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Analytical Method Validation Develop Protocols that Survive the
Analytical Method Validation Develop Protocols that Survive the

... Define Intended Use • Identify critical process steps and related assays • Is this used for characterization only? – Or will this lead to a testing requirement and be held to a specification? • How important is continued characterization testing? – Do they need to be ongoing as part of release or u ...
BERBERIS ARISTATA TETRACHLORIDE INDUCED HEPATOTOXICITY IN RATS
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... rifampicin, isoniazid etc. used in medical therapy. Hepatotoxic drugs can injure the hepatocyte by generating free-radical or metabolic intermediate that causes peroxidation of lipid membrane resulting in liver cell injury [1]. Efforts have been made to search for effective hepatoprotective agents h ...
Curcuminoid drug interactions
Curcuminoid drug interactions

... valuable in the prevention and treatment of many different degenerative diseases. As curcuminoids are often taken as supplements by some population groups, it may be asked whether this can lead to changes in the pharmacokinetics or pharmacodynamics of other drugs taken at the same time. It is partic ...
IFU - Beckman Coulter
IFU - Beckman Coulter

... SYNCHRON® Systems Drugs of Abuse Testing (DAT) Urine Calibrators, is intended for the qualitative determination of opiates in human urine at a cutoff value of 2000 ng/mL.1 The OP2 assay provides a rapid screening procedure for determining the presence of the analyte in urine. This test provides only ...
Alcohol, Tobacco and Other Drugs
Alcohol, Tobacco and Other Drugs

... When people use two or more drugs at the same time it is called ‘polydrug use’. Polydrug use is risky because the effects are hard to control, and this can lead to overdose. Mixing drugs from the same group can increase the effect. Mixing drugs from different groups can mask the effects: this might ...
Reaction Phenotyping Methods using Recombinant Enzymes and
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... • Correlate rates of metabolism of NCE vs CYP-probe substrate activity in panel and/or CYP abundance in panel - unknown & reference activity/abundance • Labor intensive, typically carried out in development stage. Used to confirm results from HLM inhibition & recombinant CYP studies • Works best whe ...


... We are, however, unaware of the evidence showing that the fine particle fraction does not contribute to the overall anti-asthma effect. On the contrary, budesonide Turbuhaler has a higher fine particle dose than budesonide P-MDI and evidence of a better clinical effect [2, 6]. If the fine particle f ...
In silico site of metabolism prediction for human UGT
In silico site of metabolism prediction for human UGT

... Overfitting often occurs when a model uses more terms than necessary (Hawkins, 2004). Because the degree of degeneracy of our defined descriptors can be high, models built using all of them could be easily overfitting. Therefore, it is important to select a subset of relevant and non-redundant featu ...
What is the equivalent dose of oral prednisolone to intravenous (IV)
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... The British National Formulary (BNF) includes a table on equivalent anti-inflammatory doses of glucocorticoids (2). It does not take account of mineralocorticoid effects nor does it take account of variations in the duration of action (2). From the literature, prednisolone 5mg is approximately equiv ...
FROM DISULFIRAM TO ANTABUSE: THE INVENTION OF A DRUG
FROM DISULFIRAM TO ANTABUSE: THE INVENTION OF A DRUG

... Bull. Hist. Chem., VOLUME 33, Number 2 (2008) However, some twenty years later, disulfiram was introduced in the developing rubber industry to accelerate the vulcanization of rubber (6). The substance proved effective and was widely used in the vulcanization of both natural rubber and synthetic ru ...
ANTI- INFLAMMATORY AND ANALGESIC ACTIVITY OF TAMARIX GALLICA  Research Article CHATURVEDI S
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... to the local accumulation of plasmatic fluid and blood cells1.Any form of injury to the human body can elicit a series of chemical changes in the injured area. Earlier inflammation was contemplated as a single disease caused by disturbances of body fluids. However, according to the modern concept, i ...
Basics Pharmacology Review - Dr. Roland Halil
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... In particular, in the area of R&D, Takeda made investments that are essential to sustainable growth in the future and continued efforts to improve R&D productivity. Efforts include obtaining approvals for late-stage pipeline products and creating new drugs by intensively allocating resources to core ...
Drugs on Skeletal Muscle
Drugs on Skeletal Muscle

... stimulation and on the putative transmitter (ACh), and they were able to reinforce the theory that tubocurarine blocked the effects of ACh rather than prevent its release from nerves. As basic neuromuscular pharmacology was still being developed, tubocurarine was introduced into anesthesia (beginnin ...
Curriculum Vitae
Curriculum Vitae

... Jansonius), and genetic engineering techniques. Also, the structure and function of a new DNA binding protein, the DgdR repressor, which has been cloned and expressed in E. coli in our lab, is under study. DNA binding by the DgdR protein is regulated by certain dialkylglycine amino acids. These stud ...
expected output
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... To produce industrial chemists who can work as quality controllers (from raw material and intermediate product to final product) in every sector of the industry. To produce a personal capable to work in research laboratories, standardization laboratories, clinical laboratories, college and universit ...
Probing the active site of homoserine trans
Probing the active site of homoserine trans

