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.
The analysis of a chemical substance by inserting a sample into a carrier stream of reagent using a sample injection valve that propels the sample downstream where mixing occurs in a coiled tube, then passes into a flow-through detector and a recorder or other data handling device.
Solid dosage forms, of varying weight, size, and shape, which may be molded or compressed, and which contain a medicinal substance in pure or diluted form. (Dorland, 28th ed)
Solution titration in which the end point is read from the electrode-potential variations with the concentrations of potential determining ions. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
Homogeneous liquid preparations that contain one or more chemical substances dissolved, i.e., molecularly dispersed, in a suitable solvent or mixture of mutually miscible solvents. For reasons of their ingredients, method of preparation, or use, they do not fall into another group of products.
A phenothiazine with actions similar to CHLORPROMAZINE but with less antipsychotic activity. It is primarily used in short-term treatment of disturbed behavior and as an antiemetic.
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.
Completed forms of the pharmaceutical preparation in which prescribed doses of medication are included. They are designed to resist action by gastric fluids, prevent vomiting and nausea, reduce or alleviate the undesirable taste and smells associated with oral administration, achieve a high concentration of drug at target site, or produce a delayed or long-acting drug effect.
Drugs intended for DENTISTRY.
Electric conductors through which electric currents enter or leave a medium, whether it be an electrolytic solution, solid, molten mass, gas, or vacuum.
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)
Macrocyclic polyethers with the repeating unit of (-CH2-CH2-O)n where n is greater than 2 and some oxygens may be replaced by nitrogen, sulfur or phosphorus. These compounds are useful for coordinating CATIONS. The nomenclature uses a prefix to indicate the size of the ring and a suffix for the number of heteroatoms.
A polyvinyl resin used extensively in the manufacture of plastics, including medical devices, tubing, and other packaging. It is also used as a rubber substitute.
Chemistry dealing with the composition and preparation of agents having PHARMACOLOGIC ACTIONS or diagnostic use.
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)
The presence of organisms, or any foreign material that makes a drug preparation impure.
An element of the rare earth family of metals. It has the atomic symbol Ce, atomic number 58, and atomic weight 140.12. Cerium is a malleable metal used in industrial applications.
Liquid chromatographic techniques which feature high inlet pressures, high sensitivity, and high speed.
An electrochemical technique for measuring the current that flows in solution as a function of an applied voltage. The observed polarographic wave, resulting from the electrochemical response, depends on the way voltage is applied (linear sweep or differential pulse) and the type of electrode used. Usually a mercury drop electrode is used.
Concentration or quantity that is derived from the smallest measure that can be detected with reasonable certainty for a given analytical procedure.
The application of scientific knowledge or technology to pharmacy and the pharmaceutical industry. It includes methods, techniques, and instrumentation in the manufacture, preparation, compounding, dispensing, packaging, and storing of drugs and other preparations used in diagnostic and determinative procedures, and in the treatment of patients.
The study of chemical changes resulting from electrical action and electrical activity resulting from chemical changes.
Substances made up of an aggregation of small particles, as that obtained by grinding or trituration of a solid drug. In pharmacy it is a form in which substances are administered. (From Dorland, 28th ed)
The art or process of comparing photometrically the relative intensities of the light in different parts of the spectrum.
The chemical and physical integrity of a pharmaceutical product.
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.
Hard or soft soluble containers used for the oral administration of medicine.
Methodologies used for the isolation, identification, detection, and quantitation of chemical substances.
A thiazide diuretic often considered the prototypical member of this class. It reduces the reabsorption of electrolytes from the renal tubules. This results in increased excretion of water and electrolytes, including sodium, potassium, chloride, and magnesium. It is used in the treatment of several disorders including edema, hypertension, diabetes insipidus, and hypoparathyroidism.
Artificially produced membranes, such as semipermeable membranes used in artificial kidney dialysis (RENAL DIALYSIS), monomolecular and bimolecular membranes used as models to simulate biological CELL MEMBRANES. These membranes are also used in the process of GUIDED TISSUE REGENERATION.
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 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.
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)
A nonmetallic element with atomic symbol C, atomic number 6, and atomic weight [12.0096; 12.0116]. It may occur as several different allotropes including DIAMOND; CHARCOAL; and GRAPHITE; and as SOOT from incompletely burned fuel.
Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.
Agents that are used to stimulate evacuation of the bowels.
A component of the CLASSICAL COMPLEMENT PATHWAY. C2 is cleaved by activated COMPLEMENT C1S into COMPLEMENT C2B and COMPLEMENT C2A. C2a, the COOH-terminal fragment containing a SERINE PROTEASE, combines with COMPLEMENT C4B to form C4b2a (CLASSICAL PATHWAY C3 CONVERTASE) and subsequent C4b2a3b (CLASSICAL PATHWAY C5 CONVERTASE).
Exclusive legal rights or privileges applied to inventions, plants, etc.
Dosage forms of a drug that act over a period of time by controlled-release processes or technology.
The first complement component to act in the activation of CLASSICAL COMPLEMENT PATHWAY. It is a calcium-dependent trimolecular complex made up of three subcomponents: COMPLEMENT C1Q; COMPLEMENT C1R; and COMPLEMENT C1S at 1:2:2 ratios. When the intact C1 binds to at least two antibodies (involving C1q), C1r and C1s are sequentially activated, leading to subsequent steps in the cascade of COMPLEMENT ACTIVATION.
A thin-walled distention of the alimentary tract protruding just outside the body cavity in the distal end of the neck (esophagus), used for the temporary storage of food and water.
Drugs manufactured and sold with the intent to misrepresent its origin, authenticity, chemical composition, and or efficacy. Counterfeit drugs may contain inappropriate quantities of ingredients not listed on the label or package. In order to further deceive the consumer, the packaging, container, or labeling, may be inaccurate, incorrect, or fake.
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)
A specialized agency of the United Nations designed as a coordinating authority on international health work; its aim is to promote the attainment of the highest possible level of health by all peoples.
The interaction of persons or groups of persons representing various nations in the pursuit of a common goal or interest.
A method of measuring the effects of a biologically active substance using an intermediate in vivo or in vitro tissue or cell model under controlled conditions. It includes virulence studies in animal fetuses in utero, mouse convulsion bioassay of insulin, quantitation of tumor-initiator systems in mouse skin, calculation of potentiating effects of a hormonal factor in an isolated strip of contracting stomach muscle, etc.
Physiological disturbances in normal sexual performance in either the male or the female.
Disturbances in sexual desire and the psychophysiologic changes that characterize the sexual response cycle and cause marked distress and interpersonal difficulty. (APA, DSM-IV, 1994)
The presence of an infectious agent on instruments, prostheses, or other inanimate articles.
The psychic drive or energy associated with sexual instinct in the broad sense (pleasure and love-object seeking). It may also connote the psychic energy associated with instincts in general that motivate behavior.
The inability in the male to have a PENILE ERECTION due to psychological or organ dysfunction.
The preparation, mixing, and assembling of a drug. (From Remington, The Science and Practice of Pharmacy, 19th ed, p1814)
Usage of a single needle among two or more people for injecting drugs. Needle sharing is a high-risk behavior for contracting infectious disease.

The gas-liquid chromatograph and the electron capture detection in equine drug testing. (1/3191)

Three gas-liquid chromatographic (G.L.C.) procedures discussed have been designed around the four "esses" of detection tests--speed, sensitivity, simplicity, and specificity. These techniques are admirably applicable to the very low plasma drug levels encountered in blood testing under pre-race conditions. The methods are equally applicable to post-race testing procedures, where both blood and urine samples are tested. Drugs can only rarely be detected by the electron capture detector (E.C.D.) without a prior derivatization step, which conveys to the drug(s) high electron affinity. Because of broad applicability, two derivatizing agents, heptafluorobutyric (HFBA) and pentafluorpropionic (PFPA) anhydrides are employed. The three techniques, allowing broad coverage of various drug classes are: 1) direct derivatization of drugs to form strongly electron capturing amides and esters. 2) reductive fragmentation of drugs with lithium aluminum hydride to form alcohols, with conversion to ester derivatives. 3) oxidative fragmentation of drugs with potassium dichromate to form derivatizable groups, followed by direct derivatization.  (+info)

Report on use of XAD resins in racing chemistry. (2/3191)

This report comprises a summary of the work done with XAD resin extraction by racing chemists and reported in the Association of Official Racing Chemists publications. It is apparent that the use of XAD resins is becoming more popular in racing laboratories as a technique for routine screening and also for the extraction of certain conjugated drugs. Most laboratories employ variations on the original Brinkmann Drug-Skreen Technique. Comparisons of the efficiency of extraction of drugs from horse urine by XAD-2 resin and by chloroform column extraction indicate that some drugs can be extracted with equal or greater efficiency by the resin technique.  (+info)

Racing problems in the U.S.A. (3/3191)

The major problems of racing in the United States at the present time are caused by too much racing. This has led to too few horses and small fields. Consequently many owners and trainers are trying to enter their horses too frequently and to race them when they are not really fit to run. The desire to race horses as frequently as possible has led to constant pressure from horsemen through their organizations for so called "permissive medication". Started in the state of Colorado approximately ten years ago this has grown until finally there are only a few states, notably New York and New Jersey that have resisted the pressure. The drug that gave the opening wedge to permissive medication was phenylbutazone, but this in many states has led to the inclusion of other drugs including analgesics and drugs that veterinarians claim are needed for therapeutic purposes. Some states have endeavoured to control phenylbutazone medication by quantitation and while lower limits cause little difficulty, maximum allowable limits have caused problems and are not practical. While there has been no publicity to my knowledge about frusemide (furosemide, lasix) the abuse of this drug for so called "bleeders" is an example that may seriously interfere with drug detection in urine and its use should be confined to proven "bleeders" (i.e. horses suffering from epistaxis). Pre-race blood testing began roughly ten years ago at the harness tracks and has been resisted by our flat tracks rather successfully up to the present time. The blood testing methods and those used by the same laboratories in post-race urine testing is inadequate and will not detect many illegal drugs.  (+info)

Doping control in Japan. An automated extraction procedure for the doping test. (4/3191)

Horse racing in Japan consists of two systems, the National (10 racecourses) and the Regional public racing (32 racecourses) having about 2,500 racing meetings in total per year. Urine or saliva samples for dope testing are collected by the officials from thw winner, second and third, and transported to the laboratory in a frozen state. In 1975, 76, 117 samples were analyzed by this laboratory. The laboratory provides the following four methods of analysis, which are variously combined by request. (1) Method for detection of drugs extracted by chloroform from alkalinized sample. (2) Methods for detection of camphor and its derivatives. (3) Method for detection of barbiturates. (4) Method for detection of ethanol. These methods consist of screening, mainly by thin layer chromatography and confirmatory tests using ultra violet spectrophotometry, gas chromatography and mass spectrometry combined with gas chromatography. In the screening test of doping drugs, alkalinized samples are extracted with chloroform. In order to automate the extraction procedure, the authors contrived a new automatic extractor. They also devised a means of pH adjustment of horse urine by using buffer solution and an efficient mechanism of evaporation of organic solvent. Analytical data obtained by the automatic extractor are presented in this paper. In 1972, we started research work to automate the extraction procedure in method (1) above, and the Automatic Extractor has been in use in routine work since last July. One hundred and twnety samples per hour are extracted automatically by three automatic extractors. The analytical data using this apparatus is presented below.  (+info)

The antidoping control in horseraces in Italy. (5/3191)

The results and the improvement of the analytical procedures adopted for the control of doping in horses will be reported. This control has been systematically carried out in Italy for about 10 years in the laboratories of Italian Federation of Sport and Medicine in which the biological samples for the control of doping in various sport activities (football, cycling, athletics etc.) are also examined. In this way it is possible to use the same instruments for all these similar problems and compare the results. The analytical procedure is based on the following steps: 1) Extraction of the samples (mainly urine but sometimes blood or saliva). 2) Screening tests by thin-layer chromatography. 3) Confirmatory tests by gas chromatography on different columns and also by gas chromatography coupled with mass spectrometry. These single steps will be separately discussed, and practical problems encountered will be presented.  (+info)

Less common "doping" agents and substances encountered during routine screening for drugs. (6/3191)

The chromatographic and spectroscopic properties of several unusual substances which have been detected in the "alkaloidal" chloroform extract from racehorse urine and saliva samples are reported. Some of these substances have been identified by combined gas chromatography-mass spectrometry and the source of the substance is stated where this is known. Other substances whose identity is not known have been detected and their mass spectra show characteristic amine fragments. The occurrence of these unidentified substances is more frequent in aged urine samples and it would therefore appear that they are associated with putrefaction.  (+info)

Does the availability of prescribed drugs affect rates of self poisoning? (7/3191)

