A plant genus of the family APIACEAE. Members contain COUMARINS.
The removal of a soluble component from a liquid mixture by contact with a second liquid, immiscible with the carrier liquid, in which the component is preferentially soluble. (McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)
Separation of a mixture in successive stages, each stage removing from the mixture some proportion of one of the substances, for example by differential solubility in water-solvent mixtures. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
An extraction method that separates analytes using a solid phase and a liquid phase. It is used for preparative sample cleanup before analysis by CHROMATOGRAPHY and other analytical methods.
A microanalytical technique combining mass spectrometry and gas chromatography for the qualitative as well as quantitative determinations of compounds.
Chromatographic techniques in which the mobile phase is a liquid.
Liquids that dissolve other substances (solutes), generally solids, without any change in chemical composition, as, water containing sugar. (Grant & Hackh's Chemical Dictionary, 5th ed)
A type of stress exerted uniformly in all directions. Its measure is the force exerted per unit area. (McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)
Liquid chromatographic techniques which feature high inlet pressures, high sensitivity, and high speed.
Salts that melt below 100 C. Their low VOLATILIZATION can be an advantage over volatile organic solvents.
Materials in intermediate state between solid and liquid.
The surgical removal of a tooth. (Dorland, 28th ed)
A mass spectrometry technique using two (MS/MS) or more mass analyzers. With two in tandem, the precursor ions are mass-selected by a first mass analyzer, and focused into a collision region where they are then fragmented into product ions which are then characterized by a second mass analyzer. A variety of techniques are used to separate the compounds, ionize them, and introduce them to the first mass analyzer. For example, for in GC-MS/MS, GAS CHROMATOGRAPHY-MASS SPECTROMETRY is involved in separating relatively small compounds by GAS CHROMATOGRAPHY prior to injecting them into an ionization chamber for the mass selection.
An analytical method used in determining the identity of a chemical based on its mass using mass analyzers/mass spectrometers.
The removal of a cataractous CRYSTALLINE LENS from the eye.
A mass spectrometry technique used for analysis of nonvolatile compounds such as proteins and macromolecules. The technique involves preparing electrically charged droplets from analyte molecules dissolved in solvent. The electrically charged droplets enter a vacuum chamber where the solvent is evaporated. Evaporation of solvent reduces the droplet size, thereby increasing the coulombic repulsion within the droplet. As the charged droplets get smaller, the excess charge within them causes them to disintegrate and release analyte molecules. The volatilized analyte molecules are then analyzed by mass spectrometry.
Artificial respiration (RESPIRATION, ARTIFICIAL) using an oxygenated fluid.
The statistical reproducibility of measurements (often in a clinical context), including the testing of instrumentation or techniques to obtain reproducible results. The concept includes reproducibility of physiological measurements, which may be used to develop rules to assess probability or prognosis, or response to a stimulus; reproducibility of occurrence of a condition; and reproducibility of experimental results.
A basis of value established for the measure of quantity, weight, extent or quality, e.g. weight standards, standard solutions, methods, techniques, and procedures used in diagnosis and therapy.
Determination, by measurement or comparison with a standard, of the correct value of each scale reading on a meter or other measuring instrument; or determination of the settings of a control device that correspond to particular values of voltage, current, frequency or other output.
A CHROMATOGRAPHY method using supercritical fluid, usually carbon dioxide under very high pressure (around 73 atmospheres or 1070 psi at room temperature) as the mobile phase. Other solvents are sometimes added as modifiers. This is used both for analytical (SFC) and extraction (SFE) purposes.
Concentration or quantity that is derived from the smallest measure that can be detected with reasonable certainty for a given analytical procedure.
Determination of the spectra of ultraviolet absorption by specific molecules in gases or liquids, for example Cl2, SO2, NO2, CS2, ozone, mercury vapor, and various unsaturated compounds. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
The selective extraction of deciduous teeth during the stage of mixed dentition in accordance with the shedding and eruption of the teeth. It is done over an extended period to allow autonomous adjustment to relieve crowding of the dental arches during the eruption of the lateral incisors, canines, and premolars, eventually involving the extraction of the first premolar teeth. (Dorland, 28th ed)
Methodologies used for the isolation, identification, detection, and quantitation of chemical substances.
A chromatography technique in which the stationary phase is composed of a non-polar substance with a polar mobile phase, in contrast to normal-phase chromatography in which the stationary phase is a polar substance with a non-polar mobile phase.
Fractionation of a vaporized sample as a consequence of partition between a mobile gaseous phase and a stationary phase held in a column. Two types are gas-solid chromatography, where the fixed phase is a solid, and gas-liquid, in which the stationary phase is a nonvolatile liquid supported on an inert solid matrix.
A clear, odorless, tasteless liquid that is essential for most animal and plant life and is an excellent solvent for many substances. The chemical formula is hydrogen oxide (H2O). (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
Substances used for the detection, identification, analysis, etc. of chemical, biological, or pathologic processes or conditions. Indicators are substances that change in physical appearance, e.g., color, at or approaching the endpoint of a chemical titration, e.g., on the passage between acidity and alkalinity. Reagents are substances used for the detection or determination of another substance by chemical or microscopical means, especially analysis. Types of reagents are precipitants, solvents, oxidizers, reducers, fluxes, and colorimetric reagents. (From Grant & Hackh's Chemical Dictionary, 5th ed, p301, p499)
Procedures for collecting, preserving, and transporting of specimens sufficiently stable to provide accurate and precise results suitable for clinical interpretation.
Detection of drugs that have been abused, overused, or misused, including legal and illegal drugs. Urine screening is the usual method of detection.
Elements of limited time intervals, contributing to particular results or situations.
Concentrated pharmaceutical preparations of plants obtained by removing active constituents with a suitable solvent, which is evaporated away, and adjusting the residue to a prescribed standard.
The property of objects that determines the direction of heat flow when they are placed in direct thermal contact. The temperature is the energy of microscopic motions (vibrational and translational) of the particles of atoms.
A commonly used laboratory solvent. It was previously used as an anesthetic, but was banned from use in the U.S. due to its suspected carcinogenicity.
A colorless, flammable liquid used in the manufacture of FORMALDEHYDE and ACETIC ACID, in chemical synthesis, antifreeze, and as a solvent. Ingestion of methanol is toxic and may cause blindness.
Compounds in which a methyl group is attached to the cyano moiety.
Miniaturized methods of liquid-liquid extraction.
Any liquid or solid preparation made specifically for the growth, storage, or transport of microorganisms or other types of cells. The variety of media that exist allow for the culturing of specific microorganisms and cell types, such as differential media, selective media, test media, and defined media. Solid media consist of liquid media that have been solidified with an agent such as AGAR or GELATIN.
The normality of a solution with respect to HYDROGEN ions; H+. It is related to acidity measurements in most cases by pH = log 1/2[1/(H+)], where (H+) is the hydrogen ion concentration in gram equivalents per liter of solution. (McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
Chromatography on thin layers of adsorbents rather than in columns. The adsorbent can be alumina, silica gel, silicates, charcoals, or cellulose. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
Use of various chemical separation and extraction methods, such as SOLID PHASE EXTRACTION; CHROMATOGRAPHY; and SUPERCRITICAL FLUID EXTRACTION; to prepare samples for analytical measurement of components.
The application of medical knowledge to questions of law.
A series of steps taken in order to conduct research.
The development and use of techniques and equipment to study or perform chemical reactions, with small quantities of materials, frequently less than a milligram or a milliliter.
Controlled operation of an apparatus, process, or system by mechanical or electronic devices that take the place of human organs of observation, effort, and decision. (From Webster's Collegiate Dictionary, 1993)
A solventless sample preparation method, invented in 1989, that uses a fused silica fiber which is coated with a stationary phase. It is used for sample cleanup before using other analytical methods.
The location of the atoms, groups or ions relative to one another in a molecule, as well as the number, type and location of covalent bonds.
The rate dynamics in chemical or physical systems.
Domesticated bovine animals of the genus Bos, usually kept on a farm or ranch and used for the production of meat or dairy products or for heavy labor.
The chemical and physical integrity of a pharmaceutical product.
A hollow part of the alveolar process of the MAXILLA or MANDIBLE where each tooth fits and is attached via the periodontal ligament.
The aftermost permanent tooth on each side in the maxilla and mandible.
Benzene derivatives that include one or more hydroxyl groups attached to the ring structure.
Liquid components of living organisms.
Removal of an implanted therapeutic or prosthetic device.
The ability of a substance to be dissolved, i.e. to form a solution with another substance. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)
Electrophoresis in which a polyacrylamide gel is used as the diffusion medium.
Six-carbon saturated hydrocarbon group of the methane series. Include isomers and derivatives. Various polyneuropathies are caused by hexane poisoning.
Liquids transforming into solids by the removal of heat.
That portion of the electromagnetic spectrum from the UHF (ultrahigh frequency) radio waves and extending into the INFRARED RAYS frequencies.
The sum of the weight of all the atoms in a molecule.
Liquid perfluorinated carbon compounds which may or may not contain a hetero atom such as nitrogen, oxygen or sulfur, but do not contain another halogen or hydrogen atom. This concept includes fluorocarbon emulsions and fluorocarbon blood substitutes.
In vitro method for producing large amounts of specific DNA or RNA fragments of defined length and sequence from small amounts of short oligonucleotide flanking sequences (primers). The essential steps include thermal denaturation of the double-stranded target molecules, annealing of the primers to their complementary sequences, and extension of the annealed primers by enzymatic synthesis with DNA polymerase. The reaction is efficient, specific, and extremely sensitive. Uses for the reaction include disease diagnosis, detection of difficult-to-isolate pathogens, mutation analysis, genetic testing, DNA sequencing, and analyzing evolutionary relationships.
The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION.
Separation technique in which the stationary phase consists of ion exchange resins. The resins contain loosely held small ions that easily exchange places with other small ions of like charge present in solutions washed over the resins.
The homogeneous mixtures formed by the mixing of a solid, liquid, or gaseous substance (solute) with a liquid (the solvent), from which the dissolved substances can be recovered by physical processes. (From Grant & Hackh's Chemical Dictionary, 5th ed)
Spectroscopic method of measuring the magnetic moment of elementary particles such as atomic nuclei, protons or electrons. It is employed in clinical applications such as NMR Tomography (MAGNETIC RESONANCE IMAGING).
The chemical alteration of an exogenous substance by or in a biological system. The alteration may inactivate the compound or it may result in the production of an active metabolite of an inactive parent compound. The alterations may be divided into METABOLIC DETOXICATION, PHASE I and METABOLIC DETOXICATION, PHASE II.
Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed)
A change of a substance from one form or state to another.
Organic compounds that generally contain an amino (-NH2) and a carboxyl (-COOH) group. Twenty alpha-amino acids are the subunits which are polymerized to form proteins.
Computer processing of a language with rules that reflect and describe current usage rather than prescribed usage.
A system for verifying and maintaining a desired level of quality in a product or process by careful planning, use of proper equipment, continued inspection, and corrective action as required. (Random House Unabridged Dictionary, 2d ed)
The application of TOXICOLOGY knowledge to questions of law.
Pesticides or their breakdown products remaining in the environment following their normal use or accidental contamination.
A large lobed glandular organ in the abdomen of vertebrates that is responsible for detoxification, metabolism, synthesis and storage of various substances.
Chromatography on non-ionic gels without regard to the mechanism of solute discrimination.
The systematic study of the complete complement of proteins (PROTEOME) of organisms.
A non-crystalline form of silicon oxide that has absorptive properties. It is commonly used as a desiccating agent and as a stationary phase for CHROMATOGRAPHY. The fully hydrated form of silica gel has distinct properties and is referred to as SILICIC ACID.
Measurement and evaluation of the components of substances to be taken as FOOD.
Classic quantitative assay for detection of antigen-antibody reactions using a radioactively labeled substance (radioligand) either directly or indirectly to measure the binding of the unlabeled substance to a specific antibody or other receptor system. Non-immunogenic substances (e.g., haptens) can be measured if coupled to larger carrier proteins (e.g., bovine gamma-globulin or human serum albumin) capable of inducing antibody formation.
The phenomenon whereby compounds whose molecules have the same number and kind of atoms and the same atomic arrangement, but differ in their spatial relationships. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed)
A procedure consisting of a sequence of algebraic formulas and/or logical steps to calculate or determine a given task.
A mass spectrometric technique that is used for the analysis of large biomolecules. Analyte molecules are embedded in an excess matrix of small organic molecules that show a high resonant absorption at the laser wavelength used. The matrix absorbs the laser energy, thus inducing a soft disintegration of the sample-matrix mixture into free (gas phase) matrix and analyte molecules and molecular ions. In general, only molecular ions of the analyte molecules are produced, and almost no fragmentation occurs. This makes the method well suited for molecular weight determinations and mixture analysis.
Drugs intended for human or veterinary use, presented in their finished dosage form. Included here are materials used in the preparation and/or formulation of the finished dosage form.
Any of various animals that constitute the family Suidae and comprise stout-bodied, short-legged omnivorous mammals with thick skin, usually covered with coarse bristles, a rather long mobile snout, and small tail. Included are the genera Babyrousa, Phacochoerus (wart hogs), and Sus, the latter containing the domestic pig (see SUS SCROFA).
A clear, colorless liquid rapidly absorbed from the gastrointestinal tract and distributed throughout the body. It has bactericidal activity and is used often as a topical disinfectant. It is widely used as a solvent and preservative in pharmaceutical preparations as well as serving as the primary ingredient in ALCOHOLIC BEVERAGES.

