STUDY OF EFFECTS OF POSTCOMPRESSION CURING ON KOLLIDON SR BASED FLOATING TABLETS
... curing at temperature above Tg significantly improved film formation which could reduce the permeability of the film and avoid accelerated and irreproducible dissolution results.13 KSR which contains 80 % of polyvinylacetate (PVAc) polymer is amorphous in nature and has got unus ...
... curing at temperature above Tg significantly improved film formation which could reduce the permeability of the film and avoid accelerated and irreproducible dissolution results.13 KSR which contains 80 % of polyvinylacetate (PVAc) polymer is amorphous in nature and has got unus ...
Basics Pharmacology Review - Dr. Roland Halil
... Pharmacist, Bruyere Academic FHT Assistant Professor, Dept Family Medicine, U of Ottawa March 2015 ...
... Pharmacist, Bruyere Academic FHT Assistant Professor, Dept Family Medicine, U of Ottawa March 2015 ...
mRNA Transcript Diversity Creates New Opportunities for
... Article, publication date, and citation information can be found at http://molpharm.aspetjournals.org. http://dx.doi.org/10.1124/mol.111.076604. ...
... Article, publication date, and citation information can be found at http://molpharm.aspetjournals.org. http://dx.doi.org/10.1124/mol.111.076604. ...
Abbreviations and Symbols for Chemical Names of Special Interest
... are built up from these units. The standardization of treatment will involve certain unimportant changes in the (as yet partly developed) systems for individual groups. This standardization is desirable for two reasons. a) The work of authors, editors, and readers is made simpler if the same princip ...
... are built up from these units. The standardization of treatment will involve certain unimportant changes in the (as yet partly developed) systems for individual groups. This standardization is desirable for two reasons. a) The work of authors, editors, and readers is made simpler if the same princip ...
SUPERGEN INC (Form: DEFA14A, Received: 04/12
... The following contains the presentation slides of the Investor and Analyst presentation by SuperGen, Inc. (“SuperGen” or the “Company”) and Astex Therapeutics Ltd. (“Astex”) on April 12, 2011, relating to the proposed acquisition of Astex by SuperGen pursuant to the terms of an Implementation Agreem ...
... The following contains the presentation slides of the Investor and Analyst presentation by SuperGen, Inc. (“SuperGen” or the “Company”) and Astex Therapeutics Ltd. (“Astex”) on April 12, 2011, relating to the proposed acquisition of Astex by SuperGen pursuant to the terms of an Implementation Agreem ...
PREPARATION AND UTILITY OF SUB-MICRON LACTOSE, A
... For many years lactose has been widely utilised as an excipient in Dry Powder Inhalers to improve both the dosing consistency and the drug respirability from the device(1). In MDIs, the requirements for dosing consistency and respirability are still paramount, however the use of bulking agents in th ...
... For many years lactose has been widely utilised as an excipient in Dry Powder Inhalers to improve both the dosing consistency and the drug respirability from the device(1). In MDIs, the requirements for dosing consistency and respirability are still paramount, however the use of bulking agents in th ...
Protein Binding Drug-Drug Interaction between Warfarin and
... The both compounds warfarin and tizoxanide bind predominantly to albumins and, most probably, competed for the same binding site of the protein. Albumins have two main drug binding sites characterized as Sudlow site I and Sudlow site II [8]. These sites bind drugs selectively. Warfarin primarily bin ...
... The both compounds warfarin and tizoxanide bind predominantly to albumins and, most probably, competed for the same binding site of the protein. Albumins have two main drug binding sites characterized as Sudlow site I and Sudlow site II [8]. These sites bind drugs selectively. Warfarin primarily bin ...
Juillerat et al, (2013) Nanotest paper online early
... chemotherapeutic NPs are presently under pre-clinical development, in clinical use, or under advanced clinical trials (Juillerat-Jeanneret, 2006; Schütz et al., 2013a; Schütz et al., 2013b) (Table 1). After drug delivery, the most represented area of application is diagnostic imaging, including in m ...
