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Poisoning and Drug Overdose
Poisoning and Drug Overdose

... Copyright © 2004 by The McGraw-Hill Companies, Inc. All rights reserved. Printed in the United States of America. Except as permitted under the United States Copyright Act of 1976, no part of this publication may be reproduced or distributed in any form or by any means, or stored in a data base or r ...
ANTILIPEMICS 2012 - students [Read
ANTILIPEMICS 2012 - students [Read

... • good oral absorption • non-CYP hepatic metabolism • renal excretion • T1/2 - 2hr / 80hr • IR - TID, SR - double-dose OD / OD ...
A Closer Look at the Risks vs. Benefits of Kava (Piper methysticum)
A Closer Look at the Risks vs. Benefits of Kava (Piper methysticum)

... complementary and herbal treatments for anxiety disorders. The complementary treatment was distinguished by using any self-help treatment not generally upheld in the health system. Each treatment was evaluated for its effectiveness in reducing anxiety symptoms in generalized and specific anxiety dis ...


... and cardiothoracic surgery [5]. There have been many reviews of the clinical use of tramadol for pain management [5,7,13]. In general, tramadol has been described as a centrally-acting opioid analgesic with potency/efficacy similar to that of pethidine but has compared favourably to various analgesi ...
troubleshooting guide drugs of abuse
troubleshooting guide drugs of abuse

... The purpose of this guide is to assist our partners in troubleshooting any foreseen or unforeseen events that may occur while running N.C.S drugs of Abuse tests. All N.C.S drug of abuse panels are rapid visual immunoassay for the qualitative detection of drug and drug metabolites in human urine. All ...
The safety of hydroquinone
The safety of hydroquinone

... The in vivo absorption study cited by FDA measured the absorption of 2% hydroquinone in a 71% ethanol vehicle through the forehead skin of 6 adult male volunteers. This preparation was 57% absorbed following a single topical exposure of 24 hours’ duration. When a sunscreen was added, absorption fell ...
Safety Assessment of Alumina and Aluminum Hydroxide as Used in
Safety Assessment of Alumina and Aluminum Hydroxide as Used in

... the ingredients that are being reviewed here for safe use in cosmetics. And we would like to see that discussion developed and put in the report, and that the report be tabled so that the Panel can get a chance to look at the discussion. Our concern is alumina is a very important ingredient in cosme ...
BIOAVAILABILITY ENHANCEMENT TECHNIQUES OF HERBAL MEDICINE: A CASE EXAMPLE OF CURCUMIN
BIOAVAILABILITY ENHANCEMENT TECHNIQUES OF HERBAL MEDICINE: A CASE EXAMPLE OF CURCUMIN

... Curcumin was characterized as an excellent molecule among many naturally occurring compounds for treatment and prevention of a wide variety of human diseases especially for cancer therapeutics. It was proved to be safe even used at very high dose. However, due to its very low bioavailability, curcum ...
Glucosamine sulfate.fm
Glucosamine sulfate.fm

... synovial fluid [11]. However, it also exerts specific pharmacological effects on osteoarthritic cartilage and chondrocytes. Glucosamine base must be salified for pharmaceutical use, and glucosamine sulfate is the salt that was originally developed as a prescription drug and used in the vast majority ...
$doc.title

... sites have been found in most areas of the human brain, but they appear to be most abundant in the hypothalamus. There are many reports in the literature relating sleep disturbances to lower levels of nightly melatonin excretion, a common occurrence in old age which has also reportedly been a findin ...
Complete Program - Mathematics and Computer Science
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... Limitations in resources have prevented our department from offering a traditional laboratory for the non-majors introductory chemistry course. Instead, the authors have developed in-class demonstrations which provide students an opportunity to record observations and data, analyze and graph data, a ...
The C. elegans model in toxicity testing
The C. elegans model in toxicity testing

... ABSTRACT: Caenorhabditis elegans is a small nematode that can be maintained at low cost and handled using standard in vitro techniques. Unlike toxicity testing using cell cultures, C. elegans toxicity assays provide data from a whole animal with intact and metabolically active digestive, reproductiv ...
11146027
11146027

