGRAPHY; and ECHOCARDIOGRAPHY, to visually display echoes received from irradiated tissues.
Infections resulting from the implantation of prosthetic devices. The infections may be acquired from intraoperative contamination (early) or hematogenously acquired from other sites (late).
Small encapsulated gas bubbles (diameters of micrometers) that can be used as CONTRAST MEDIA, and in other diagnostic and therapeutic applications. Upon exposure to sufficiently intense ultrasound, microbubbles will cavitate, rupture, disappear, release gas content. Such characteristics of the microbubbles can be used to enhance diagnostic tests, dissolve blood clots, and deliver drugs or genes for therapy.
The use of focused, high-frequency sound waves to produce local hyperthermia in certain diseased or injured parts of the body or to destroy the diseased tissue.
The use of focused, high-frequency sound waves to destroy tissue. It is sometimes used in conjunction with but is distinct from INTERVENTIONAL ULTRASONOGRAPHY.
Artificial substitutes for body parts, and materials inserted into tissue for functional, cosmetic, or therapeutic purposes. Prostheses can be functional, as in the case of artificial arms and legs, or cosmetic, as in the case of an artificial eye. Implants, all surgically inserted or grafted into the body, tend to be used therapeutically. IMPLANTS, EXPERIMENTAL is available for those used experimentally.
A genus of BROWN ALGAE, in the family Alariaceae, native to Japan, Korea, and China. The edible SEAWEED Undaria pinnatifida is also called wakame.
Replacement for an elbow joint.
Techniques to partition various components of the cell into SUBCELLULAR FRACTIONS.
Techniques used in studying bacteria.
Liquids transforming into solids by the removal of heat.
Artificial, single or multilaminar vesicles (made from lecithins or other lipids) that are used for the delivery of a variety of biological molecules or molecular complexes to cells, for example, drug delivery and gene transfer. They are also used to study membranes and membrane proteins.
Techniques used in microbiology.
Procedures for collecting, preserving, and transporting of specimens sufficiently stable to provide accurate and precise results suitable for clinical interpretation.

Isolation of Staphylococcus aureus from sputum in cystic fibrosis. (1/631)

The success in the isolation of Staphylococcus aureus of different methods of sputum processing was investigated in 60 specimens collected from 14 patients with cystic fibrosis during a seven-month period. Fifty specimens (83%) from 11 patients yielded Staph. aureus by one or more methods. Direct plating of purulent portions of sputum on to media designed for general use in respiratory infections gave unsatisfactory results (35% yield of Staph. aureus). Some increase in isolations was obtained with preliminary liquefaction of sputum; but the best results were given by the addition of a medium selective for staphylococci (mannitol salt agar, BBL) or by initial sonication of sputum (each 83% yield). Seven of the 11 strains of Staph. aureus were thymidine-dependent and otherwise atypical in laboratory characteristics; these were isolated from patients who had received co-trimoxazole.  (+info)

Partial characterization of a major autolysin from Mycobacterium phlei. (2/631)

Autolytic enzyme profiles of fast- and slow-growing mycobacteria were examined using SDS-PAGE zymography with incorporated mycobacterial peptidoglycan sacculi as substrate. Each species tested (Mycobacterium phlei, Mycobacterium smegmatis, Mycobacterium aurum, Mycobacterium fortuitum and Mycobacterium kansasii) appeared to produce a different set of enzymes on the basis of differing number and molecular masses. A major autolysin from M. phlei was purified to apparent homogeneity by DEAE-cellulose chromatography, preparative gel electrophoresis and Mono Q FPLC. This enzyme had an estimated molecular mass of 38 kDa, an isoelectric point of 5.5 and a pH optimum of pH 7.5. Digestion of purified peptidoglycan by the enzyme resulted in the appearance of reducing sugars, suggesting that the 38 kDa autolysin is a beta-glycosidase. Partial internal amino acid sequence of the autolysin was determined and should facilitate identification, cloning and overexpression of the encoding gene.  (+info)

Involvement of outer-membrane proteins in the aggregation of Azospirillum brasilense. (3/631)

