A REVIEW ON BIOAVAILABILITY AND BIOEQUIVALENCE TRIALS AND ITS NECESSITY
... Bioequivalence gained increasing attention during the last 40 years after it became evident that marketed products having the same amounts of the drug may exhibit marked differences in their therapeutic responses. Generally, these differences were well correlated to dis ...
... Bioequivalence gained increasing attention during the last 40 years after it became evident that marketed products having the same amounts of the drug may exhibit marked differences in their therapeutic responses. Generally, these differences were well correlated to dis ...
DESIGN AND EVALUATION OF CONTROLLED RELEASE TABLETS OF LIPID LOWERING
... release matrix tablets of Nicotinic acid (NA). The tablets were prepared by wet granulation method and the prepared tablets of NA will remain intact up to 2 hrs even in pH 1.2 due to eudragit S100 and its release is not only initiated but tact fully retarded up to 12 hrs and were found to be superio ...
... release matrix tablets of Nicotinic acid (NA). The tablets were prepared by wet granulation method and the prepared tablets of NA will remain intact up to 2 hrs even in pH 1.2 due to eudragit S100 and its release is not only initiated but tact fully retarded up to 12 hrs and were found to be superio ...
Product Development Issues of Powders for Injection
... primary pack allows the formulation of drugs that are thermolabile or unstable in aqueous solution. However, lyophilization normally yields an amorphous or partially amorphous product, which leads to solid-state instability (3). A more-stable crystalline stage can be obtained by crystallization in a ...
... primary pack allows the formulation of drugs that are thermolabile or unstable in aqueous solution. However, lyophilization normally yields an amorphous or partially amorphous product, which leads to solid-state instability (3). A more-stable crystalline stage can be obtained by crystallization in a ...
DEVELOPMENT & VALIDATION OF STABILITY INDICATING HPLC METHOD FOR DETERMINATION OF SOLIFENACIN IN BULK FORMULATIONS
... A stability indicating, isocratic, rapid, specific, and sensitive high performance liquid chromatographic (HPLC) method was developed and validated for determination of Solifenacin in bulk drug. The quantitative determination of SOLIFENACIN was performed on a Hypersil C8 (250mm × 4.6 mm i.d., 5 µ ...
... A stability indicating, isocratic, rapid, specific, and sensitive high performance liquid chromatographic (HPLC) method was developed and validated for determination of Solifenacin in bulk drug. The quantitative determination of SOLIFENACIN was performed on a Hypersil C8 (250mm × 4.6 mm i.d., 5 µ ...
Direct to Consumer Advertising for Prescription Drugs
... selection of specific drugs for patients should be based upon the recommendations of physicians familiar with the illnesses of their specific patients. We are concerned that advertising will result in increased consumption of these drugs; though their use may neither be appropriate nor necessary. A ...
... selection of specific drugs for patients should be based upon the recommendations of physicians familiar with the illnesses of their specific patients. We are concerned that advertising will result in increased consumption of these drugs; though their use may neither be appropriate nor necessary. A ...
Meditechnicalities
... Every implementation gives additional insight into technical issues that need to be addressed to optimize the MEDITECH environment. This session will focus on lessons learned in Magic, CS and 6.0 installations of Pharmacy and pharmacy related modules. It will include discussion on how to add additio ...
... Every implementation gives additional insight into technical issues that need to be addressed to optimize the MEDITECH environment. This session will focus on lessons learned in Magic, CS and 6.0 installations of Pharmacy and pharmacy related modules. It will include discussion on how to add additio ...
Article 07-10: Carcinogenicity of Lipid-lowering Drugs
... “For patients not at high short-term risk of CHD death, especially patients with life expectancies of more than 10 to 20 years, pharmacologic treatment [with lipid-lowering drugs] probably should be avoided.” 10) It is possible that these drugs are not carcinogenic, but rather that it is the lower c ...
... “For patients not at high short-term risk of CHD death, especially patients with life expectancies of more than 10 to 20 years, pharmacologic treatment [with lipid-lowering drugs] probably should be avoided.” 10) It is possible that these drugs are not carcinogenic, but rather that it is the lower c ...
SBN Investor Presentation
... drugs precisely based on a detailed understanding of the structure of the drug target – an approach known as structure-based drug design (SBDD). By this method, Heptares aims to design and develop superior medicines that are more effective, with better selectivity and fewer side effects. Heptares ap ...
