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LN_ch06
LN_ch06

... Balanced Chemical Equations  Chemical Equations must be balanced There must be equal numbers of atoms of each element on both sides of the equation (both sides of the arrow) ►1. Write the correct symbols and formulas for all of the _______ and ____________. ►2. Count the number of each type of __ ...
Toward 2015
Toward 2015

... description of the pharmacovigilance system used by the marketing authorization holder with respect to its authorized medicinal products. The purpose of the PSMF is to improve the oversight and accountability of pharmacovigilance data. Many companies have already had some experience with the PSMF be ...
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pdf

... witnessed a huge leap in our understanding of the basic biological processes that contribute to many human disorders. However, this has not been paralled by an increase in the number of approved new molecular entities. From 1950 to 2008, the FDA approved 1222 new drugs including biologicals (Munos, ...
Clinical Relevance of Drug Releases Testing
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Codeine and paracetamol use in children
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Extension of agreement on Telmisartan (Micardis
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DEVELOPMENT AND VALIDATION OF UV SPECTROPHOTOMETRIC METHOD FOR
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Revised Pharm. D. Curriculum 2013
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... In order to select a new cheap, effective alternative natural suspending agent for pharmaceutical suspensions Raj D et al., performed comparative studies between the Leucaena Latisiliqua seed gum and other gums like tragacanth, acacia. Leucaena Latisiliqua seed was boiled and the seed gum was extrac ...
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... Dissymmetry, asymmetry and chirality- simple and alternating axis of symmetry- Conditions for optical activity, Isotopic asymmetric variation and specific rotation of the same compound in sign and magnitude under different conditions. Relative and absolute configurations. Sequence rule– R and S nota ...
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... chemically adding or removing chemical elements, and changes them into other materials. Chemical weathering consists of chemical reactions, most of which involve water. ...
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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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