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Biomedical aspects of chiral molecules
Biomedical aspects of chiral molecules

... CYP1A2 and CYP3A4 (Pohl et al. 1976). With regard to genetic polymorphism, these have some clinical relevance (Schwarz 2003). ...
Knowledge Discovery in Academic Drug Discovery Programs
Knowledge Discovery in Academic Drug Discovery Programs

... With enough understanding of the underlying cause of a disease, one or a few related “targets” for a potential new medicine will be identified. A target is generally a single molecule, such as a gene or protein, which is involved in a particular ...
Revealing the paradox of drug reward in human evolution
Revealing the paradox of drug reward in human evolution

... compounds are rewarding. It is therefore important to stress that these and other addictive drugs appear to have evolved only because they successfully deterred, not rewarded or reinforced, plant consumption. Among drugs of abuse, the data are particularly clear for nicotine, an alkaloid that binds ...
Pharmacology
Pharmacology

... pediatrics) and many other disciplines. Pharmacology is characterized by wide range of contents and profound theories, making it an indispensable course for medical and pharmaceutical research as well as clinical and production practice. The goal of pharmacology includes: 1) to clarify the action of ...
Toxicokinetics and analytical toxicology of amphetamine
Toxicokinetics and analytical toxicology of amphetamine

... The phase I and II metabolites of the designer drugs methylenedioxyamphetamine (MDA), R,S-methylenedioxymethamphetamine (MDMA), R,S-methylenedioxyethylamphetamine (MDE), R,S-benzodioxazolylbutanamine (BDB) and R,S-N-methyl-benzodioxazolylbutanamine (MBDB) were identified by gas chromatography-mass s ...
gcse biology - School
gcse biology - School

... In schools and college laboratories, cultures should be incubated at a maximum temperature of 25oC to prevent the growth of pathogens – in industry, higher temps can produce a more rapid growth rate. ...
Microsponges as Innovative Drug Delivery Systems
Microsponges as Innovative Drug Delivery Systems

... circulation in significant amounts is a challenging area of research. Topical application of drugs suffers many problems. Ointments, which are often aesthetically unappealing faces the problems like greasiness, stickiness and often result in lack of patient compliance. These vehicles require high co ...
STUDIES ON DISSOLUTION ENHANCEMENT OF LOVASTATIN USING SOLUPLUS BY SOLID
STUDIES ON DISSOLUTION ENHANCEMENT OF LOVASTATIN USING SOLUPLUS BY SOLID

... For a successful formulation, various formulation parameters that play a crucial role are aqueous solubility; stability at ambient temperature and humidity, photo-stability, compatibility with solvents etc. Among all these, Solubility is the most important property for developing formulations. The p ...
Adverse Drug Reactions and Interactions
Adverse Drug Reactions and Interactions

... Active tubular secretion is the other important excretory process in the kidney. Weak electrolytes (acids and bases) are secreted into the proximal tubular fluid and digoxin may be secreted by the distal tubule. This is an energy-dependent process and drugs can be effectively cleared, with a tubular ...
Available through Online Review Article www.ijptonline.com
Available through Online Review Article www.ijptonline.com

... therapeutically effective and nontoxic for extended period of time. This goal can be achieved by formulation of sustained release formulation. Microsponge is a common technique used in the production of sustained release dosage forms. Microsponge based drug delivery system has received considerable ...
Polymorph Impact on the Bioavailability and Stability of Poorly
Polymorph Impact on the Bioavailability and Stability of Poorly

... particle size to nanodimensions [5,6]. Including or dispersing the poorly soluble drug in a carrier such as a cyclodextrin [7,8] or a polymer (solid dispersion) [9] are also common applied approaches. Modifications in the solid state, conversion from one polymorph to another [10], solvation/hydratio ...
the full case study to learn more
the full case study to learn more

... • Polymorphisms in transporters and enzymes can affect drug distribution and elimination. For example, CYP2D6 activity increases when multiple gene copies arise. A wide variety of drug toxicities and/or efficacies can be affected by variations in the CYP2D6 status, such as tamoxifen. CYP2D6 status c ...
Prodrugs:
Prodrugs:

... transformation, to the active drug that exerts the intended therapeutic effect(s)". Ideally, the prodrug should be converted to the parent drug as soon as it reach its goal, and then followed by the subsequent rapid metabolism and/or elimination of the released active group. Prodrug design can be hi ...
Drug Groupings and Workflow Options for the Processing and Review of Concomitant Medication Data
Drug Groupings and Workflow Options for the Processing and Review of Concomitant Medication Data

... Figure 3 Examples for selected search conditions within various drug groupings ...
TRANSDERMAL DRUG DELIVERY SYSTEMS
TRANSDERMAL DRUG DELIVERY SYSTEMS

... it is well known that the pressure sensitive adhesive used to produce intimate contact with the skin is more often the source of cutaneous reactivity & not the drug. many of the inactive ingredients used in topical pharmaceutical dosage forms have the ability to alter the barrier function of the ski ...
Lipid-based Dosage Forms - American Association of
Lipid-based Dosage Forms - American Association of

