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New Psychoactive Substances
New Psychoactive Substances

... many parts of the world. The emergence of NPS (referring to a new substance that has not yet been scheduled under one of the international drug conventions) has lead to an extraordinary diversity of substances on the market available to new generations of users and raises some fundamental questions ...
Replacement of a Thiourea-S with an Amidine
Replacement of a Thiourea-S with an Amidine

... The reactivity of the Pt-Sthiourea bond and its cis labilizing effect on chloride are potential contributors to the increased cysteine reactivity of PT-ACRAMTU (2) compared to analogue 1. The rationale for incorporating a thiourea-based nonleaving group in the original design was to enhance the reac ...
FORMULATION AND EVALUATION OF LOSARTAN POTASSIUM SUSTAINED RELEASE TABLETS  Research Article
FORMULATION AND EVALUATION OF LOSARTAN POTASSIUM SUSTAINED RELEASE TABLETS Research Article

... Losartan potassium is a potent antihypertensive drug which is a highly specific Angiotensin II Type/AT 1 receptor antagonist. It is readily absorbed from the gastro intestinal tract, having oral bioavailability 33% and plasma elimination half life from 1.5 to 2.5 hours. The present study is an attem ...
Sample pages 2 PDF
Sample pages 2 PDF

... mixtures of molecules that represent linear combinations of behaviors of subsystems, giving an organized structure approximating the overall system. Actually, this structure will be referred as an artificial organic network because it is inspired on carbon based networks, especially studied on organ ...
Research Notes - California Workers` Compensation Institute
Research Notes - California Workers` Compensation Institute

... combinations of various substances, at least one of which is a primary acting pharmaceutical drug and others which are often more inert in nature. Compound drugs, however, are medications produced by mixing various component parts, including one or more drugs, while co-packs consist of a drug and a ...
Physical Property
Physical Property

Antifungals - ACH Pediatric Residents
Antifungals - ACH Pediatric Residents

...  Less infusion –related toxicities, less renal toxicities  Main use is in patients with pre-existing renal impairment  Also in those who fail conventional ampho b therapy, or are unable to tolerate ...
chemical labelling - The University of Sydney
chemical labelling - The University of Sydney

... and any relevant hazard statements. Where reasonably practical, also provide precautionary statements. Reference can be made to the SDS (Figure 3). For very small sample containers or vials containing material with similar risks, which may not have room for an individual label, attach a label to the ...
Curriculum Vitae
Curriculum Vitae

... Study the expressional regulation and the kinetics of transporters, enzymes (phase I and II), and proteins involved in drug metabolism and disposition. Characterize the metabolic stability, metabolite identification, inhibition/induction kinetics, enzyme mapping, formation of reactive metabolites, a ...
Mechanism of Drug Action and Drug Targets Receptors
Mechanism of Drug Action and Drug Targets Receptors

... muscarine (a mushroom alkaloid) causes the same response as acetylcholine. There are several subtypes of muscarinic acetylcholine receptors present in different cell types; all are coupled to G proteins, but they induce different responses. The M2 receptor present in heart muscle activates a Gi prot ...
The study includes drug abuse patients
The study includes drug abuse patients

... Occupational therapy practitioners intervene in a wide variety of settings with people who abuse substances. Recognition of the effect that the substance abuse has had on the occupational functioning of the individual and the family is a unique dimension that the occupational therapist brings to the ...
Proposed Course Structure and Syllabus. B. Pharmacy
Proposed Course Structure and Syllabus. B. Pharmacy

... Computation of analytical results, significant figures, concept of error, precision, accuracy, standard deviation, rejection of doubtful values with special reference to volumetric analysis. Calibration of analytical equipment used in volumetric analysis. UNIT-II (a) Theory of Neutralization Titrati ...
Chinese Traditional Medicines Face Crucial Challenges in the New
Chinese Traditional Medicines Face Crucial Challenges in the New

... formulated as the drugs that are applied clinically according to the traditional medical theories, most of which are used in the form of formulations, such as traditional Chinese drugs, Mongolian medicines, Tibetan medicines, and Uighur medicines. Modern plant medicines (natural medicines) are defin ...


