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UV SPECTROPHOTOMETRIC METHOD FOR DETERMINATION OF ONDANSETRON
UV SPECTROPHOTOMETRIC METHOD FOR DETERMINATION OF ONDANSETRON

... A simple, rapid, precise, accurate and sensitive analytical method was developed for the UV spectrophotometric assay of ondansetron. The drug obeyed the Beer’s law and showed good correlation. It showed absorption maxima at 248 nm in saline. The linearity was observed between 5 – 25 µg mL-1. The res ...
Full Text PDF - Science and Education Publishing
Full Text PDF - Science and Education Publishing

... lauryl Sulphate (SLS) on transdermal absorption of 2-Methyl-2-phenoxy-propionic acid (MPA) was evaluated with aid of response surface methodology (RSM) based formulations. The prepared formulations were characterised and subsequently subjected to diffusion cell experiments through a well-established ...
Reduction in Medication Errors: The Fentora Case Study
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... increases in these errors in the first 3 years of marketing are likely related to an increase in use and market penetration by Fentora. Most interesting, however, is the leveling off of reports shortly thereafter and then the rapid fall from a peak of 73 reports in year 3 to 6 reports in year 6. Ano ...
sustained and controlled drug delivery system - as a part
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... dosage form. Risk of dose dumping, usually SRDDS contain drug amount that is 3-4 times more than conventional formulations. Sometimes this large quantity of drug may get rapidly released leading to toxicity. • Reduced drug absorption may delay onset of action. The effect of food on drug absorption. ...
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... Vancomycin was kept as a ‘reserve’ antibiotic and was usually prescribed only when other drugs proved to be inactive. However, even in spite of its relatively ...
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...  Disposable gowns made of fabric that has low permeability to the agents in use, with closed fonts and cuffs,intended for single use.  Powder free gloves, labeled and tested for drugs used with chemotherapy , made of latex, nitrile or neoprene.  Face and eye protection when splashing is possible. ...
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Unit 2 Objectives - Chemistry of Life
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Guidance for NCAP FA-713 Chemical Container HCS 2012 Labeling

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... • Prototype of Non-depolarizing is tubocurarine (new generation: pancuronium and gallamine). • Mechanism of Action: In small clinical doses they act the predominantly at the nicotinic receptor site to block ACh. • At higher does they can block prejunctional Na channels thereby decreasing ACh release ...
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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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