Highly efficient microscale purification of glycerophospholipids by microfluidic cell lysis and lipid extraction for lipidomics profiling. (1/73)

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Rapid and sensitive determination of udenafil in plasma by LC-MS/MS for intranasal pharmacokinetic study in rats. (2/73)

A rapid and sensitive analytical method for udenafil in rat plasma was developed and validated using liquid chromatography-tandem mass spectrometry (LC-MS/MS). This chromatographic procedure was then applied to the in vivo pharmacokinetic studies in rats for determining the advantages of intranasal administration of the drug over oral administration. Using liquid-liquid extraction (LLE), udenafil and the internal standard (IS) sildenafil were extracted with dichloromethane from 100 mul of plasma samples. Chromatographic separation was performed using Pursuit XRS C(1)(8) column (50 mm x 2.1 mm, i.d., 3 mum, Varian Inc., CA, U.S.A.) with an isocratic mobile phase consisting of acetonitrile and 10 mM ammonium acetate (90 : 10, v/v) at a flow rate of 0.2 ml/min over a total run time of 2.5 min. Detection and quantification was performed by mass spectrometry using the multiple reaction-monitoring mode at m/z 517.4-->283.1 for udenafil and m/z 475.3-->100.0 for IS. Results showed that the developed method was sensitive and specific for udenafil. Linearity was obtained in the range of 0.5-1000 ng/ml. The coefficient of variation of both intra- and inter-day validation were below 11.6% and the intra- and inter-day accuracy ranged from 91.5 to 109.9%. Udenafil concentration was successfully measured from plasma after intranasal as well as after intravenous or oral administration at clinical dose (1.67 mg/kg) in rats. Moreover, the T(max) values obtained from pharmacokinetic studies suggested that administration of udenafil intranasally could be more effective than by the oral route.  (+info)

Comparison of analytical methods and residue patterns of pymetrozine in Aster scaber. (3/73)

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Determination of acrylamide in starch-based foods by HPLC with pre-column ultraviolet derivatization. (4/73)

A new method is developed for the determination of acrylamide in starch-based foods. The method included the extraction of acrylamide with water, defatting with hexane, derivatization with potassium bromate (KBrO(3)) and potassium bromide (KBr), liquid-liquid extraction with ethyl acetate-hexane (4:1), and concentration. The final analyte (2-bromopropenamide, 2-BPA) is analyzed by high-performance liquid chromatography coupled with diode array detection for quantification and by gas chromatography coupled to mass spectrometry for confirmation. The chromatographic analysis is performed on an ODS-3 C(18) column, and good retention and peak response of acrylamide are achieved under the optimal conditions. The limit of detection and quantitation are estimated to be 15 and 50 mug/kg, respectively. The recoveries of acrylamide from the commercial samples are spiked at levels of 50-1000 mug/kg, and range between 89.6 and 102.0%. These results show that this method should be regarded as a new, low-cost, and robust alternative for conventional investigation of acrylamide.  (+info)

Enhanced sensitivity of LC-MS analysis of permethylated N-glycans through online purification. (5/73)

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Liquid-phase-based separation systems for depletion, prefractionation and enrichment of proteins in biological fluids and matrices for in-depth proteomics analysis--an update covering the period 2008-2011. (6/73)

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Determination of cediranib in mouse plasma and brain tissue using high-performance liquid chromatography-mass spectrometry. (7/73)

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Investigation of figopitant and its metabolites in rat tissue by combining whole-body autoradiography with liquid extraction surface analysis mass spectrometry. (8/73)

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"Heracleum" is a genus of plants in the family Apiaceae, also known as the carrot or parsley family. Many species in this genus are large herbaceous plants native to Europe and Asia, with some found in North America. One well-known species is Heracleum persicum, commonly called "giant hogweed," which can grow up to 15 feet tall and has been identified as an invasive species in certain regions.

The sap of giant hogweed contains toxic compounds that can cause phytophotodermatitis, a skin reaction characterized by redness, pain, itching, and blistering when the affected area is exposed to sunlight. This reaction can be severe and may result in scarring or long-term sensitivity to light. It's essential to exercise caution when handling or coming into contact with giant hogweed or any other members of the Heracleum genus.

In a medical context, it's crucial to differentiate between 'Heracleum' as a plant genus and 'heracleum' as a term used in anatomy. In anatomy, 'heracleum' refers to a muscle in certain animals, specifically the external abdominal oblique muscle in ruminants like cows and sheep. However, this usage is not directly related to human medicine or healthcare.

Liquid-liquid extraction, also known as solvent extraction or partitioning, is a method used in chemistry to separate and purify compounds based on their relative solubilities in two different immiscible liquids. In this process, a solution containing the target compound is mixed with a second solvent in which the compound of interest has greater solubility. After mixing, the two liquids are allowed to separate into distinct layers based on their differences in density. The desired compound will then preferentially partition into the second solvent layer, allowing for its separation from other components in the original solution. This process can be repeated multiple times to increase the purity of the extracted compound. It is commonly used in various fields including pharmaceuticals, biochemistry, and environmental science for the extraction and isolation of organic compounds.

Chemical fractionation is a process used in analytical chemistry to separate and isolate individual components or fractions from a mixture based on their chemical properties. This technique typically involves the use of various chemical reactions, such as precipitation, extraction, or chromatography, to selectively interact with specific components in the mixture and purify them.

In the context of medical research or clinical analysis, chemical fractionation may be used to isolate and identify individual compounds in a complex biological sample, such as blood, urine, or tissue. For example, fractionating a urine sample might involve separating out various metabolites, proteins, or other molecules based on their solubility, charge, or other chemical properties, allowing researchers to study the individual components and their roles in health and disease.

It's worth noting that while chemical fractionation can be a powerful tool for analyzing complex mixtures, it can also be time-consuming and technically challenging, requiring specialized equipment and expertise to perform accurately and reliably.

Solid-phase extraction (SPE) is a method used in analytical chemistry and biochemistry to extract, separate, or clean up specific components from a complex matrix, such as a biological sample. It involves the use of a solid phase, typically a packed bed of sorbent material, held within a cartridge or column. The sample mixture is passed through the column, and the components of interest are selectively retained by the sorbent while other components pass through.

The analytes can then be eluted from the sorbent using a small volume of a suitable solvent, resulting in a more concentrated and purified fraction that can be analyzed using various techniques such as high-performance liquid chromatography (HPLC), gas chromatography (GC), or mass spectrometry.

The solid phase used in SPE can vary depending on the nature of the analytes and the matrix, with different sorbents offering varying degrees of selectivity and capacity for specific compounds. Commonly used sorbents include silica-based materials, polymeric resins, and ion exchange materials.

Overall, solid-phase extraction is a powerful tool in sample preparation, allowing for the isolation and concentration of target analytes from complex matrices, thereby improving the sensitivity and selectivity of downstream analytical techniques.

Gas Chromatography-Mass Spectrometry (GC-MS) is a powerful analytical technique that combines the separating power of gas chromatography with the identification capabilities of mass spectrometry. This method is used to separate, identify, and quantify different components in complex mixtures.

In GC-MS, the mixture is first vaporized and carried through a long, narrow column by an inert gas (carrier gas). The various components in the mixture interact differently with the stationary phase inside the column, leading to their separation based on their partition coefficients between the mobile and stationary phases. As each component elutes from the column, it is then introduced into the mass spectrometer for analysis.

The mass spectrometer ionizes the sample, breaks it down into smaller fragments, and measures the mass-to-charge ratio of these fragments. This information is used to generate a mass spectrum, which serves as a unique "fingerprint" for each compound. By comparing the generated mass spectra with reference libraries or known standards, analysts can identify and quantify the components present in the original mixture.

GC-MS has wide applications in various fields such as forensics, environmental analysis, drug testing, and research laboratories due to its high sensitivity, specificity, and ability to analyze volatile and semi-volatile compounds.

Liquid chromatography (LC) is a type of chromatography technique used to separate, identify, and quantify the components in a mixture. In this method, the sample mixture is dissolved in a liquid solvent (the mobile phase) and then passed through a stationary phase, which can be a solid or a liquid that is held in place by a solid support.

The components of the mixture interact differently with the stationary phase and the mobile phase, causing them to separate as they move through the system. The separated components are then detected and measured using various detection techniques, such as ultraviolet (UV) absorbance or mass spectrometry.

Liquid chromatography is widely used in many areas of science and medicine, including drug development, environmental analysis, food safety testing, and clinical diagnostics. It can be used to separate and analyze a wide range of compounds, from small molecules like drugs and metabolites to large biomolecules like proteins and nucleic acids.

Solvents, in a medical context, are substances that are capable of dissolving or dispersing other materials, often used in the preparation of medications and solutions. They are commonly organic chemicals that can liquefy various substances, making it possible to administer them in different forms, such as oral solutions, topical creams, or injectable drugs.

However, it is essential to recognize that solvents may pose health risks if mishandled or misused, particularly when they contain volatile organic compounds (VOCs). Prolonged exposure to these VOCs can lead to adverse health effects, including respiratory issues, neurological damage, and even cancer. Therefore, it is crucial to handle solvents with care and follow safety guidelines to minimize potential health hazards.

In medical terms, pressure is defined as the force applied per unit area on an object or body surface. It is often measured in millimeters of mercury (mmHg) in clinical settings. For example, blood pressure is the force exerted by circulating blood on the walls of the arteries and is recorded as two numbers: systolic pressure (when the heart beats and pushes blood out) and diastolic pressure (when the heart rests between beats).