... manufacturing. Drugs with low melting points or poor compression properties, or low dosage forms are all difficult to process using conventional approaches, especially when the drug is liquid at ambient temperature. Lipid-based formulations can be filled into hard or soft capsules[24]. Design of Lip ...
Drug Interactions—Principles, Examples and Clinical Consequences
Drug Interactions—Principles, Examples and Clinical Consequences

... necessary to prescribe several drugs for one patient at a time. As a consequence, the average 65-year-old patient is on five drugs simultaneously (1). Prescription peaks in the 75- to 84-year-old group; a European study showed among patients with a mean age of 81 years that 34% to 68% were taking si ...
Speech - Cannabis Skunk Sense
Speech - Cannabis Skunk Sense

... want facts. This pathetic effort is a waste of time and public money. Harm reduction has its place in treatment one-to-one with known users - a short-term strategy on the road to abstinence, e.g. gradually reducing the dose. But never in the classroom where harm reduction tips can and sometimes do a ...
Benefit-Risk Assessments in Rare Disorders
Benefit-Risk Assessments in Rare Disorders

... Benefit-risk assessments are essential to the Food and Drug Administration’s (FDA) regulatory process for approving therapeutic products, and to informing the patient and physician selection or rejection of approved products. This paper examines the similarities and differences between benefit-risk ...
Interactions of Grapefruit Juice with Drugs
Interactions of Grapefruit Juice with Drugs

... is seen when bioavailability and plasma concentration increase without the need for an increase in the dose, the dosing frequency or the cost of drug therapy4. Cyclosporin has low oral bioavailability because of significant intestinal metabolism. The drug is not rapidly metabolised by CYP3A4 but has ...
Binder1 Hodgson Tut 17Feb
Binder1 Hodgson Tut 17Feb

... taken to achieve this level is found. If a 50% reduction in concentration is used, the time taken is the half-life (t1/2); this will be constant whatever starting drug concentration is used. Another time period that can be used to describe the curve is the time constant (t). This is the point at whi ...
IN SILICO DISCOVERY PROCESS  Review Article  E.N BHARATH*, S.N MANJULA, A. VIJAYCHAND 
IN SILICO DISCOVERY PROCESS  Review Article  E.N BHARATH*, S.N MANJULA, A. VIJAYCHAND 

... Stagnation:  Challenge  and  Opportunity  on  the  Critical  Path  to  New  Medical  Products9 Modeling and simulation  could play a key role in  overcoming this innovation deficit.  It noted that while spending on  biomedical research  has increased greatly  over the  last decade, the  submission o ...
Computational Biology
Computational Biology

... Specific example: protein kinases Phosphorylation of Ser, Thr, and Tyr residues is a primary mechanism for regulating protein function in eukaryotic cells. Protein kinases, the enzymes that catalyze these reactions, regulate essentially all cellular processes and have thus emerged as therapeutic ta ...
Drug and Chem-informatics Databases - BIDD
Drug and Chem-informatics Databases - BIDD

... chemicals. A user may enter compound identifiers such as Chemical Name, CAS Registry Number, Molecular Formula, Classification Code, Locator Code, and Structure or Substructure. New searchable features include search and display by Toxicity indicators such as Median Lethal Dose (LD50), by Physical/C ...
Pricing and Patents of HIV/AIDS Drugs in Developing Countries
Pricing and Patents of HIV/AIDS Drugs in Developing Countries

... under nonpatent regimes drives drug prices to be related to per capita income across countries, but also that multinational drug firms have effectively tiered their prices to per capita income across countries when drugs are under patent regime. Finally, we find that drug firms set a very high initi ...
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Orphan drug

An orphan drug is a pharmaceutical agent that has been developed specifically to treat a rare medical condition, the condition itself being referred to as an orphan disease.In the US and EU it is easier to gain marketing approval for an orphan drug, and there may be other financial incentives, such as extended exclusivity periods, all intended to encourage the development of drugs which might otherwise lack a sufficient profit motive. The assignment of orphan status to a disease and to any drugs developed to treat it is a matter of public policy in many countries, and has resulted in medical breakthroughs that may not have otherwise been achieved due to the economics of drug research and development.According to Thomson Reuters in their 2012 publication ""The Economic Power of Orphan Drugs"", there has been increased investing in orphan drug Research and Development partly due to the U. S. Orphan Drug Act (ODA) 1983 and similar Acts in other regions of the world and also driven by ""high-profile philanthropic funding."" The period between 2001 to 2011 was the ""most productive period in the history of orphan drug development, in terms of average annual orphan drug designations and orphan drug approvals."" For the same decade the compound annual growth rate (CAGR) of the orphan drugs was an ""impressive 25.8 percent, compared to only 20.1 percent for a matched control group of non-orphan drugs."" By 2012 the market for orphan drugs was worth USD$637 million compared to the USD$638 million matched control group of non-orphan drugs, Thomson Reuters.By 2012, ""the revenue-generating potential of orphan drugs [was] as great as for non-orphan drugs, even though patient populations for rare diseases are significantly smaller. Moreover, we suggest that orphan drugs have greater profitability when considered in the full context of developmental drivers including government financial incentives, smaller clinical trial sizes, shorter clinical trial times and higher rates of regulatory success.""
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