The trends in self-poisoning rates and in rates of prescribing of the major drug groups were compared. Over the period 1981-91, barbiturate prescribing and self poisoning both fell by 80%; for antidepressants, prescribing increased by over 40% and self poisoning by 30%; for antipsychotics, both rose by 30%; for benzodiazepines, poisoning fell by 30% and prescribing by 20%. Even for analgesic drugs, which are also available over the counter, there was a correspondence between changes in self poisoning and prescribing. The availability of prescribed drugs is directly related to their use for self poisoning. Restricting the availability of these drugs is a possible preventative strategy, although further research on this is needed.  (+info)

Drug-protein binding and blood-brain barrier permeability. (8/3191)

The permeability surface area (PS) product, an index of permeability of the blood-brain barrier (BBB), was measured by using the in situ perfusion method. In the cerebral circulation, the fraction of drug that permeates into the brain through the BBB is not only the unbound fraction but also the fraction dissociated from the protein in the perfusate. The sum of these two fractions, the apparent exchangeable fraction, was estimated by fitting the parameters of the BBB permeability under the condition of varying BSA concentrations in the perfusate. The unbound fraction of drugs in a buffer containing 0.5 mM BSA was measured by using the ultrafiltration method in vitro, and the apparent exchangeable fraction was measured in vivo by using the intracarotid artery injection method. The apparent exchange fraction was 100% for S-8510, 96.5% for diazepam, 90.9% for caffeine, 38.3% for S-312-d, 33.1% for propranolol, and 6.68% for (+)-S-145 Na, and each of these was higher than the corresponding unbound fraction in vitro in all drugs. The apparent exchangeable fractions, for example, were 8 times higher for diazepam and 38 times for S-312-d than the unbound fractions in vitro. The apparent exchangeable fraction of drugs was also estimated from the parameters obtained with the perfusion method. Because drugs can be infused for an arbitrary length of time in the perfusion method, substances with low permeability can be measured. The apparent exchangeable fractions obtained with this method were almost the same as those obtained with the intracarotid artery injection method.  (+info)

