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Artemisia annua (Asteraceae) Description of the plant Plant parts
Artemisia annua (Asteraceae) Description of the plant Plant parts

... Hepatocarcinoma cells (SMMC-7721) were treated with essential oil of A.annua 100 µg/ml for 24h. By this treatment apoptosis was induced, verified by light and electronic microscopy and Giemsa stain. The apoptosis was observed by condensated cytoplasm, fragmentation of nuclear chromatin and apoptosis ...
A SURVEY BASED STUDY IN CURRENT SCENARIO OF GENERIC AND... Research Article
A SURVEY BASED STUDY IN CURRENT SCENARIO OF GENERIC AND... Research Article

... a branded generic. Branded generic drugs have names derived from a combination of the manufacturer’s name and the non-proprietary name. This enables the manufacturer to market the product in a way similar to the proprietary product [2]. Generic drugs are cheaper in comparison to branded drugs becaus ...
BSc Chemistry Syllabus - St. Xavier`s College
BSc Chemistry Syllabus - St. Xavier`s College

... a. To learn preparations reactions and properties of alkane, alkene and alkynes. b. To learn estimation of nitrogen and molecular weight determination of organic acids and bases c. To learn basics of selected organic reactions and mechanisms d. To understand the atomic structure e. To learn the appl ...
GHB - CAP Members
GHB - CAP Members

... medical use in treatment in the United States, and a lack of accepted safety for use under medical supervision. GHB products are Schedule III substances under the Controlled Substances Act. In addition, GBL is a List I chemical. It was placed on Schedule I of the Controlled Substances Act in March 2 ...
Alaris Medley Pump Module 8100 Version 7
Alaris Medley Pump Module 8100 Version 7

... facilities that utilize infusion pumps for the delivery of fluids, medications, blood, and blood products using continuous or intermittent delivery through clinically acceptable routes of administration; such as, intravenous (IV), intra-arterial (IA), subcutaneous, epidural, enteral, or irrigation o ...
Zidovudine Concentration in Brain Extracellular Fluid Measured by
Zidovudine Concentration in Brain Extracellular Fluid Measured by

... in the concentration of drug between the inflow and outflow. Thus, recovery is inversely related to the perfusate flow rate. Molecular weight, charge, shape, and protein binding of a drug will influence recovery. Microdialysis membrane surface area, composition, and MWCO can be selected to accommoda ...
Prevalence and nature of adverse drug events and the potential for
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... Personal identity number Abstract database of psychological literature Statistics Sweden Standard deviation Swedish Prescribed Drug Register Sub-therapeutic effect of drug therapy Therapeutic failure Morbidity due to drug-related untreated indication Care Data Warehouse of Östergötland World Health ...
Chemotherapy extravasation guideline
Chemotherapy extravasation guideline

... hyaluronic acid and by this mechanism enhances the systemic uptake of the infiltrated cytotoxic. It is routinely used with vinca-alkaloids and its use has been advocated with other agents such as paclitaxel. It is unlikely to cause harm to surrounding tissue. Its use in extravasation injuries is unl ...
Choosing a Regimen for Treatment of Latent Tuberculosis Latent
Choosing a Regimen for Treatment of Latent Tuberculosis Latent

... -Least costly DOT regimen -↓ side effects than INH BIW -Promising completion rates ...
as a PDF
as a PDF

... potent and selective inhibitors against this CYP isoform are indispensible tools. With use of recombinant CYP2J2 enzyme, screening of substrate and inhibitor of this CYP isoform can be performed, because specific substrate can be useful for profiling CYP2J2 inhibition of drug candidates in vitro in ...
- International Journal Of Pharmaceutical Sciences And
- International Journal Of Pharmaceutical Sciences And

... up of the small leaflets composing the doubly compound leaves. Remarkably, the touch response is not restricted to the stimulated leaflet, but can propagate to all the neighboring leaflets of the leaf. A complex electrical signal can be responded by the epidermal cell of plants and animals and capable ...
Forced Degradation of Ibuprofen in Bulk Drug and Tablets
Forced Degradation of Ibuprofen in Bulk Drug and Tablets

... recommended storage conditions and establish retest periods and shelf lives (1). Assay analytical methods for evaluating the stability of drug substance or drug product should be specific and selective and should detect quantitative changes in drug substance and drug product over time (2). The speci ...
Wrightia tinctoria R. Br. - Journal of Coastal Life Medicine
Wrightia tinctoria R. Br. - Journal of Coastal Life Medicine

