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CE Prn - WF Professional Associates
CE Prn - WF Professional Associates

... as sterile formulations for injection, inhalation, or ophthalmic application may become contaminated with bacteria, fungi, or other pathogens. Compounded drugs for pediatric or elderly patients may cause problems that were not anticipated due to the frailty of the patient. Long acting compounded pro ...
6 points each
6 points each

... nM, similar to Ki values for serotonin and dopamine receptors. Developing a drug with relatively less affinity for α1 adrenergic receptors would probably reduce the side effect of orthostatic hypotension ...
USP`s Role in Patient Safety Goals: Objectives
USP`s Role in Patient Safety Goals: Objectives

... States Pharmacopeia (USP) and allied reports. For the most part, these are standards and supporting information that speak to how practitioners within healthcare systems should adjust their processes and practices to promote safe medication use. At times, USP product standards call for the adjustmen ...
Interaction of Plant Extracts with Central Nervous System Receptors
Interaction of Plant Extracts with Central Nervous System Receptors

... constitutively active molecules, which can cause alterations in ligand binding, receptor desensitization and recycling, potentially resulting in onset of disease [13,14]. There are a large number of studies demonstrating direct effect of plant extracts and/or their compounds on GPCRs and ion channel ...
Anesthetics-3
Anesthetics-3

... damage or initiate immune mediated responses. ...
Full Text
Full Text

... as “any component other than the active ingredient in a drug product” (FDA 2011). These various compounds may be used in drug formulations for a number of functions related to the preparation and stability of the physical dosage form or the delivery of active ingredients (Rowe et al. 2009). Excipien ...
© Jones and Bartlett Publishers, LLC. NOT FOR SALE OR
© Jones and Bartlett Publishers, LLC. NOT FOR SALE OR

... New drugs are coming on the market all the time that offer health benefits and successful treatments of medical conditions. EMS providers need to be aware of the dangers of drug use—such as with patients who have good intentions but who use their medications inappropriately and thus experience a har ...
Functional Group Characteristics and Roles
Functional Group Characteristics and Roles

... group. As shown in Figure 2-1, bethanechol and simvastatin have an additional methyl group as compared to acetylcholine and lovastatin, respectively. The methyl group in bethanchol offers several advantages for bethanechol over acetylcholine as acetylcholine non-selectively interacts with both musca ...
Why test for Hydrocodone and Hydromorphone?
Why test for Hydrocodone and Hydromorphone?

... Hydrocodone is one of the most misused prescription drugs on the market, according to the Drug Enforcement Administration (1). It is a semi-synthetic opioid, most commonly known as Vicodin® and is prescribed as a cough suppressant and for the treatment of moderate to severe pain. One of its metaboli ...
Cost Containment Strategies for Precription Drugs
Cost Containment Strategies for Precription Drugs

... to this issue. According to news accounts, some insurance companies responded by making it difficult for patients to obtain competing prescriptions once a drug in its class becomes available over-the-counter. Some large insurers responded to this change by moving competing drugs (Allegra and Zyrtec) ...
Behavioural and neurochemical changes induced by stress
Behavioural and neurochemical changes induced by stress

... of the neurokinin-2 (NK2) receptor antagonist saredutant (SR48968) in rats tested in the forced swim test (FST), by analysing hippocampal brain-derived neurotrophic factor (BDNF) and plasma corticosterone [as index of hypothalamic-pituitary-adrenal (HPA) axis activity]. Male Wistar rats received thr ...
Resource Manual
Resource Manual

... They can also stunt the height of growing adolescents. The oral drugs are more like to cause liver toxicity, but cancers, heart disease, and emotional problems can also occur. Some of the most commonly prescribed steroids are Anadrol, danazol, and Winstrol (taken in pill form); and boldenone, dihydr ...
Coupling Data Mining and Laboratory Experiments to Discover Drug
Coupling Data Mining and Laboratory Experiments to Discover Drug

... ime stepwise from 0.1 to 100 m M. The concentrations ...
Training Curriculum on Drug Addiction Counseling Training Manual
Training Curriculum on Drug Addiction Counseling Training Manual

... Say: There are various drug classifications. These are somewhat arbitrary groupings, but they provide a useful reference tool for approximating relative drug effects, possible risks, and potential withdrawal features. The classification in this slide shows how these drugs affect the brain. Classific ...
The Usefulness of a Closed-system Device for the Mixing of
The Usefulness of a Closed-system Device for the Mixing of

