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Antimicrobial Pharmacokinetics and Pharmacodynamics
Antimicrobial Pharmacokinetics and Pharmacodynamics

... because of the dilution of samples with intracellular contents. Techniques that directly extract interstitial fluid, such as subcutaneously implanted cotton threads or more recently microdialysis methods, demonstrate high (3-lactam concentrations in this tissue compartment that are similar to free d ...
Problems of anabolic steroids in sport.
Problems of anabolic steroids in sport.

... Sumner (1974) developed antisera (see Fig. 4) with the desired specificity for certain characteristic features of various types of anabolic steroids. The appropriate antibodies were made by attaching an anabolic steroid e.g. 17-α methyltestosterone by covalent links to a pure protein and injecting t ...
and 7-hydroxymethotrexate
and 7-hydroxymethotrexate

... The elevation in metabolite plasma concentration cannot be only attributed to the increase in metabolic clearance of MTX, but also to the decrease in the total body clearance of the metabolite. The total body clearance of the major metabolite 7-OHMTX in the PIP-treated rabbits significantly decreas ...
SCLEROTIUM ROLFSII AND ANTIFUNGAL ACTIVITY  Research Article   
SCLEROTIUM ROLFSII AND ANTIFUNGAL ACTIVITY  Research Article   

... nausea,  electrolyte  imbalance  and  nephrotoxicity  are  of  great  concern.  It  is  thought  that  the  aggregated  form  of  AmB,  which  is  largely responsible for membrane damage, brings about these side‐ effects18. In order to mitigate these side effects several drug delivery  systems such  ...
organonitrogen compounds i. amines
organonitrogen compounds i. amines

... as topical anaesthetics (cocaine). With the possible exception of caffeine, all may be described as potentially poisonous enough to warrant great care in their use. Although some of these compounds are used as natural medicinals, an entire industry has developed in an effort to produce synthetic ana ...
NEEDLE FREE INJECTION SYSTEM: A REVIEW  Review Article
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... Needle free technology (Jet injectors), were developed in the 1930s and used widely over 50 years in mass vaccination programs in patients suffering from smallpox, polio, and measles. Mechanical compression is used to force (generated by a compressed gas typically air, CO2 or nitrogen) fluid through ...
OCR AS Level Chemistry B (Salters) H033
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... Our new AS Level Chemistry B (Salters) qualification builds on our existing popular course. We’ve based the redevelopment of our AS level sciences on an understanding of what works well in centres large and small and have updated areas of content and assessment where stakeholders have identified tha ...
full text pdf - Department of Physical Chemistry
full text pdf - Department of Physical Chemistry

... darkness a well determined time (15 minutes) to assure a complete oxidation of the drug. Subsequently, 1.5 mL of 500 ppm methyl orange solution was added to each volumetric flask and diluted to the mark with double distilled water. The UV-VIS spectrum of each solution was recorded in the range 600-3 ...
Research Report Series: MDMA (Ecstasy) Abuse
Research Report Series: MDMA (Ecstasy) Abuse

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MICHIGAN NEWBORN SCREENING PROGRAM  ANNUAL REPORT
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... NBS is a process of early identification of health conditions followed by their subsequent timely treatment before the onset of disease processes thereby minimizing the risk of long-term sequelae. Depending on the condition, potential outcomes of disorders in the NBS panel include but are not limite ...
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Macromolecules in Biological System.doc
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The first miracle drugs : how the sulfa drugs transformed medicine
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... motif?) that I can only begin to acknowledge here. Funding for research, and for the invaluable leaves from teaching that make it possible, has come at different times from the National Science Foundation (SES 81-11985 and SES-8409848), the National Institutes of Health (NIH-R01 LM04231), the John S ...
RP-HPLC Analysis of Aspirin - Indian Journal of Pharmaceutical
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... Antifungal activities of different extracts of Millingtonia hortensis were investigated against various fungal pathogens. Methanol extract was found to have stronger activity than fluconazole against yeast like fungi: 4 fold against Candida krusei with 4 µg/ml minimal inhibitory concentration and 2 ...
R.W. Moreadith, T.X. Viegas, M.D. Bentley, J.M. Harris, Z. Fang, K
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... result the polymer influences the properties of the newly conjugated molecule. They have also been used to enable other types of drug delivery systems such as liposomes, micelles and dendrimers where they provide stealth-like properties. One of the first studies with drug conjugation was reported by ...
sanofi-aventis Canada Inc. Date of Revision: 2150 St. Elzear Blvd. West
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Stoichiometry - Chemistry 11
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... Stoichiometry Stoichiometry is the calculation of quantitative (measurable) relationships of the reactants and products in a balanced chemical reaction (chemicals). It can be used to calculate quantities such as the amount of products that can be produced with the given reactants and percent yield. ...
Antiseizure drugs
Antiseizure drugs

... of phenytoin. However, it is also commonly used for Rx of mania and trigeminal neuralgia. Pharmacokinetics available as an oral form only Well absorbed 80 % protein bound Strong inducing agent including its own (can lead to failure of other drugs e.g. oral contraceptives, warfarin, etc. Metabolized ...
Gabapentin - Renal Pharmacy Group
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PEGylation of Biopharmaceuticals: A Review of Chemistry and
PEGylation of Biopharmaceuticals: A Review of Chemistry and

... E-mail address: [email protected] (P.L. Turecek). ...
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... raw materials must be sterile and pyrogen free, (2) preparation in sterile system: working areas equipped with laminar flow and (3) use of sterile containers. Some issues related to phospholipids need attention.12,13 The liposomes based on crude egg yolk phospholipids are not very stable. The cost o ...
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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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