... drugs precisely based on a detailed understanding of the structure of the drug target – an approach known as structure-based drug design (SBDD). By this method, Heptares aims to design and develop superior medicines that are more effective, with better selectivity and fewer side effects. Heptares ap ...
Suitable dosage forms for paediatric medicine
... More precise pump to select the most adapted dilution for children before infusion. During their illness the most important for children is their pain and they are afraid of all that could be an aggression (injection, perfusion….) Use of nitrogen protoxide or « fentanyl »patch (manually dose-are ...
... More precise pump to select the most adapted dilution for children before infusion. During their illness the most important for children is their pain and they are afraid of all that could be an aggression (injection, perfusion….) Use of nitrogen protoxide or « fentanyl »patch (manually dose-are ...
Chemistry Midterm Review 2006
... 12. Name five indicators of a chemical reaction. 13. Define the words “reactant” and “product”. In a chemical equation, where are the reactants located? Where are the products located? What separates them from each other? 14. Classify each as a physical or chemical change: food spoiling, water boils ...
... 12. Name five indicators of a chemical reaction. 13. Define the words “reactant” and “product”. In a chemical equation, where are the reactants located? Where are the products located? What separates them from each other? 14. Classify each as a physical or chemical change: food spoiling, water boils ...
DrugLecture2001
... • Animals work at high rates to obtain ICSS • ICSS enhances the rewarding properties of food, water, sex • Animals prefer ICSS over food, water, sex • Areas of the brain that best support ICSS are those of the natural reward circuits ...
... • Animals work at high rates to obtain ICSS • ICSS enhances the rewarding properties of food, water, sex • Animals prefer ICSS over food, water, sex • Areas of the brain that best support ICSS are those of the natural reward circuits ...
SYLLABUS FOR B. PHARM. - All India Council For Technical
... Algebra : Equations reducible to quadratics, simultaneous equations (linear and quadratic), Determinants, properties of solution of simultaneous equations by Cramer's rule, matrices, definition of special kinds of matrices, arithmetic operations on matrices, inverse of a matrix, solution of simultan ...
... Algebra : Equations reducible to quadratics, simultaneous equations (linear and quadratic), Determinants, properties of solution of simultaneous equations by Cramer's rule, matrices, definition of special kinds of matrices, arithmetic operations on matrices, inverse of a matrix, solution of simultan ...
Insight DOA Panel 6.1
... 1. Sensitivity : THC in the INSIGHT DOA Panel 6.1 detects THC at concentrations equal to or greater than 50 ng/ml. AMP in the INSIGHT DOA Panel 6.1 detects amphetamine at concentrations equal to or greater than 1000 ng/ml. BAR in the INSIGHT DOA Panel 6.1 detects barbiturates at concentrations equal ...
... 1. Sensitivity : THC in the INSIGHT DOA Panel 6.1 detects THC at concentrations equal to or greater than 50 ng/ml. AMP in the INSIGHT DOA Panel 6.1 detects amphetamine at concentrations equal to or greater than 1000 ng/ml. BAR in the INSIGHT DOA Panel 6.1 detects barbiturates at concentrations equal ...
Vol 1. Issue 1, April 2006 - The University of the West Indies at Mona
... Generics have made a significant impact in the provision of better healthcare. A 2002 survey conducted in USA reported that nearly a quarter (24 percent) of the survey respondents said they have not been able to afford a prescription medication when there was no generic available. Jamaica’s drug pol ...
... Generics have made a significant impact in the provision of better healthcare. A 2002 survey conducted in USA reported that nearly a quarter (24 percent) of the survey respondents said they have not been able to afford a prescription medication when there was no generic available. Jamaica’s drug pol ...
urine drug test information sheet barbiturates
... Background: Barbiturates are a group of drugs that act as central nervous system depressants. Opiates, benzodiazepines and alcohol are also CNS depressants, and like their use, the effect seems to the user as an overall sense of calm. Barbiturates were introduced in 1903, dominating the sedative-hyp ...
... Background: Barbiturates are a group of drugs that act as central nervous system depressants. Opiates, benzodiazepines and alcohol are also CNS depressants, and like their use, the effect seems to the user as an overall sense of calm. Barbiturates were introduced in 1903, dominating the sedative-hyp ...
Misuse of amphetamines and related drugs
... This article discusses the misuse of drugs which act as stimulants, an effect mainly produced by enhancement of the central transmission of catecholamines, particularly dopamine. Stimulant misuse is extremely widespread in the UK and elsewhere, but primary users of such drugs present relatively rare ...