Pressure can also refer to the pressure exerted on a wound or incision to help control bleeding, or the pressure inside the skull or spinal canal. High or low pressure in different body systems can indicate various medical conditions and require appropriate treatment.

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

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

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

Ionic liquids are not a medical term, but rather a term used in the field of chemistry and physics. They refer to salts that exist in the liquid state at temperatures below 100 degrees Celsius. Ionic liquids are composed entirely of ions and have unique properties such as low volatility, high thermal stability, and good conductivity, making them useful in various applications including chemical reactions, energy storage, and biomedical devices. However, they do not have a direct relation to medical definitions or healthcare.

Liquid crystals (LCs) are not exclusive to the medical field, but they do have important applications in medicine, particularly in the development of display technologies for medical devices. Here is a general definition:

Liquid crystals are a state of matter that possess properties between those of conventional liquids and solid crystals. They can flow like liquids but have molecules oriented in a way that they can reflect light, creating birefringence. This unique property makes them useful in various applications, such as LCDs (liquid crystal displays) found in many electronic devices, including medical equipment.

In the context of medicine, liquid crystals are primarily used in LCD screens for medical devices like monitors, imaging systems, and diagnostic equipment. They enable high-resolution, clear, and adjustable visualization of medical images, which is crucial for accurate diagnosis and treatment planning.

Tooth extraction is a dental procedure in which a tooth that is damaged or poses a threat to oral health is removed from its socket in the jawbone. This may be necessary due to various reasons such as severe tooth decay, gum disease, fractured teeth, crowded teeth, or for orthodontic treatment purposes. The procedure is performed by a dentist or an oral surgeon, under local anesthesia to numb the area around the tooth, ensuring minimal discomfort during the extraction process.

Tandem mass spectrometry (MS/MS) is a technique used to identify and quantify specific molecules, such as proteins or metabolites, within complex mixtures. This method uses two or more sequential mass analyzers to first separate ions based on their mass-to-charge ratio and then further fragment the selected ions into smaller pieces for additional analysis. The fragmentation patterns generated in MS/MS experiments can be used to determine the structure and identity of the original molecule, making it a powerful tool in various fields such as proteomics, metabolomics, and forensic science.

Mass spectrometry (MS) is an analytical technique used to identify and quantify the chemical components of a mixture or compound. It works by ionizing the sample, generating charged molecules or fragments, and then measuring their mass-to-charge ratio in a vacuum. The resulting mass spectrum provides information about the molecular weight and structure of the analytes, allowing for identification and characterization.

In simpler terms, mass spectrometry is a method used to determine what chemicals are present in a sample and in what quantities, by converting the chemicals into ions, measuring their masses, and generating a spectrum that shows the relative abundances of each ion type.

Cataract extraction is a surgical procedure that involves removing the cloudy lens (cataract) from the eye. This procedure is typically performed to restore vision impairment caused by cataracts and improve overall quality of life. There are two primary methods for cataract extraction:

1. Phacoemulsification: This is the most common method used today. It involves making a small incision in the front part of the eye (cornea), inserting an ultrasonic probe to break up the cloudy lens into tiny pieces, and then removing those pieces with suction. After removing the cataract, an artificial intraocular lens (IOL) is inserted to replace the natural lens and help focus light onto the retina.

2. Extracapsular Cataract Extraction: In this method, a larger incision is made on the side of the cornea, allowing the surgeon to remove the cloudy lens in one piece without breaking it up. The back part of the lens capsule is left intact to support the IOL. This technique is less common and typically reserved for more advanced cataracts or when phacoemulsification cannot be performed.

Recovery from cataract extraction usually involves using eye drops to prevent infection and inflammation, as well as protecting the eye with a shield or glasses during sleep for a few weeks after surgery. Most people experience improved vision within a few days to a week following the procedure.

Mass spectrometry with electrospray ionization (ESI-MS) is an analytical technique used to identify and quantify chemical species in a sample based on the mass-to-charge ratio of charged particles. In ESI-MS, analytes are ionized through the use of an electrospray, where a liquid sample is introduced through a metal capillary needle at high voltage, creating an aerosol of charged droplets. As the solvent evaporates, the analyte molecules become charged and can be directed into a mass spectrometer for analysis.

ESI-MS is particularly useful for the analysis of large biomolecules such as proteins, peptides, and nucleic acids, due to its ability to gently ionize these species without fragmentation. The technique provides information about the molecular weight and charge state of the analytes, which can be used to infer their identity and structure. Additionally, ESI-MS can be interfaced with separation techniques such as liquid chromatography (LC) for further purification and characterization of complex samples.

Liquid ventilation is a medical procedure that involves the use of an oxygen-rich liquid, such as perfluorocarbons (PFCs), to replace air in the lungs. This technique is used to improve gas exchange and lung function in patients with severe respiratory distress syndrome (RDS) or other forms of acute lung injury.

During liquid ventilation, the liquid is instilled into the lungs through a special endotracheal tube, causing the alveoli (tiny air sacs in the lungs) to fill up and float in the liquid. The PFCs used in liquid ventilation are capable of dissolving large amounts of oxygen and carbon dioxide, allowing for efficient gas exchange between the lungs and the bloodstream.

The use of liquid ventilation has been shown to improve lung compliance, reduce lung injury, and decrease the need for mechanical ventilation in some patients with severe respiratory distress. However, further research is needed to fully understand its potential benefits and risks.

Reproducibility of results in a medical context refers to the ability to obtain consistent and comparable findings when a particular experiment or study is repeated, either by the same researcher or by different researchers, following the same experimental protocol. It is an essential principle in scientific research that helps to ensure the validity and reliability of research findings.

In medical research, reproducibility of results is crucial for establishing the effectiveness and safety of new treatments, interventions, or diagnostic tools. It involves conducting well-designed studies with adequate sample sizes, appropriate statistical analyses, and transparent reporting of methods and findings to allow other researchers to replicate the study and confirm or refute the results.

The lack of reproducibility in medical research has become a significant concern in recent years, as several high-profile studies have failed to produce consistent findings when replicated by other researchers. This has led to increased scrutiny of research practices and a call for greater transparency, rigor, and standardization in the conduct and reporting of medical research.

Reference standards in a medical context refer to the established and widely accepted norms or benchmarks used to compare, evaluate, or measure the performance, accuracy, or effectiveness of diagnostic tests, treatments, or procedures. These standards are often based on extensive research, clinical trials, and expert consensus, and they help ensure that healthcare practices meet certain quality and safety thresholds.

For example, in laboratory medicine, reference standards may consist of well-characterized samples with known concentrations of analytes (such as chemicals or biological markers) that are used to calibrate instruments and validate testing methods. In clinical practice, reference standards may take the form of evidence-based guidelines or best practices that define appropriate care for specific conditions or patient populations.

By adhering to these reference standards, healthcare professionals can help minimize variability in test results, reduce errors, improve diagnostic accuracy, and ensure that patients receive consistent, high-quality care.

In the context of medicine and medical devices, calibration refers to the process of checking, adjusting, or confirming the accuracy of a measurement instrument or system. This is typically done by comparing the measurements taken by the device being calibrated to those taken by a reference standard of known accuracy. The goal of calibration is to ensure that the medical device is providing accurate and reliable measurements, which is critical for making proper diagnoses and delivering effective treatment. Regular calibration is an important part of quality assurance and helps to maintain the overall performance and safety of medical devices.

Chromatography, supercritical fluid (SFC) is a type of chromatographic technique that uses supercritical fluids as the mobile phase to separate and analyze components of a mixture. A supercritical fluid is a substance that is maintained at temperatures and pressures above its critical point, where it exhibits properties of both a gas and a liquid, making it an ideal medium for separations due to its low viscosity, high diffusivity, and tuneable solvating strength.

In SFC, the supercritical fluid, typically carbon dioxide (CO2) due to its mild critical point conditions, is used to elute analytes from a stationary phase, such as a silica or polymer-based column. The interactions between the analytes and the stationary phase, along with the properties of the supercritical fluid, determine the separation efficiency and resolution of the technique.

SFC has several advantages over traditional liquid chromatography (LC) techniques, including faster analysis times, lower solvent consumption, and the ability to analyze a wider range of polar and nonpolar compounds. SFC is commonly used in the pharmaceutical industry for drug discovery and development, as well as in environmental, food, and chemical analyses.

The 'Limit of Detection' (LOD) is a term used in laboratory medicine and clinical chemistry to describe the lowest concentration or quantity of an analyte (the substance being measured) that can be reliably distinguished from zero or blank value, with a specified level of confidence. It is typically expressed as a concentration or amount and represents the minimum amount of analyte that must be present in a sample for the assay to produce a response that is statistically different from a blank or zero calibrator.

The LOD is an important parameter in analytical method validation, as it helps to define the range of concentrations over which the assay can accurately and precisely measure the analyte. It is determined based on statistical analysis of the data generated during method development and validation, taking into account factors such as the variability of the assay and the signal-to-noise ratio.

It's important to note that LOD should not be confused with the 'Limit of Quantification' (LOQ), which is the lowest concentration or quantity of an analyte that can be measured with acceptable precision and accuracy. LOQ is typically higher than LOD, as it requires a greater level of confidence in the measurement.

Spectrophotometry, Ultraviolet (UV-Vis) is a type of spectrophotometry that measures how much ultraviolet (UV) and visible light is absorbed or transmitted by a sample. It uses a device called a spectrophotometer to measure the intensity of light at different wavelengths as it passes through a sample. The resulting data can be used to determine the concentration of specific components within the sample, identify unknown substances, or evaluate the physical and chemical properties of materials.

UV-Vis spectroscopy is widely used in various fields such as chemistry, biology, pharmaceuticals, and environmental science. It can detect a wide range of substances including organic compounds, metal ions, proteins, nucleic acids, and dyes. The technique is non-destructive, meaning that the sample remains unchanged after the measurement.

In UV-Vis spectroscopy, the sample is placed in a cuvette or other container, and light from a source is directed through it. The light then passes through a monochromator, which separates it into its component wavelengths. The monochromatic light is then directed through the sample, and the intensity of the transmitted or absorbed light is measured by a detector.

The resulting absorption spectrum can provide information about the concentration and identity of the components in the sample. For example, if a compound has a known absorption maximum at a specific wavelength, its concentration can be determined by measuring the absorbance at that wavelength and comparing it to a standard curve.

Overall, UV-Vis spectrophotometry is a versatile and powerful analytical technique for quantitative and qualitative analysis of various samples in different fields.

"Serial extraction" is not a widely recognized or established term in medical or dental literature. However, within the context of dentistry, it could potentially refer to the sequential removal of multiple teeth during separate appointments. This approach may be used when extracting multiple problematic teeth to minimize the risk of complications such as excessive bleeding, swelling, or infection that can arise from removing numerous teeth at once. It is essential to consult a dental professional for a precise understanding and application of this term in a medical context.