A bioassay was developed to investigate biological factors involved in the aggregation of Azospirillum brasilense strain Cd. Cells were grown for 24 h under aggregation-inducing and non-aggregation-inducing conditions (high and low C:N, respectively) and sonicated for 20 s. The cells were washed by centrifugation and resuspended in potassium phosphate buffer containing the two types of sonication extract. A greater extent of aggregation and higher flocculation were observed after 2-3 h incubation in the presence of sonicates from cells grown at high C:N (H-cells) compared to cells grown at low C:N. Flocculation did not occur after incubation of these cells in phosphate buffer. Boiled or proteinase K-treated sonicates originating from H-cells had lower aggregation-inducing capacity. After fractionation of the crude sonicate, both the outer-membrane protein (OMP) and the total membrane (mostly OMP) fractions possessed relatively high aggregation specific activities. The aggregation-inducing capacity of the OMP fraction strongly correlated with its protein concentration in the bioassay. Treatment of this fraction with proteinase K also decreased its aggregation-inducing activity. These findings suggest that OMPs are involved in the aggregation process of cells of A. brasilense.  (+info)

Physical and biological properties of cationic triesters of phosphatidylcholine. (4/631)

The properties of a new class of phospholipids, alkyl phosphocholine triesters, are described. These compounds were prepared from phosphatidylcholines through substitution of the phosphate oxygen by reaction with alkyl trifluoromethylsulfonates. Their unusual behavior is ascribed to their net positive charge and absence of intermolecular hydrogen bonding. The O-ethyl, unsaturated derivatives hydrated to generate large, unilamellar liposomes. The phase transition temperature of the saturated derivatives is very similar to that of the precursor phosphatidylcholine and quite insensitive to ionic strength. The dissociation of single molecules from bilayers is unusually facile, as revealed by the surface activity of aqueous liposome dispersions. Vesicles of cationic phospholipids fused with vesicles of anionic lipids. Liquid crystalline cationic phospholipids such as 1, 2-dioleoyl-sn-glycero-3-ethylphosphocholine triflate formed normal lipid bilayers in aqueous phases that interacted with short, linear DNA and supercoiled plasmid DNA to form a sandwich-structured complex in which bilayers were separated by strands of DNA. DNA in a 1:1 (mol) complex with cationic lipid was shielded from the aqueous phase, but was released by neutralizing the cationic charge with anionic lipid. DNA-lipid complexes transfected DNA into cells very effectively. Transfection efficiency depended upon the form of the lipid dispersion used to generate DNA-lipid complexes; in the case of the O-ethyl derivative described here, large vesicle preparations in the liquid crystalline phase were most effective.  (+info)

Alamethicin-mediated fusion of lecithin vesicles. (5/631)

It was recently shown that alamethicin greatly facilitates the fusion of small, sonicated, lecithin bilayer vesicles. In the present work the details of this fusion process have been followed by monitoring the inner and outer choline methyl signals separately by proton magnetic resonance spectroscopy. It is shown that during the alamethicine-induced fusion some of the antibiotic molecules become translocated from the extravesicular aqueous medium into the enclosed intravesicular space, and these alamethicine molecules were found to affect the choline methyl signals from the inner half of the bilayer only. No evidence was obtained for transmembrane coupling of the two halves of the bilayer in the presence of alamethicin or for any effects that might be construed as due to incorporation of alamethicin molecules into the hydrophobic core of the bilayer.  (+info)

Differential determination of phospholipase A(2) and PAF-acetylhydrolase in biological fluids using fluorescent substrates. (6/631)

The purpose of the present study was the development and evaluation of a fluorimetric method for the screening and differential determination of phospholipase A(2) and PAF-acetylhydrolase in bronchoalveolar lavage (BAL) fluid and serum. Phospholipase A(2) was determined using C(12)-NBD-PC in the presence of Ca(2+), from the slope of the fluorescence enhancement due to the formation of C(12)-NBD-fatty acid. PAF-acetylhydrolase was determined using C(6)-NBD-PC, from the slope of the curve due to C(6)-NBD-fatty acid formation in the absence of Ca(2+). The results were confirmed after TLC analysis. The method's selectivity was evaluated by comparing to radiometric measurements. Light scattering did not interfere and inner filter effects was not observed under our experimental conditions. The effects of pH, temperature, and Ca(2+) were investigated. Protein caused an increase in the background fluorescence of both NBD-PCs. The standard curves of both NBD-fatty acids exhibited the same slope. Linearity extended at least up to 4. 5 nmoles per ml of reaction mixture at the normal pH 7.4. The fluorescence of the NBD-fatty acids remained stable for increasing concentrations of BAL fluid and serum and for BSA up to 100 microg/ml of reaction mixture. Porcine pancreatic PLase A(2) showed preference for C(12)-NBD-PC in the presence of Ca(2+), while without Ca(2+), serum PAF-AcH hydrolyzed only C(6)-NBD-PC. The method is highly sensitive, accurate, and reproducible and can be applied for the differential determination of phospholipase A(2) and PAF-acetylhydrolase activities in BAL fluid and serum.  (+info)

