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... Safety Features • Consultation Paper – All prescription products must contain safety features – to identify an individual pack of medicinal products ('unique identifier') – verify whether the outer packaging has been tampered with (tamper evidence) ...
TASTE MASKED CHEWABLE DISPERSIBLE TABLET OF ATOMOXETINE HYDROCHLORIDE  Research Article HUDA.I.G*
TASTE MASKED CHEWABLE DISPERSIBLE TABLET OF ATOMOXETINE HYDROCHLORIDE Research Article HUDA.I.G*

... In the present work, chewable dispersible tablets of Atomoxetine Hydrochloride were designed by preparing taste masked granulate of Atomoxetine Hydrochloride with Eudragit EPO. The taste masked granulate was prepared by the batch process in Rapid Mixer Granulator using Eudragit EPO with a drug: Avic ...
EXTEMPORANEOUS PREPARATION OF PAEDIATRIC ORAL
EXTEMPORANEOUS PREPARATION OF PAEDIATRIC ORAL

... In addition, physical and microbiological stability of the suspension preparations was assessed. Individually weighed oral powders, manually filled capsules and unit dose syringes were prepared either by using nifedipine drug powder or a crushed commercial tablet. A reproducible and validated stabil ...
Anti-emetic activity of four species of Genus Cassia in chicks
Anti-emetic activity of four species of Genus Cassia in chicks

... intestine and prevent their further ingestion. Emesis is a complex process which comprise of three phases pre - ejection phase (gastric relaxation and retro-peristalsis) , retching (rhythmic action of respiratory muscles preceding vomiting and consisting of contraction of abdominal , intercostals an ...
Senior Scientist Computational Biology - Pharma
Senior Scientist Computational Biology - Pharma

... validating clinically important therapeutic targets; high throughput screening systems combined with diverse and focused compound libraries for discovering new drug leads; computational and medicinal chemistry for optimizing drug candidates; in vitro and in vivo models of disease for preclinical eva ...
Quantity Dependent Sentencing Ranges, the Drug
Quantity Dependent Sentencing Ranges, the Drug

... 841(b) attaches penalties to § 841(a) unlawful conduct. For certain controlled substances the penalties include not only maximum but also mandatory minimum terms of imprisonment. The severity of the § 841(b) penalties are greatly dependent on facts beyond the generic controlled substance conduct des ...


... That the conditions included in the monograph, under which the ...
Document
Document

... CO2 (37.8 g). This is reasonable because each carbon in CO2 has two oxygen atoms associated with it, while in C6H12O6 each carbon has only one oxygen atom associated with it and two hydrogen atoms, which are much lighter than oxygen. Therefore the mass of glucose produced should be less than the mas ...
the concept of the therapeutic window in the choice of h1
the concept of the therapeutic window in the choice of h1

... almost 12 times the recommended daily dose.1 By contrast, the H1 antihistamine loratadine has a very narrow therapeutic window, with the clinically recommended dose of 10 mg appearing to be both the minimally effective dose and the maximum tolerated dose.4,5 Whereas interactions or dose adjustments ...
Formulation of Effervescent Ibuprofen
Formulation of Effervescent Ibuprofen

... acid to prostaglandin H2 (PGH2). PGH2, in turn, is converted by other enzymes to several other prostaglandins (which are mediators of pain, inflammation, and fever) and to thromboxane A2 (which stimulates platelet aggregation, leading to the formation of blood clots). Like aspirin and indometacin, i ...
Discovery of Selective and Potent Inhibitors of Palmitoylation
Discovery of Selective and Potent Inhibitors of Palmitoylation

... face where it acts as a receptor for antiproliferative factor (APF) [37] [or presumably its other two known ligands, tissue plasminogen activator [54] and surfactant protein A [55]]. With‐ out surface expression of CKAP4, APF is unable to initiate a wide range of downstream ef‐ fects, including halt ...
The role of metabolic inhibition
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FORMULATION OF RAPID MOUTH DISSOLVING TABLETS OF CETIRIZINE di HCL USING  SUBLIMATION METHOD  Research Article   
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... The agreement between calculation and experimental mass change values suggested in the above scheme, was very good; the largest difference was only 1.76%. The formation of the oxides by thermal decomposition of the double sul®tes are also in agreement with the Xray powder diffraction patterns. On th ...
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... ocular and dermal exposure may occur during these processes when handling the powder form of the notified chemical. After formulation, dermal contamination would be considered to be the main route of occupational exposure to liquids or semi-liquids. Local exhaust ventilation is in place over the wei ...
Chitosan LipoSan Ultra
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... this product. Chitosan may interfere with the absorption of fat-soluble vitamin supplements and should be taken at a separate time than vitamins A, D, E or K. Individuals with intestinal malabsorption syndromes should not use chitosan. This product should not be taken by individuals with a shellfish ...
The rise and fall of the COX-2 inhibitors
The rise and fall of the COX-2 inhibitors

... essential to ensure that rapid and appropriate responses are made to potential safety issues related to medicinal products. The various regulatory restriction of the COX-2 inhibitors go to show the extreme importance of post-market surveillance which include Phase 4 studies, epidemiological studies ...
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... Registered dentists are legally entitled to prescribe from the entirety of the British National Formulary (BNF) and BNF for Children (BNFC). However, dental prescribing within the National Health Service (NHS) is restricted to those drugs contained within the List of Dental Preparations in the Denta ...
Powerpoint template for scientific posters (Swarthmore College)
Powerpoint template for scientific posters (Swarthmore College)

... could potentially slow cancer development, lessen the likelihood of heart disease, and aid in diabetes. ...
In vitro - In vivo Correlation: From Theory to
In vitro - In vivo Correlation: From Theory to

... drug substance is a key element both in establishing the initial feasibility of any formulation program and in the subsequent interpretation of the observed in vivo absorption characteristics of a given dosage form. The physicochemical characteristics of the drug substance itself, in the context of ...
DME Drugs And Supplies - National Government Services
DME Drugs And Supplies - National Government Services

... employees, agents, and staff make no representation, warranty, or guarantee that this compilation of Medicare information is error-free and will bear no responsibility or liability for the results or consequences of the use of this material. Although every reasonable effort has been made to assure t ...
Indole alkaloids
Indole alkaloids

... • is the dried whole plant of catharanthus roseus. F. Apocynaceae. • Folklore uses as an oral hypoglycemic agent. • It contain 150 alkaloids, the most important are the anticancer agents vincristine and vinblastine. • These are complex bisindole (dimeric indole) natural products present in small qua ...
A GESTALT OF ABZYMES Review Article K. BABU NAGESWARARAO
A GESTALT OF ABZYMES Review Article K. BABU NAGESWARARAO

... the repetition of ADEPT treatments. The concomitant administration of immunosuppressant will allow for slightly more repetitions of the therapy, but still only allowing two to three cycles of treatments. However, when compared to free drug administration, ADEPT can achieve higher concentrations of d ...
pharmaceutical compounding-nonsterile preparations
pharmaceutical compounding-nonsterile preparations

... is specifically designated for compounding of prescriptions. This space shall provide for the orderly placement of equipment and materials to prevent mixups among ingredients, containers, labels, in-process materials, and finished preparations and is designed, arranged, and used to prevent adventiti ...
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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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