Analytical chemistry techniques are a collection of methods and tools used to identify and quantify the chemical composition of matter. These techniques can be used to analyze the presence and amount of various chemicals in a sample, including ions, molecules, and atoms. Some common analytical chemistry techniques include:

1. Spectroscopy: This technique uses the interaction between electromagnetic radiation and matter to identify and quantify chemical species. There are many different types of spectroscopy, including UV-Vis, infrared (IR), fluorescence, and nuclear magnetic resonance (NMR) spectroscopy.
2. Chromatography: This technique separates the components of a mixture based on their physical or chemical properties, such as size, charge, or polarity. Common types of chromatography include gas chromatography (GC), liquid chromatography (LC), and thin-layer chromatography (TLC).
3. Mass spectrometry: This technique uses the mass-to-charge ratio of ions to identify and quantify chemical species. It can be used in combination with other techniques, such as GC or LC, to provide structural information about unknown compounds.
4. Electrochemical methods: These techniques use the movement of electrons to measure the concentration of chemical species. Examples include potentiometry, voltammetry, and amperometry.
5. Thermal analysis: This technique uses changes in the physical or chemical properties of a sample as it is heated or cooled to identify and quantify chemical species. Examples include differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA).

These are just a few examples of the many analytical chemistry techniques that are available. Each technique has its own strengths and limitations, and the choice of which to use will depend on the specific needs of the analysis.

Reverse-phase chromatography is a type of liquid chromatography that is commonly used in analytical chemistry and biochemistry to separate, identify, and purify complex mixtures of chemicals or biological molecules. In this technique, the stationary phase is a nonpolar solid, such as octadecyl silica (ODS) or C18, which is coated with a polar solvent, while the mobile phase is a nonpolar solvent, such as methanol or acetonitrile.

The term "reverse-phase" refers to the fact that the polarity of the stationary and mobile phases is reversed compared to normal-phase chromatography. In normal-phase chromatography, the stationary phase is polar and the mobile phase is nonpolar, which results in the separation of analytes based on their polarity. However, in reverse-phase chromatography, the stationary phase is nonpolar and the mobile phase is polar, which means that the separation of analytes is based on their hydrophobicity or hydrophilicity.

In reverse-phase chromatography, hydrophobic molecules elute more slowly than hydrophilic molecules because they have a stronger affinity for the nonpolar stationary phase. The retention time of an analyte can be adjusted by changing the composition of the mobile phase or the pH of the solution. This technique is widely used in the analysis of drugs, metabolites, peptides, proteins, and other biological molecules.

Chromatography, gas (GC) is a type of chromatographic technique used to separate, identify, and analyze volatile compounds or vapors. In this method, the sample mixture is vaporized and carried through a column packed with a stationary phase by an inert gas (carrier gas). The components of the mixture get separated based on their partitioning between the mobile and stationary phases due to differences in their adsorption/desorption rates or solubility.

The separated components elute at different times, depending on their interaction with the stationary phase, which can be detected and quantified by various detection systems like flame ionization detector (FID), thermal conductivity detector (TCD), electron capture detector (ECD), or mass spectrometer (MS). Gas chromatography is widely used in fields such as chemistry, biochemistry, environmental science, forensics, and food analysis.

Medical definitions of water generally describe it as a colorless, odorless, tasteless liquid that is essential for all forms of life. It is a universal solvent, making it an excellent medium for transporting nutrients and waste products within the body. Water constitutes about 50-70% of an individual's body weight, depending on factors such as age, sex, and muscle mass.

In medical terms, water has several important functions in the human body:

1. Regulation of body temperature through perspiration and respiration.
2. Acting as a lubricant for joints and tissues.
3. Facilitating digestion by helping to break down food particles.
4. Transporting nutrients, oxygen, and waste products throughout the body.
5. Helping to maintain healthy skin and mucous membranes.
6. Assisting in the regulation of various bodily functions, such as blood pressure and heart rate.

Dehydration can occur when an individual does not consume enough water or loses too much fluid due to illness, exercise, or other factors. This can lead to a variety of symptoms, including dry mouth, fatigue, dizziness, and confusion. Severe dehydration can be life-threatening if left untreated.

Indicators and reagents are terms commonly used in the field of clinical chemistry and laboratory medicine. Here are their definitions:

1. Indicator: An indicator is a substance that changes its color or other physical properties in response to a chemical change, such as a change in pH, oxidation-reduction potential, or the presence of a particular ion or molecule. Indicators are often used in laboratory tests to monitor or signal the progress of a reaction or to indicate the end point of a titration. A familiar example is the use of phenolphthalein as a pH indicator in acid-base titrations, which turns pink in basic solutions and colorless in acidic solutions.

2. Reagent: A reagent is a substance that is added to a system (such as a sample or a reaction mixture) to bring about a chemical reaction, test for the presence or absence of a particular component, or measure the concentration of a specific analyte. Reagents are typically chemicals with well-defined and consistent properties, allowing them to be used reliably in analytical procedures. Examples of reagents include enzymes, antibodies, dyes, metal ions, and organic compounds. In laboratory settings, reagents are often prepared and standardized according to strict protocols to ensure their quality and performance in diagnostic tests and research applications.

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.

Substance abuse detection refers to the process of identifying the use or misuse of psychoactive substances, such as alcohol, illicit drugs, or prescription medications, in an individual. This can be done through various methods, including:

1. Physical examination: A healthcare professional may look for signs of substance abuse, such as track marks, enlarged pupils, or unusual behavior.
2. Laboratory tests: Urine, blood, hair, or saliva samples can be analyzed to detect the presence of drugs or their metabolites. These tests can provide information about recent use (hours to days) or longer-term use (up to several months).
3. Self-report measures: Individuals may be asked to complete questionnaires or interviews about their substance use patterns and behaviors.
4. Observational assessments: In some cases, such as in a treatment setting, healthcare professionals may observe an individual's behavior over time to identify patterns of substance abuse.

Substance abuse detection is often used in clinical, workplace, or legal settings to assess individuals for potential substance use disorders, monitor treatment progress, or ensure compliance with laws or regulations.

In the field of medicine, "time factors" refer to the duration of symptoms or time elapsed since the onset of a medical condition, which can have significant implications for diagnosis and treatment. Understanding time factors is crucial in determining the progression of a disease, evaluating the effectiveness of treatments, and making critical decisions regarding patient care.

For example, in stroke management, "time is brain," meaning that rapid intervention within a specific time frame (usually within 4.5 hours) is essential to administering tissue plasminogen activator (tPA), a clot-busting drug that can minimize brain damage and improve patient outcomes. Similarly, in trauma care, the "golden hour" concept emphasizes the importance of providing definitive care within the first 60 minutes after injury to increase survival rates and reduce morbidity.

Time factors also play a role in monitoring the progression of chronic conditions like diabetes or heart disease, where regular follow-ups and assessments help determine appropriate treatment adjustments and prevent complications. In infectious diseases, time factors are crucial for initiating antibiotic therapy and identifying potential outbreaks to control their spread.

Overall, "time factors" encompass the significance of recognizing and acting promptly in various medical scenarios to optimize patient outcomes and provide effective care.

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

Temperature, in a medical context, is a measure of the degree of hotness or coldness of a body or environment. It is usually measured using a thermometer and reported in degrees Celsius (°C), degrees Fahrenheit (°F), or kelvin (K). In the human body, normal core temperature ranges from about 36.5-37.5°C (97.7-99.5°F) when measured rectally, and can vary slightly depending on factors such as time of day, physical activity, and menstrual cycle. Elevated body temperature is a common sign of infection or inflammation, while abnormally low body temperature can indicate hypothermia or other medical conditions.

Chloroform is a volatile, clear, and nonflammable liquid with a mild, sweet, and aromatic odor. Its chemical formula is CHCl3, consisting of one carbon atom, one hydrogen atom, and three chlorine atoms. Chloroform is a trihalomethane, which means it contains three halogens (chlorine) in its molecular structure.

In the medical field, chloroform has been historically used as an inhaled general anesthetic agent due to its ability to produce unconsciousness and insensibility to pain quickly. However, its use as a surgical anesthetic has largely been abandoned because of several safety concerns, including its potential to cause cardiac arrhythmias, liver and kidney damage, and a condition called "chloroform hepatopathy" with prolonged or repeated exposure.

Currently, chloroform is not used as a therapeutic agent in medicine but may still be encountered in laboratory settings for various research purposes. It's also possible to find traces of chloroform in drinking water due to its formation during the disinfection process using chlorine-based compounds.

Methanol, also known as methyl alcohol or wood alcohol, is a volatile, colorless, flammable liquid with a distinctive odor similar to that of ethanol (drinking alcohol). It is used in various industrial applications such as the production of formaldehyde, acetic acid, and other chemicals. In the medical field, methanol is considered a toxic alcohol that can cause severe intoxication and metabolic disturbances when ingested or improperly consumed. Methanol poisoning can lead to neurological symptoms, blindness, and even death if not treated promptly and effectively.

Acetonitrile is an organic compound with the formula CH3CN. It is a colorless liquid that is used as a solvent and in the production of various chemicals. Acetonitrile is weakly basic and polar, and it has a unique smell that is often described as unpleasant or sweet.

Acetonitrile is not considered to be a medication or a drug, so it does not have a medical definition. However, it is sometimes used in the medical field as a solvent for various applications, such as in the preparation of pharmaceutical products or in laboratory research. It is important to handle acetonitrile with care, as it can be harmful if swallowed, inhaled, or contacted with the skin.

Liquid-phase microextraction (LPME) is a sample preparation technique used in analytical chemistry and clinical laboratory medicine. It is a miniaturized version of traditional liquid-liquid extraction, which involves the separation of analytes from a sample matrix based on their partitioning between two immiscible liquids.

In LPME, a small volume (microliters to nanoliters) of an organic extractant phase is placed in a micro-syringe or contained within a porous membrane or hollow fiber. This extractant phase is then introduced into a larger sample solution, where analytes partition from the aqueous sample matrix into the organic phase due to their higher solubility in the organic solvent. After equilibrium has been reached, the extractant phase is withdrawn and analyzed for the presence of the target analytes using various analytical techniques such as gas chromatography (GC), high-performance liquid chromatography (HPLC), or mass spectrometry (MS).

LPME offers several advantages over traditional liquid-liquid extraction, including reduced solvent consumption, lower cost, shorter analysis time, and higher enrichment factors. It is commonly used for the preconcentration and cleanup of environmental, biological, and clinical samples prior to analysis.

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

Hydrogen-ion concentration, also known as pH, is a measure of the acidity or basicity of a solution. It is defined as the negative logarithm (to the base 10) of the hydrogen ion activity in a solution. The standard unit of measurement is the pH unit. A pH of 7 is neutral, less than 7 is acidic, and greater than 7 is basic.

In medical terms, hydrogen-ion concentration is important for maintaining homeostasis within the body. For example, in the stomach, a high hydrogen-ion concentration (low pH) is necessary for the digestion of food. However, in other parts of the body such as blood, a high hydrogen-ion concentration can be harmful and lead to acidosis. Conversely, a low hydrogen-ion concentration (high pH) in the blood can lead to alkalosis. Both acidosis and alkalosis can have serious consequences on various organ systems if not corrected.

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

Thin-layer chromatography (TLC) is a type of chromatography used to separate, identify, and quantify the components of a mixture. In TLC, the sample is applied as a small spot onto a thin layer of adsorbent material, such as silica gel or alumina, which is coated on a flat, rigid support like a glass plate. The plate is then placed in a developing chamber containing a mobile phase, typically a mixture of solvents.

As the mobile phase moves up the plate by capillary action, it interacts with the stationary phase and the components of the sample. Different components of the mixture travel at different rates due to their varying interactions with the stationary and mobile phases, resulting in distinct spots on the plate. The distance each component travels can be measured and compared to known standards to identify and quantify the components of the mixture.

TLC is a simple, rapid, and cost-effective technique that is widely used in various fields, including forensics, pharmaceuticals, and research laboratories. It allows for the separation and analysis of complex mixtures with high resolution and sensitivity, making it an essential tool in many analytical applications.

