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Optimized and Validated Spectrophotometric Methods for the
Optimized and Validated Spectrophotometric Methods for the

... Three new visible spectrophotometric methods which are simple, sensitive and cost-effective are proposed for the determination of gatifloxacin (GTF) using N-bromosuccinimide (NBS), and three dyes, thymol blue, indigo carmine and methyl orange as reagents. The methods engross the addition of a known ...
THESPESIA POPULNEA LINN.  Review Article MOHINI A. PHANSE*,
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... determine the anti-ulcer potential of the terpenoid fraction from the leaves of T. populnea. The terpenoid fraction of leaves of T. populnea were tested orally at the doses of 50, 100 and 200 mg/kg, on gastric ulcerations experimentally induced by pylorus ligation, aspirin induced ulcer, aspirin ind ...
LYOPHILIZED GLICLAZIDE­POLOXAMER SOLID DISPERSIONS FOR ENHANCEMENT OF  IN­ VITRO DISSOLUTION AND IN­VIVO BIOAVAILABILITY 
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... diseases with lower drug doses (Cokol et al. 2011). For example, trimethoprim and sulfamethaxozole, which are both folic acid biosynthesis inhibitors, have long been used together for treating bacterial infections due to their synergistic interactions. Although use of synergistic drug pairs has grea ...
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abstract book - Marmara Üniversitesi
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... be used as indispensable tools in biomedical research. Many local folk medıcınes contain natural products of plant origin, which remain a largely untapped reservoir of natural compounds with novel chemical structures and biological activities. One common objective of practicing research in the field ...
A Four Pillars Approach to Methamphetamine
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... to the public. Amphetamine was used for weight control, for athletic performance and endurance, for treating mild depression, and to help truckers complete their long hauls without falling asleep. Methamphetamine was widely marketed to women for weight loss and to treat depression.5 The first instan ...
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... of tolerance and sensitization. These findings, in turn, may be generalizable to humans and ultimately prove to be useful in helping a person overcome drug addiction. Tolerance is a key element of drug addiction because as one continues to use a drug, the effectiveness of the drug tends to decrease, ...
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Article Strength of Selection Pressure Is an

... diseases with lower drug doses (Cokol et al. 2011). For example, trimethoprim and sulfamethaxozole, which are both folic acid biosynthesis inhibitors, have long been used together for treating bacterial infections due to their synergistic interactions. Although use of synergistic drug pairs has grea ...


... were corrected by dividing them by this value to determine the true inhaled masses. The quality of colistin extraction was also verified by studying reference filters on which known amounts of non-nebulized colistin had been deposited. Indeed, using bacteriological methods similar to those applied t ...
Antibiotic Drug Delivery Systems for the Intracellular
Antibiotic Drug Delivery Systems for the Intracellular

... ity, biodegradability, and biocompatibility, making it suitable for use in biomedical and pharmaceutical formulations. This approach will allow reviving old antibiotics rendered useless by resistance or toxicity, rescuing the last line therapy antibiotics by increasing the therapeutic index, widenin ...
STUDY GUIDE
STUDY GUIDE

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PHAR 7633 Chapter 21 Non-Linear Pharmacokinetic
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... Student Objectives for this Chapter To draw the scheme and write the differential equations for compartmental pharmacokinetic models with non-linear metabolism elimination To understand the process of parallel pathways as it applies with one or more non-linear pathways To define and use the paramete ...
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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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