Reconstitution of D-glucose transport catalyzed by a protein fraction from human erythrocytes in sonicated liposomes. (7/631)

A protein fraction was obtained from human erythrocyte ghosts by solubilization with Triton X-100 or octylglucoside. Triton X-100 was removed from the protein by Bio-Beads SM-2 and octylglucoside, by diafiltration. The solubilized protein fraction catalyzed D-glucose uptake when reconstituted in sonicated liposomes. The uptake was time dependent and inhibited by mercuric ions or cytochalasin B. The results indicate that the uptake represents transport of the sugar into the liposomes rather than binding to the reconstituted liposomes.  (+info)

Sonicated diagnostic immunoblot for bartonellosis. (8/631)

Two simple Bartonella bacilliformis immunoblot preparation methods were developed. Antigen was prepared by two different methods: sonication of whole organisms or glycine extraction. Both methods were then tested for sensitivity and specificity. Well-defined control sera were utilized in the development of these diagnostic immunoblots, and possible cross-reactions were thoroughly examined. Sera investigated for cross-reaction with these diagnostic antigens were drawn from patients with brucellosis, chlamydiosis, Q fever, and cat scratch disease, all of whom were from regions where bartonellosis is not endemic. While both immunoblots yielded reasonable sensitivity and high specificity, we recommend the use of the sonicated immunoblot, which has a higher sensitivity when used to detect acute disease and produces fewer cross-reactions. The sonicated immunoblot reported here is 94% sensitive to chronic bartonellosis and 70% sensitive to acute bartonellosis. In a healthy group, it is 100% specific. This immunoblot preparation requires a simple sonication protocol for the harvesting of B. bacilliformis antigens and is well suited for use in regions of endemicity.  (+info)

Sonication is a medical and laboratory term that refers to the use of ultrasound waves to agitate particles in a liquid. This process is often used in medical and scientific research to break down or disrupt cells, tissue, or other substances that are being studied. The high-frequency sound waves create standing waves that cause the particles in the liquid to vibrate, which can lead to cavitation (the formation and collapse of bubbles) and ultimately result in the disruption of the cell membranes or other structures. This technique is commonly used in procedures such as sonication of blood cultures to release microorganisms from clots, enhancing their growth in culture media and facilitating their identification.

Ultrasonics is a branch of physics and acoustics that deals with the study and application of sound waves with frequencies higher than the upper limit of human hearing, typically 20 kilohertz or above. In the field of medicine, ultrasonics is commonly used in diagnostic and therapeutic applications through the use of medical ultrasound.

Diagnostic medical ultrasound, also known as sonography, uses high-frequency sound waves to produce images of internal organs, tissues, and bodily structures. A transducer probe emits and receives sound waves that bounce off body structures and reflect back to the probe, creating echoes that are then processed into an image. This technology is widely used in various medical specialties, such as obstetrics and gynecology, cardiology, radiology, and vascular medicine, to diagnose a range of conditions and monitor the health of organs and tissues.

Therapeutic ultrasound, on the other hand, uses lower-frequency sound waves to generate heat within body tissues, promoting healing, increasing local blood flow, and reducing pain and inflammation. This modality is often used in physical therapy and rehabilitation settings to treat soft tissue injuries, joint pain, and musculoskeletal disorders.

In summary, ultrasonics in medicine refers to the use of high-frequency sound waves for diagnostic and therapeutic purposes, providing valuable information about internal body structures and facilitating healing processes.

Prosthesis-related infections, also known as prosthetic joint infections (PJIs), are infections that occur around or within a prosthetic device, such as an artificial joint. These infections can be caused by bacteria, fungi, or other microorganisms and can lead to serious complications if not treated promptly and effectively.

Prosthesis-related infections can occur soon after the implantation of the prosthetic device (early infection) or months or even years later (late infection). Early infections are often caused by bacteria that enter the surgical site during the procedure, while late infections may be caused by hematogenous seeding (i.e., when bacteria from another source spread through the bloodstream and settle in the prosthetic device) or by contamination during a subsequent medical procedure.

Symptoms of prosthesis-related infections can include pain, swelling, redness, warmth, and drainage around the affected area. In some cases, patients may also experience fever, chills, or fatigue. Diagnosis typically involves a combination of clinical evaluation, laboratory tests (such as blood cultures, joint fluid analysis, and tissue biopsy), and imaging studies (such as X-rays, CT scans, or MRI).

Treatment of prosthesis-related infections usually involves a combination of antibiotics and surgical intervention. The specific treatment approach will depend on the type and severity of the infection, as well as the patient's overall health status. In some cases, it may be necessary to remove or replace the affected prosthetic device.