... chemotherapeutic NPs are presently under pre-clinical development, in clinical use, or under advanced clinical trials (Juillerat-Jeanneret, 2006; Schütz et al., 2013a; Schütz et al., 2013b) (Table 1). After drug delivery, the most represented area of application is diagnostic imaging, including in m ...
process development and optimization for moisture activated dry
... typically have a size range between 0.2 and 4.0 mm, depending on their subsequent use.2 Granulation method can be broadly classified into two types: Wet granulation and Dry granulation. Wet granulation technique is receiving great significance, because direct compression method is not most suitable ...
... typically have a size range between 0.2 and 4.0 mm, depending on their subsequent use.2 Granulation method can be broadly classified into two types: Wet granulation and Dry granulation. Wet granulation technique is receiving great significance, because direct compression method is not most suitable ...
CHOICE BASED CREDIT SYSTEM B. Sc. WITH CHEMISTRY
... 1. Estimation of sodium carbonate and sodium hydrogen carbonate present in a mixture. 2. Estimation of oxalic acid by titrating it with KMnO4. 3. Estimation of water of crystallization in Mohr’s salt by titrating with KMnO4. 4. Estimation of Fe (II) ions by titrating it with K2Cr2O7 using internal i ...
... 1. Estimation of sodium carbonate and sodium hydrogen carbonate present in a mixture. 2. Estimation of oxalic acid by titrating it with KMnO4. 3. Estimation of water of crystallization in Mohr’s salt by titrating with KMnO4. 4. Estimation of Fe (II) ions by titrating it with K2Cr2O7 using internal i ...
Influence of CYP2D6 genotype on the
... of functional activity of CYP2D6 may lead to an impaired metabolism of many drugs, such as VEN, resulting in high plasma drug concentrations, lack of therapeutic response and/or an increased risk for side-effects. Another risk group is individuals who have a substantially increased metabolism, e.g. ...
... of functional activity of CYP2D6 may lead to an impaired metabolism of many drugs, such as VEN, resulting in high plasma drug concentrations, lack of therapeutic response and/or an increased risk for side-effects. Another risk group is individuals who have a substantially increased metabolism, e.g. ...
Preventing Occupational Exposure to Antineoplastic and Other
... The area of new drug development is rapidly evolving as unique approaches are being taken to treat cancer and other serious diseases. Defining Hazardous Drugs Hazardous drugs include those used for cancer chemotherapy, antiviral drugs, hormones, some bioengineered drugs, and other miscellaneous drug ...
... The area of new drug development is rapidly evolving as unique approaches are being taken to treat cancer and other serious diseases. Defining Hazardous Drugs Hazardous drugs include those used for cancer chemotherapy, antiviral drugs, hormones, some bioengineered drugs, and other miscellaneous drug ...
Orphan_Drugs_RTF
... The US Orphan Drug Act of 1983 pioneered the regulation of this type of medicines, and its success encouraged other countries to enact similar legislation. Among these new orphan drug laws is the one that was drafted in the European Union in 2000. This paper attempts to scrutinize some of the key po ...
... The US Orphan Drug Act of 1983 pioneered the regulation of this type of medicines, and its success encouraged other countries to enact similar legislation. Among these new orphan drug laws is the one that was drafted in the European Union in 2000. This paper attempts to scrutinize some of the key po ...
Compliance, Validation, and Related Processes
... • The use of healthy volunteers to document the rate of absorption and excretion from the body of a compound's active ingredients. • Companies conduct bioavailability studies both at the beginning of human testing and just prior to marketing to show that the formulation used to demonstrate safety an ...
... • The use of healthy volunteers to document the rate of absorption and excretion from the body of a compound's active ingredients. • Companies conduct bioavailability studies both at the beginning of human testing and just prior to marketing to show that the formulation used to demonstrate safety an ...
Relationship between objective responses in phase I trials and
... Background: Although the evaluation of new investigational drugs in phase I, II and III trials requires considerable time and patient resources, only a few of these drugs are ultimately established as anticancer drugs. Materials and methods: We collected papers of phase I trials by a Medline search ...