Analytical sample preparation methods refer to the procedures and techniques used to manipulate and treat samples in order to make them suitable for analysis by an analytical instrument. The main goal of these methods is to isolate, concentrate, and purify the analytes of interest from a complex matrix, while also minimizing interference and improving the accuracy, precision, and sensitivity of the analysis.

Some common analytical sample preparation methods include:

1. Extraction: This involves separating the analyte from the sample matrix using a solvent or other medium. Examples include liquid-liquid extraction (LLE), solid-phase extraction (SPE), and microwave-assisted extraction (MAE).
2. Purification: This step is used to remove impurities and interfering substances from the sample. Common methods include column chromatography, gel permeation chromatography, and distillation.
3. Derivatization: This involves chemically modifying the analyte to improve its detectability or stability. Examples include silylation, acetylation, and esterification.
4. Digestion: This step is used to break down complex samples into smaller, more manageable components. Examples include acid digestion, dry ashing, and microwave digestion.
5. Concentration: This step is used to increase the amount of analyte in the sample, making it easier to detect. Examples include evaporation, lyophilization, and rotary evaporation.

These methods are widely used in various fields such as forensics, environmental science, food analysis, pharmaceuticals, and clinical diagnostics to ensure accurate and reliable results.

Forensic medicine, also known as legal medicine or medical jurisprudence, is a branch of medicine that deals with the application of medical knowledge to legal issues and questions. It involves the examination, interpretation, and analysis of medical evidence for use in courts of law. This may include determining the cause and manner of death, identifying injuries or diseases, assessing the effects of substances or treatments, and evaluating the competency or capacity of individuals. Forensic medicine is often used in criminal investigations and court cases, but it can also be applied to civil matters such as personal injury claims or medical malpractice suits.

In the context of medical research, "methods" refers to the specific procedures or techniques used in conducting a study or experiment. This includes details on how data was collected, what measurements were taken, and what statistical analyses were performed. The methods section of a medical paper allows other researchers to replicate the study if they choose to do so. It is considered one of the key components of a well-written research article, as it provides transparency and helps establish the validity of the findings.

I'm sorry for any confusion, but "Microchemistry" is not a commonly used term in medicine. It is, however, a branch of chemistry that deals with the separation, identification, and analysis of chemical substances in minute quantities. This field can be applied in various scientific disciplines, including forensic science, environmental science, and materials science.

In the medical field, you might encounter similar concepts under terms like "microanalysis" or "clinical chemistry," which refer to the identification and measurement of chemical components in body fluids (like blood or urine) for diagnostic purposes. But again, "Microchemistry" is not a standard term used in this context.

Automation in the medical context refers to the use of technology and programming to allow machines or devices to operate with minimal human intervention. This can include various types of medical equipment, such as laboratory analyzers, imaging devices, and robotic surgical systems. Automation can help improve efficiency, accuracy, and safety in healthcare settings by reducing the potential for human error and allowing healthcare professionals to focus on higher-level tasks. It is important to note that while automation has many benefits, it is also essential to ensure that appropriate safeguards are in place to prevent accidents and maintain quality of care.

Solid-phase microextraction (SPME) is an advanced technique used in analytical chemistry for the preparation and extraction of samples. It's not exclusively a medical term, but it does have applications in clinical and medical research. Here's a definition:

Solid-phase microextraction (SPME) is a solvent-free sample preparation technique that integrates sampling, extraction, concentration, and cleanup into a single step. It involves the use of a fused-silica fiber, which is coated with a thin layer of a stationary phase, such as polydimethylsiloxane (PDMS) or polyacrylate. This fiber is exposed to the sample matrix, allowing the analytes (compounds of interest) to be adsorbed or absorbed onto the coating. After the extraction step, the fiber is then inserted into a gas chromatograph or high-performance liquid chromatograph for analysis. SPME is widely used in various fields, including environmental monitoring, food analysis, and biomedical research, due to its simplicity, rapidity, and low cost. In the medical field, it can be applied for the analysis of drugs, metabolites, or other compounds in biological samples such as blood, urine, or tissue.

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

In the context of medicine and pharmacology, "kinetics" refers to the study of how a drug moves throughout the body, including its absorption, distribution, metabolism, and excretion (often abbreviated as ADME). This field is called "pharmacokinetics."

1. Absorption: This is the process of a drug moving from its site of administration into the bloodstream. Factors such as the route of administration (e.g., oral, intravenous, etc.), formulation, and individual physiological differences can affect absorption.

2. Distribution: Once a drug is in the bloodstream, it gets distributed throughout the body to various tissues and organs. This process is influenced by factors like blood flow, protein binding, and lipid solubility of the drug.

3. Metabolism: Drugs are often chemically modified in the body, typically in the liver, through processes known as metabolism. These changes can lead to the formation of active or inactive metabolites, which may then be further distributed, excreted, or undergo additional metabolic transformations.

4. Excretion: This is the process by which drugs and their metabolites are eliminated from the body, primarily through the kidneys (urine) and the liver (bile).

Understanding the kinetics of a drug is crucial for determining its optimal dosing regimen, potential interactions with other medications or foods, and any necessary adjustments for special populations like pediatric or geriatric patients, or those with impaired renal or hepatic function.

"Cattle" is a term used in the agricultural and veterinary fields to refer to domesticated animals of the genus *Bos*, primarily *Bos taurus* (European cattle) and *Bos indicus* (Zebu). These animals are often raised for meat, milk, leather, and labor. They are also known as bovines or cows (for females), bulls (intact males), and steers/bullocks (castrated males). However, in a strict medical definition, "cattle" does not apply to humans or other animals.

Drug stability refers to the ability of a pharmaceutical drug product to maintain its physical, chemical, and biological properties during storage and use, under specified conditions. A stable drug product retains its desired quality, purity, strength, and performance throughout its shelf life. Factors that can affect drug stability include temperature, humidity, light exposure, and container compatibility. Maintaining drug stability is crucial to ensure the safety and efficacy of medications for patients.

A tooth socket, also known as an alveolus (plural: alveoli), refers to the hollow cavity or space in the jawbone where a tooth is anchored. The tooth socket is part of the alveolar process, which is the curved part of the maxilla or mandible that contains multiple tooth sockets for the upper and lower teeth, respectively.

Each tooth socket has a specialized tissue called the periodontal ligament, which attaches the root of the tooth to the surrounding bone. This ligament helps absorb forces generated during biting and chewing, allowing for comfortable and efficient mastication while also maintaining the tooth's position within the jawbone. The tooth socket is responsible for providing support, stability, and nourishment to the tooth through its blood vessels and nerves.

A third molar is the most posterior of the three molars present in an adult human dental arch. They are also commonly known as wisdom teeth, due to their late eruption period which usually occurs between the ages of 17-25, a time traditionally associated with gaining maturity and wisdom.

Anatomically, third molars have four cusps, making them the largest of all the teeth. However, not everyone develops third molars; some people may have one, two, three or no third molars at all. In many cases, third molars do not have enough space to fully erupt and align properly with the rest of the teeth, leading to impaction, infection, or other dental health issues. As a result, third molars are often extracted if they cause problems or if there is a risk they will cause problems in the future.

Phenols, also known as phenolic acids or phenol derivatives, are a class of chemical compounds consisting of a hydroxyl group (-OH) attached to an aromatic hydrocarbon ring. In the context of medicine and biology, phenols are often referred to as a type of antioxidant that can be found in various foods and plants.

Phenols have the ability to neutralize free radicals, which are unstable molecules that can cause damage to cells and contribute to the development of chronic diseases such as cancer, heart disease, and neurodegenerative disorders. Some common examples of phenolic compounds include gallic acid, caffeic acid, ferulic acid, and ellagic acid, among many others.

Phenols can also have various pharmacological activities, including anti-inflammatory, antimicrobial, and analgesic effects. However, some phenolic compounds can also be toxic or irritating to the body in high concentrations, so their use as therapeutic agents must be carefully monitored and controlled.

Body fluids refer to the various liquids that can be found within and circulating throughout the human body. These fluids include, but are not limited to:

1. Blood: A fluid that carries oxygen, nutrients, hormones, and waste products throughout the body via the cardiovascular system. It is composed of red and white blood cells suspended in plasma.
2. Lymph: A clear-to-white fluid that circulates through the lymphatic system, helping to remove waste products, bacteria, and damaged cells from tissues while also playing a crucial role in the immune system.
3. Interstitial fluid: Also known as tissue fluid or extracellular fluid, it is the fluid that surrounds the cells in the body's tissues, allowing for nutrient exchange and waste removal between cells and blood vessels.
4. Cerebrospinal fluid (CSF): A clear, colorless fluid that circulates around the brain and spinal cord, providing protection, cushioning, and nutrients to these delicate structures while also removing waste products.
5. Pleural fluid: A small amount of lubricating fluid found in the pleural space between the lungs and the chest wall, allowing for smooth movement during respiration.
6. Pericardial fluid: A small amount of lubricating fluid found within the pericardial sac surrounding the heart, reducing friction during heart contractions.
7. Synovial fluid: A viscous, lubricating fluid found in joint spaces, allowing for smooth movement and protecting the articular cartilage from wear and tear.
8. Urine: A waste product produced by the kidneys, consisting of water, urea, creatinine, and various ions, which is excreted through the urinary system.
9. Gastrointestinal secretions: Fluids produced by the digestive system, including saliva, gastric juice, bile, pancreatic juice, and intestinal secretions, which aid in digestion, absorption, and elimination of food particles.
10. Reproductive fluids: Secretions from the male (semen) and female (cervical mucus, vaginal lubrication) reproductive systems that facilitate fertilization and reproduction.

"Device Removal" in a medical context generally refers to the surgical or nonsurgical removal of a medical device that has been previously implanted in a patient's body. The purpose of removing the device may vary, depending on the individual case. Some common reasons for device removal include infection, malfunction, rejection, or when the device is no longer needed.

Examples of medical devices that may require removal include pacemakers, implantable cardioverter-defibrillators (ICDs), artificial joints, orthopedic hardware, breast implants, cochlear implants, and intrauterine devices (IUDs). The procedure for device removal will depend on the type of device, its location in the body, and the reason for its removal.

It is important to note that device removal carries certain risks, such as bleeding, infection, damage to surrounding tissues, or complications related to anesthesia. Therefore, the decision to remove a medical device should be made carefully, considering both the potential benefits and risks of the procedure.

Solubility is a fundamental concept in pharmaceutical sciences and medicine, which refers to the maximum amount of a substance (solute) that can be dissolved in a given quantity of solvent (usually water) at a specific temperature and pressure. Solubility is typically expressed as mass of solute per volume or mass of solvent (e.g., grams per liter, milligrams per milliliter). The process of dissolving a solute in a solvent results in a homogeneous solution where the solute particles are dispersed uniformly throughout the solvent.

Understanding the solubility of drugs is crucial for their formulation, administration, and therapeutic effectiveness. Drugs with low solubility may not dissolve sufficiently to produce the desired pharmacological effect, while those with high solubility might lead to rapid absorption and short duration of action. Therefore, optimizing drug solubility through various techniques like particle size reduction, salt formation, or solubilization is an essential aspect of drug development and delivery.

Electrophoresis, polyacrylamide gel (EPG) is a laboratory technique used to separate and analyze complex mixtures of proteins or nucleic acids (DNA or RNA) based on their size and electrical charge. This technique utilizes a matrix made of cross-linked polyacrylamide, a type of gel, which provides a stable and uniform environment for the separation of molecules.

