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WHO Drug Information - World Health Organization
WHO Drug Information - World Health Organization

... cooperation among regulatory agencies The rapid advancement in biomedical sciences and the invention of novel therapeutic products have made it more critical than ever for medicines regulatory agencies to work together to achieve the goal of protecting and advancing public health. The 14th ICDRA re- ...
Immunoassays - OldForensics 2012-2013
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... resulted in their receipt of the Nobel Prize in Medicine in 1977. Since this introduction, immunoassays have evolved considerably. The first homogenous immunoassay (no separation step required) was the Enzyme Multiplied Immunoassay Technique (EMIT), which enabled adaptation of this assay onto automa ...
Media Kit - Perosphere
Media Kit - Perosphere

... therapies with regards to route of administration, drug interactions and predictability of bioactivity. However, the NOACs currently lack a specific reversal agent. As such concern over serious bleeding, emergency procedures and potential overdosage is heightened. We set out to rationally design, sy ...
IOSR Journal of Dental and Medical Sciences (IOSR-JDMS)
IOSR Journal of Dental and Medical Sciences (IOSR-JDMS)

... inferior alveolar nerve. The lingual nerve (tongue) is approximately twice as often involved as the inferior alveolar nerve (lip), 92 versus 42 cases. This finding is confirmed by Progrei and Thamby, which found the same distributes for the paresthesia (2000).17 The reason for this finding might be ...
Drug Testing - Mayo Medical Laboratories
Drug Testing - Mayo Medical Laboratories

... Benzodiazepines are extensively metabolized, and the parent compounds are not detected in urine. Diazepam is metabolized to nordiazepam, oxazepam, and temazepam; all may be detected after diazepam use. Diazepam > Nordiazepam, Oxazepam, and Temazepam Chlordiazepoxide is metabolized to nordiazepam and ...
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A Treatise on Collinsonia canadensis
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Evaluation of Diuretic activity of aqueous and alcoholic rhizomes
Evaluation of Diuretic activity of aqueous and alcoholic rhizomes

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Carbinoxamine Maleate
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Beta-Adrenoceptor Antagonists (Beta
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IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS) e-ISSN: 2278-3008, p-ISSN:2319-7676.
IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS) e-ISSN: 2278-3008, p-ISSN:2319-7676.

... 2005. The annual number of AIDS deaths can be expected to increase for many years to come, unless more effective and patient compliant anti-retroviral medications are available at affordable prices [3]. The major drawbacks of antiretroviral drugs for the treatment of AIDS are their adverse side effe ...
Safety Considerations in Phase 1 Trials - M
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... • Is there information regarding quality of investigational products? – Formulations should be well characterized with respect to purity, potency, stability, and sterility (if applicable) ...
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... All drugs used for the immobilization, capture, and translocation of wild animals in South Africa are registered or controlled under the Medicines and Related Substances Control Act No. 101 of 1965. The Act provides that all medicinal substances be placed into nine schedules, representing four main ...
ON THE EMERGENCE OF BIOLOGICAL COMPLEXITY: LIFE AS A
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... explanation for this process of complexification is of course Darwinian evolution – the operation of natural selection. In attempting to bridge between biology and chemistry, Eigen (1971) proposed that the very same process of Darwinian evolution that operated at the biological level must have initi ...
Ahead of print online version Moxidectin causes adult worm
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... Abstract: Moxidectin is a macrocyclic lactone belonging to milbemycin family closely related to ivermectin and is currently progressing towards Phase III clinical trial against human infection with the filaria Onchocerca volvulus (Leuckart, 1894). There is a single report on the microfilaricidal and ...
Marijuana: What you need to know
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... Research indicates that students do not remember what they have learned when they are “high”. “It is estimated that 9 percent of people who use marijuana will become dependent on it. The number goes up to about 1 in 6 in those who start using young (in their teens) and to 25-50 percent among daily u ...
Clinical Drug Testing in Primary Care Manual
Clinical Drug Testing in Primary Care Manual

... practitioners need when deciding whether to introduce drug testing in their practices and gives guidance on implementing drug testing.  The TAP does not address drug testing for law enforcement or legal purposes, nor does it include testing for the use of anabolic steroids or performance­enhancing s ...
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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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