Microbubbles are tiny gas-filled microspheres, typically made up of a gas core (such as air or perfluorocarbon) encapsulated by a stabilizing shell (often a phospholipid or protein). They range in size from 1 to 10 micrometers in diameter and are used in various medical applications.

In diagnostic imaging, microbubbles serve as contrast agents for ultrasound examinations. When injected into the bloodstream, they enhance the echogenicity of blood, improving visualization of vasculature, tissue perfusion, and detection of abnormalities such as tumors or lesions.

In therapeutic applications, microbubbles can be utilized in targeted drug delivery systems, where they are loaded with drugs or genes and then mechanically destroyed using ultrasound to release their cargo locally at the target site. This approach allows for more precise and controlled drug administration while minimizing systemic side effects.

Ultrasonic therapy, also known as therapeutic ultrasound, is a treatment method used in physical therapy and rehabilitation that utilizes sound waves with frequencies higher than the upper limit of human hearing. In most cases, the frequency ranges from 800,000 to 2,000,000 Hz (cycles per second).

During ultrasonic therapy, a small device called a transducer is placed in direct contact with the patient's skin. The transducer emits ultrasonic waves that are primarily absorbed by soft tissues directly beneath the skin's surface, including muscles, tendons, and ligaments. These sound waves cause microscopic vibrations in the tissue molecules, which can produce various therapeutic effects:

1. Deep heating: The vibration of tissue molecules generates heat within the treated area, increasing local blood flow, reducing muscle tension, and promoting healing. This effect is particularly beneficial for treating chronic pain, muscle spasms, joint stiffness, and soft tissue injuries.
2. Cavitation: High-intensity ultrasonic waves can create tiny gas bubbles in the fluid surrounding the tissue cells. When these bubbles collapse (a process called cavitation), they generate intense localized pressure that may help break down scar tissue, reduce adhesions, and improve tissue mobility.
3. Non-thermal effects: Low-intensity ultrasonic waves can stimulate cellular processes without causing significant heating. These non-thermal effects include enhanced metabolism, increased collagen production, and improved nutrient exchange in the treated tissues, which may contribute to faster healing and tissue regeneration.

Ultrasonic therapy is generally considered safe when performed by a trained healthcare professional. However, it should be avoided in certain situations, such as over areas with malignant tumors, infected tissues, or near metal implants (due to the risk of heating). Pregnant women should also avoid therapeutic ultrasound, especially during the first trimester, due to potential risks to fetal development.

High-Intensity Focused Ultrasound (HIFU) ablation is a minimally invasive medical procedure that uses high-frequency ultrasound energy to generate heat and destroy targeted tissue. The ultrasound beam is focused on a specific point within the body, raising the temperature at that spot to between 65 and 90°C, which causes coagulative necrosis and ablation of the targeted tissue.

HIFU ablation is often used in the treatment of various types of tumors, including prostate, liver, kidney, and breast cancer. It can also be used to treat benign conditions such as uterine fibroids. The procedure does not require incisions, which reduces the risk of complications and speeds up recovery time compared to traditional surgical procedures.

During the procedure, an ultrasound probe is inserted into the body and positioned near the targeted tissue. High-intensity ultrasound waves are then emitted from the probe and focused on a small area within the tissue. The energy from the ultrasound waves causes the temperature at the focal point to rise rapidly, destroying the targeted tissue.

HIFU ablation is typically performed as an outpatient procedure, and patients can usually return to their normal activities within a few days. However, the effectiveness of HIFU ablation varies depending on the size and location of the tumor, as well as other factors. Therefore, it is important for patients to discuss the potential benefits and risks of HIFU ablation with their healthcare provider before undergoing the procedure.

Prostheses: Artificial substitutes or replacements for missing body parts, such as limbs, eyes, or teeth. They are designed to restore the function, appearance, or mobility of the lost part. Prosthetic devices can be categorized into several types, including:

1. External prostheses: Devices that are attached to the outside of the body, like artificial arms, legs, hands, and feet. These may be further classified into:
a. Cosmetic or aesthetic prostheses: Primarily designed to improve the appearance of the affected area.
b. Functional prostheses: Designed to help restore the functionality and mobility of the lost limb.
2. Internal prostheses: Implanted artificial parts that replace missing internal organs, bones, or tissues, such as heart valves, hip joints, or intraocular lenses.