In this process:

1. The polyacrylamide gel is prepared by mixing acrylamide monomers with a cross-linking agent (bis-acrylamide) and a catalyst (ammonium persulfate) in the presence of a buffer solution.
2. The gel is then poured into a mold and allowed to polymerize, forming a solid matrix with uniform pore sizes that depend on the concentration of acrylamide used. Higher concentrations result in smaller pores, providing better resolution for separating smaller molecules.
3. Once the gel has set, it is placed in an electrophoresis apparatus containing a buffer solution. Samples containing the mixture of proteins or nucleic acids are loaded into wells on the top of the gel.
4. An electric field is applied across the gel, causing the negatively charged molecules to migrate towards the positive electrode (anode) while positively charged molecules move toward the negative electrode (cathode). The rate of migration depends on the size, charge, and shape of the molecules.
5. Smaller molecules move faster through the gel matrix and will migrate farther from the origin compared to larger molecules, resulting in separation based on size. Proteins and nucleic acids can be selectively stained after electrophoresis to visualize the separated bands.

EPG is widely used in various research fields, including molecular biology, genetics, proteomics, and forensic science, for applications such as protein characterization, DNA fragment analysis, cloning, mutation detection, and quality control of nucleic acid or protein samples.

Heptanes are a group of hydrocarbons that are composed of straight-chain or branched arrangements of six carbon atoms and are commonly found in gasoline. They are colorless liquids at room temperature with a characteristic odor. In a medical context, exposure to heptanes can occur through inhalation, skin contact, or ingestion, and can cause symptoms such as headache, dizziness, nausea, and irritation of the eyes, nose, and throat. Chronic exposure has been linked to more serious health effects, including neurological damage and cancer. Proper handling and use of heptanes, as well as adequate ventilation, are important to minimize exposure and potential health risks.

"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.

I'm sorry for any confusion, but "microwaves" is not a term typically used in medical definitions. Microwaves are a form of electromagnetic radiation with wavelengths ranging from one meter to one millimeter; they are commonly used in communication devices and home appliances such as microwave ovens. If you have any questions related to health or medicine, please provide more context so I can give you a more accurate response.

Molecular weight, also known as molecular mass, is the mass of a molecule. It is expressed in units of atomic mass units (amu) or daltons (Da). Molecular weight is calculated by adding up the atomic weights of each atom in a molecule. It is a useful property in chemistry and biology, as it can be used to determine the concentration of a substance in a solution, or to calculate the amount of a substance that will react with another in a chemical reaction.

I'm sorry for any confusion, but "Fluorocarbons" are not typically associated with medical definitions. Fluorocarbons are chemical compounds that contain carbon atoms bonded to fluorine atoms. They are often used in a variety of applications including refrigerants, fire extinguishing agents, and in the manufacturing of Teflon and other non-stick coatings.

If you have any medical terms or concepts you'd like me to define or explain, please let me know!

Polymerase Chain Reaction (PCR) is a laboratory technique used to amplify specific regions of DNA. It enables the production of thousands to millions of copies of a particular DNA sequence in a rapid and efficient manner, making it an essential tool in various fields such as molecular biology, medical diagnostics, forensic science, and research.

The PCR process involves repeated cycles of heating and cooling to separate the DNA strands, allow primers (short sequences of single-stranded DNA) to attach to the target regions, and extend these primers using an enzyme called Taq polymerase, resulting in the exponential amplification of the desired DNA segment.

In a medical context, PCR is often used for detecting and quantifying specific pathogens (viruses, bacteria, fungi, or parasites) in clinical samples, identifying genetic mutations or polymorphisms associated with diseases, monitoring disease progression, and evaluating treatment effectiveness.

An amino acid sequence is the specific order of amino acids in a protein or peptide molecule, formed by the linking of the amino group (-NH2) of one amino acid to the carboxyl group (-COOH) of another amino acid through a peptide bond. The sequence is determined by the genetic code and is unique to each type of protein or peptide. It plays a crucial role in determining the three-dimensional structure and function of proteins.

Ion exchange chromatography is a type of chromatography technique used to separate and analyze charged molecules (ions) based on their ability to exchange bound ions in a solid resin or gel with ions of similar charge in the mobile phase. The stationary phase, often called an ion exchanger, contains fixed ated functional groups that can attract counter-ions of opposite charge from the sample mixture.

In this technique, the sample is loaded onto an ion exchange column containing the charged resin or gel. As the sample moves through the column, ions in the sample compete for binding sites on the stationary phase with ions already present in the column. The ions that bind most strongly to the stationary phase will elute (come off) slower than those that bind more weakly.

Ion exchange chromatography can be performed using either cation exchangers, which exchange positive ions (cations), or anion exchangers, which exchange negative ions (anions). The pH and ionic strength of the mobile phase can be adjusted to control the binding and elution of specific ions.

Ion exchange chromatography is widely used in various applications such as water treatment, protein purification, and chemical analysis.

In the context of medical terminology, "solutions" refers to a homogeneous mixture of two or more substances, in which one substance (the solute) is uniformly distributed within another substance (the solvent). The solvent is typically the greater component of the solution and is capable of dissolving the solute.

Solutions can be classified based on the physical state of the solvent and solute. For instance, a solution in which both the solvent and solute are liquids is called a liquid solution or simply a solution. A solid solution is one where the solvent is a solid and the solute is either a gas, liquid, or solid. Similarly, a gas solution refers to a mixture where the solvent is a gas and the solute can be a gas, liquid, or solid.

In medical applications, solutions are often used as vehicles for administering medications, such as intravenous (IV) fluids, oral rehydration solutions, eye drops, and topical creams or ointments. The composition of these solutions is carefully controlled to ensure the appropriate concentration and delivery of the active ingredients.

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

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

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

Biotransformation is the metabolic modification of a chemical compound, typically a xenobiotic (a foreign chemical substance found within an living organism), by a biological system. This process often involves enzymatic conversion of the parent compound to one or more metabolites, which may be more or less active, toxic, or mutagenic than the original substance.

In the context of pharmacology and toxicology, biotransformation is an important aspect of drug metabolism and elimination from the body. The liver is the primary site of biotransformation, but other organs such as the kidneys, lungs, and gastrointestinal tract can also play a role.

Biotransformation can occur in two phases: phase I reactions involve functionalization of the parent compound through oxidation, reduction, or hydrolysis, while phase II reactions involve conjugation of the metabolite with endogenous molecules such as glucuronic acid, sulfate, or acetate to increase its water solubility and facilitate excretion.

Sensitivity and specificity are statistical measures used to describe the performance of a diagnostic test or screening tool in identifying true positive and true negative results.

* Sensitivity refers to the proportion of people who have a particular condition (true positives) who are correctly identified by the test. It is also known as the "true positive rate" or "recall." A highly sensitive test will identify most or all of the people with the condition, but may also produce more false positives.
* Specificity refers to the proportion of people who do not have a particular condition (true negatives) who are correctly identified by the test. It is also known as the "true negative rate." A highly specific test will identify most or all of the people without the condition, but may also produce more false negatives.

In medical testing, both sensitivity and specificity are important considerations when evaluating a diagnostic test. High sensitivity is desirable for screening tests that aim to identify as many cases of a condition as possible, while high specificity is desirable for confirmatory tests that aim to rule out the condition in people who do not have it.

It's worth noting that sensitivity and specificity are often influenced by factors such as the prevalence of the condition in the population being tested, the threshold used to define a positive result, and the reliability and validity of the test itself. Therefore, it's important to consider these factors when interpreting the results of a diagnostic test.

A phase transition in the context of medicine and physiology often refers to the transformation of a substance or matter from one state to another within the body, typically in relation to temperature or pressure changes. However, I couldn't find a widely accepted medical definition for "phase transition."

In physics and chemistry, a phase transition is a process where a thermodynamic system changes from one phase or state of matter to another, such as:

1. Solid to liquid (melting)
2. Liquid to gas (vaporization)
3. Gas to liquid (condensation)
4. Solid to gas (sublimation)
5. Changes between different crystalline structures of the same substance (polymorphic phase transitions)

While not a direct medical definition, these concepts are relevant in various biochemical and physiological processes, such as protein folding, cell membrane fluidity, and temperature regulation in the body.

Amino acids are organic compounds that serve as the building blocks of proteins. They consist of a central carbon atom, also known as the alpha carbon, which is bonded to an amino group (-NH2), a carboxyl group (-COOH), a hydrogen atom (H), and a variable side chain (R group). The R group can be composed of various combinations of atoms such as hydrogen, oxygen, sulfur, nitrogen, and carbon, which determine the unique properties of each amino acid.

There are 20 standard amino acids that are encoded by the genetic code and incorporated into proteins during translation. These include:

1. Alanine (Ala)
2. Arginine (Arg)
3. Asparagine (Asn)
4. Aspartic acid (Asp)
5. Cysteine (Cys)
6. Glutamine (Gln)
7. Glutamic acid (Glu)
8. Glycine (Gly)
9. Histidine (His)
10. Isoleucine (Ile)
11. Leucine (Leu)
12. Lysine (Lys)
13. Methionine (Met)
14. Phenylalanine (Phe)
15. Proline (Pro)
16. Serine (Ser)
17. Threonine (Thr)
18. Tryptophan (Trp)
19. Tyrosine (Tyr)
20. Valine (Val)

Additionally, there are several non-standard or modified amino acids that can be incorporated into proteins through post-translational modifications, such as hydroxylation, methylation, and phosphorylation. These modifications expand the functional diversity of proteins and play crucial roles in various cellular processes.

Amino acids are essential for numerous biological functions, including protein synthesis, enzyme catalysis, neurotransmitter production, energy metabolism, and immune response regulation. Some amino acids can be synthesized by the human body (non-essential), while others must be obtained through dietary sources (essential).

I'm sorry for any confusion, but "Natural Language Processing" (NLP) is actually a subfield of artificial intelligence that focuses on the interaction between computers and human language. It involves developing algorithms and software to understand, interpret, and generate human language in a valuable way.

In a medical context, NLP can be used to analyze electronic health records, clinical notes, and other forms of medical documentation to extract meaningful information, support clinical decision-making, and improve patient care. For example, NLP can help identify patients at risk for certain conditions, monitor treatment responses, and detect adverse drug events.

However, NLP is not a medical term or concept itself, so it doesn't have a specific medical definition.

"Quality control" is a term that is used in many industries, including healthcare and medicine, to describe the systematic process of ensuring that products or services meet certain standards and regulations. In the context of healthcare, quality control often refers to the measures taken to ensure that the care provided to patients is safe, effective, and consistent. This can include processes such as:

1. Implementing standardized protocols and guidelines for care
2. Training and educating staff to follow these protocols
3. Regularly monitoring and evaluating the outcomes of care
4. Making improvements to processes and systems based on data and feedback
5. Ensuring that equipment and supplies are maintained and functioning properly
6. Implementing systems for reporting and addressing safety concerns or errors.

The goal of quality control in healthcare is to provide high-quality, patient-centered care that meets the needs and expectations of patients, while also protecting their safety and well-being.

Forensic Toxicology is a branch of toxicology that applies scientific methods and techniques to investigate and provide information about the presence, identity, concentration, and effects of drugs, poisons, or other chemicals in biological specimens (such as blood, urine, tissues) within a legal context. It is often used in criminal investigations, medical examinations, and workplace drug testing to determine the cause of death, poisoning, impairment, or other health effects related to exposure to toxic substances. Forensic toxicologists may also provide expert testimony in court based on their findings.