... The best one-parametric model contains 1st order valence-connectivity index for which the R2 value comes to be 0.8513. The systematic addition of topological indices gave three bi-parametric correlations which were found statistically better than the mono-parametric correlations. However the best bi ...
Interpretation of "Identical Medicinal Ingredient
Interpretation of "Identical Medicinal Ingredient

... solution, then a conclusion of “chemical identity” has to questioned for different ‘solvates’. ...
NEUROPHARMACOLOGY
NEUROPHARMACOLOGY

... d) Abrupt withdrawal: causes a mild abstinence syndrome that includes hyperphagia, hypersomnolence; fatigue, irritability and depression may last for months e) Treatment: after withdrawal: dopaminergic agonists or tricyclic antidepressants are being tested ...
Brief Note on the Development of Biotechnology
Brief Note on the Development of Biotechnology

... caused by effects of food. In the last century the artisanal craft processes of food technology were more and more mechanised, which was the beginning of industrial food production. In parallel, at the end of the 19th century, organic chemistry gained ground in the synthesis of pharmaceuticals over ...
Amiodarone - GEOCITIES.ws
Amiodarone - GEOCITIES.ws

... b/c when you get amiodarone LD you’re also getting a big dose of iodine as well since it’s part of molecule. the hyperthyroidism will subside once LD is over, you don’t have to tx it. It on drug for long time, years,almost all drugs develop hyperT the reason for that is b/c of B blocking property of ...
Effects and Risks Associated with Novel Psychoactive Substances
Effects and Risks Associated with Novel Psychoactive Substances

... medical research, derivatives of such substances, or previously approved drugs for human consumption. They can be classified by their major effects as sedatives, stimulants, or hallucinogens, or by their chemical structure (e1). Commerce in these substances occupies a legal gray area (2). In Germany ...
Approaches using molecular imaging... PET in Clinical microdose
Approaches using molecular imaging... PET in Clinical microdose

... radioisotope, since it allows for imaging durations of up to 10 hours. A considerable drawback, however, stems from the fact that relatively few drug molecules contain fluorine in their native structure. Consequently, despite the rather short half-life of 11C (20.4 min), the majority of PET microdose ...
Chemical Equations and Reactions
Chemical Equations and Reactions

... • First balance the atoms of elements that are combined and that appear only once on each side of the equation. • Balance polyatomic ions that appear on both sides of the equation as single units. • Balance H atoms and O atoms after atoms of all other elements have been balanced. ...
Balancing Chemical Equations
Balancing Chemical Equations

... There are 3 Cl’s in the reactants and 2 Cl’s in the products The least common multiple between 3 and 2 is…6 In order to make 6 Cl’s on each side, put the coefficient 2 in front of the AlCl3 and the coefficient 3 in front of the CaCl2. ...
FORMULATION AND EVALUATION OF PH TRIGGERED IN SITU OPHTHALMIC GEL... MOXIFLOXACIN HYDROCHLORIDE  Research Article
FORMULATION AND EVALUATION OF PH TRIGGERED IN SITU OPHTHALMIC GEL... MOXIFLOXACIN HYDROCHLORIDE Research Article

... fluoroquinolone antibiotic, Moxifloxacin hydrochloride. Polyacrylic acid (Carbopol 934) was used as gelling agent in combination with hydroxy propyl methyl cellulose(k15M) as viscosifying agent. Benzalkonium chloride in suitable concentration was used as preservative. The formulations were sterilize ...
22-7. Antibacterials
22-7. Antibacterials

... the presence of of IgE antibodies in serum is a useful indicator of reactions mediated by these antibodies, i.e. immediate (type 1) reactions. Additionally, an intradermal test for allergy may be performed; appearance of wheal reaction ...
Transdermal drug delivery: Past, present, future trends
Transdermal drug delivery: Past, present, future trends

... ISSN: 0976-7126 steroid fludroxycortide is absorbed systemically but this is not the desired action. The first commercially available prescription patch was approved by the U.S. Food and Drug Administration in December 1979. These patches administered scopolamine for motion sickness10-16. Developmen ...
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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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