Implants: Medical devices or substances that are intentionally placed inside the body to replace or support a missing or damaged biological structure, deliver medication, monitor physiological functions, or enhance bodily functions. Examples of implants include:

1. Orthopedic implants: Devices used to replace or reinforce damaged bones, joints, or cartilage, such as knee or hip replacements.
2. Cardiovascular implants: Devices that help support or regulate heart function, like pacemakers, defibrillators, and artificial heart valves.
3. Dental implants: Artificial tooth roots that are placed into the jawbone to support dental prostheses, such as crowns, bridges, or dentures.
4. Neurological implants: Devices used to stimulate nerves, brain structures, or spinal cord tissues to treat various neurological conditions, like deep brain stimulators for Parkinson's disease or cochlear implants for hearing loss.
5. Ophthalmic implants: Artificial lenses that are placed inside the eye to replace a damaged or removed natural lens, such as intraocular lenses used in cataract surgery.

Undaria is a type of brown seaweed that belongs to the family Alariaceae. The scientific name for this species is Undaria pinnatifida, and it is also commonly known as wakame in Japan. This seaweed is native to the coasts of Japan, Korea, and China, but has been introduced and become invasive in other parts of the world, such as Europe and New Zealand.

Undaria is a popular ingredient in Asian cuisine, particularly in miso soup and salads. It is also used in traditional medicine in some countries. In recent years, Undaria has gained attention for its potential health benefits, including its high content of dietary fiber, omega-3 fatty acids, iodine, and various minerals and vitamins. Some studies have suggested that Undaria may have anti-inflammatory, antioxidant, and anticancer properties, although more research is needed to confirm these effects and establish safe and effective dosages.

It's worth noting that while Undaria has potential health benefits, it can also accumulate heavy metals and other pollutants from the environment, so it's important to source it from reputable suppliers and consume it in moderation.

An elbow prosthesis is a medical device that is used to replace all or part of the elbow joint during a surgical procedure called elbow arthroplasty or elbow replacement. The prosthesis typically consists of a metal component that replaces the humerus (upper arm bone) and another metal or plastic component that replaces the ulna (forearm bone). These components are designed to articulate with each other in a way that replicates the normal movement of the elbow joint, allowing for flexion, extension, and rotation.

Elbow prostheses may be used to treat a variety of conditions, including severe arthritis, fractures, tumors, or other injuries that have damaged the elbow joint beyond repair. The goal of elbow replacement surgery is to relieve pain, restore function, and improve the patient's quality of life.

There are several different types of elbow prostheses available, each with its own unique design features and benefits. Some prostheses are designed to be fixed in place using cement, while others use a press-fit or semi-constrained design that allows for some degree of natural movement between the components. The choice of prosthesis will depend on several factors, including the patient's age, activity level, and overall health.

After surgery, patients typically undergo a period of rehabilitation to help them regain strength and mobility in their elbow. This may involve physical therapy, exercises, and other treatments designed to promote healing and prevent complications. With proper care and follow-up, most patients can expect to enjoy improved function and reduced pain following elbow replacement surgery with an elbow prosthesis.

Cell fractionation is a laboratory technique used to separate different cellular components or organelles based on their size, density, and other physical properties. This process involves breaking open the cell (usually through homogenization), and then separating the various components using various methods such as centrifugation, filtration, and ultracentrifugation.

The resulting fractions can include the cytoplasm, mitochondria, nuclei, endoplasmic reticulum, Golgi apparatus, lysosomes, peroxisomes, and other organelles. Each fraction can then be analyzed separately to study the biochemical and functional properties of the individual components.

Cell fractionation is a valuable tool in cell biology research, allowing scientists to study the structure, function, and interactions of various cellular components in a more detailed and precise manner.

Bacteriological techniques refer to the various methods and procedures used in the laboratory for the cultivation, identification, and study of bacteria. These techniques are essential in fields such as medicine, biotechnology, and research. Here are some common bacteriological techniques:

1. **Sterilization**: This is a process that eliminates or kills all forms of life, including bacteria, viruses, fungi, and spores. Common sterilization methods include autoclaving (using steam under pressure), dry heat (in an oven), chemical sterilants, and radiation.

2. **Aseptic Technique**: This refers to practices used to prevent contamination of sterile materials or environments with microorganisms. It includes the use of sterile equipment, gloves, and lab coats, as well as techniques such as flaming, alcohol swabbing, and using aseptic transfer devices.

3. **Media Preparation**: This involves the preparation of nutrient-rich substances that support bacterial growth. There are various types of media, including solid (agar), liquid (broth), and semi-solid (e.g., stab agar). The choice of medium depends on the type of bacteria being cultured and the purpose of the investigation.

