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ANALYTICAL METHOD DEVELOPMENT AND METHOD VALIDATION FOR THE ESTIMATION
ANALYTICAL METHOD DEVELOPMENT AND METHOD VALIDATION FOR THE ESTIMATION

... and accurate and can thereby easily adopted for routine quality control analysis. The results of this analysis confirmed that the proposed method was suitable for determination of drug in pharmaceutical formulation with virtually no interference of additives. Hence the proposed method can be success ...
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... Modern synthetic medicines are very effective in curing diseases but also cause a number of side effects. Crude drugs are less efficient with respect to cure of diseases but are relatively free from side effects. Parasites have been of concern to the medical field for centuries and the helminths con ...
laman web smk raja perempuan, ipoh
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... 2. explain the construction of the alkane series (straight and branched) and IUPAC nomenclature of alkanes for C1 to C5 3. name alkyl groups derived from alkanes and identify primary, secondary , tertiary and quartenary carbons. 4. explain the homolytic cleavage of bonds which produces free radicals ...
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... more than 700 times more potent than the parent compound. This suggests that the O-demethylated metabolite may account for most of tramadol‟s opiate-mediated analgesic activity (Gillen et al., 2000)3. A range of other pharmacological actions have been attributed to tramadol. In particular, it has be ...
Hidden Dangers: Herbal and Dietary Supplement Induced
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... plant species. It was translated in many languages and served as the primary pharmacopeia for over 1500 years. The native people of Africa, South Pacific Islands and the Americas also had plant centered healing traditions. Traditionally herbal products made of stems, roots, bark, leaves, berries, se ...
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... At present, no one immobilizing agent is able to achieve all the above mentioned properties.40 As a result the primary immobilization agent (the primary agent is the one that produces the most marked central nervous system (CNS) depression, such as the opioid compounds or the cyclohexamines) needs t ...
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... model to provide explanatory power and to assess how various variables influence the development of addiction. Predictive validity refers to the model’s ability to produce valid predictions about the human form of addiction based on results from the animal model (Koob and Le Moal, 2006). Another rea ...
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... Report) indicated that there were 2,400 exposures of tramadol reported to control centers, of those, 108 resulted in a major medical outcome and 8 resulted in death. Long- term administration of tramadol for management of pain, as well as its use as an acceptable alternative in persons with drug- se ...
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... on the extract has highlighted some important components that might play roles in this process while few more are yet to be identified. Once the active components are identified and a proper biochemical basis of their action is defined, these components may be used even for newer purposes (Chakrabor ...
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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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