Pesticide residues refer to the remaining pesticide chemicals, including their metabolites and degradation products, that are present in or on food commodities or environmental samples after a pesticide application has ended. These residues can result from agricultural use, such as spraying crops to control pests, or from non-agricultural uses, like treating buildings for termite control.

Regulatory agencies establish maximum residue limits (MRLs) to ensure that the levels of pesticide residues in food and feed are below those that may pose a risk to human health. Monitoring programs are in place to check compliance with these MRLs, and enforcement actions can be taken if violations occur.

It's important to note that not all pesticide residues are harmful, as some pesticides degrade into harmless compounds over time or leave behind residues below levels of concern for human health. However, long-term exposure to even low levels of certain pesticide residues may still pose a risk and should be avoided when possible.

The liver is a large, solid organ located in the upper right portion of the abdomen, beneath the diaphragm and above the stomach. It plays a vital role in several bodily functions, including:

1. Metabolism: The liver helps to metabolize carbohydrates, fats, and proteins from the food we eat into energy and nutrients that our bodies can use.
2. Detoxification: The liver detoxifies harmful substances in the body by breaking them down into less toxic forms or excreting them through bile.
3. Synthesis: The liver synthesizes important proteins, such as albumin and clotting factors, that are necessary for proper bodily function.
4. Storage: The liver stores glucose, vitamins, and minerals that can be released when the body needs them.
5. Bile production: The liver produces bile, a digestive juice that helps to break down fats in the small intestine.
6. Immune function: The liver plays a role in the immune system by filtering out bacteria and other harmful substances from the blood.

Overall, the liver is an essential organ that plays a critical role in maintaining overall health and well-being.

Gel chromatography is a type of liquid chromatography that separates molecules based on their size or molecular weight. It uses a stationary phase that consists of a gel matrix made up of cross-linked polymers, such as dextran, agarose, or polyacrylamide. The gel matrix contains pores of various sizes, which allow smaller molecules to penetrate deeper into the matrix while larger molecules are excluded.

In gel chromatography, a mixture of molecules is loaded onto the top of the gel column and eluted with a solvent that moves down the column by gravity or pressure. As the sample components move down the column, they interact with the gel matrix and get separated based on their size. Smaller molecules can enter the pores of the gel and take longer to elute, while larger molecules are excluded from the pores and elute more quickly.

Gel chromatography is commonly used to separate and purify proteins, nucleic acids, and other biomolecules based on their size and molecular weight. It is also used in the analysis of polymers, colloids, and other materials with a wide range of applications in chemistry, biology, and medicine.

Proteomics is the large-scale study and analysis of proteins, including their structures, functions, interactions, modifications, and abundance, in a given cell, tissue, or organism. It involves the identification and quantification of all expressed proteins in a biological sample, as well as the characterization of post-translational modifications, protein-protein interactions, and functional pathways. Proteomics can provide valuable insights into various biological processes, diseases, and drug responses, and has applications in basic research, biomedicine, and clinical diagnostics. The field combines various techniques from molecular biology, chemistry, physics, and bioinformatics to study proteins at a systems level.

Silica gel is not typically considered a medical term, but it is often used in medical contexts. Silica gel is a form of silicon dioxide (SiO2), which is a naturally occurring mineral. It is usually produced in a porous form, with a large surface area and high absorption capacity.

In the medical field, silica gel is sometimes used as a desiccant in packaging to protect sterile medical supplies from moisture during storage and transportation. This helps maintain the sterility of the products and ensures their effectiveness when they are used. Silica gel can also be found in some medical devices, such as wound dressings, where it can help absorb excess exudate and maintain a moist environment that promotes healing.

It is important to note that silica gel should not be ingested or inhaled, as it can cause irritation to the respiratory and gastrointestinal tracts.

"Food analysis" is not a medical term per se, but it falls under the broader field of food science and nutrition. Food analysis refers to the laboratory methods and techniques used to determine the composition and quality of food products. This can include testing for nutrients (such as proteins, fats, carbohydrates, vitamins, and minerals), contaminants (like heavy metals, pesticides, or allergens), and other components that may affect the safety, quality, or authenticity of food.

The results of food analysis can be used to ensure compliance with regulatory standards, develop new food products, assess the nutritional value of diets, investigate food-borne illnesses, and monitor trends in food consumption. While not a medical definition, food analysis is an important tool for promoting public health and preventing diet-related diseases.

Radioimmunoassay (RIA) is a highly sensitive analytical technique used in clinical and research laboratories to measure concentrations of various substances, such as hormones, vitamins, drugs, or tumor markers, in biological samples like blood, urine, or tissues. The method relies on the specific interaction between an antibody and its corresponding antigen, combined with the use of radioisotopes to quantify the amount of bound antigen.

In a typical RIA procedure, a known quantity of a radiolabeled antigen (also called tracer) is added to a sample containing an unknown concentration of the same unlabeled antigen. The mixture is then incubated with a specific antibody that binds to the antigen. During the incubation period, the antibody forms complexes with both the radiolabeled and unlabeled antigens.

After the incubation, the unbound (free) radiolabeled antigen is separated from the antibody-antigen complexes, usually through a precipitation or separation step involving centrifugation, filtration, or chromatography. The amount of radioactivity in the pellet (containing the antibody-antigen complexes) is then measured using a gamma counter or other suitable radiation detection device.

The concentration of the unlabeled antigen in the sample can be determined by comparing the ratio of bound to free radiolabeled antigen in the sample to a standard curve generated from known concentrations of unlabeled antigen and their corresponding bound/free ratios. The higher the concentration of unlabeled antigen in the sample, the lower the amount of radiolabeled antigen that will bind to the antibody, resulting in a lower bound/free ratio.

Radioimmunoassays offer high sensitivity, specificity, and accuracy, making them valuable tools for detecting and quantifying low levels of various substances in biological samples. However, due to concerns about radiation safety and waste disposal, alternative non-isotopic immunoassay techniques like enzyme-linked immunosorbent assays (ELISAs) have become more popular in recent years.

Stereoisomerism is a type of isomerism (structural arrangement of atoms) in which molecules have the same molecular formula and sequence of bonded atoms, but differ in the three-dimensional orientation of their atoms in space. This occurs when the molecule contains asymmetric carbon atoms or other rigid structures that prevent free rotation, leading to distinct spatial arrangements of groups of atoms around a central point. Stereoisomers can have different chemical and physical properties, such as optical activity, boiling points, and reactivities, due to differences in their shape and the way they interact with other molecules.

There are two main types of stereoisomerism: enantiomers (mirror-image isomers) and diastereomers (non-mirror-image isomers). Enantiomers are pairs of stereoisomers that are mirror images of each other, but cannot be superimposed on one another. Diastereomers, on the other hand, are non-mirror-image stereoisomers that have different physical and chemical properties.

Stereoisomerism is an important concept in chemistry and biology, as it can affect the biological activity of molecules, such as drugs and natural products. For example, some enantiomers of a drug may be active, while others are inactive or even toxic. Therefore, understanding stereoisomerism is crucial for designing and synthesizing effective and safe drugs.

An algorithm is not a medical term, but rather a concept from computer science and mathematics. In the context of medicine, algorithms are often used to describe step-by-step procedures for diagnosing or managing medical conditions. These procedures typically involve a series of rules or decision points that help healthcare professionals make informed decisions about patient care.

For example, an algorithm for diagnosing a particular type of heart disease might involve taking a patient's medical history, performing a physical exam, ordering certain diagnostic tests, and interpreting the results in a specific way. By following this algorithm, healthcare professionals can ensure that they are using a consistent and evidence-based approach to making a diagnosis.

Algorithms can also be used to guide treatment decisions. For instance, an algorithm for managing diabetes might involve setting target blood sugar levels, recommending certain medications or lifestyle changes based on the patient's individual needs, and monitoring the patient's response to treatment over time.

Overall, algorithms are valuable tools in medicine because they help standardize clinical decision-making and ensure that patients receive high-quality care based on the latest scientific evidence.

Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry (MALDI-MS) is a type of mass spectrometry that is used to analyze large biomolecules such as proteins and peptides. In this technique, the sample is mixed with a matrix compound, which absorbs laser energy and helps to vaporize and ionize the analyte molecules.

The matrix-analyte mixture is then placed on a target plate and hit with a laser beam, causing the matrix and analyte molecules to desorb from the plate and become ionized. The ions are then accelerated through an electric field and into a mass analyzer, which separates them based on their mass-to-charge ratio.

The separated ions are then detected and recorded as a mass spectrum, which can be used to identify and quantify the analyte molecules present in the sample. MALDI-MS is particularly useful for the analysis of complex biological samples, such as tissue extracts or biological fluids, because it allows for the detection and identification of individual components within those mixtures.

Pharmaceutical preparations refer to the various forms of medicines that are produced by pharmaceutical companies, which are intended for therapeutic or prophylactic use. These preparations consist of an active ingredient (the drug) combined with excipients (inactive ingredients) in a specific formulation and dosage form.

The active ingredient is the substance that has a therapeutic effect on the body, while the excipients are added to improve the stability, palatability, bioavailability, or administration of the drug. Examples of pharmaceutical preparations include tablets, capsules, solutions, suspensions, emulsions, ointments, creams, and injections.

The production of pharmaceutical preparations involves a series of steps that ensure the quality, safety, and efficacy of the final product. These steps include the selection and testing of raw materials, formulation development, manufacturing, packaging, labeling, and storage. Each step is governed by strict regulations and guidelines to ensure that the final product meets the required standards for use in medical practice.

"Swine" is a common term used to refer to even-toed ungulates of the family Suidae, including domestic pigs and wild boars. However, in a medical context, "swine" often appears in the phrase "swine flu," which is a strain of influenza virus that typically infects pigs but can also cause illness in humans. The 2009 H1N1 pandemic was caused by a new strain of swine-origin influenza A virus, which was commonly referred to as "swine flu." It's important to note that this virus is not transmitted through eating cooked pork products; it spreads from person to person, mainly through respiratory droplets produced when an infected person coughs or sneezes.

Ethanol is the medical term for pure alcohol, which is a colorless, clear, volatile, flammable liquid with a characteristic odor and burning taste. It is the type of alcohol that is found in alcoholic beverages and is produced by the fermentation of sugars by yeasts.

In the medical field, ethanol is used as an antiseptic and disinfectant, and it is also used as a solvent for various medicinal preparations. It has central nervous system depressant properties and is sometimes used as a sedative or to induce sleep. However, excessive consumption of ethanol can lead to alcohol intoxication, which can cause a range of negative health effects, including impaired judgment, coordination, and memory, as well as an increased risk of accidents, injuries, and chronic diseases such as liver disease and addiction.