4. **Inoculation**: This is the process of introducing a bacterial culture into a medium. It can be done using a loop, swab, or needle. The inoculum should be taken from a pure culture to avoid contamination.

5. **Incubation**: After inoculation, the bacteria are allowed to grow under controlled conditions of temperature, humidity, and atmospheric composition. This process is called incubation.

6. **Staining and Microscopy**: Bacteria are too small to be seen with the naked eye. Therefore, they need to be stained and observed under a microscope. Gram staining is a common method used to differentiate between two major groups of bacteria based on their cell wall composition.

7. **Biochemical Tests**: These are tests used to identify specific bacterial species based on their biochemical characteristics, such as their ability to ferment certain sugars, produce particular enzymes, or resist certain antibiotics.

8. **Molecular Techniques**: Advanced techniques like PCR and DNA sequencing can provide more precise identification of bacteria. They can also be used for genetic analysis and epidemiological studies.

Remember, handling microorganisms requires careful attention to biosafety procedures to prevent accidental infection or environmental contamination.

"Freezing" is a term used in the medical field to describe a phenomenon that can occur in certain neurological conditions, most notably in Parkinson's disease. It refers to a sudden and temporary inability to move or initiate movement, often triggered by environmental factors such as narrow spaces, turning, or approaching a destination. This can increase the risk of falls and make daily activities challenging for affected individuals.

Freezing is also known as "freezing of gait" (FOG) when it specifically affects a person's ability to walk. During FOG episodes, the person may feel like their feet are glued to the ground, making it difficult to take steps forward. This can be very distressing and debilitating for those affected.

It is important to note that "freezing" has different meanings in different medical contexts, such as in the field of orthopedics, where it may refer to a loss of joint motion due to stiffness or inflammation. Always consult with a healthcare professional for accurate information tailored to your specific situation.

Liposomes are artificially prepared, small, spherical vesicles composed of one or more lipid bilayers that enclose an aqueous compartment. They can encapsulate both hydrophilic and hydrophobic drugs, making them useful for drug delivery applications in the medical field. The lipid bilayer structure of liposomes is similar to that of biological membranes, which allows them to merge with and deliver their contents into cells. This property makes liposomes a valuable tool in delivering drugs directly to targeted sites within the body, improving drug efficacy while minimizing side effects.

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.

Specimen handling is a set of procedures and practices followed in the collection, storage, transportation, and processing of medical samples or specimens (e.g., blood, tissue, urine, etc.) for laboratory analysis. Proper specimen handling ensures accurate test results, patient safety, and data integrity. It includes:

1. Correct labeling of the specimen container with required patient information.
2. Using appropriate containers and materials to collect, store, and transport the specimen.
3. Following proper collection techniques to avoid contamination or damage to the specimen.
4. Adhering to specific storage conditions (temperature, time, etc.) before testing.
5. Ensuring secure and timely transportation of the specimen to the laboratory.
6. Properly documenting all steps in the handling process for traceability and quality assurance.