A comprehensive introduction for scientists engaged in new drug development, analysis, and approvals Each year the pharmaceutical industry worldwide recruits thousands of recent science graduates especially chemistry, analytical chemistry, pharmacy, and pharmaceutical majors into its ranks. However, because of their limited background in pharmaceutical analysis most of those new recruits find making the transition from academia to industry very difficult. Designed to assist both recent graduates, as well as experienced chemists or scientists with limited regulatory, compendial or pharmaceutical analysis background, make that transition, Pharmaceutical Analysis for Small Molecules is a concise, yet comprehensive introduction to the drug development process and analysis of chemically synthesized, small molecule drugs. It features contributions by distinguished experts in the field, including editor and author, Dr. Behnam Davani, an analytical chemist with decades of technical management and ...
Title:A UPLC-MS/MS Method for Simultaneous Determination of Six Bioactive Compounds in Rat Plasma, and its Application to Pharmacokinetic Studies of Naoshuantong Granule in Rats. VOLUME: 15 ISSUE: 3. Author(s):Ping Wang, Shenmeng Jiang, Yu Zhao, Shuo Sun, Xiaoli Wen, Xingjie Guo* and Zhen Jiang*. Affiliation:Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, Liaoning Province, Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, Liaoning Province, Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, Liaoning Province, Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, Liaoning Province, Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, Liaoning Province, Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang ...
This study presents the evaluation of seven pharmaceutical compounds belonging to different commonly used therapeutic classes in seawater samples from coastal areas of Gran Canaria Island. The target compounds include atenolol (antihypertensive), acetaminophen (analgesic), norfloxacin and ciprofloxacin (antibiotics), carbamazepine (antiepileptic) and ketoprofen and diclofenac (anti-inflammatory). Solid phase extraction (SPE) was used for the extraction and preconcentration of the samples, and liquid chromatography tandem mass spectrometry (LC-MS/MS) was used for the determination of the compounds. Under optimal conditions, the recoveries obtained were in the range of 78.3% to 98.2%, and the relative standard deviations were less than 11.8%. The detection and quantification limits of the method were in the ranges of 0.1-2.8 and 0.3-9.3 ng·L−1, respectively. The developed method was applied to evaluate the presence of these pharmaceutical compounds in seawater from four outfalls in Gran Canaria Island
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ABSTRACT. The aim of this study is to present a Quick and Easy formula for the calculations of percent spike recovery of drug samples. Currently there are several cumbersome methods used in the determination of percent spike recovery in pharmaceutical analyses performed in various laboratories including the FDA laboratories around the world and especially in USA. In this paper we have compared the Quick & Easy Method using Pals formula against the method suggested by ORA Manual. The efficacy of this new formula has been demonstrated by seven examples including the main example of Pilocarpine hydrochloride discussed in detail. This Quick & Easy method is very simple, efficient and convenient way of determining percent spike recoveries and RPD values of duplicate spike solutions in drug analyses by HPLC, GC or UV methods. The simplicity of the method saves time and effort when compared to the existing method. Keywords: Pals formula, ORA Manual. ...
Current Pharmaceutical Analysis publishes authoritative reviews, written by experts in the field on all the most recent advances in pharmaceutical and biomedical analysis. All aspects of the field are represented including drug analysis, analytical methodology and instrumentation. The journal is essential to all involved in pharmaceutical, biochemical and clinical analysis.. ...
Pharmaceutical Drugs are defined as chemical substances used for treating, curing and preventing different types of diseases. Commonly referred as medicines or medication, pharmaceutical drugs are used in the medical diagnosis, treatment, prevention or curing disease. For varied diseases, physical ailments, there are a wide range of pharmaceutical drugs which are available over the counter (OTC) or with doctors advise.
Our GMP pharmaceutical laboratories provide chemistry, manufacturing and controls (CMC) analytical laboratory services in accordance with current Good Manufacturing Practice (cGMP). Intertek provides cGMP compliant pharmaceutical analysis services that meet the requirements of regulatory authorities worldwide. Laboratory services supporting GMP and CMC requirements range from early development characterization, formulation support analysis, stability testing and method development and method validation through to GMP batch release testing. Our experienced scientists can support your development or manufacturing activities for both small molecule pharmaceuticals and biopharmaceuticals such as proteins, monoclonal antibodies and vaccines. Our GMP laboratory teams have extensive experience with drug delivery systems, drug device combinations and a wide range of medical devices.. cGMP Compliant Analytical Laboratories:. ...
Capillary Electrophoresis (CE) | Separation Science Pharmaceutical Analysis (www.pharma-sci.com) offers free learning from the experts covering methods, applications, webinars, videos, tutorials for pharmaceutical and biopharmaceutical analysis users of chromatography, mass spectrometry, sample preparation and related analytical techniques.
Useni Reddy Mallu is an editor of Edelweiss Pharma Analytic Acta journal, whose research interests currently includes Pharmaceutical Analysis, Pharmaceutical Regulatory affairs and Drug delivery system.
Pharmaceutical Analysis, 978-3-659-63956-2, This research focuses on the in vitro evaluation of commercially available marketed antacid preparation (tablet) in Bangladesh. This research work deals with chewable non - systemic antacid preparations which are usually used in combination. We have done our experimental work by measuring the acid - neutralizing capacity in two ways. These are simple complexometric titration method and pH measurement method. Then we compare those results. Then we have done assay of those antacid preparations. And we also work various tests for evaluation of tablet. These are weight variation test, thickness and diameter, hardness test. Ultimately our goal is to know about those antacid preparation (tablet) are maintain BP specification and they are how much acceptable.
This title simplifies the understanding of the basic principles of Pharmaceutical Analysis by bridging the gap between the basics and complex topics such as spectrometry, chromatography, and various thermal analysis techniques. The title is a must-read for pharmacy graduates.
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Molecular Spectroscopy Market by Technology (NMR (FT - UV-VIS spectroscopy is routinely These bonds absorb the energy in the form of ultraviolet or visible light to Course in Pharmaceutical Analysis
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polysaccharide (9.522) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [triterpene (5.647) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [ganoderic acid (5.384) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [lucidenic acid (2.999) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [Gl-PS (2.998) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [lanostanoid (2.645) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [ergosterol (2.234) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [laccase (2.230) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [proteoglycan (1.997) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [F3 (1.993) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [terpenoid (1.987) (E)Literature evidences(S)STITCH: Chemical-Protein Interactions] [more] [Help ...
Capillary Electrophoresis (CE) was explored as a means for physicochemical and biopharmaceutical characterisation of small drug molecules. Special attention was paid to the characterisation of acid-base and lipophilic properties of drug compounds by analysing their migration behaviour in different CE systems. The thesis comprises an overview of the field together with separate studies on the different topics.. The utility of CE for the determination of pKa of labile drug compounds was investigated. A general methodology was developed comprising key steps such as the use of a stabilising sample diluent, electromigration injection, and analyte characterisation by UV-Vis spectroscopy. The methodology was successfully applied for two sets of drug compounds, labile at low and high pH, respectively.. CE was also evaluated for experimental modelling of passive intestinal membrane permeability by studying analyte migration in liposomal, microemulsion and micellar electrolytes. Good correlation is ...
An analytical method for the simultaneous determination of eight pharmaceutical compounds in biosolids from urban wastewater treatment plants (WWTPs) was developed and validated. The compounds evaluated were non-steroidal anti-inflammatory drugs (naproxen, diclofenac, and ibuprofen), lipid regulators (clofibric acid), and antibiotics (sulfathiazole, sulfapyridine, sulfamethazine, and sulfamethoxazole). Ultrasound assisted extraction with a water-methanol solvent mixture (1:1, v:v) was performed and the compounds were then determined by liquid chromatography coupled with tandem mass spectrometry. The design of the method was based on the application of the standard addition calibration methodology to reduce matrix interferences. Validation procedures were conducted with rabbit excrements as blank samples. Recoveries of the target analytes ranged from 76 to 131% in spiked samples at 50, 200 or 1000 ng g−1 dry weight (dw). The relative standard deviations were in the range of 5-15% and the method ...
HPLC Application #15626: Pharmaceutical Compounds by Luna 3µ C18(2) MercuryMS Cartridge 20 x 4.0mm. Column used: Luna® 3 µm C18(2) 100 Å, LC Column 20 x 4 mm, Mercury, Ea Part#: 00M-4251-D0-CE
TY - JOUR. T1 - High-throughput screening for drugs of abuse and pharmaceutical drugs in hair by liquid-chromatography-high resolution mass spectrometry (LC-HRMS). AU - Pascali, Vincenzo Lorenzo. AU - Strano Rossi, Sabina. AU - Odoardi, Sara. AU - Valentini, Valeria. AU - De Giovanni, Nadia. PY - 2017. Y1 - 2017. N2 - A liquid chromatography-high resolution mass spectrometry (LC-HRMS) method for the simultaneous screening in hair samples of drugs of abuse and medicaments was developed. Target analytes screened using a single extraction and analytical run were opiates, cocaine, amphetamines and amphetamine-like substances, ketamine and analogues, cannabinoids, both natural and synthetic, cathinones, piperazines, ephedrines and others new psychoactive substances not pertaining to these classes; pharmaceutical drugs such as antipsychotics, antiepileptics, antidepressants, benzodiazepines and analogues, anorectics, stimulants, drugs for the erectile dysfunction. The multiresidual method involved ...
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HEALTHY LIFE PHARMA PVT. LTD., a WHO GMP Certified Company, Manufacturer, Supplier, Exporter of Generic Pharmaceutical Drugs based in Mumbai, Maharashtra, India & offering best quality Generic Pharmaceutical Drugs to our clients.
China Pharmaceutical Drug Glimepiride 93479-97-1 for Treating Diabetes, Find details about China Glimepiride, 93479-97-1 from Pharmaceutical Drug Glimepiride 93479-97-1 for Treating Diabetes - Wuhan Lianshangwang Technology Co., Ltd.
A method is disclosed for delivering molecules such as pharmaceutical drugs and nucleic acids into skeletal muscle in vivo. The pharmaceutical drug or nucleic acid is first injected into the muscle at
TY - JOUR. T1 - Drug compound characterization by mass spectrometry imaging in cancer tissue. AU - Kwon, Ho Jeong. AU - Kim, Yonghyo. AU - Sugihara, Yutaka. AU - Baldetorp, Bo. AU - Welinder, Charlotte. AU - Watanabe, Ken Ichi. AU - Nishimura, Toshihide. AU - Malm, Johan. AU - Török, Szilvia. AU - Döme, Balázs. AU - Végvári, Ákos. AU - Gustavsson, Lena. AU - Fehniger, Thomas E.. AU - Marko-Varga, György. PY - 2015/9/22. Y1 - 2015/9/22. N2 - MALDI mass spectrometry imaging (MSI) provides a technology platform that allows the accurate visualization of unlabeled small molecules within the two-dimensional spaces of tissue samples. MSI has proven to be a powerful tool-box concept in the development of new drugs. MSI allows unlabeled drug compounds and drug metabolites to be detected and identified and quantified according to their mass-to-charge ratios (m/z) at high resolution in complex tissue environments. Such drug characterization in situ, by both spatial and temporal behaviors within ...
Expertise:. » Isolation, characterization and evaluation of bioactive constituents from herbal extracts using bioactivity guided fractionation. » Computer aided Drug Design (in silico analysis), synthesis and pharmacological evaluation (in vitro analysis) » Resolution of drugs, including enzymatic resolution and its monitoring. » Chiral chromatography » Forced degradation studies, Impurity profiling and development of stability indicating assays. » Analytical method development and validation » Synthesis, purification and characterization of impurities/metabolites. » Structural Elucidation using spectroscopic techniques » Bioanalytical method development and validation; Therapeutic Drug Monitoring » Drug metabolism and pharmacokinetic analysis » Herbal Analysis » In vitro analysis for antibacterial, antifungal and antiamoebic activity Go to TOP ...
A rapid and simple method of spectrophotometric estimation Empagliflozin in UV-region was developed and validated according to International Conference on Harmonization (ICH Q2 R1) guidelines. The standard and sample solutions were prepared using ethanol and water. The maximum absorbance (?max) was obtained at 223 nm. The calibration curve was linear in the range of 1-30µg/ml. The %RSD for intra and inter-day precision was found to be 0.29 and 0.39 respectively. Recovery studies of Empagliflozin were within 99.20% to 99.49 and assay was found to be 99.87% and LOD and LOQ was found to be 0.10 and 0.33 respectively. The %RSD for robustness was found to be between 0.20 and %RSD for ruggedness was found to be 0.03. The proposed method was found to be rapid, precise, accurate and can be adaptable for routine analysis of Empagliflozin bulk and marketed dosage forms.
In the Laboratory of Drug Quality and Registration (DruQuaR) fundamental and applied research is carried out in the fields of pharmaceutical analytics and regulatory affairs.. Our general research goal is studying the functional quality of pharmaceuticals and related products. Emphasis is placed on the following, more specific topics:. ...
In the present study, a new, simple and cheap shaker-assisted deep eutectic solvent microextraction (SA-DESME) procedure was developed for extraction of paracetamol in synthetic urea and pharmaceutical samples prior to its determination by UV-VIS spectrophotometer. The SA-DES-ME procedure is based on the selective extraction of paracetamol which deep eutectic solvents (DESs) prepared with choline chloride (ChCI)/betaine (Bet) and different hydrogen bond donors (HBDs).The DESs was used as the extraction solvent for the separation of the paracetamol-containing complex from the sample solution. Optimum values of experimental parameters were determined by univariate optimization method. Under optimum conditions, analytical results such as good linearity (50-800 mu g L-1), quantitative recoveries (94.2-107.1%), low detection limit (14.9 mu g L-1), and high sensitivity enhancement factor (135) were obtained using the proposed method. Additionally, the relative standard deviations (RSDs%) were less ...