... and is used in scorpion sting and snakebite[23]. In Nasik district of Maharashtra state of India, infusion of bark is administered to mothers for a week to increase lactation[24]. People inhabiting in Seshachalam hills of Andhra Pradesh, India apply a paste of crushed stem bark along with bark of Ai ...
Interactions with Antineoplastic Agents Used in Veterinary Medicine
Interactions with Antineoplastic Agents Used in Veterinary Medicine

... Chapter 012 (edited file)—“Tables 12B-1 and 12B-2” 6/30/2017, Page 10 of 39, 0 Figure(s), 2 Table(s), 0 Box(es) ...
Medical Marijuana And Methadone Treatment Programs Jassin M
Medical Marijuana And Methadone Treatment Programs Jassin M

... analgesia. According to the Drug Enforcement Administration (DEA), an 8 10 mg dose of methadone is similar in analgesic effects to a 10 mg dose of morphine.14 As with other opioid analgesics, its pain relief lasts anywhere from 4 - 8 hours. When it is absorbed, methadone is distributed to the kidney ...
Mrs - Vitrodiagnostic.com
Mrs - Vitrodiagnostic.com

... and protein with an osmolality less than or equal to that of plasma (Paxton, 1979). Also present in saliva is a certain amount of cell debris arising from the epithelial cells of the mouth together with food residues (Caddy, 1984). The osmolality is principally determined by the type of gland and by ...
Drug Allergy: An Updated Practice Parameter
Drug Allergy: An Updated Practice Parameter

... mechanisms are not thought to be involved, and a scientific explanation for such exaggerated responses has not been established (eg, aspirin-induced tinnitus at low doses). • Drug idiosyncrasy is an abnormal and unexpected effect that is unrelated to the intended pharmacologic action of a drug and h ...
Health Needs Assessment – Drug and Alcohol
Health Needs Assessment – Drug and Alcohol

... (representing 39.80% of activity), followed by prescription opioids (37.7%) and codeine (15.2%). For context, in the Central Queensland area, service activity data for opioid treatment identifies cannabis as the primary drug of concern, followed by heroin and morphine. In the Wide Bay Area – the pri ...
LC-Tandem MS Detection of Covalent Binding of Acetaminophen to
LC-Tandem MS Detection of Covalent Binding of Acetaminophen to

... 120.07 (immonium ion of phenylalanine). To further characterise the NAPQI-CPF product, and to enable quantification of NAPQI-CPF in patient samples, a large scale synthesis was performed. Acetaminophen (32 mg) was oxidised to NAPQI in 75 mL chloroform, as described above, and stirred vigorously for ...
CONTROLLED SUBSTANCES
CONTROLLED SUBSTANCES

... by the federal food and drug administration as a drug, and contains any quantity of the following substances, their salts, isomers (whether optical, positional, or geometric), homologues (analogs), and salts of isomers and homologues (analogs), unless specifically excepted, whenever the existence of ...
Master-Thesis
Master-Thesis

... Insufficient law enforcement and insufficient penalties As well as missing regulations and weak authorities will lead to the prospering of undesired counterfeit activities, insufficient law enforcement and insufficient penalties will lead to this effect. If counterfeiters are not persecuted, may it ...
BIOLOGICAL EVALUATION OF OPIOIDS, STIMULANTS, AND
BIOLOGICAL EVALUATION OF OPIOIDS, STIMULANTS, AND

... receptors, yet are weakly active, or inactive, in antinociceptive assays. For example NIH 11139 (N-8hydroxyoctyl) had good affinity at all three receptors, but was only active in the antiwrithing assay in mice. This was demonstrated not to be delta agonist mediated through the lack of antagonism wi ...
Express Scripts 2015 Drug Trend Report
Express Scripts 2015 Drug Trend Report

... dollars are spent on specialty, rather than traditional, medications. In the late ‘80s and early ‘90s, most drug development and spend was on traditional, potential drugs in development mostly oral, small-molecule solid drugs used to treat conditions such as heartburn/ulcer, depression and diabetes. ...
Distinct profiling of antimicrobial peptide families
Distinct profiling of antimicrobial peptide families

... the design of new AMPs (Juretic et al., 2011). A number of methods have been proposed to identify and characterize AMPs using compositional characteristics of their amino acid sequences and information extracted from sequence alignment (Lata et al., 2007, 2010; Wang et al., 2011). However, the activ ...
Update on Serotonin - Mayo Medical Laboratories
Update on Serotonin - Mayo Medical Laboratories

... toxicity. Patients who are ultrarapid metabolizers may benefit from increased doses or conversion to other drugs that are not primarily metabolized by CYP2D6. A complicating factor in correlating CYP2D6 genotype with phenotype is that many drugs (or their metabolites) may reduce CYP2D6 catalytic act ...
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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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