... and wipe samples were obtained was to be 20 μL and the concen­ for contamination detection. tration of the sample was diluted Medical cotton (4 x 4 cm), wetted to match the concentration in with 1ml of ultra-purified water which there was linearity shown was used to wipe the surfaces of for the purp ...
SPECTROPHOTOMETRIC DETERMINATION OF PIZOTIFEN MALEATE IN BULK DRUG AND TABLETS
SPECTROPHOTOMETRIC DETERMINATION OF PIZOTIFEN MALEATE IN BULK DRUG AND TABLETS

... Objective: Three sensitive spectrophotometric methods are presented for the assay of pizotifen maleate (PZT) in bulk drug and pharmaceutical formulation (tablets) using N-bromosuccinimide (NBS) and three dyes, methyl orange, amaranth and indigo carmine, as reagents. Methods: The methods involve the ...
Basics Pharmacology Review - Dr. Roland Halil
Basics Pharmacology Review - Dr. Roland Halil

... (Partially adapted from slides by Marc Riachi, R.Ph.) ...
Product Monograph - Paladin Labs Inc.
Product Monograph - Paladin Labs Inc.

... Hepatic Function: Hepatotoxicity, a rare adverse reaction, has an estimated frequency of 0.10.2% in patients treated with propylthiouracil. Propylthiouracil-induced hepatotoxicity is not dose-related and is thought to be idiosyncratic with an autoimmune component. Hepatocellular necrosis and fulmina ...
SYNTHESIS AND CHARACTERIZATION OF NEW AZO DYE (1
SYNTHESIS AND CHARACTERIZATION OF NEW AZO DYE (1

... spectrophotometer .The purity of the dye was cheeked by TLC using the solvent system (Sec.Butanol-wateracetic acid) (2:2:1).The melting point of the purified dye was measured in an open capillary tube. 2-Study of anti bacterial activity of dye. ...
calibration - Beckman Coulter
calibration - Beckman Coulter

... 600/800 System(s) and SYNCHRON® Systems Drugs of Abuse Testing (DAT) Urine Calibrators, is intended for the qualitative determination of opiates in human urine at a cutoff value of 2000 ng/mL. 1 The OP2 assay provides a rapid screening procedure for determining the presence of the analyte in urine. ...
Two simple animal models of intraocular pressure elevation for testing
Two simple animal models of intraocular pressure elevation for testing

... On day 28, the IOP lowering effect of bilateral single drop application of latanoprost (0.002%)4 or brimonidine/timolol (0.2%/0.25%) was evaluated in high IOP rats. The naive group and an induced group treated with bilateral single drop application of 0.9% NaCl served as controls (n=10 per group). I ...
Chapter 3: Effects Of Amphetamine-Type Stimulants
Chapter 3: Effects Of Amphetamine-Type Stimulants

... As already noted, investigating psychiatric problems associated with ecstasy is difficult due to high rates of polydrug use among those presenting with psychiatric symptoms and the possibility of pre-existing problems. To date, most research has investigated the proposed link between MDMA use and de ...
DEVELOPMENT AND EVALUATION OF PARACETAMOL TASTE MASKED ORALLY
DEVELOPMENT AND EVALUATION OF PARACETAMOL TASTE MASKED ORALLY

... The purpose of this research was to mask the intensely bitter taste of paracetamol and to formulate the orally disintegrating tablets (ODTs). TasteMasked orally disintegrating tablets of paracetamol were prepared by Flash Tab Technology. Taste masked granules of paracetamol were prepared by coating ...
Alexander Fleming and the discovery of Penicillin
Alexander Fleming and the discovery of Penicillin

... human body (in vivo) to kill bacteria effectively. Many clinical tests were inconclusive, probably because it had been used as a surface antiseptic. In the 1930s, Fleming’s trials occasionally showed more promise, and he continued until 1940 to try to interest a chemist skilled enough to further ref ...
340B Drug Discount Program: Expansion Issues, Diversion
340B Drug Discount Program: Expansion Issues, Diversion

... Allegations of manufacturers not making enough product available to 340B entities at 340B prices – GAO stated that “36 of the 61 stakeholders we interviewed did not report any effect on covered entities’ or non-340B providers’ access to drugs related to manufacturers’ distribution of drugs at 340B p ...
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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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