508834031 - EP 3345600 A4 20190410 - MIRABEGRON-CONTAINING TABLET, METHOD FOR PRODUCING MIRABEGRON-CONTAINING PHARMACEUTICAL PREPARATION AND METHOD FOR PRODUCING MIRABEGRON-CONTAINING GRANULATED PRODUCT - [origin: EP3345600A1] [Problem] To provide a mirabegron-containing tablet which retains the amorphous state of mirabegron after long-term storage; a mirabegron-containing pharmaceutical preparation capable of retaining mirabegron purity by preventing analog formation during storage; a method for producing a mirabegron-containing pharmaceutical preparation; and a method for producing a mirabegron-containing granulated product. [Solution] According to one embodiment of the present invention, provided is a mirabegron-containing pharmaceutical preparation, characterized in comprising mirabegron, and hypromellose and polyvinyl pyrrolidone. The mirabegron-containing pharmaceutical preparation may comprise a spray-dried granulated product comprising the mirabegron and the hypromellose and the polyvinyl
This moment version of a world bestseller has been thoroughly redesigned and broadly rewritten take into consideration the recent caliber via layout (QbD) and lifecycle ideas in pharmaceutical manufacturing.. As within the first variation, the elemental specifications for analytical technique validation are lined, however the moment variation describes how those are utilized systematically in the course of the whole analytical lifecycle. QbD ideas require adoption of a scientific method of improvement and validation that commence with predefined ambitions. For analytical equipment those predefined goals are verified as an Analytical goal Profile (ATP). The booklet chapters are aligned with lately brought criteria and instructions for production methods validation and stick with the 3 levels of the analytical lifecycle: technique layout, strategy functionality Qualification, and persisted technique functionality Verification. Case stories and examples from the pharmaceutical illustrate the ...
A simple, accurate, precise, sensitive and a highly selective ultra violet spectrophotometric method has been developed for the simultaneous estimation of in bulk and solid dosage form. The estimation of Zidovudine was carried out at 266 nm. The developed method was validated for linearity, range, precision, recovery studies and interference study for mixture. All these parameters showed the adaptability of the method for the quality control analysis of the drug in bulk and in marketed formulations.
Micellar liquid chromatography (MLC) is an analytical technique belonging to the wide range of reversed-phase liquid chromatographic (RP-LC) separation techniques. MLC with the use of surfactant solutions above its critical micellar concentration (CMC) and the addition of organic modifiers is currently an important analytical tool with still growing theoretical considerations and practical applications in pharmaceutical analysis of drugs and other biologically active compounds. The use of MLC as an alternative, relatively much faster in comparison to conventional chromatographic separation techniques has several advantages, especially as being suitable for screening pharmaceutical analysis. The analytical data received from MLC analysis are considered a useful source of information to predict passive drug absorption, drug transport and other pharmacokinetics and physicochemical measures of pharmaceutical substances. In the review several MLC assays for determination of drugs and other active ...
Crystallinity and Why It Is Important for Pharmaceuticals. The term crystalline is used to describe solids in which the atoms or molecules are arranged in an ordered manner. For many pharmaceuticals, the crystalline form is more kinetically stable than the amorphous form, which typically results in crystalline solids being less soluble, and therefore less bioavailable than their amorphous counterparts. The influence that crystallinity has over the solubility of a solid is what makes this an important factor when manufacturing pharmaceuticals, as those which are supposed to be fast-acting should be readily soluble in the body, while slow-acting drugs should dissolve relatively slowly. This has been shown to be the case in previous studies of bioavailability of APIs in the literature (3-5). Because of this, it is important to be able to control the crystallinity of a drug and monitor it. However, the crystallinity of a sample cannot be assumed to be simply either 100% ordered or 100% amorphous. ...
Ottergemsesteenweg 460, 9000 Ghent (Belgium). Phone: + 32 (0)9 264.81.01. E-mail: [email protected] PhD Research:. Title: Somatropin derivatives for imaging and treatment of GH-R expressing melanoma. Summary:. Melanoma is considered to be one of the deadliest cancers worldwide. Originating from melanocytes in skin and mucosa with metastasis to other organs, it is difficult to treat. Human growth hormone (hGH) and the growth hormone-receptor (GHR) are normally involved in regulatory processes like metabolism, balanced growth, and cell differentiation. However, the human GHR was found to be over-expressed in i.a. different melanoma cell lines and may thus play a role in metastasis and invasion of human melanoma. Derivates of somatropin (i.e. recombinantly produced hGH) show potential to visualize and treat these types of cancer in humans.. The main goal of this research is to develop a tumor-selective protein drug for use in diagnosis and treatment of melanoma. Somatropin and its ...
Dr Khaled H Assi obtained his BSc in the Sciences of Chemistry in 1994 and was awarded the PhD in pharmaceutical analysis by the University of Bradford, in 1999.. He then took up a post doctoral post at university of Bradford between 1999-2001 working on the inhaled therapies. His post doctoral program was extended for one more year through an awarded grant from Glaxo SmithKline joint with Professor H Chrystyn .. In 2002, he was accepted a research fellowship at Bradford School of Pharmacy. Dr Assi was appointed as a Lecturer at the Bradford School of Pharmacy, in July 2004 and has continued developing his research in the inhaled therapies area. In this position he is teaching the pharmacy and pharmaceutical management students at different levels. The modules he delivers cover the area of pharmaceutical analysis, Quality assurance and quality control of pharmaceuticals.. He is also active in the research. His research interests cover the inhalation therapies and developing of pharmaceutical and ...
|p|Get an introduction to pharmaceuticals from drug discovery to manufacture, and learn to use the  tools needed for their analysis.|/p|
This 2-day HPLC course is aimed at those who are new to the technique of HPLC and want to use it for the analysis of pharmaceuticals. The training course is delivered at your companys site by the MTS trainer. A pre-training visit may be arranged during which the MTS trainer will discuss the content of the training course with you to ensure that the HPLC training is fully tailored to your needs.
Purchase the latest market research you need on the Pharmaceutical Industry in India. Click here to find the reports from reputable publishers.
Paper analytical devices (PADs) are test cards that can quickly determine whether a drug tablet contains the correct medicines. They are cheap and easy to use. They dont require power, chemicals, solvents, or any expensive instruments, so they can be deployed rapidly at large scale whereever a problem with pharmaceutical quality is suspected.
MILAN, December 4, 2012 /PRNewswire/ --. Last month, 55 of Europes biggest players from across the pharmaceutical drug discovery sector convened for two-and-a-half days as they attended the most disruptive event of the year - GDS Internationals fourth Next Generation Pharmaceutical Drug Discovery summit (NGP DD EU), held at the Meliá Milano Hotel, Milan, Italy.. Europe has been an enduring force in the pharmaceutical industry for decades. However, increased competition due in part to globalisation, economic recession and ICT advancements has levelled the playing field for drug discovery. Wise investment and innovative new technologies are subsequently proving key to staying ahead of competitors. With this in mind, GDS International has created an award to recognise exceptional talent within the sector.. Selected as the winners by a panel of 20 senior executives from the R&D functions of global biopharma companies, Paul ORiordan - CEO of Synexa Life Sciences, and Henning Steinhagen - SVP Head ...
McCarthy , Kelly LLP lawyers have represented individuals that have been injured by a variety of pharmaceutical drugs. Our lawyers have many years of experience litigating cases against manufacturers of defective product including members of the pharmaceutical industry. McCarthy , Kelly LLP lawyers and staff represent individuals who were injured through the use of pharmaceutical drugs and provide our clients with up-to-date information about the drug and their legal options.. ...
In the past, people used herbs as a form of treatment for illness. Nowadays, the mainstream belief is that they are not as effective and not worth taking. For each health issue people use pharmaceutical drugs. This is because effectiveness of each herb and their use has not been studied deeply to determine how effective it can be. On the other hand, pharmaceutical drugs are attempted to mimic a compound that occurs naturally in nature (herbs). They can also bring the risk of side effects.. According to stats released by the American Association of Poison Control Centers, no deaths have been reported due to the use and consumption of herbs. However, pharmaceutical drugs and physician prescribed medications kill approximately one million Americans each year. It is important to note that herbal medicines can be lethal in extreme doses it appears their safety is much greater than that of pharmaceutical drugs.. Pharmaceutical drugs can have side effects on human health. For example antibiotics in ...
LI Song;NI Hai-tao;SHENG Xia;TANG Shou-yan;LU Wen-jing;CHENG Chun-yan;LI Wei;FAN Guo-rong;SUN Ying-hao;GCP Office,Department of Urology,Changhai Hospital,Second Military Medical University;Department of Pharmaceutical Analysis,School of Pharmacy,Second Military Medical University & Key Laboratory of Shanghai Drug(Chinese Materia Medica)Metabolism Research;Department of Pharmaceutical Analysis,School of Pharmacy,Shenyang Pharmaceutical University;Department of Histology and Embryology,College of Basic Medical Sciences,Second Military Medical University; ...
Science Citation Index Expanded, Journal Citation Reports/Science Edition, Index to Scientific Reviews®, Biochemistry & Biophysics Citation Index®, ISI Alerting Service, Scopus, EMBASE, Chemical Abstracts Service/SciFinder, ProQuest, ChemWeb, Google Scholar, EMBiology, PubsHub, Genamics JournalSeek, Cabells Directory, MediaFinder®-Standard Periodical Directory, J-Gate, CNKI Scholar, Suweco CZ, TOC Premier, EBSCO and Ulrichs Periodicals Directory.. ...
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McKesson Corporation (McKesson), one of the nations largest distributors of pharmaceutical drugs, agreed to pay a record $150 million civil penalty for alleged violations of the Controlled Substances Act (CSA), the Justice Department announced today. The nationwide settlement requires McKesson to suspend sales of controlled substances from distribution centers in Colorado, Ohio, Michigan and Florida for multiple years. The staged suspensions are among the most severe sanctions ever agreed to by a Drug Enforcement Administration (DEA) registered distributor. The settlement also imposes new and enhanced compliance obligations on McKessons distribution system. In 2008, McKesson agreed to a $13.25 million civil penalty and administrative agreement for similar violations. In this case, the government alleged again that McKesson failed to design and implement an effective system to detect and report suspicious orders for controlled substances distributed to its independent and small chain pharmacy ...
These people all knew why talking therapies are better than pharmaceutical drugs in the treatment of depression. They have described so much more succinctly the power of the mind over our mental health than ever I could ...
Wholesale Trader of Pharmaceutical Drugs - Dexmethasone Injection 5ml, Dexmethasone Injection 10ml offered by Vinson Pharma (A Div. Of Vintek Pharmaceutials), Chandigarh.
Rodent Research-6 (RR-6) is a two-fold investigation that will study the effectiveness of both the drug compound and the nano-channel drug delivery implant HOUSTON, TX, January 27, 2018 /24-7PressRelease/ - Extended spaceflight takes a toll on many systems within the human body, including the musculoskeletal system. An investigation aboard the International Space Station will examine a drug compound and drug delivery system aimed at preventing, slowing, or even reversing muscular breakdown, both in space and on Earth.. Rodent Research-6 (RR-6) is a two-fold investigation that will study the effectiveness of both the drug compound and the nano-channel drug delivery implant, for their use in the treatment of muscle loss in future spaceflight, and in the treatment of patients with muscle wasting diseases or conditions on Earth.. The drug compound will be administered through a device implanted beneath the skin, allowing for a constant, steady delivery of the drug.. The unique aspect of the mission ...
0187]Pharmaceutical agent as used herein refers to any of a variety of drugs or pharmaceutical compounds that can be used as active agents to prevent or treat a disease (meaning any treatment of a disease in a mammal, including preventing the disease, i.e. causing the clinical symptoms of the disease not to develop; inhibiting the disease, i.e. arresting the development of clinical symptoms; and/or relieving the disease, i.e. causing the regression of clinical symptoms). It is possible that the pharmaceutical agents of the invention may also comprise two or more drugs or pharmaceutical compounds. Pharmaceutical agents, include but are not limited to antirestenotic agents, antidiabetics, analgesics, antiinflammatory agents, antirheumatics, antihypotensive agents, antihypertensive agents, psychoactive drugs, tranquilizers, antiemetics, muscle relaxants, glucocorticoids, agents for treating ulcerative colitis or Crohns disease, antiallergics, antibiotics, antiepileptics, anticoagulants, ...
TABLE-US-00016 TABLE 3 LEVOSALBUTAMOL S04 - Form III Peak No. 2θ (deg) d (A) Height Height % FWHM 1 5.496 16.0657 2337 41.8 0.206 2 6.901 12.799 320 5.7 0.295 3 7.340 12.034 1938 34.6 0.217 4 8.181 10.7983 2348 42.0 0.645 5 8.399 10.5187 5559 99.4 0.251 6 10.978 8.0527 577 10.3 0.190 7 11.758 7.5203 978 17.5 0.178 8 12.778 6.9221 365 6.5 0.186 9 14.298 6.1895 565 10.1 0.233 10 14.701 6.0206 428 7.7 0.165 11 16.321 5.4266 4839 86.5 0.292 12 16.981 5.2172 498 8.9 0.134 13 17.980 4.9293 1110 19.8 0.319 14 18.180 4.8758 1421 25.4 0.532 15 18.660 4.7512 4455 79.6 0.432 16 18.860 4.7013 3247 58.0 0.243 17 19.189 4.6215 636 11.4 0.100 18 20.179 4.3969 797 14.2 0.529 19 20.720 4.2833 2355 42.1 0.315 20 22.019 4.0335 5594 100.0 0.306 21 22.219 3.9976 2598 46.4 0.595 22 23.121 3.8436 761 13.6 0.563 23 23.640 3.7604 2729 48.8 0.460 24 23.858 3.7265 2189 39.1 0.547 25 24.638 3.6103 654 11.7 0.168 26 25.339 3.5120 1235 22.1 0.276 27 25.721 3.4607 445 8.0 0.215 28 26.299 3.3859 414 7.4 0.352 29 26.518 3.3585 ...
According to the Gate-Control Theory of pain: a)we cannot control the gate through which pain enters or is emitted back from the brain b)the gate for pain is open only for survival instincts c)pain cannot pass through these special ...
The production of salt or cocrystalline forms is a common approach to alter the physicochemical properties of pharmaceutical compounds. The goal of this work was to evaluate the impact of anion choice (succinate, adipate, and sulfate) on the physicochemical characteristics of salbutamol forms. Novel crystals of salbutamol were produced by solvent evaporation: a cocrystal of salbutamol hemiadipate with adipic acid (salbutamol adipate, SA), salbutamol hemisuccinate tetramethanolate (SSU.MeOH), and its desolvated form (SSU). The crystalline materials obtained were characterized using thermal, X-ray, nuclear magnetic resonance, Fourier transform infrared spectroscopy, dynamic vapor sorption (DVS), and elemental analysis. The crystal forms of SA and SSU.MeOH were determined to be triclinic, (P?i), and monoclinic, (P21/n), respectively. DVS analysis confirmed that SSU and SA do not undergo hydration under increased relative humidity. Both thermal and elemental analyses confirmed the stoichiometry of ...
