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FLOATING SYSTEMS: A NOVEL APPROACH TOWARDS GASTRORETENTIVE DRUG DELIVERY  SYSTEMS  Review Article 
FLOATING SYSTEMS: A NOVEL APPROACH TOWARDS GASTRORETENTIVE DRUG DELIVERY  SYSTEMS  Review Article 

... development  of  several  novel  drug  delivery  systems  (NDDS)  that  could revolutionize method of medication and provide a number of  therapeutic  benefits2.  The  most  important  objectives  of  these  new  drug  delivery  systems  are:  First,  it  would  be  single  dose,  which  releases  t ...
www.ijpbs.com Rishikesh S Deshmukh*et al Int J Pharm Bio Sci
www.ijpbs.com Rishikesh S Deshmukh*et al Int J Pharm Bio Sci

... use of these metallic compounds. The synthetic dyes were much brighter, cheaper, more uniform, more stable (in their reactions to high processing temperatures, acids, carbon dioxide, storage and light) and more potent (i.e., less could be used to gain the same effect) than anything seen before, and ...
High-Risk Medications Attributed to Falls in Older Adults
High-Risk Medications Attributed to Falls in Older Adults

... 1. Ferreri, S et al. Methodology of an ongoing, randomized controlled trial to prevent falls through enhanced pharmaceutical care. Am J Geriatr. Pharmacother. 2008;6:61-81. 2. Leipzig RM, Cumming RG, Tinetti ME. Drugs and falls in older people: A systematic review and meta-analysis l. Psychotropic d ...
Has ethical clearance been obtained from your institution
Has ethical clearance been obtained from your institution

Presentation - Chronice Myeloid Leukemia
Presentation - Chronice Myeloid Leukemia

... NICE: clinical effectiveness – how well does something work in comparison with what we already use? AND cost effectiveness – how much more life or quality of life do we get for the extra money spent? A positive NICE appraisal has to be funded by the NHS: as the budget is fixed, something else has to ...
DESIGN DEVELOPMENT AND EVALUATION OF MATRIX TABLETS OF AMBROXOL Original Article
DESIGN DEVELOPMENT AND EVALUATION OF MATRIX TABLETS OF AMBROXOL Original Article

... geometrically modified systems. Many of these systems are not produced in a form that is amenable to large-scale manufacturing processes and the cost of formulation development, raw materials and manufacturing technology are among the principal factors in CR delivery systems for oral dosing [4]. The ...
Revised section Chapter Page  Heading / subheading
Revised section Chapter Page Heading / subheading

... supplements/cranberry Products for women/vaginal antifungal drugs Topical ophthalmic products/Dry eye products/Artifical tear solutions Otic products/prevention o swimmer‟s ear ...
Formulation and Evaluation of Terbutaline Sulphate Loaded
Formulation and Evaluation of Terbutaline Sulphate Loaded

... as the solid and sub-micron sized drug carriers that are less than 100nm in diameter. The main aim behind the synthesis of nanoparticles is to control the drug release from the formulations by altering the pharmacokinetic properties to enhance pharmacodynamic properties of drugs at the target site.5 ...
IT IS ELEMENTARY - the OLLI at UCI Blog
IT IS ELEMENTARY - the OLLI at UCI Blog

... and animal origin • These elements or their very simple compounds can kill—most commonly by interfering with cellular access to oxygen • Nitrogen N2 • Carbon dioxide CO2 • Carbon monoxide CO • Hydrogen cyanide HCN ...
pdf
pdf

... information. Network approaches have proven useful for organizing these high-dimensional biological data sets and extracting meaningful information,10 and the term network pharmacology or systems pharmacology has been coined.11 Interestingly, a high-throughput electronic-biology approach based on in ...
MicroDose Therapeutx and Moerae Matrix Announce
MicroDose Therapeutx and Moerae Matrix Announce

... another extremely important disease area.”  MMI‐0100  is  a  selective  inhibitor  of  MAPKAP  kinase  2  (MK2),  a  key  terminal  kinase  in  the  transforming growth factor beta (TGF‐)/p38 signaling pathway.  By targeting a terminal kinase,  MMI‐0100 has the potential for greater specificity of a ...
Bridging Studies
Bridging Studies