Small unilamellar vesicles (SUVs) can be made by sonication of a dispersion of large multilamellar vesicles (LMVs). Sonication ... Sonication is the act of applying sound energy to agitate particles in a sample, for various purposes such as the extraction of ... Sonication can be used to remove dissolved gases from liquids (degassing) by sonicating the liquid while it is under a vacuum. ... Sonication can be used to speed dissolution, by breaking intermolecular interactions. It is especially useful when it is not ...
Reflux pretreatment-mediated sonication: A new universal route to obtain 2D quantum dots on Materials Today - the gateway for ... Reflux pretreatment-mediated sonication: A new universal route to obtain 2D quantum dots. Volume 22, Issue , Page 17-24 , ... Home » Materials chemistry » Journal articles » Reflux pretreatment-mediated sonication: A new universal route to obtain 2D ... Herein, for the first time, we demonstrate a reflux pretreatment-mediated sonication approach to produce a series of ultrathin ...
Sonication është aplikimi i ultrazërit me performancë të lartë për të homogjenizuar, shpërndarë dhe emulsifikuar lëngje ose për ... Tema Utrasonike: "Sonication - Aplikime dhe Avantazhe" Sonication (quhet edhe ultrasonication) është aplikimi i frekuencave të ... Efektet e sonication në përçueshmëri dhe vlerën pH të ujit. Përçueshmëria dhe vlera e pH e ujit mund të ndikohen në mënyrë ... Lexoni më shumë për avantazhet e shumëfishta të sonication dhe mësoni se si procesi juaj mund të përfitojnë nga aplikimi i ...
... përçueshmëri uje i distiluar elektricitet elektrodë elektroliza ... Sonicating ujë me ultrasonikator i tipit sondë UP400St: Sonication rrit përçueshmërinë elektrike të ujit ... fuqi të lartë përçueshmëri e rritur vlera e rritur e pH vlera e pH sonikimi i tipit sondë Sondë tip ultrasonicator Sonication ...
If I make an emulsion w/ solventless HTE and water using a sonicator, would I be able to use silica and alumina in a Buchner to filter out some fats and lipids and then separate whats left when the emulsion breaks at th…
... well explore the reasons why high pressure homogenization is more effective for cannabis processing than sonication. ... Using Sonication for Cannabis Processing. Sonication uses sound energy to disrupt the molecular bonds that hold cells together ... Cannabis Processing: Sonication vs. High Pressure Homogenization. Posted by Bryan Colwell on Aug 17, 2022 12:45:00 PM ... While sonication is effective for small batch samples of delicate materials, it is not especially suitable for processing large ...
i. Sonication. Disruption of LMV suspensions using sonic energy (sonication) typically produces small, unilamellar vesicles ( ... For more information on sonication, read "Morrissey Lab Protocol for Preparing Phospholipid Vesicles (SUV) by Sonication." ... Sonication of an LMV dispersion is accomplished by placing a test tube containing the suspension in a bath sonicator (or ... Sonication tips also tend to release titanium particles into the lipid suspension which must be removed by centrifugation prior ...
Exporter of Ultrasonic Probe Sonicators For Ultrasonic Liquid Sonication For Food Industry, Beverages Industry from Pune, India ... Applications of Ultrasonic Liquid Sonication in the Food & Beverages Industry 1. Extraction and infusion: Ultrasonic sonication ... Ultrasonic sonication can remove dissolved gases from liquids, a process known as degassing. It is employed in the production ... Ultrasonic liquid sonication can be used for efficient mixing and homogenization, resulting in uniform product consistency. It ...
title = "Sonication can reduce β-lactamase activity",. keywords = "Bacteria/enzymology, Sonication, Ultrasonics, beta-Lactamase ... Sonication can reduce β-lactamase activity. / Nichols, Wright W.; Hewinson, R. Glyn. Yn: Journal of Antimicrobial Chemotherapy ... Nichols, W. W., & Hewinson, R. G. (1989). Sonication can reduce β-lactamase activity. Journal of Antimicrobial Chemotherapy, 24 ... Sonication can reduce β-lactamase activity. Journal of Antimicrobial Chemotherapy. 1989 Gor 1;24(1):81-82. doi: 10.1093/jac/ ...
The Sonication-MicroAssembly (SMA) method of de novo DNA barcoding. The SMA strategy relies on sonication of amplicons followed ... Figure 4: Sonication-MicroAssembly (SMA) method for high throughput matK reference barcoding.. ... We next explored a Sonication-MicroAssembly (SMA) strategy for de novo barcoding of matK and longer barcodes. Here, barcode ... P.G. was responsible for optimization of amplicon sonication prior to library preparation and contributed to writing of the ...
Articles related to sonication are open access to read here. ...
Hello! Here is a list of recent publications the PhD students of COSMIC have been involved with. Hopefully you will find something of interest 🙂 Continuous flow synthesis of menthol via tandem cyclisation-hydrogenation of citronellal catalysed by scrap catalytic converters. (Alessio Zuliani, Camilla Maria Cova, Roberta Manno, Victor Sebastian, Antonio A. Romero and Rafael Luque) A continuous flow synthesis of menthol .... Read More » ...
Stir and sonication time. To obtain a stable microemulsion, solutions were mixed to obtain a similar Weber number of 1400, as ... Figure 3 depicts a peak in turbidity at 45 seconds of sonication, indicating that the solution was stable and had the smallest ... The solution was then sonicated* for varying amounts of time at a maximum amplitude of 30%. Immediately after sonication, PEG ... Figure 3: Emulsion turbidity as a function of sonication time. The highest turbidity occurred at 45 seconds, indicating the ...