Introduction: Drug checking as a part of drug harm-reduction strategies represents an essential aspect of public health policies. It focuses on rapid identification of drugs that individuals intend to use during night events, in order to implement health-protective behaviors. Chemical drug analysis techniques vary considerably, from simple colorimetric reagents to advanced forensic methods such as gas chromatography/mass spectrometry (GC/MS).Materials and Methods: In 2019, drug-check services were offered at some night events in Umbria (Central Italy). One hundred and twenty attendees directly delivered unidentified substances to a harm-reduction worker, who collected a few milligrams of the substances on ceramic plates and added a drop of colorimetric reagent. Multiple reagents were used to increase the diagnostic capacity of a substance, which may react with a specific drug or a few drugs. Later, a fraction of the samples was analyzed by GC/MS. The concordance of the results obtained using these two
SRS pharma, India is a Pharmaceutical Manufacturer & Exporter of quality drugs. SRS Pharmaceutical Manufactures drugs like ACE Inhibitors,Hypertensives, Calcium Channel Blockers etc.
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Arlington, TX (PRWEB) September 07, 2016 -- Registration is now open for Serious Science: Advanced Course in Blood Drug Analysis and Trial Advocacy, an
The goal of this PhD work is to evaluate the possibilities of supercritical fluid chromatography (SFC) in the pharmaceutical analysis. This chromatographic approach will be used to develop analytical methods for numerous types of drugs (including chiral ones) in pharmaceutical formulations. Some inventive strategies will be developed to maximize performance and apply SFC to the widest possible range of molecules. The performance of SFC will be systematically compared to liquid chromatography (LC). In parallel, the PhD candidate will also have the opportunity to couple SFC with single quadrupole(MS), triple quadrupole (MS/MS) and high resolution (QqTOF/MS) mass spectrometers available in our laboratory. This instrumental setup will be used for the determination of drugs and metabolites in complex matrixes, such as biological fluids.. ...
Start Over You searched for: Languages Spanish ✖Remove constraint Languages: Spanish Languages French ✖Remove constraint Languages: French Languages Italian ✖Remove constraint Languages: Italian Copyright Public domain ✖Remove constraint Copyright: Public domain Subjects Pharmaceutical Preparations -- administration & dosage ✖Remove constraint Subjects: Pharmaceutical Preparations -- administration & dosage Titles How to get the best results from using Dr. Miles Nervine Liquid ✖Remove constraint Titles: How to get the best results from using Dr. Miles Nervine Liquid Dates by Range 1900-1949 ✖Remove constraint Dates by Range: 1900-1949 ...
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The 2016-2021 World Outlook for Pharmaceutical Preparations Affecting the Central Nervous System and Sense Organs The 2016-2021 World Outlook for Pharmaceutical Preparations Affecting the Central - Market research report and industry analysis - 9157883
Author: Allen Loyd V Jr, Year: 2019, Abstract: Process analytical technology was introduced by the U. S. Food and Drug Administration about 20 years ago to assist the pharmaceutical industry in making changes that should reduce batch failures, ensure performance, and enhance quality. Its premise is that
Professor David Woolfson holds the Chair in Pharmaceutics (Drug Delivery). He is a graduate in Pharmacy from Queens and is a registered pharmacist. Prof. Woolfson founded the McClay Research Centre for Pharmaceutical Sciences, from initial concept through to raising of the necessary funding. Starting as a lecturer in pharmaceutical analysis, he was appointed Reader in Pharmaceutical Sciences in 1991 and to the Chair in Pharmaceutics in 1995. He is Head of the School of Pharmacy at Queens.. Prof. Woolfson became a member of the British Pharmacopoeia Commission (BPC) in 1997 and was appointed as Chair of the BPC in 2006. The Commission is responsible under the UK Medicines Act for the annual publication of the British Pharmacopoeia., which sets legally enforceable quality standards for medicinal chemicals, drugs and formulated products. He has extensive experience of work in the European Pharmacopoeia Commission (EPC) as leader of the UK delegation and formerly UK Expert on Formulated Medicinal ...
PI & PI Biotech Inc. is mainly engaged in the custom synthesis, separation and purification of drug Impurities, highly pure natural compounds and APIs & intermediates, and pharmaceutical analysis.
2015 was a good year for innovation in medicine in both the EU and the US, according to data published on Monday (4 January).. The European Medicines Agency (EMA) recommended 93 new products, including generics, up from 82 in 2014. Across the Atlantic, the Food and Drug Administration (FDA) approved 45 novel drugs, four more than in 2014 and the most since the all-time record of 53 set in 1996.. But despite the rosy statistics and the prospect for further progress in 2016, the pharmaceuticals industry faces challenges, with increased political focus on drug pricing having punctured both biotech and specialty pharma valuations in recent months.. The prospect of Hillary Clinton becoming president of the United States could further undermine confidence in the sectors profitability in 2016, given her pledge to rein in drug costs. But any changes in the US pricing model are likely to be gradual, according to Bernstein analyst Tim Anderson.. Big pharmaceutical companies, meanwhile, are still ...
Del Mar Photonics offer a handheld infrared spectrometer based on the acousto-optic tunable filter (AOTF). This instrument is about the size and weight of a video camera, and can be battery operated. This unique, patented device is all solid-state with no moving parts. It has been sold for a wide variety of applications such as liquid fuel analysis, pharmaceutical analysis, gas monitoring and plastic analysis. Miniature AOTF infrared spectrometer uses a crystal of tellurium dioxide to scan the wavelength. Light from a light source enters the crystal, and is diffracted into specific wavelengths. These wavelengths are determined by the frequency of the electrical input to the crystal. Since there are no moving parts, the wavelength scanning can be extremely fast. In addition, specific wavelengths can be chosen by software according to the required algorithm, and therefore can be modified without changing the hardware. After the infrared radiation reflects off of the sample, it is converted into an ...
Del Mar Photonics offer a handheld infrared spectrometer based on the acousto-optic tunable filter (AOTF). This instrument is about the size and weight of a video camera, and can be battery operated. This unique, patented device is all solid-state with no moving parts. It has been sold for a wide variety of applications such as liquid fuel analysis, pharmaceutical analysis, gas monitoring and plastic analysis. Miniature AOTF infrared spectrometer uses a crystal of tellurium dioxide to scan the wavelength. Light from a light source enters the crystal, and is diffracted into specific wavelengths. These wavelengths are determined by the frequency of the electrical input to the crystal. Since there are no moving parts, the wavelength scanning can be extremely fast. In addition, specific wavelengths can be chosen by software according to the required algorithm, and therefore can be modified without changing the hardware. After the infrared radiation reflects off of the sample, it is converted into an ...
Received:10-07-2016 Revised: 12-08-2016 Accepted:18-08-2016 *Corresponding author: Shakeena G, Department of Pharmaceutical Analysis and Quality Assurance, Green Royal..
Researchers at Yangzhou University in China have employed fluorophotometry - a process used for quality control and pharmaceutical analysis - to deter
IMGT?, the worldwide ImMunoGeneTics information program? (http://www. and useful data released within the immunogenetics field keeps growing and involves fundamental exponentially, scientific, veterinary, and pharmaceutical analysis. The accurate amount of potential proteins types of the antigen receptors, immunoglobulins (IG) and T cell receptors (TR) is nearly unlimited. The repertoire of every individual is normally approximated to comprise about 1012 different IG (or antibodies) and TR, as well as the restricting factor is the amount of B and T cells an organism is normally genetically programmed to create. This huge variety is normally natural to the especially complex and exclusive molecular synthesis and genetics from the antigen receptor stores. This includes natural mechanisms such as for example DNA molecular rearrangements in multiple loci (three for IG and four for TR in human beings) situated on different chromosomes (four in human beings), nucleotide deletions and insertions on the ...
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The analysis of large intact proteins and complex biological samples containing drug molecules is a common complicated task for many scientists. However, due to the importance of these molecules, there is a growing interest in pharmaceutical and medicinal research to develop rapid, highly sensitive and efficient analytical techniques. The advantages of capillary electrophoresis (CE) in combination with mass spectrometry (MS) provide a powerful analytical tool. However, further improvement and development of these techniques are required to extend their utility and to meet the challenges of selected analytes. Thus, the scope of this thesis deals with the development of novel analytical methods to achieve efficient and high performance analysis of peptides, intact proteins, digests of complex samples and basic pharmaceutical drug compounds in biological matrices.. Implementation of CE for routine analysis of proteins and complex samples is constrained by the partial adsorption to the capillary ...
Ketoconazole containing medications, Ketoconazole indications and usages ATC and ICD codes, combinations with other active ingredients and trade names information from Drugs-about.com
Ferrous Sulfate containing medications, Ferrous Sulfate indications and usages ATC and ICD codes, combinations with other active ingredients and trade names information from Drugs-about.com
Pharmaceutical preparations[edit]. Main article: Gonadotropin preparations. There are various preparations of gonadotropins for ... Besides the aforementioned legitimate pharmaceutical drugs, there are fad diet or quack preparations, which are illegal in ... There are various preparations of gonadotropins for therapeutic use, mainly as fertility medication. There are also fad diet or ...
of Pharmaceutical Sciences (1993). The Extra Pharmacopoeia. Pharmaceutical Press. p. 800. ISBN 978-0-85369-300-0. Monalazone ... Multi-ingredient preparations. Malun. RÖMPP Lexikon Chemie. 10. Auflage, 1996-1999. Thieme. 16 July 2014. pp. 2000-2001. ISBN ... 185-. ISBN 978-0-7514-0499-9. Martindale W, Royal Pharmaceutical Society of Great Britain. Dept. ...
Pharmaceutical dosage forms 250-252.........................................Commercial preparations. Patent medicines 355-356 ... Pharmaceutical substances (Plant, animal, and inorganic) 189-190.........................................Assay methods. ...
779-. ISBN 978-3-88763-075-1. Locum R (1961). "Latest Pharmaceutical Preparations" (PDF). The Central African Journal of ... "Anadrol-50" (PDF). Meda Pharmaceuticals. December 2006. Archived from the original (PDF) on 11 June 2014. Retrieved 8 January ...
... and in pharmaceutical preparations. Sigma-Aldrich Co., Ammonium bromide. Retrieved on 2013-07-20. Pradyot Patnaik. Handbook of ...
There are several categories of active ingredients that may be best administered in the form of effervescent preparations: ... Stahl, Harald (Apr 1, 2003). "Effervescent Dosage Manufacturing". Pharmaceutical Technology Europe. PharmTech. 15 (4). W. A. ... Dubogrey, Ilya (2013). "Putting the Fizz into Formulation". European Pharmaceutical Contractor (Autumn). "Formulated ... Effervescent tablets have been used as products of the pharmaceutical and dietary industries for over two centuries. Vitamin ...
Pharmaceutical, veterinary and sanitary preparations; dietetic substances adapted for medical use, food for babies; plasters, ... Bleaching preparations and other substances for laundry use; cleaning; polishing; scouring and abrasive preparations; soaps; ... flour and preparations made from cereals, bread, pastry and confectionery, ices; honey, treacle; yeast, baking powder; salt, ... syrups and other preparations for making beverages Class 33 .Alcoholic beverages(except beers) Class 34 . Tobacco, smokers' ...
Pharmaceutical preparations which contain tartrazine]". Allergol Immunopathol (Madr). 9 (1): 45-54. Elhkim MO, Héraud F, Bemrah ... Types of pharmaceutical products that may contain tartrazine include vitamins, antacids, cold medications (including cough ... The Canadian Compendium of Pharmaceuticals and Specialties (CPS), a prescribing reference book for health professionals, ... "Electrochemical Studies on a Pharmaceutical Azo Dye: Tartrazine". Industrial & Engineering Chemistry Research. 42 (2): 243-247 ...
Pharmaceutical Press. p. 960. PROPRIETARY PREPARATIONS CONTAINING OESTRADIOL MONOBENZOATE. Benztrone (Paines & Byrne). ... 377-. ISBN 978-80-247-2639-7. Injection of estrogenic preparations - Injectable preparations are AGOFOLLIN, inj. 5 mg ( ... of each of the above preparations, a woman would typically remain free of symptoms for 10 days. This could, however, be as much ... CIBA's range of hormone preparations has been increased with the advent of "Sistocyclin", one ampoule of which contains 200 mg ...
... pharmaceutical and medical History, or the Substances employed in Medicine ; 3. The pharmaceutical Preparations and ... The Edinburgh new Dispensatory : containing 1. The Elements of pharmaceutical Chemistry ; 2. The Materia Medica; or the natural ...
"International Nonproprietary Names for Pharmaceutical Preparations. Recommended International Non-Proprietary Names (Rec. I.N.N ... Lactulose is contraindicated in case of galactosemia, as most preparations contain the monosaccharide galactose due to its ...
"International Non-Proprietary Names for Pharmaceutical Preparations. Recommended International Non-Proprietary Names (Rec. I.N. ...
Pharmaceutical and Chemical Preparations, Etc. (Third Edition.). J. Allen, D. Francis. Tiger Balm: Heritage, archived from the ... Liniment (from the Latin linere, to anoint), or embrocation, is a medicated topical preparation for application to the skin. ... Nine oils: a 19th-century preparation used on both horses and humans. Although druggists' books sometimes specified recipes, ...
Thesaurus of Proprietary Preparations and Pharmaceutical Specialties: Including "patent" Medicines, Proprietary Pharmaceuticals ... Pharmaceutical and Chemical Preparations, Etc (3rd ed.). J. Allen, D. Francis. Gentilcore, David (1998). Healers and Healing in ... Água de Inglaterra: a name used for preparations using the bark of the cinchona tree, used to treat malaria in Portugal from ... New York: Pharmaceutical Products Press. p. 154. ISBN 9780789018458. Watson, Ronald Ross; Preedy, Victor R. (2008). Botanical ...
World Health Organization (December 1959). "International Non-Proprietary Names for Pharmaceutical Preparations). Recommended ... 2009). "Antiparkinsonian Drugs". Martindale: The Complete Drug Reference (36th ed.). London: Pharmaceutical Press. p. 797. ISBN ...
"International Non-Proprietary Names for Pharmaceutical Preparations. Recommended International Non-Proprietary Names: List 3" ( ...
Pharmaceutical and Chemical Preparations, Etc. (Third Edition.). J. Allen, D. Francis. http://www.mspong.org/cyclopedia/ ... In the 19th century, the nine oils was a preparation, or liniment, which was rubbed into the skin to relieve aches, such as ... According to one 19th-century druggists' book, oils used in the preparation included: train oil; that is, whale oil or the oil ... preparations did not contain these ingredients, and in fact it is possible that the name "nine oils" never referred to any ...
"Unauthorised pharmaceutical preparations trafficking on the internet". Newsnow (in Greek). Archived from the original on 2020- ... aspects for licenses and online sale of pharmaceutical products". Healthweb (in Greek). Archived from the original on 2021-01- ...
... only approved pharmaceutical preparations are included. (3): The availability of pharmaceutical estradiol products differs by ... Vermeulen A (1975). "Longacting steroid preparations". Acta Clin Belg. 30 (1): 48-55. doi:10.1080/17843286.1975.11716973. PMID ... 2009). "Sex hormones and their modulators". Martindale: The Complete Drug Reference (36th ed.). London: Pharmaceutical Press. p ... William Andrew Publishing (22 October 2013). Pharmaceutical Manufacturing Encyclopedia. Elsevier. pp. 2934-2935. ISBN 978-0- ...