... Extrapolation and Similarity • If the bridging study shows that dose response, safety and efficacy in the new region are similar, then the study is readily interpreted as capable of “bridging” the foreign data • If a bridging study, properly executed, indicates that a different dose in the new regio ...
RefresherMedical-7PoisoningsOverdose
RefresherMedical-7PoisoningsOverdose

... • Can be lethal with other CNS depressants especially alcohol • Look like other CNS depressant overdoses ...
Large-Scale Elucidation of Drug Response Pathways in Humans
Large-Scale Elucidation of Drug Response Pathways in Humans

... interactions with drug-response gene expression data; and (ii) a meta-analysis of the inferred drug-response subnetworks to elucidate probable signaling pathways that are supported by multiple subnetworks (Fig. 1). In the first phase, we assembled a human physical interaction network, comprised of p ...
FLUNIXAMINE | nOnStEROIDAl AntI
FLUNIXAMINE | nOnStEROIDAl AntI

... Horse: Flunixin is four times as potent on a mg-per-mg transient and disappear without antidotal medication within basis as phenylbutazone as measured by the reduction a few minutes. Do not use in horses showing hypersensitivity in lameness and swelling in the horse. Plasma half-life to flunixin meg ...
New (and emerging) Psychoactive Substances (NPS)
New (and emerging) Psychoactive Substances (NPS)

... methamphetamine and MDMA are examples of phenethylamines that are controlled under the 1971 Convention of Psychotropic Substances. Examples of phenethylamine new or emerging substances in Australia include the 2C and NBOMe series. The 2C series are a group of psychedelic phenethylamines, with 2C-B b ...
Types of exudate Serous
Types of exudate Serous

... • Exudates it is an inflammatory extra vascular fluid that has a high protein concentration, cellular debris and an specific gravity above 1.020. There is also disturbance in the normal permeability of small blood vessels in the area of injury. ...
the PDF file to learn more
the PDF file to learn more

... consisting in developing allosteric modulators and biased ligands (BLs) are now emerging. Indeed, all GPCR agonists do not always uniformly activate all signalling pathways mediated by a given receptor. BLs therefore constitute a novel approach to more selectively activate a receptor for the develop ...
C u t t i n g   E...
C u t t i n g E...

... vincristine, and prednisone (CHOP-based) treatment protocols,1-5 most eventually relapse and require rescue therapy, which is designed to re-induce remission in cases of relapsed lymphoma. Some relapsed dogs become refractory to additional chemotherapy protocols, with lymphoma persisting despite mul ...
Faculty of Chemical Technology and Biotechnology
Faculty of Chemical Technology and Biotechnology

... The subject of chemistry. Material, the structure of the material, mixtures, energy and mass conservation. Atoms, molecules, elements compounds, ions, mol. Chemical formula, stoichiometry, concentration and its measurement. Chemical reactions and their types. Redox reactions, oxidation number acid- ...
Corel Ventura - untitled.chp
Corel Ventura - untitled.chp

... throughout the world, would not have treatments for their diseases. This further underscores the moral and health significance of the ODA. Before its enactment in 1983, only ten products for the treatment of rare diseases were approved for use in the US.12 Since then, over 1,100 medicinal products h ...
pdf file - 366KB
pdf file - 366KB

... and search the Display File list to access the catalytic site. Although some target enzyme active sites are not available from PDB files, it is possible to estimate how strongly a molecule will bind to a catalytic site by selecting the ligand’s surface contacts favorably interacting with specific fu ...
Drug reaction with eosinophilia and systemic symptoms
Drug reaction with eosinophilia and systemic symptoms

... the disappearance of exanthema and correction of laboratory parameters (eosinophilia and liver tests). Two weeks after discharge, she again presented a maculopapular exanthema associated with a fever up to 38°C, without other symptoms. On the suspicion of a reactivation of DRESS syndrome, she was ho ...
Drug Abuse Education Course
Drug Abuse Education Course

... • The effects are felt within minutes of smoking, peak within 20 minutes, and last for two or three hours. • THC is stored in fatty tissue like the brain, liver and reproductive organs. • 2-3 days after use, 50% of the original dose is still present in those tissues. ...
Highlights - IEA
Highlights - IEA

... chemical/kraft mills, mechanical mills, and paper mills (without virgin pulp production), chemical/kraft mills generally have the largest on-site fuel use, which is mainly biomass-based. However, a mechanical mill uses large amounts of electricity, implying that the primary energy use of the mechani ...
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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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