... Hypertension and dyslipidemia may frequently coexist, and together have an increase in coronary heart disease related events. Combination therapy of rosuvastatin calcium and amlodipine besylate, effective for the control of hypertension by substantially reducing blood pressure and cholesterol levels ...
Pharmacology of platelet inhibition in humans: implications of the
Pharmacology of platelet inhibition in humans: implications of the

... ABSTRACT The current dispute over the effects of "low" vs "high"doses of aspirin should take into consideration the pharmacokinetics of this drug. In fact, different pharmaceutical formulations of aspirin may deliver little or no aspirin to the systemic blood. This was the case, for instance, in hea ...
Pharmacological and Pharmaceutical Profile of Valsartan: A Review
Pharmacological and Pharmaceutical Profile of Valsartan: A Review

... beneficial effects are related to inhibition of Angiotensin II by blockade of AT1 receptor. Valsartan is an orally active Angiotensin II receptor type 1 antagonist which causes reduction in blood pressure and is used in treatment of hypertension. It was first developed by Novartis and has a wide mar ...
Link - Bahagian Perkhidmatan Farmasi
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... and resources. We are optimistic that as NMUS matures, there will be more chapters deliberated and the data processing methodologies will constantly refined, future MSOM reports will continue to produce accurate and reliable statistics on Malaysian medicines consumption at all time. We sincerely hop ...
Cytochrome P450 and Polymorphism - uni
Cytochrome P450 and Polymorphism - uni

... Uptake of orally administered drug proceeds after the stomach passage via the small intestine. ...
European guidelines for quality assurance in colorectal cancer
European guidelines for quality assurance in colorectal cancer

... Authors, contributors, editors and reviewers serve in their individual capacities as experts and not as representatives of their government or any other organisation with which they are affiliated. Affiliations are provided for identification purposes only. Minor pertinent interests are not listed. ...
CYP 2D6 Polymorphism
CYP 2D6 Polymorphism

... Uptake of orally administered drug proceeds after the stomach passage via the small intestine. In the liver, a series of metabolic transformation occurs. ...
A Unique Delivery Vehicle for Topically Applied Formulations
A Unique Delivery Vehicle for Topically Applied Formulations

... respectively, are both thermolabile (temperature-sensitive) steroid hydroethanolic foams (containing about 60% ethanol).9,10 Evoclin (Stiefel) is another hydroethanolic foam, comprising 1% clindamycin, which is indicated for acne.11-12 Stiefel, a GSK company further markets four emollient foams, na ...
Kratom - NeuroSoup
Kratom - NeuroSoup

... this   alkaloid.   Given   that   nearly   all   the   chemical   studies   of   kratom   have   been   done   on   the   assumption   that   mitragynine   was   the   most   important   alkaloid,   and   that   nearly   all   pharmacological ...
Drug utilisation sub-committee (DUSC)
Drug utilisation sub-committee (DUSC)

... Medicare for payment of a subsidy by the Government, with an estimate of under general copayment prescriptions based on dispensing data from a sample of pharmacies to the end of March 2012, replaced by actual under copayment data from DHS Medicare from 1 April 2012. The DUSC database also includes a ...
101-Chem
101-Chem

... 1. Determine mass in g of each element 2. Convert mass in g to moles 3. Divide all quantities by smallest number of moles to get smallest ratio of moles 4. Convert any non-integers into integer numbers.  If number ends in decimal equivalent of fraction, multiply all quantities by least common denom ...
Determination of Solubility Parameters of Ibuprofen and Ibuprofen
Determination of Solubility Parameters of Ibuprofen and Ibuprofen

... obtained when using group contribution method of Fedors. The partial solubility parameters values also did not differ much between methods. The largest value in the case of the dispersion solubility parameter was obtained by using the group contribution method of Hoftyzer and Van Krevelen and the sm ...
Drug interactions involving warfarin
Drug interactions involving warfarin

... Warfarin has been the mainstay of oral anticoagulant therapy for the past 60 years and it is most commonly used to treat or prevent thrombosis or thromboembolism in patients with venous thromboembolism, atrial fibrillation and prosthetic heart valves.1 However, this drug is efficacious only when the ...
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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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