... (LLE), also known as solvent extraction and partitioning, is a method to separate compounds or metal ... Liquid-liquid extraction is possible in non-aqueous systems: In a system consisting of a molten metal in contact with molten ... After performing liquid-liquid extraction, a quantitative measure must be taken to determine the ratio of the solution's total ... Success of liquid-liquid extraction is measured through separation factors and decontamination factors. The best way to ...
A reactive liquid extraction process is a liquid-liquid extraction process that is intensified through a mechanism involving a ... Tamada, J. A.; Kertes, A. S.; King, C. J. "Extraction of carboxylic acids with amine extractants. 1. equilibria and law of mass ...
... is a subclass of liquid-liquid extractions and involves the separation of chemical species from other ... "Liquid liquid extractions" (PDF). Minnesota State University. "Acid-Base Extraction". Chemistry LibreTexts. 2013-10-03. ... Chromatography Extraction Multiphasic liquid Separating funnel "Acid-Base Extraction". Chemistry LibreTexts. 2013-10-03. ... A separatory funnel is commonly used to perform an acid-base extraction. Acid-base extraction utilizes the difference in ...
... liquid-liquid extraction; adsorption and ion exchange; gas-solid, liquid-solid and solid-solid operations; biochemical ...
He was known for his research on liquid-liquid extraction at Alagappa College of Technology, Anna University, and his ... G. S. Laddha; T. E. Degaleesan (1978). Transport phenomena in liquid extraction. McGraw-Hill. G. S. Laddha (1976). Towards the ... liquid_extraction.html?id=2spTAAAAMAAJ&redir_esc=y (All articles with dead external links, Articles with dead external links ...
"Nomenclature for liquid-liquid distribution (solvent extraction)". Pure Appl. Chem. IUPAC. 65 (11): 2373-2396. doi:10.1351/ ... 2004). Solvent Extraction Principles and Practice ( (2nd. ed.). Boca Raton, Fla.: CRC Press. ISBN 978-0-8247-5063-3. Buck, R. P ... This is particularly true in gas-liquid chromatography where column lengths up to 60 m are possible, providing a very large ... In ion-exchange chromatography the selectivity coefficient is defined in a slightly different way Solvent extraction is used to ...
Stauffer, E.; Dolan, J.; Newman, R. (2008). "Extraction of Ignitable Liquid Residues from Fire Debris". Fire Debris Analysis. ... Some of the most common methods include solvent extraction, headspace extraction, and adsorption extraction which in itself has ... It is important to understand that an ignitable liquid is a liquid that will readily ignite when exposed to an ignition source ... but it could also be present at a scene as an ignitable liquid due to gasoline being a common fuel. Although ignitable liquids ...
... the Liquid Solvent Extraction Process by British Coal; and the Brown Coal Liquefaction Process of Japan have been developed. ... Liquid yields of pyrolysis and Karrick processes are generally low for practical use for synthetic liquid fuel production. ... gas-to-liquids (GTL) or biomass-to-liquids (BTL), depending on the initial feedstock. At least three projects (Ohio River Clean ... However, the produced liquids are mostly a by-product and the main product is semi-coke, a solid and smokeless fuel. The COED ...
Extraction is effective to separate immiscible liquid phases. Filtration is effective to separate dispersed particles that are ... Centrifugation, extraction, and filtration are examples of methods which separate material in different phases. Centrifugation ... Analytical methods used on liquid phases might include distillation or one of a variety of chromatographic separation methods. ... Chomatography separates components of a liquid or gaseous mixture according to differences in retention time as the mixture ...
... the Liquid Solvent Extraction Process by British Coal; and the Brown Coal Liquefaction Process of Japan have been developed. ... Liquid yields of pyrolysis and the Karrick process are generally considered too low for practical use for synthetic liquid fuel ... Coal liquefaction is a process of converting coal into liquid hydrocarbons: liquid fuels and petrochemicals. This process is ... However, any produced liquids are mostly a by-product and the main product is semi-coke - a solid and smokeless fuel. The COED ...
It is an example of liquid-liquid extraction. The process takes advantage of two liquid-state properties of zinc. The first is ... If gold is present in the liquid lead, it can also be removed and isolated by the same process. The process was patented by ... When zinc is added to liquid lead that contains silver as a contaminant, the silver preferentially migrates into the zinc. ...
It is based on liquid-liquid extraction ion-exchange. PUREX is applied to spent nuclear fuel, which consists primarily of very ... The other is from the medium-active cycle in which the uranium and plutonium are refined by a second extraction with tributyl ... Uranium is then stripped from the kerosene solution by back-extraction into nitric acid at a concentration around 0.2 M. The ... J.H. Burns (1983). "Solvent-extraction complexes of the uranyl ion. 2. Crystal and molecular structures of catena-bis(.mu.-di-n ...
Laskin J, Lanekoff I (January 2016). "Ambient Mass Spectrometry Imaging Using Direct Liquid Extraction Techniques". Analytical ... an ambient method for liquid-extraction surface sampling in mass spectrometry". The Analyst. 135 (9): 2233-2236. Bibcode: ... The liquid bridge is maintained by continuous flow of the solvent and the contact area between the solvent bridge and sample ... In this technique, analytes are desorbed into a liquid bridge formed between two capillaries and the sampling surface. Unlike ...
Analytes are then extracted from the sample into the solvent droplet by a solid-liquid extraction mechanism. After a 3 second ... The MasSpec Pen can further be categorized as a solid-liquid extraction based ambient ionization method, described as methods ... The system collects biological molecules from a tissue sample surface via a solid-liquid extraction mechanism and transports ... ISBN 978-1-84973-926-9. Laskin J, Lanekoff I (January 2016). "Ambient Mass Spectrometry Imaging Using Direct Liquid Extraction ...
... are a type of liquid-liquid extraction equipment; examples of this class of extraction equipment is used at the ... Special use in nuclear industries for fuel reprocessing, where spent fuel from reactors is subjected to solvent extraction. A ... But, because of radioactivity, and frequent maintenance required for mechanical agitators, pulsing is used in extraction ...
The yield of this process is approximately 95%. The purification takes place with a liquid-gas-phase extraction. In the ... GHB has biphasic effects, a euphoric effect at low doses (the reason for the term liquid ecstasy), and a sedative effect at ... The concentration detected was approximately 5 μg/mL and was easily observed using a simple extraction technique followed by GC ... Gamma-butyrolactone (GBL) or γ-butyrolactone, is a hygroscopic colorless, water-miscible liquid with a weak characteristic odor ...
"Oilfield produced water treatment by liquid-liquid extraction: A review". Journal of Petroleum Science and Engineering. 199: ... "Oil and Gas Extraction Effluent Guidelines". EPA. 2019-05-15. Development Document for Final Effluent Limitations Guidelines ... or used as a medium for heat extraction. Water that is produced along with the hydrocarbons is generally brackish and saline ... a term used in the oil industry or geothermal industry to describe water that is produced as a byproduct during the extraction ...
It is further refined through aqueous-solvent liquid-liquid extraction. Crack is usually smoked in a glass pipe, and once ... Alternatively, coca leaves can be infused in liquid and consumed like tea. Coca tea, an infusion of coca leaves, is also a ... After extraction from the plant, and further processing into cocaine hydrochloride (powdered cocaine), the drug is administered ... A chemical analysis by solid-phase extraction and gas chromatography-mass spectrometry (SPE-GC/MS) of Peruvian and Bolivian tea ...
ISBN 978-0-9678550-9-7. Rice NM, Irving HM, Leonard MA (1993). "Nomenclature for liquid-liquid distribution (solvent extraction ... Thus, the concentration of A remaining in an aqueous solution after i extractions with an organic solvent can be found using ... even after a number of solvent extractions have occurred. They also provide guidance in choosing the most efficient way to ...
Liquid-liquid extraction can be also performed or countercurrent chromatography. Solid phase extraction can also be made on C18 ... high-pressure liquid extraction or use of ethanol in an immersion extractor. The extraction conditions (temperature, extraction ... Other techniques are ultrasonic extraction, heat reflux extraction, microwave-assisted extraction, critical carbon dioxide, ... Alonso-Salces RM, Korta E, Barranco A, Berrueta LA, Gallo B, Vicente F (November 2001). "Pressurized liquid extraction for the ...
This way, the extraction of the solute is enhanced. While during conventional liquid-liquid extraction the solvent and the ... The setup would consist of a packed column or a fluidized bed rather than liquid-liquid extraction equipment with additional ... Also, the impregnation step decreases the solvent loss into the aqueous phase compared to liquid-liquid extraction. This ... The basic principle combines adsorption, chromatography and liquid-liquid extraction. The principle of Solvent Impregnated ...
Bruce W. Baldwin, Kasey R. Bunker, Thoman S. Kuntzleman (2019). "Extraction of Dyes Contained in Glow Sticks Using Liquid CO2 ... The liquid is then allowed to travel up the chalk; polar dyes would tend to stick to the chalk and not travel significantly ... In this case, non polar dyes would dissolve in the liquid CO2 and other dyes would be attracted to cotton. Retardation factor ... Further, dyes in glow sticks can also be extracted using liquid carbon dioxide (CO2) as an environmentally friendly or green ...
... see liquid-liquid extraction. It is possible to extract a solute from one liquid phase to another without a chemical reaction. ... The process of gas or liquid which penetrate into the body of adsorbent is commonly known as absorption. If absorption is a ... liquid or solid) of the material in which it is taken up." A more general term is sorption, which covers absorption, adsorption ... liquid or solid material. This is a different process from adsorption, since molecules undergoing absorption are taken up by ...
Barros, Sam; Atkinson, William; Piduru, Naag (2015). "Extraction of Liquid Water from the Exhaust of a Diesel Engine". SAE ... "Quantitation of polycyclic aromatic hydrocarbons in diesel exhaust particulate matter by high-performance liquid chromatography ...
Modern methods of production include liquid-liquid extraction using common solvents such as hexane, petroleum ether, chloroform ... "Solvent Extraction of Egg Oil of From Liquid Egg Yolk" (PDF). Tini M, Jewell UR, Camenisch G, Chilov D, Gassmann M (2002). " ... Warren, M. W.; Brown, H. G.; Davis, D. R. (2014). "Solvent extraction of lipid components from egg yolk solids". Journal of the ...
Separatory funnels are used in liquid-liquid extractions. Borosilicate glass is one of the most common materials of choice for ... When used with filter paper, filter funnels, Buchner and Hirsch funnels can be used to remove fine particles from a liquid in a ...
Separatory funnels are used in liquid-liquid extractions. The Tullgren funnel is used to collect arthropods from plant litter ... To channel liquids or fine-grained substances into containers with a small opening. Used for pouring liquids or powder through ... A funnel is a tube or pipe that is wide at the top and narrow at the bottom, used for guiding liquid or powder into a small ... Used in transferring liquids in small containers. Funnels known as killing cones are used to slaughter individual birds in ...
... (SPE) is a solid-liquid extractive technique, by which compounds that are dissolved or suspended in a ... Hennion, Marie-Claire (1999). "Solid-phase extraction: method development, sorbents, and coupling with liquid chromatography". ... Analytical laboratories use solid phase extraction to concentrate and purify samples for analysis. Solid phase extraction can ... is a solid phase extraction technique that involves the use of a fiber coated with an extracting phase, that can be a liquid ( ...
Today, liquid solvent extraction procedures involving selective complexation of Th4+ are used. For example, following alkaline ... Solvent extraction may also be used to separate out the thorium and uranium, by dissolving the resultant filter cake in nitric ... Thorium forms eutectic mixtures with chromium and uranium, and it is completely miscible in both solid and liquid states with ... There are two categories of thorium minerals for thorium extraction: primary and secondary. Primary deposits occur in acidic ...
Ionic liquids have been considered as solvents in a variety of liquid-liquid extraction processes, but never commercialized. ... "Room temperature ionic liquids as novel media for 'clean' liquid-liquid extraction". Chem. Commun. (16): 1765-1766. doi:10.1039 ... Finally, ionic liquids can be mixed with other ionic liquids, water, or amines to achieve different properties in terms of ... Ionic liquids, which are salts that exist as liquids near room temperature, are polar, nonvolatile materials that have been ...
It may be used for the shale oil extraction and coal liquefaction. Other liquids extraction processes from solid fuels are ...

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