Kunieda, Takehisa; Takizawa, Takeo (1977). "Convenient preparation of tetraarylbutatrienes". Chemical & Pharmaceutical Bulletin ...
Supplements and pharmaceutical preparationsEdit. Water extraction is the traditional method for preparation of the plant. ... In Germany, kava-based pharmaceutical preparations are currently prescription drugs. Furthermore, patient and professional ... Traditional preparationEdit. Kava is consumed in various ways throughout the Pacific Ocean cultures of Polynesia, Vanuatu, ... Pharmaceutical and herbal supplement companies extract kavalactones from the kava plant using solvents such as supercritical ...
Many of the preparations were pharmaceutical in nature. Tyrocinium Chymicum, Jean Beguinus, Richard Russell (Translator), ...
Wesołowski, M. (1982). "Thermal decomposition of pharmaceutical preparations containing inorganic components". Microchimica ... Norwich Eaton Pharmaceuticals was acquired by Procter and Gamble in 1982. As of 1946 and 1959, Canadian advertisements placed ...
International Non-Proprietary Names for Pharmaceutical Preparations - Rec. I.N.N. List 6 Servin, Frédérique S.; Sear, John W. ( ... although a lipid emulsion preparation (of equivalent strength) has also been introduced. Etomidate was originally formulated as ...
"The Leonurine and its preparation". An Hui New Star Pharmaceutical Development Co. 2008. Archived from the original on 2008-05- ...
The rights to the drug belong to the Russian pharmaceutical company NPK ECHO ("НПК ЭХО"). It is not approved for sale in the ... Mirzoian RS, Gan'shina TS (1989). "[The new cerebrovascular preparation pikamilon]". Farmakologiia I Toksikologiia (in Russian ... However, as recently as 2020, picamilon has been found in pharmaceutical dosages in over-the-counter supplements in the US. One ... Pharmaceutical Bulletin. 32 (10): 4089-95. doi:10.1248/cpb.32.4089. PMID 6529802.[permanent dead link] Avula B, Chittiboyina AG ...
Royal Pharmaceutical Society of Great Britain. Pharmacist prescribing. *^ Cipolle RJ, Strand LM, Morley PC. Pharmaceutical care ... It now includes extensive didactic clinical preparation, a full year of hands-on practice experience in a wider array of ... Royal Pharmaceutical Society History of the Society Accessed 18 January 2012 *^ General Pharmaceutical Council Registering as a ... It is not unusual for pharmaceutical studies majors to work in other fields such as the pharmaceutical industry or in hospitals ...
"International Nonproprietary Names for Pharmaceutical Preparations List #3" (PDF). WHO Chronicle. 13 (12): 463-474. December ... The case was part of the reshaping of the US pharmaceutical market that occurred in the 1990s, to favor generic entry. Although ... Chien C (2003). "Cheap Drugs at What Price to Innovation: Does the Compulsory Licensing of Pharmaceuticals Hurt Innovation?". ... British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. p. 759. ISBN 9780857113382. "Dicyclomine ...
... is used in nutraceutical and pharmaceutical preparations. Magnesium chloride (E511) is an important ... "Highly Reactive Magnesium for the Preparation of Grignard Reagents: 1-Norbornane Acid", Organic Syntheses, Collected Volume 6, ... coagulant used in the preparation of tofu from soy milk. In Japan it is sold as nigari (にがり, derived from the Japanese word for ...
The Dakin-West reaction provides an efficient method for preparation of certain methyl ketones from carboxylic acids.[16] ... Ketones are produced on massive scales in industry as solvents, polymer precursors, and pharmaceuticals. In terms of scale, the ... Many methods exist for the preparation of ketones in industrial scale and academic laboratories. Ketones are also produced in ...
... and helped to author the Pharmacopoeia Londinensis in 1618-a directory of standardized pharmaceutical preparations given by the ...
Interactions with conventional pharmaceuticals. Forms of alternative medicine that are biologically active can be dangerous ... Homeopathic preparations, termed "remedies", are extremely dilute, often far beyond the point where a single molecule of the ... There is also an increase in conspiracy theories toward conventional medicine and pharmaceutical companies,[34] mistrust of ... In addition, in most countries, alternative therapies (in contrast to pharmaceuticals) can be marketed without any proof of ...
... are marketed for academic and pharmaceutical research. The scanners are apparently based on microminiature scintillators and ... for specially adapted on-site chemical synthesis apparatus to produce the radiopharmaceuticals after radioisotope preparation. ...
Topical and oral preparations of nicotinamide (the amide form of vitamin B3) are alternative medical treatments.[147] ... "Current Pharmaceutical Design. 5 (9): 707-23. PMID 10495361. Archived from the original on 27 February 2020. Retrieved 21 ... Madan RK, Levitt J (April 2014). "A review of toxicity from topical salicylic acid preparations". Journal of the American ... Topical and oral preparations of zinc are suggested treatments for acne; evidence to support their use for this purpose is ...
This article is about levothyroxine as a pharmaceutical drug. For its role as a hormone, see Thyroid hormone. ... Antithyroid preparations. Thyroid peroxidase. inhibitors (thioamide). *Thiouracils *Propylthiouracil#. *Methylthiouracil. * ...
... in preparation for human clinical trials, this technology was further developed by Tocagen (a pharmaceutical company primarily ...
Sano H.; Ogawa H. (1975). "Preparation and application nitrogen containing active carbons". Osaka Kogyo Gijutsu Shirenjo. 26 (5 ... Filtration over activated carbon is used in large scale fine chemical and pharmaceutical processes for the same purpose. The ... Petrov N.; Budinova T.; Razvigorova M.; Ekinci E.; Yardim F.; Minkova V. (2000). "Preparation and characterization of carbon ... However, some broad classification is made for general purpose based on their size, preparation methods, and industrial ...
One such pharmaceutical application is in the synthesis of SIB-1508Y, which is more commonly known as Altinicline. Altinicline ... Preparation of 1,3-Decadiyne" (PDF), Organic Synthesis, 84: 77-87, doi:10.15227/orgsyn.084.0077, PMC 2901882 , PMID 20628544 ... There are other recent examples of the use of aryl iodides for the preparation of intermediates under typical Sonogashira ... Its applications include pharmaceuticals, natural products, organic materials, and nanomaterials. Specific examples include its ...
Journal of Pharmaceutical and Biomedical Analysis. 37 (4): 631-828. doi:10.1016/j.jpba.2004.11.051. PMID 15797781.. ... "all herbal preparations should be checked for toxic chemical residues to allay consumer fears of exposure to known neuro- ...
... preparations of a given formulation, as opposed to preparation for a specific patient, is known as "non-traditional ... So economies of scale, not lack of skill or knowledge, produced the modern pharmaceutical industry. With the turn of the 20th ... In the field of pharmacy, compounding (performed in compounding pharmacies) is preparation of a custom formulation of a ... International Journal of Pharmaceutical Compounding. *Drug Compounding: FDA Authority and Possible Issues for Congress from the ...
Pharmaceuticals[edit]. Recognizing that approximately 50% of commercial pharmaceuticals are organic salts, ionic liquid forms ... They can be functionalized to act as acids, bases, or ligands, and are precursors salts in the preparation of stable carbenes. ... Ionic Liquid Salt Forms of Active Pharmaceutical Ingredients: A Position Paper". Pharmaceutical Research. 27 (4): 521-526. doi: ... ILs can extract specific compounds from plants for pharmaceutical, nutritional and cosmetic applications, such as the ...
Gomelsky, A.; Dmochowski, RR (2003). "Antibiotic prophylaxis in urologic prosthetic surgery". Current Pharmaceutical Design. 9 ... Traditional strategies to combat infections aim at decreasing skin colony count such as scrubbing skin preparation with alcohol ... The use of an antibiotic-coated implant and a no-touch surgical technique with skin preparation measures and peri-operative ...
Medical Science and Medical Industry: The Formation of the American Pharmaceutical Industry (1987) ... Published housekeeping guides included instructions in medical care and the preparation of common remedies. Nursing was ...
... high performance thin layer chromatography method for determination of yohimbine hydrochloride in pharmaceutical preparations" ... Year Book of the American Pharmaceutical Association. American Pharmaceutical Association. 1914. p. 564. Retrieved 2015-05-04. ... Yohimbe is the common English name for the tree species P. johimbe and, by extension, the name of a medicinal preparation made ... Some brands sold over-the-counter were found to contain more yohimbine per serving than a standard pharmaceutical dose;[8]:368 ...
"Journal of Pharmacy & Pharmaceutical Sciences. 11 (1): 77-87. doi:10.18433/J39G6V. PMID 18445366.. ... Scutellaria baicalensis in particular is a common component of many preparations.[8] Its root, known as Radix Scutellariae, is ... Journal of Pharmaceutical and Biomedical Analysis. 63: 120-7. doi:10.1016/j.jpba.2012.01.027. PMID 22342658.. ... Pharmaceutical Bulletin. 34 (8): 1198-203. doi:10.1248/bpb.34.1198. PMID 21804206.. ...
International Journal of Pharmaceutical Compounding, Winter 2006. Retrieved 2009-01-03.. *^ The Extra Pharmacopeia Martindale. ... its preparations, derivatives, alkaloids and salts, although an exception is made for poppyseed.[40] ... London: The Pharmaceutical Press, 1958, page 924. *^ "International Narcotics Control Bureau, Technical Reports, 2008, Part IV ... The second is to produce opium for use mainly by the pharmaceutical industry.[4] The third is to produce other alkaloids, ...
SupprelinLA, by Endo Pharmaceuticals, Inc.. *Information of use of Zoladex in prostate cancer ... Preparations. *Follicle-stimulating hormone. *Human chorionic gonadotropin. *Luteinizing hormone. *Menotropin. *Urofollitropin ...
Pharmaceutical Services Branch, Guide to poisons and therapeutic goods legislation for medical practitioners and dentists, ... progesterone preparations, norethisterone/ethinylestradiol ('OrthoNovum 7/7/7'), St. John's Wort, phenytoin, and systemic ... In the United States, a special procedure is required to obtain the pharmaceutical. In most other countries, a consent form is ... British National Formulary (47th ed.). London: British Medical Association and Royal Pharmaceutical Society of Great Britain. ...
The Western pharmaceutical term is Oviductus Ranae. ... Preparation[edit]. Hasma cooked with jujubes fruits. Hasma ...
Materials chemistry is the preparation, characterization, and understanding of substances with a useful function. The field is ... and the various pharmaceuticals. ...
... plant-based preparation for use in beverages (ID 4210, 4211); Carica papaya L. (ID 2007); "fish protein" (ID 651); acidic water ... pharmaceuticals, art, furniture polish and more.[43] ...
ISIC 5231 retail sales of pharmaceutical and medical goods, cosmetic and toilet articles ... 2424 soap and detergents, cleaning preparations, perfumes. *2430 men's and women's inner garments, shaving gels, deodorants ...
Pharmaceutical Press. *↑ 2,0 2,1 2,2 Combs G.F. Jr. (1998). The vitamins; Fundamental aspects in nutrition and health. Second ... 2001). »Similar therapeutic serum levels attained with emulsified and oil-based preparations of coenzyme Q10«. Asia Pacific ...
... among them Northeast Pharmaceutical Group and North China Pharmaceutical Group, and agreed to temporarily stop production in ... Food preparation[edit]. Vitamin C chemically decomposes under certain conditions, many of which may occur during the cooking of ... Traditionally, the main producers were BASF/Takeda, DSM, Merck and the China Pharmaceutical Group Ltd. of the People's Republic ... British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. p. 1049. ISBN 9780857113382. .. ...
Stewart JM (2003). "Bradykinin antagonists as anti-cancer agents". Current Pharmaceutical Design. 9 (25): 2036-42. doi:10.2174/ ... they discovered the powerful hypotensive effects of bradykinin in animal preparations. Bradykinin was detected in the blood ... Journal of Pharmaceutical Sciences. 71 (10): 1172-4. doi:10.1002/jps.2600711024. PMID 7143219.. ...
Lomb/Valeant Pharmaceuticals), Amphadase (Amphastar Pharmaceuticals), and Wydase. Wydase, however, is no longer manufactured. ... although most hyaluronidase preparations are contaminated with large amounts of angiogenic growth factors.[15] ...
The "Ecole de Pharmacie", nowadays the "Faculté de Pharmacie" (University of pharmaceutical sciences) of Paris, stands 4, ... raw opium was used in diverse preparations known as laudanum (see Thomas de Quincey's "Confessions of an English Opium-Eater ... some types of flies from Spain had a reputation for inducing aphrodisiac effects when used in preparations after having been ... Deputy Professor in History of pharmaceutical matters (1811) then Professor (1814) then Administrator-Treasurer (1824) at the ...
It was also a precursor in the preparation of cortisone. When Marker found that there was a similar structure to sarsasapogenin ... Businesspeople in the pharmaceutical industry. *University of Maryland, College Park alumni. *People from Hagerstown, Maryland ...
Scientific American is the essential guide to the most awe-inspiring advances in science and technology, explaining how they change our understanding of the world and shape our lives.
Expert Advisory Panel on the International Pharmacopoeia and Pharmaceutical Preparations. The Expert Advisory Panel on the ... Expert Committee on Specifications for Pharmaceutical Preparations (ECSPP). ... International Pharmacopoeia and Pharmaceutical Preparations is the largest expert advisory panel within WHO. It consists of ... more than 70 members conversant with quality assurance in the area of quality assurance of pharmaceuticals. ...
According to the Paperwork Reduction Act of 1995, no persons are required to respond to a collection of information unless it displays a valid OMB control number. The valid OMB control number for this information collection is 0990-0379. The time required to complete this information collection is estimated to average 5 minutes per response, including the time to review instructions, search existing data resources, gather the data needed, and complete and review the information collection. If you have comments concerning the accuracy of the time estimate(s) or suggestions for improving this form, please write to: U.S. Department of Health & Human Services, OS/OCIO/PRA, 200 Independence Ave., S.W., Suite 336-E, Washington D.C. 20201, Attention: PRA Reports Clearance Officer ...
Pharmaceuticals--mfg ; * Pills, pharmaceutical--mfg * Pituitary gland pharmaceutical preparations--mfg * Poultry and animal ... Syrups, pharmaceutical--mfg * Tablets, pharmaceutical--mfg * Thyroid preparations--mfg * Tinctures, pharmaceutical--mfg * ... Barbituric acid pharmaceutical preparations--mfg * Belladonna pharmaceutical preparations--mfg * Botanical extracts: powdered, ... Powders, pharmaceutical--mfg * Procaine pharmaceutical preparations--mfg * Proprietary drug products--mfg * Remedies, human and ...
... was 288 Units (Enterprises). Discover more data with NationMaster! ... How does Poland perform in the Pharmaceutical industry?. Basic Pharmaceutical Products and Pharmaceutical Preparations ... Total Hours Worked in Basic Pharmaceutical Products and Pharmaceutical Preparations in Poland ... Pharmaceutical Preparations Number of Enterprises Units (Enterprises) - 2008 to 2019. Since 2014, Poland Pharmaceutical ...
Pharmaceutical compositions which release the active ingredient slowly are based upon a growth factor or hormone as active ... 6. A method for administering a pharmaceutical preparation to a patient in need thereof comprising administering to said ... The present invention relates to a pharmaceutical preparation comprising at least one receptor/binding protein and a ... The preparation containing IGF-I binding protein resulted in a retardation of release compared to the preparation without IGF-I ...
Organic Chemistry Pharmaceutical Chemical Chemical Preparation These keywords were added by machine and not by the authors. ...
