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September 2006 - Highmark Blue Shield
September 2006 - Highmark Blue Shield

... • Ambrisentan is to be used for the treatment of pulmonary arterial hypertension (WHO Group I) in members with WHO functional Class II or III symptoms, AND • Ambrisentan may be used alone or in combination with calcium channel blockers, angiotensin converting enzyme (ACE) inhibitors, diuretics, digo ...
Chemical Dynamics at Surfaces
Chemical Dynamics at Surfaces

... Irving Langmuir was born in Brooklyn, New York, on January 31, 1881, as the third of four sons of Charles Langmuir and Sadie, neé Comings. His early education was obtained in various schools and institutes in the USA, and in Paris (1892-1895). He graduated as a metallurgical engineer from the School ...
Document
Document

... previously used acetylcysteine infusion, used to treat paracetamol poisoning.2 We now examine carboplatin, used to treat cancer. Acetylcysteine bags are made up on the ward by staff who are not used to making up infusions, whereas carboplatin is made up by trained pharmacy staff in controlled and st ...
euphorbia neriifolia linn: a phytopharmacological review
euphorbia neriifolia linn: a phytopharmacological review

... In recent era of globalization, Medicinal plants have attracted global interest. Now a day medicinal plants are part and parcel of human society to combat diseases, from the dawn of civilization1. Medicinal plants have been of great importance to the health care needs of individuals & Communities. I ...
FORMULATION, CHARACTERIZATION AND COMPARATIVE IN VITRO IN VIVO EVALUATION
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... The following study involves formulation and evaluation of simple highly drug loaded matrix tablets of theophylline anhydrous (THF) containing ethylcellulose (EC) polymer as a release retardant at low concentrations (1- 9 %w/w) using wet granulation technique. An optimum formula was chosen on the ba ...
Using Arrays to Quickly Perform Fuzzy Merge Look-ups: Case Studies in Efficiency
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Session 9: Central Nervous System Depressants
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Guide to Good Prescribing - World Health Organization
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Preventing and Curing Infectious Diseases: Carbohydrate
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... Based on the automated synthesis platform,1 that has been generalized 2-4 and commercialized5 we have created a series of vaccine candidates that are nearing clinical trials. In addition, synthetic oligosaccharides serve as tools to create monoclonal antibodies6 and to establish glycan microarrays t ...
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... In certain embodiments of the aspect, the one or more suitable anticancer therapies or medical procedures is selected from treatment with a chemotherapeutic agent (e.g. chemotherapeutic drug), radiation treatment (e.g. x-ray, -ray, or electron, proton, neutron, or  particle beam), hyperthermia hea ...
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... Change in specifications of the drug product or API Change in test procedures linked with a change in specification Change in dimensions of a sustained release formulation Major changes in manufacture of the drug product Change from wet granulation to direct compression of dry powder Site change to ...
Appendix 5 - Cancer Care Ontario
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IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS)

... liquid chromatography has been developed and validated for the related substance and estimation of Eslicarbazepine acetate in bulk and pharmaceutical dosage form. The chromatographic separations were achieved using a High performance liquid chromatography (Inertsil ODS 3V 150 mm, 4.6 mm, 5µm) employ ...
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... promote CB1 receptor internalization. To ensure a better comparison with our previous report on the effects of JWH018 and to account for differences in passage number and other cell culture variables, we tested JWH018 alongside our analyses of CP47,497-C8 and JWH073. Fig. 4A shows the time course of ...
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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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