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Pharmacodynamics – How Drugs Work
Pharmacodynamics – How Drugs Work

... A full agonist is one that is capable of producing a maximal response, when it binds to a sufficient number of receptors. In contrast, a partial agonist cannot produce the maximal response of which the tissue is capable, even when it binds to the same number of receptors as a full agonist binds to w ...
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... Since  origin  of  human’s  life,  plants  continue  to  play  a  curative  and  therapeutic  role  in  preserving  human  health  against  disease  and  decay.  The  widespread  use  of  herbal  remedies  and  healthcare  preparations, such as those described in ancient texts like the Vedas  and th ...
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... unpleasant reaction, resulting from an intervention related to the use of a medicinal product, which predicts hazard from future administration and warrants prevention or specific treatment, or alteration of the dosage regimen, or withdrawal of the product.” The term “adverse effect” is preferable t ...
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... bath and fasten the long ligature to the side writing lever so that the lever is horizontal. The lever is then correctly adjusted. Check that the gut is vertical and not rubbing on the side of the bath. Move the whole bath apparatus so that the side writing lever makes contact with the drum on the k ...
ISOLATED RABBIT JEJUNUM PREPARATION
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... bath and fasten the long ligature to the side writing lever so that the lever is horizontal. The lever is then correctly adjusted. Check that the gut is vertical and not rubbing on the side of the bath. Move the whole bath apparatus so that the side writing lever makes contact with the drum on the k ...
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... • Amphetamines stimulate dopamine synapses by increasing the release of dopamine from the presynaptic terminal. • Cocaine blocks the reuptake of dopamine, norepinephrine, and serotonin. • Methylphenidate (Ritalin) also blocks the reuptake of dopamine but in a more gradual and more controlled rate. – ...
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... size and degradation in the gastric environment of gut. Recently, phospholipid-complex technique has unveiled in addressing these stumbling blocks either by enhancing the solubilizing capacity or its potentiating ability to pass through the biological membranes and it also protects the active herbal ...
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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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