WHO Expert Committee on Specifications for Pharmaceutical Preparations; World Health Organization (‎World Health Organization, ... World Health Organization; WHO Expert Committee on Specifications for Pharmaceutical Preparations (‎World Health Organization, ... 1966)‎. International non-proprietary names for pharmaceutical preparations: general principles. World Health Organization. ... Forty-sixth report of the WHO Expert Committee on Specifications for Pharmaceutical Preparations  ...
Belgium Basic Pharmaceutical Products and Pharmaceutical Preparations Turnover Per Employee rose 3.9% in 2019, from a year ... Pharmaceutical Preparations Labour Cost Per Employee FTE Since 2014 Switzerland Pharmaceutical Preparations Labour Cost Per ... Pharmaceutical Preparations Turnover Per Employee In 2019 Switzerland was ranked number 1 in Pharmaceutical Preparations ... Basic Pharmaceutical Products and Pharmaceutical Preparations Turnover Per Employee. This key economic indicator for the ...
Barbituric acid pharmaceutical preparations. Pituitary gland pharmaceutical preparations. Belladonna pharmaceutical ... pharmaceutical preparations promoted primarily to the public. Adrenal pharmaceutical preparations. Liniments. Analgesics. Lip ... Industry: 2834-Pharmaceutical Preparations. Establishments primarily engaged in manufacturing, fabricating, or processing drugs ... Products of this industry consist of two important lines, namely: (1) pharmaceutical preparations promoted primarily to the ...
The Expert Committee on Specifications for Pharmaceutical Preparations reviews developments in the quality assurance of ... procedures governing the assessment of pharmaceutical products for procurement by United Nations agencies and for assessing the ...
This invention relates to the preparation of a transdermal delivery system. The preparation is designed to deliver therapeutic ... the drugs or other pharmaceutical preparations by definition, are not isotonic with mammalian blood. ... Topical drug preparations. 1999-04-27. Drizen et al.. 424/488. 5731339. Methods and formulations for modulating the human ... A transdermal preparation of Alprostadil is prepared in the manner of Example 1 with the following components: ...
Regional pharmaceutical preparation for biological and chemical terrorism.. Mrvos R1, Piposzar JD, Stein TM, Locasto D, ... An important element in a biological or chemical terrorist event is the availability of the pharmaceuticals and the capability ... Assisting in the development, implementation, and procurement of a pharmaceutical cache is yet another role. ... one of the roles of the poison center was to determine the pharmaceutical needs of the community in the event of a terrorist ...
Said preparation releases a medicinal compound in a sigmoid type dissolution pattern irrespective of the PH of a dissolution ... A controlled release pharmaceutical preparation comprising a core containing a medicinal compound and a coating layer ... Therefore, the pharmaceutical preparation of the present invention is useful as a pharmaceutical preparation wherein the ... For example, following two pharmaceutical preparations have been known. One is a sustained release pharmaceutical preparation ( ...
Equipment Type: Other pharmaceutical preparations, acting on skin, for human use Industry: Pharmaceutical and medicine ... 2019 Global Forecast for Other pharmaceutical preparations, acting on skin, for human use (2020-2025 Outlook)-Manufacturing & ... Equipment Type: Other pharmaceutical preparations, acting on skin, for human use. Industry: Pharmaceutical and medicine ... The 2019 Global Forecast for Other pharmaceutical preparations, acting on skin, for human use (2020-2025 Outlook)-Manufacturing ...
Those of the BP, based on the performance of established well-preserved BP preparations, are not mandatory but provide guidance ... for multi-dose sterile products but BP and draft EP tests include also criteria for topical and liquid oral preparations. ...
... and an external preparation containing the above composition as a base. ... Dicyclohexylalkanes, their preparation, cosmetic and pharmaceutical formulations containing these compounds, and their use as ... Taro Pharmaceutical Industries Ltd.. Spill resistant pharmaceutical system. US7662855 *. 9 Nov 2004. 16 Feb 2010. Imaginative ... Spill resistant pharmaceutical compositions in semi-solid form. US6572880 *. 3 Jan 2001. 3 Jun 2003. Pharmaceutical ...
Buy Specifications for Pharmaceutical Preparations: 30th Report by World Health Organization(WHO) from Waterstones today! Click ... Specifications for Pharmaceutical Preparations: 30th Report - Technical Report Series (Paperback). World Health Organization( ...
Flavouring preparations meet EC/1334/2008, Art. 3.2(d) guidelines.. Hemp Flavouring Preparation (THC-free) - 50% CBD equivalent ...
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You have to register before you can post on our forums or use our advanced features. Register Now! Its Free and Fast!. Already registered? Login now below.. ...
Regeneron Pharmaceuticals Inc. Tarrytown. NY. 325412 - Pharmaceutical Preparation Manufacturing This U.S. industry comprises ... Penicillin preparations manufacturing. 325412. 325412. 325412. Pharmaceutical preparations (e.g., capsules, liniments, ... Sodium chloride pharmaceutical preparations manufacturing. 325412. 325412. 325412. Sodium salicylate preparations manufacturing ... 325412 - Pharmaceutical Preparation Manufacturing Top Businesses by Revenue for 325412:. Novartis Corporation. East Hanover. NJ ...
... for treatment of irritable bowel ... Group A (n = 30) were treated by acupuncture combined with microorganism pharmaceutical preparations, group B (n = 35) by oral ... Clinical observation on acupuncture combined with microorganism pharmaceutical preparations for treatment of irritable bowel ... CONCLUSION: Acupuncture combined with microorganism pharmaceutical preparations has a better therapeutic effect on irritable ...
... by weight within the preparation, and is sta ... The present invention provides a lyophilized preparation of ... which can be conventionally added as an additive for pharmaceutical preparations, may be added to the lyophilized preparation ... As a preparation of stabilized amrubicin, a preparation incorporated with L-cysteine or a salt thereof has been known (e.g., ... 2. The stabilized preparation according to claim 1, wherein the water content within the preparation is in the range of 0 to ...
"Pharmaceutical Preparations" by people in Harvard Catalyst Profiles by year, and whether "Pharmaceutical Preparations" was a ... "Pharmaceutical Preparations" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH ( ... Below are the most recent publications written about "Pharmaceutical Preparations" by people in Profiles. ... Below are MeSH descriptors whose meaning is more general than "Pharmaceutical Preparations". ...
This statistic shows the number of enterprises in the manufacture of pharmaceutical preparations industry in Switzerland from ... Latvia: number of pharmaceutical preparations manufacturers 2008-2016. *Czech Republic: number of pharmaceutical preparations ... Latvia: number of pharmaceutical preparations manufacturers 2008-2016. *Czech Republic: number of pharmaceutical preparations ... Turkey: number of pharmaceutical preparations manufacturers 2009-2014. *UK: number of pharmaceutical preparations manufacturers ...
This study covers the latent demand outlook for oxytocic pharmaceutical preparations across the regions of China, including ... Oxytocic pharmaceutical preparations is specifically defined as follows:. 325412D187 Genito-urinary preparations, oxytocics. ... In order to estimate the latent demand for oxytocic pharmaceutical preparations across the regions and cities of China, I used ... Based on the aggregate view of oxytocic pharmaceutical preparations as defined above, data were then collected for as many ...
... Anna ... Liquid matrices such as beverages, drops, mouthwashes, and pharmaceutical preparations often have physicochemical properties ... Luckily, it is highly unlikely that as many as five dyes are used in a single preparation so it is our suggestion that a ... Other components of liquid preparations, including surfactants, vitamins, preservatives, and flavors, do not interfere. Due to ...
... which comprises administering a powdery preparation in unit dosage form to the nasal cavity of a human being requiring ... A powdery pharmaceutical composition and a powdery preparation in unit dosage form for application to the mucosa of the nasal ... Aventis Pharmaceuticals Inc.. Aqueous-based pharmaceutical composition. US7994197. 26 Ago 2009. 9 Ago 2011. Map Pharmaceuticals ... A powdery pharmaceutical composition and a powdery preparation in unit dosage form for application to the mucosa of the nasal ...
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  • Identification and determination of oxytetracycline, tiamulin, lincomycin, and spectinomycin in veterinary preparations by thin-layer chromatography/densitometry. (molecularstation.com)
  • Regarding the quality control of medicines, a validated microbiological assay for determination of orbifloxacin in pharmaceutical formulations has not as yet been reported. (mdpi.com)
  • The developed procedures were applied for the determination of ranitidine in river water and pharmaceutical preparations. (rsc.org)
  • developed and validated for simultaneous determination of RPG and metformin hydrochloride MTF in original fixed dose combination tablet preparations using a zero-crossing first-derivative for RPG and fourth-derivative for MTF accurately. (scirp.org)
  • A simple, selective and sensitive spectrophotometric method is described by the determination of menadione (or menadione sodium bisulfite) in bulk samples and pharmaceutical preparations. (eurekamag.com)
  • In this study, a simple, fast and sensitive method was developed for the determination of escitalopram by capillary electrophoresis in pharmaceutical preparations. (alliedacademies.org)
  • Therefore analytical methods for the determination of sulfonamides in pharmaceuticals and biological samples are of great importance. (eurekaselect.com)
  • A controlled release pharmaceutical preparation comprising a core containing a medicinal compound and a coating layer containing a water-repellent salt and a water-insoluble and slightly water-permeable acrylic polymer having trimethylammoniumethyl group. (google.com.au)
  • Said preparation releases a medicinal compound. (google.com.au)
  • Said preparation releases a medicinal compound in a sigmoid type dissolution pattern irrespective of the PH of a dissolution medium. (google.com.au)
  • 4. The pharmaceutical preparation of claim 1, wherein another coating layer made of at least one material selected from the group consisting of ethylcellulose, hydroxypropylcellulose and a medicinal compound is provided around the coating layer on the surface of the core. (google.com.au)
  • The present invention relates to a controlled release pharmaceutical preparation, and more particularly to a so-called sigmoid type controlled release pharmaceutical preparation (Sigmoidal-Releasing System) from which a medicinal compound rapidly dissolves after a certain lag time. (google.com.au)
  • Hitherto, concerning pharmaceutical preparations containing medicinal compounds, there have been various attempts to maintain their effects after the administration. (google.com.au)
  • And the other is a sustained release pharmaceutical preparation (see Japanese Unexamined Patent Publication No. 193913/1985) in which a core containing a medicinal active ingredient and an organic acid is spray-coated with an ethanol solution of an acrylic polymer having trimethylammoniumethyl group. (google.com.au)
  • However, although these pharmaceutical preparations are suitable for releasing medicinal active ingredients gradually after the administration, they have a problem that the starting of the dissolution of their medicinal active ingredients can hardly be controlled. (google.com.au)
  • On the other hand, it is known in the field of the pharmaceutical preparation that an increase in the thickness of the coating layer results in a delay of the starting of the dissolution of a medicinal active ingredient. (google.com.au)
  • An object of this invention is to provide a controlled release pharmaceutical preparation giving a so-called sigmoid type dissolution pattern wherein a lag time until the starting of the dissolution of a medicinal compound and the rate of the following dissolution can be controlled and the rate of the dissolution of the medicinal compound does not depend on the pH of a medium for the dissolution. (google.com.au)
  • This pharmaceutical preparation can be prepared by dissolving the above-mentioned water-soluble polymeric substance and medicinal agent in an organic solvent, casting the resultant solution, and removing the organic solvent by drying to obtain a pharmaceutical preparation in the form of a film or sheet. (google.ch)
  • The increasing contamination of freshwater with pharmaceuticals, surfactants, pesticides and other organic compounds are of major concern. (arctichealth.org)
  • This application note describes results obtained using a liquid handling-based automation system for the sample preparation of compounds to be analyzed by LC-MS/MS and applied to the monitoring of multiple classes of pharmaceutical and illicit drugs. (technologynetworks.com)
  • The Expert Committee on Specifications for Pharmaceutical Preparations reviews developments in the quality assurance of medicines and provides advice and recommendations to help combat problems caused by counterfeit and substandard medicines. (who.int)
  • on the compounding of sterile preparations. (ijpc.com)
  • The Galenical preparations of the British pharmacopoeia : a handbook for medical and pharmaceutical students / by C.O. Hawthorne. (wellcomecollection.org)
  • Credit: The Galenical preparations of the British pharmacopoeia : a handbook for medical and pharmaceutical students / by C.O. Hawthorne. (wellcomecollection.org)
  • This industry includes establishments primarily engaged in manufacturing, fabricating, or processing drugs in pharmaceutical preparations for human or veterinary use. (warc.com)
  • This invention relates to a base composition capable of increasing the percutaneous absorption of drugs, to a pharmaceutical composition for external use in which said base composition is used, and to a method of promoting the percutaneous absorption of drugs. (google.com.au)
  • Catalent, Inc, a leading global provider of advanced delivery technologies and development solutions for drugs, biologics and consumer health products, has announced that it is acquiring Juniper Pharmaceuticals, including its Nottingham, UK-based Juniper Pharma Services division. (specchemonline.com)
  • Results indicated that 73% of the solid formulations failed to meet the acceptance criteria for active pharmaceutical ingredient (API) and in-flight degradation rates for most drugs were consistently higher than those from matching-lot ground controls. (nsbri.org)
  • In particular, provided is a compound of formula (I), or a pharmaceutically acceptable salt, stereoisomer or solvate thereof, a preparation method therefor and a use thereof in the preparation of drugs for treating pain. (sumobrain.com)
  • According to a STADA press release on Monday, Biopharma's pharmaceutical business will become an integral part of STADA in Ukraine and has strong growth potential in the production of high-quality prescription and OTC drugs. (interfax.com.ua)
  • Together with the corresponding closure systems, they serve for packaging of pharmaceutical preparations which are not intended for parenteral use. (complianceonline.com)
  • In 2019 Mexico was number 35 in Total Number of Scientific Publications in Pharmaceutical Science reaching 43.33 Publications, compared to 40 in 2018. (nationmaster.com)
  • This statistic shows the revenue of pharmaceutical preparations manufacturing in New Zealand from 2008 to 2012, with a projection until 2018. (statista.com)
  • Drozdov, V. 2018-06-01 00:00:00 The composite Y14/siUTR, a complex consisting of cationic lipopeptide Y14 as an excipient and pharmaceutical substance of small interfering RNAtargeted against the UTR region of hepatitis C virus (siUTR), was investigated. (deepdyve.com)
  • The present invention provides a lyophilized preparation of amrubicin, which contains L-cysteine or a salt thereof and has a water content of 0 to about 4% by weight within the preparation, and is stable even in a long-term storage, and further provides a method for production of said preparation. (freepatentsonline.com)