... This article discusses the misuse of drugs which act as stimulants, an effect mainly produced by enhancement of the central transmission of catecholamines, particularly dopamine. Stimulant misuse is extremely widespread in the UK and elsewhere, but primary users of such drugs present relatively rare ...
Contents - World Health Organization
... weight gain, and edema, both of which are warning signs of heart failure; some reports were associated with poor treatment outcomes, including death, when treatment was continued. The strengthened warning advises health-care professionals to observe patients carefully for the signs and symptoms of h ...
... weight gain, and edema, both of which are warning signs of heart failure; some reports were associated with poor treatment outcomes, including death, when treatment was continued. The strengthened warning advises health-care professionals to observe patients carefully for the signs and symptoms of h ...
The impact of polypharmacology on chemical biology Albert Antolín Hernández
... Accordingly, we are witnessing an early impact of polypharmacology on drug discovery with new business models like drug repurposing already exploiting drug promiscuity and with ongoing academic efforts to rationally design multitarget drugs. Drug discovery is, slowly, becoming a more holistic endeav ...
... Accordingly, we are witnessing an early impact of polypharmacology on drug discovery with new business models like drug repurposing already exploiting drug promiscuity and with ongoing academic efforts to rationally design multitarget drugs. Drug discovery is, slowly, becoming a more holistic endeav ...
Full Text Article
... Cross-reactivity Patients that are allergic to one sulfonamide antibiotic are likely to be allergic to other sulfonamide antibiotics. Until recently, it was thought that these patients were also likely to be allergic to non-antibiotic sulfonamides (called cross-reactivity). There are important chemi ...
... Cross-reactivity Patients that are allergic to one sulfonamide antibiotic are likely to be allergic to other sulfonamide antibiotics. Until recently, it was thought that these patients were also likely to be allergic to non-antibiotic sulfonamides (called cross-reactivity). There are important chemi ...
Chapter 19
... Morphine antagonists inhibit the action of morphine by blocking receptors. Pentazocine acts as both. It is less addictive than morphine and is effective at relieving pain. Naloxone is a pure antagonist. It can be used to treat opium addicts. ...
... Morphine antagonists inhibit the action of morphine by blocking receptors. Pentazocine acts as both. It is less addictive than morphine and is effective at relieving pain. Naloxone is a pure antagonist. It can be used to treat opium addicts. ...
Drugs of Addiction - City Vision University
... To define psycho active chemicals To examine the routes that drugs take to the brain and the ways in which they affect brain chemistry To present a system for classifying these psychoactive substances. To detail the physiological effects of uppers, downers and other commonly abused drugs To ...
... To define psycho active chemicals To examine the routes that drugs take to the brain and the ways in which they affect brain chemistry To present a system for classifying these psychoactive substances. To detail the physiological effects of uppers, downers and other commonly abused drugs To ...
Ribozyme Catalysis
... • A typical drug molecule acts by docking with a target biomolecule such as an enzyme or receptor. These drugs are often chiral, and the two enantiomers may differ greatly in efficacy. ...
... • A typical drug molecule acts by docking with a target biomolecule such as an enzyme or receptor. These drugs are often chiral, and the two enantiomers may differ greatly in efficacy. ...
Download Pdf Article
... properties of LDHs opens interesting perspectives to use them for targeted drug delivery [9]. Cefotaxime is a third generation cephalosporin antibiotic; despite its high biological activity cefotaxime is less stable then the other cephalosporin derivates in aqueous solutions due to its photodegradat ...
... properties of LDHs opens interesting perspectives to use them for targeted drug delivery [9]. Cefotaxime is a third generation cephalosporin antibiotic; despite its high biological activity cefotaxime is less stable then the other cephalosporin derivates in aqueous solutions due to its photodegradat ...
Influence of Alcohol and Smoking on Drug Action
... respectively. The plasma levels of phenacetin after its oral administration are much lower in smokers when compared to non-smokers probably due to the increased presystemic gastrointestinal or hepatic metabolism. The half-life of alprazolam was also found to be reduced by 35% in smokers. The AUC of ...
... respectively. The plasma levels of phenacetin after its oral administration are much lower in smokers when compared to non-smokers probably due to the increased presystemic gastrointestinal or hepatic metabolism. The half-life of alprazolam was also found to be reduced by 35% in smokers. The AUC of ...
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.