In total, 60 samples were analysed: 20 intraoperative swabs, 20 vortex fluids, and 20 sonication fluids. Sonication fluid ... If sonication is not available, vortexing is a potential alternative. In immunocompromised patients, especially when ... Comparison of a standard probing method: intraoperative swab, with sonication, and vortex of the removed tooth, was performed ... Comparing the operational taxonomic units (OTUs) of the identified bacteria, significantly more OTUs were found in sonication ...
Sonication of both egg lecithin above Tm, and dipalmitoyl lecithin above and below Tm produces no change in the relative ... The effect of sonication on the hydrocarbon chain conformation in model membrane systems: A Raman spectroscopic study. BBA - ... Sonication of both egg lecithin above Tm, and dipalmitoyl lecithin above and below Tm produces no change in the relative ... Sonication of both egg lecithin above Tm, and dipalmitoyl lecithin above and below Tm produces no change in the relative ...
Optimum sonication duration as a process variable was determined to be 30 min which increased EE from 24.5% to 42% and zeta ... Optimum sonication duration as a process variable was determined to be 30 min which increased EE from 24.5% to 42% and zeta ... Optimum sonication duration as a process variable was determined to be 30 min which increased EE from 24.5% to 42% and zeta ... Optimum sonication duration as a process variable was determined to be 30 min which increased EE from 24.5% to 42% and zeta ...
... Xu Jun-Ming;Zhang Xiao-Bin;Chen Fei;Li Yu;Wang You-Wen ... Sonication cutting process was applied to shorten the outgrown carbon nanotubes to get aligned carbon nanotube film. With the ... Meanwhile, cobalt catalyst on the top of the carbon nanotube is cut off during the sonication. So the end-opened aligned carbon ... Rapid Growth of Aligned CNTs on AAO Template and Its Sonication Cutting[J]. Acta Phys. -Chim. Sin. 2004, 20(03), 271-274. doi: ...
The European Commission hosted several stands in which successful scientific projects financed by EU were explained to the non-expert visitors through multimedia material or games for the youths. Passionate "Marie Skłodowska-Curie Actions" fellows were available at the MSCA stand for whoever wanted to know more about the projects and the fellowships through which innovative and fruitful research is made possible.. All over the place one could feel the pride and the joy of the organizers in showing to everyone how far did the European Union go since the 9th of May 1950 when the "father of Europe" Robert Schuman in the so called "Schuman declaration" paved the way to the cooperation among European countries based on peace and solidarity so that a conflict between the countries would be "not merely unthinkable, but materially impossible". Indeed, since that day Europe has been characterized by a long period of peace and the mutual cooperation among countries is perfectly represented by the ...
Effect of hydrazine addition during sonication. Crystal Growth & Design, 13 (8). pp. 3637-3644. ISSN 1528-7483 ... importance of hydrazine addition in controlling the phase formation and growth of iron oxide nanoparticles during sonication. ...
tr., sonication or trypsin Erythrocytes (species used). Goose pH Range. 6.0-7.6 pH Optimum. ...
Sonication. 8.5. 7.5. 4.4. 2.5-18.9. 5.7 to 11.3. aCI, confidence interval.. bAdjusted for multiple comparisons by Bonferroni ...
Sonication bath.. Optical stands; linear polarizer setup. For custom rheo-optical methods (method development). ...
For such studies, a homogeneous phospholipid vesicle suspension can be prepared by extrusion or sonication,[27] or by rapid ... Batzri S, Korn ED (April 1973). "Single bilayer liposomes prepared without sonication". Biochimica et Biophysica Acta (BBA) - ...
Protein lysates were homogenated by sonication. In some experiments, phosphatase inhibitor cocktail PhosSTOP (Roche) was added ...
Effect of Sonication on Microwave Inactivation Kinetics of Enterococcus faecalis in Dairy Effluent.. Kernou, Ourdia-Nouara; ...
Sonication convenience with labware specifically designed for the PIXUL sonication workflow. ... The PIXUL 96-well Plate Washer is available to rinse the bottom of the PIXUL 96-well Plate after a sonication run to fully ... The PIXUL Multi-Sample Sonicator utilizes a proprietary Coupling Fluid to ensure sonication is delivered consistently to every ... the PIXUL Sonicator with room for the PIXUL 96-well Plate to keep the bottom of the plate clean before and after sonication ...
Nano-liposomes were made by sonication and filtration methods with molar ratios 7:3, 3:2 and ratios of 3:1 V/V Essential oil to ... The production of nanoliposomal system containing Ducrosia anethifolia (DC.) Boiss essential oil made by sonication and ... and results of nanoliposomes made by sonication with molar ratios of 7:3 and ratios of 3:1 was 224.4 to 5330 nm with 93 to 7 % ... It is important to note that the nanoliposomes produced by the sonication are smaller than filtration for use in the liposomal ...
sonication, nanoparticle, nanomaterial, dispersion, toxicology, particle size. Nanotechnology, Nanomaterials and Environmental ...
After the sonication, the mixture was filtered through filter paper (Whatman number 1), and then hexane was then removed under ...

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