  • 4. The stabilized preparation according to any one of claims 1 to 3, wherein the content of L-cysteine or a salt thereof is in the range of about 0.5 to about 250 mg to 100 mg (potency) of amrubicin or a salt thereof. (freepatentsonline.com)
  • 5. The stabilized preparation according to any one of claims 1 to 3, wherein the content of L-cysteine or a salt thereof is in the range of about 3 to about 45 mg to 100 mg (potency) of amrubicin or a salt thereof. (freepatentsonline.com)
  • 6. The stabilized preparation according to claim 1, wherein the salt of amrubicin is a hydrochloride thereof. (freepatentsonline.com)
  • 8. The stabilized preparation according to claim 1, wherein L-cysteine or a salt thereof is (1) L-cysteine in an amount of about 5 to about 20 mg, or (2) a salt of L-cysteine in an amount corresponding thereto, to 100 mg (potency) of amrubicin hydrochloride. (freepatentsonline.com)
  • 12. A method for producing a stabilized preparation as set forth in claim 1, which comprises preparing an aqueous solution containing (a) amrubicin or a salt thereof, and (b) L-cysteine or a salt thereof, sterilizing the resulting solution by aseptic filtration, and followed by lyophilizing the resultant. (freepatentsonline.com)
  • An extended release perparation of an active compound with very low solubility containing the active compound dissolved or dispersed in a semi-solid or liquid non-ionic solubilizer and whereby the amount by weight of the solubilizer is at least equal to the amount by weight of the active compound as well as a process for the preparation thereof. (google.com)
  • (EN) The present invention relates to a binder free pharmaceutical composition comprising canagliflozin or a prodrug or a pharmaceutically acceptable salt thereof, and one or more 5 pharmaceutically acceptable excipients, wherein the said composition is devoid of canagliflozin hemihydrate, and having acceptable chemical stability, polymorphic stability & comparative dissolution and bioequivalence profile to that of INVOKANA® tablets. (wipo.int)
  • Provided are a polyhydroxyphthalazinone compound, a preparation method therefor and the use thereof, wherein the general formula of the chemical structure of the polyhydroxyphthalazinone compound is as shown by formula (I). The polyhydroxyphthalazinone compound disclosed in the present invention has a good ER receptor agonistic effect, and is expected to be useful in developing a novel ER receptor agonist. (sumobrain.com)
  • The invention belongs to the technical field of pharmaceutical chemistry, and particularly pertains to benzimidazole derivatives, and preparation process and pharmaceutical uses thereof. (patents.com)
  • The 2019 Global Forecast for Other pharmaceutical preparations, acting on skin, for human use (2020-2025 Outlook)-Manufacturing & Markets Report, published by Barnes Reports, contains timely and accurate market statistics and forecasts on the market for over 140 countries. (bccresearch.com)
  • This U.S. industry comprises establishments primarily engaged in manufacturing in-vivo diagnostic substances and pharmaceutical preparations (except biological) intended for internal and external consumption in dose forms, such as ampoules, tablets, capsules, vials, ointments, powders, solutions, and suspensions. (naics.com)
  • In 2015, there were 139 enterprises manufacturing pharmaceutical preparations in Switzerland. (statista.com)
  • In 2010, revenues of pharmaceutical preparations manufacturing in New Zealand amounted to approximately 1.34 billion U.S. dollars. (statista.com)
  • The line comprised a 4000 litre reactor for final batch preparation, a 400 litre reactor for pre-mixes, and a CIP type cleaning system which, along with a SCADA control system based on manufacturing and cleaning recipes, increased the level of automation in the cleaning processes. (inoxpa.com)
  • HOUSTON, Dec. 17, 2019 /PRNewswire/ -- CNS Pharmaceuticals, Inc. (NASDAQ: CNSP) ("CNS" or the "Company"), a biotechnology company specializing in the development of novel treatments for brain tumors, today announced the completed good manufacturing practice (GMP) reprocessing of its lead drug candidate, Berubicin, with partner Anthem Biosciences Pvt. (pharmiweb.com)
  • This book is intended to serve as a resource for analysts in developing and troubleshooting sample preparation methods. (kobo.com)
  • Part Three discusses sample preparation method development for different types of dosage forms including addressing drug excipient interactions and post extraction considerations, as well as method validation and applying Quality by Design (QbD) principles to sample preparation methods. (kobo.com)
  • These developments have attracted the attention of process chemists who add metathesis reaction to a toolbox of reliable methods for production of pharmaceuticals. (teknoscienze.com)
  • The present work was aimed at developing pharmaceutical analytical methods for the components of this composite using HPLC-UV and UV spectroscopy. (deepdyve.com)
  • The compound-entrapped liposomes prepared in accordance with the disclosed methods may be used as pharmaceutical preparations. (energy.gov)
  • Methods of administering such pharmaceutical preparations are also disclosed. (energy.gov)
  • Regional pharmaceutical preparation for biological and chemical terrorism. (nih.gov)
  • An important element in a biological or chemical terrorist event is the availability of the pharmaceuticals and the capability of delivering them rapidly. (nih.gov)
  • This industry includes companies that manufacture medications, chemical contraceptive products, medical diagnostic preparations, radioactive in-vivo diagnostic substances and biotech pharmaceuticals. (marketresearch.com)
  • The degradation of the active pharmaceutical ingredient (API) and adjuvants in addition to alterations of the chemical matrix of the formulation can decrease potency and bioavailability, and increase the risk of toxicity of degraded medications. (nsbri.org)
  • The laboratory work involves production of sterile pharmaceutical preparations and microbiological quality control of finished products. (uio.no)
  • The laboratory work related to production of sterile pharmaceutical preparations needs to be approved in order for the student to be eligible to take the practical exam. (uio.no)
  • On and a half (1 ½) hours practical examination in the production of sterile pharmaceutical preparations, which is graded Passed / Not passed. (uio.no)
  • The range of PHARMIX equipment is designed for preparation of sterile pharmaceutical products. (inoxpa.com)
  • Part One covers dosage form and diluent properties that impact sample preparation of pharmaceutical dosage forms and the importance of sampling considerations in generating data representative of the drug product batch. (kobo.com)
  • Part Two reviews specific sample preparation techniques typically used with pharmaceutical dosage forms. (kobo.com)
  • Part Four examines additional topics in sample preparation including automation, investigating aberrant potency results, green chemistry considerations for sample preparation and the ideal case where no sample preparation is required for sample analysis. (kobo.com)
  • Bioanalysis of Pharmaceuticals: Sample Preparation, Separation Techniques and Mass Spectrometry is the first student textbook on the separation science and mass spectrometry of pharmaceuticals present in biological fluids with an educational presentation of the principles, concepts and applications. (separationsnow.com)
  • Automated sample preparation enables highly reproducible quantitative analyses while meeting the increased efficiency needs often required for sample processing in laboratories. (technologynetworks.com)
  • In the present review article, column and mobile phase conditions as well as sample preparation issues are taken into consideration. (eurekaselect.com)
  • Products of this industry consist of two important lines: pharmaceutical preparations promoted primarily to the dental, medical, or veterinary profession, and pharmaceutical preparations promoted primarily to the public. (warc.com)
  • Belgium Basic Pharmaceutical Products and Pharmaceutical Preparations Turnover Per Employee rose 3.9% in 2019, from a year earlier. (nationmaster.com)
  • Since 2014 Belgium Basic Pharmaceutical Products and Pharmaceutical Preparations Turnover Per Employee increased 9.7% year on year close to €934.8 Thousand. (nationmaster.com)
  • In 2019 Denmark was ranked number 3 in Basic Pharmaceutical Products and Pharmaceutical Preparations Turnover Per Employee. (nationmaster.com)
  • In 2017 France was number 7 in Basic Pharmaceutical Products and Pharmaceutical Preparations Turnover Per Employee at €464.5 Thousand, from 26 in 2016. (nationmaster.com)
  • This report includes the following guidelines of direct relevance to the United Nations Prequalification Programme for Priority Essential Medicines and for quality control laboratories: procedures governing the assessment of pharmaceutical products for procurement by United Nations agencies and for assessing the acceptability of quality control laboratories for use by United Nations agencies, as well as guidance on variations to a prequalified product dossier. (who.int)
  • The USP test is intended for multi-dose sterile products but BP and draft EP tests include also criteria for topical and liquid oral preparations. (springer.com)
  • FCS Frankfurt Cargo Services was recently granted EU good distribution practice (GDP) certification for medical products for human use-a key step in the company's goal to expand its pharmaceutical logistics activities and ramp up preparations to handle sensitive Covid-19 vaccine consignments. (pharmaceuticalcommerce.com)
  • It also includes those that manufacture medical impregnated wadding, gauze, bandages and dressings, and that prepare botanical products for pharmaceutical use. (marketresearch.com)
  • The UK's Medicines and Healthcare products Regulatory Agency (MHRA) has published an official update to pharmaceutical companies on preparations for Brexit. (specchemonline.com)
  • Salix Pharmaceuticals, Ltd., headquartered in Raleigh, North Carolina, develops and markets prescription pharmaceutical products and medical devices for the prevention and treatment of gastrointestinal diseases. (fiercebiotech.com)
  • 1. We has 7 years' exporting experience in active pharmaceutical ingredient products. (hfcletter.com)
  • Technologies like BilcareOptima TM (Ajith Nair, "Time to show your work and that includes packaging," Pharmaceutical Processing , Aug. 2012) developed by Bilcare Research are used by pharmaceutical companies to understand the factors causing the degradation of the drug products (primarily solid dosages) in the prevailing Earth conditions and use the data to model an optimum packaging. (nsbri.org)
  • This annex is the result of the Q4B process for Microbiological Examination of Non-Sterile Products: Acceptance Criteria for Pharmaceutical Preparations and Substances for Pharmaceutical Use. (gmp-compliance.org)
  • Buy Pharmaceutical Preparations Products Online at Chemist Warehouse and enjoy huge discounts across the entire range. (chemistwarehouse.com.au)
  • In 2019 Kazakhstan was number 1 in Share of Corresponding/Leading Author Scientific Publications in Pharmaceutical Science. (nationmaster.com)
  • This invention relates to a powdery pharmaceutical composition for application to the mucosa of the nasal cavity. (google.es)
  • More specifically, this invention relates to a powdery pharmaceutical composition which when administered, adheres to the nasal mucosa and absorbs the mucus on the nasal mucosa to form a viscous liquid having moderate tackiness and flowability whereby the active drug contained in it is gradually and effectively absorbed through the nasal mucosa. (google.es)
  • The invention relates to cosmetic and/or pharmaceutical preparations containing (a) UV-A filters having an enamine structure, and (b) oil components and/or emulsifiers with a polarity of between 1.0 and 4.0 Debye. (google.com)
  • The present invention relates to a pharmaceutical preparation for remedy of periodontal disease. (google.ch)
  • The present invention relates to a pharmaceutical composition comprising glycerol esters of a fatty acid, wherein the compositions are useful for the delivery. (patents.com)
  • A preparation for topical use in the therapeutic treatment of impotentia coeundi. (freepatentsonline.com)
  • Pharmaceutical compositions which release the active ingredient slowly are based upon a growth factor or hormone as active ingredient and a means for effecting slow release of the active ingredient. (google.com)
  • Those of the BP, based on the performance of established well-preserved BP preparations, are not mandatory but provide guidance for the selection of suitable antimicrobial preservatives for inclusion in formulae of the Pharmacopoeia. (springer.com)
  • HPLC can provide a valuable tool for generating highly pure preparations for characterizing the antimicrobial activities. (eurekaselect.com)
  • Robsco Search is an executive recruiting company working with pharmaceutical and biotech companies for twenty two years. (veteranownedbusiness.com)
  • and an external preparation containing the above composition as a base. (google.com.au)
  • A powdery pharmaceutical composition and a powdery preparation in unit dosage form for application to the mucosa of the nasal cavity, at least about 90% of which consists of particles having an effective particle diameter of about 20 to about 250 microns, said composition comprising a lower alkyl ether. (google.es)
  • This uncertainty in its composition causes the preparation to be little used. (drugs-forum.com)
  • Provided is a pharmaceutical preparation composition comprising a polymerized camptothecin derivative which is obtained by bonding a camptothecin derivative to. (patents.com)
  • The invention is in the field of sun protection agents and relates to new preparations which UV-A filter enamine together with oil components and / or emulsifiers of a defined polarity included. (google.com)
  • Germany's STADA pharmaceutical company is acquiring pharmaceutical business of prescription and OTC preparations of Biopharma blood product manufacturer. (interfax.com.ua)
  • Selected synthetic food dyes (tartrazine, Ponceau 4R, Brilliant Blue, orange yellow, and azorubine) were isolated from liquid preparations (mouthwashes and beverages) by Solid Phase Extraction on aminopropyl-bonded silica with diluted aqueous sodium hydroxide as an eluent. (hindawi.com)
  • How does Poland perform in the Pharmaceutical industry? (nationmaster.com)
  • Since World War II, when the U.S. drug industry was established on a permanent footing, pharmaceutical firms have enjoyed a high level of profitability. (warc.com)
  • Even with strict regulatory oversight and periodic crises, such as the Thalidomide scare of 1962, the U.S. pharmaceutical industry, or at least its major players, managed to remain both profitable and beneficial to world health while avoiding the price controls common in other industrialized nations. (warc.com)
  • The advent of the surface plasmon resonance (SPR) biosensor has led to many applications in diverse fields from the pharmaceutical industry to the life. (molecularstation.com)
  • This statistic shows the number of enterprises in the manufacture of pharmaceutical preparations industry in Switzerland from 2009 to 2016. (statista.com)
  • This study gives, however, my estimates for the latent demand, or potential industry earnings (P.I.E.), for oxytocic pharmaceutical preparations in China. (reportlinker.com)
  • This study gives, however, my estimates for the latent demand, or potential industry earnings (P.I.E.), for enema specialty laxative pharmaceutical preparations in India. (reportlinker.com)
  • CINFA entrusted INOXPA because of their experience in successfully developing solutions for Spanish pharmaceutical industry customers. (inoxpa.com)
  • INOXPA installed the new line in Cinfa's installations in accordance with good pharmaceutical industry practices. (inoxpa.com)
  • This review presents selected examples of successful application of olefin metathesis in the synthesis of active pharmaceutical ingredients from laboratories within the pharmaceutical industry. (teknoscienze.com)
  • The purpose of this paper was to prepare purified Na- bentonite with improved properties for use in the pharmaceutical industry. (geoscienceworld.org)