... [11–13]. This loss of activity at temperatures above 32 C is due to protein unfolding followed by aggregation above 42 C [14]. Recently, it was shown that HTS is an unstable protein, subject to energy-dependent, proteolytic degradation [15]. The control of HTS concentration by proteolysis constitu ...
RELAGESIC Liquid - International Ethical Labs
RELAGESIC Liquid - International Ethical Labs

... Pharmacokinetics: The behavior of the individual components is described below. Acetaminophen: Acetaminophen is rapidly absorbed from the gastrointestinal tract and is distributed throughout most body tissues. The plasma half-life is 1.25 to 3 hours, but may be increased by liver damage and followi ...
expected output
expected output

... To produce industrial chemists who can work as quality controllers (from raw material and intermediate product to final product) in every sector of the industry. To produce a personal capable to work in research laboratories, standardization laboratories, clinical laboratories, college and universit ...
SCHOOL OF CHEMICAL SCIENCES
SCHOOL OF CHEMICAL SCIENCES

... The School of Chemical Sciences (SCS), established in 1969, is one of the pioneering Schools of USM. With an academic staff of more than 30 and over 50 supporting staff, the School has been entrusted to provide professional training in chemistry to meet the demands of the industries and society. The ...
WORD - SSS Chemistry
WORD - SSS Chemistry

... The Greek who developed the idea of atoms was _______________________________ Consider the following ideas:  Compounds are made up of molecules which are combinations of atoms  All atoms of an element are the same  Atoms of different elements are different  Atoms are indivisible particles Who ca ...
RTF - South Australian Legislation
RTF - South Australian Legislation

... manufacture of a controlled drug to be a controlled precursor for the purposes of this Act. (4b) The Governor may, by regulation, declare, individually or by class, a plant that in the Governor's opinion has the potential if it, or any product of it, is smoked or consumed by, or administered to, hum ...
Ranibizumab or bevacizumab in AMD?
Ranibizumab or bevacizumab in AMD?

Syva EMIT II Plus 6-Acetylmorphine Assay
Syva EMIT II Plus 6-Acetylmorphine Assay

... The Syva® EMIT® II Plus 6-Acetylmorphine Assay (EMIT 6-AM assay) was introduced in 2011, and is available for use on several automated immunoassay platforms. The assay can be run in either a qualitative or semi-quantitative mode. In the qualitative mode, a sample containing 6-acetylmorphine (6-AM) a ...
Pharmacokinetics of Chemotherapeutic Agents in Kidney Disease
Pharmacokinetics of Chemotherapeutic Agents in Kidney Disease

... The drug is 90% protein bound within 2 hours after infusion, and 30% is excreted in the urine within 24 hours. Dosing guidelines for patients with CKD are empiric. Kintzel recommends for a creatinine clearance (CrCl) of 46–60 mL/min, give 75% of the usual dose; for a CrCl of 31–45 mL/min, give 50% o ...
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Drug discovery



In the fields of medicine, biotechnology and pharmacology, drug discovery is the process by which new candidate medications are discovered. Historically, drugs were discovered through identifying the active ingredient from traditional remedies or by serendipitous discovery. Later chemical libraries of synthetic small molecules, natural products or extracts were screened in intact cells or whole organisms to identify substances that have a desirable therapeutic effect in a process known as classical pharmacology. Since sequencing of the human genome which allowed rapid cloning and synthesis of large quantities of purified proteins, it has become common practice to use high throughput screening of large compounds libraries against isolated biological targets which are hypothesized to be disease modifying in a process known as reverse pharmacology. Hits from these screens are then tested in cells and then in animals for efficacy.Modern drug discovery involves the identification of screening hits, medicinal chemistry and optimization of those hits to increase the affinity, selectivity (to reduce the potential of side effects), efficacy/potency, metabolic stability (to increase the half-life), and oral bioavailability. Once a compound that fulfills all of these requirements has been identified, it will begin the process of drug development prior to clinical trials. One or more of these steps may, but not necessarily, involve computer-aided drug design. Modern drug discovery is thus usually a capital-intensive process that involves large investments by pharmaceutical industry corporations as well as national governments (who provide grants and loan guarantees). Despite advances in technology and understanding of biological systems, drug discovery is still a lengthy, ""expensive, difficult, and inefficient process"" with low rate of new therapeutic discovery. In 2010, the research and development cost of each new molecular entity (NME) was approximately US$1.8 billion. Drug discovery is done by pharmaceutical companies, with research assistance from universities. The ""final product"" of drug discovery is a patent on the potential drug. The drug requires very expensive Phase I, II and III clinical trials, and most of them fail. Small companies have a critical role, often then selling the rights to larger companies that have the resources to run the clinical trials.Discovering drugs that may be a commercial success, or a public health success, involves a complex interaction between investors, industry, academia, patent laws, regulatory exclusivity, marketing and the need to balance secrecy with communication. Meanwhile, for disorders whose rarity means that no large commercial success or public health effect can be expected, the orphan drug funding process ensures that people who experience those disorders can have some hope of pharmacotherapeutic advances.
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