... Background: Although the evaluation of new investigational drugs in phase I, II and III trials requires considerable time and patient resources, only a few of these drugs are ultimately established as anticancer drugs. Materials and methods: We collected papers of phase I trials by a Medline search ...
Diamondoid Molecules - University of Illinois at Chicago
... number of six-member carbon rings fused together (see Figure 1). More explicitly, they consist of repeating units of ten carbon atoms forming a tetra-cyclic cage system [1-3]. They are called "diamondoid" because their carbon-carbon framework constitutes the fundamental repeating unit in the diamond ...
... number of six-member carbon rings fused together (see Figure 1). More explicitly, they consist of repeating units of ten carbon atoms forming a tetra-cyclic cage system [1-3]. They are called "diamondoid" because their carbon-carbon framework constitutes the fundamental repeating unit in the diamond ...
1158-1161 Lovelyn Joseph 317 - International Journal of Bioassays
... electroshock seizure model in mice. Phytochemical profile of Valeriana wallichii suggests many active constituents with more than one possible mechanism of action. The interaction could be pharmacokinetic or pharmacodynamic. Large scale studies at various dose ratios and with more parameters includi ...
... electroshock seizure model in mice. Phytochemical profile of Valeriana wallichii suggests many active constituents with more than one possible mechanism of action. The interaction could be pharmacokinetic or pharmacodynamic. Large scale studies at various dose ratios and with more parameters includi ...
STABILITY INDICATING HPLC METHOD FOR SIMULTANEOUS DETERMINATION OF DROTAVERINE AND ACECLOFENAC Research Article
... Forced degradation studies were conducted separately and for the combination for DRO and ACE at a concentration of 80 µg/ml and 100 µg/ml respectively. Then the study was extended for the formulation. Forced degradation with acidic media was performed by heatin ...
... Forced degradation studies were conducted separately and for the combination for DRO and ACE at a concentration of 80 µg/ml and 100 µg/ml respectively. Then the study was extended for the formulation. Forced degradation with acidic media was performed by heatin ...
(RICiFa 2014), 18th and 19th September 2014, Córdoba (Argentine
... in the palliative setting. It is also especially appropriate where prolonged drug exposure is desirable. At present, many current anti-cancer therapies are cytostatic in nature and thus are optimally effective when given chronically for a continuous tumour exposure. However, this mechanism of action ...
... in the palliative setting. It is also especially appropriate where prolonged drug exposure is desirable. At present, many current anti-cancer therapies are cytostatic in nature and thus are optimally effective when given chronically for a continuous tumour exposure. However, this mechanism of action ...
Transdermal Fentanyl
... micro abrasions which may affect drug absorption. If site needs to be washed, do so with clear water; soaps, lotions, alcohols and other agents can also affect drug absorption. • With the recent addition of a 12.5mcg patch, use in pediatrics may increase. It is approved for use over the age of 2 ...
... micro abrasions which may affect drug absorption. If site needs to be washed, do so with clear water; soaps, lotions, alcohols and other agents can also affect drug absorption. • With the recent addition of a 12.5mcg patch, use in pediatrics may increase. It is approved for use over the age of 2 ...
PHYSICOCHEMICAL PROPERTIES OF HESPERIDIN NANOCRYSTAL Research Article RACHMAT MAULUDIN
... Fig. 1: Chemical structure of hesperidin A lot of new pharmaceutical development substance is poor solubility in aqueous environment [3-5]. In the most case, it is associated to physicochemical problem such as slowly dissolution rate and very low solubility. In recently decade, particle size reducti ...
... Fig. 1: Chemical structure of hesperidin A lot of new pharmaceutical development substance is poor solubility in aqueous environment [3-5]. In the most case, it is associated to physicochemical problem such as slowly dissolution rate and very low solubility. In recently decade, particle size reducti ...
Therapeutic applications of ricin and some alkaloids
... with Hodgkin’s disease. To establish the efficacy of such immunotoxins the most conventional method documented is by treating nude mice bearing engrafts of human tumors. The disadvantage of this system is that those tumors do not metastasize and hence only reduction in local tumor size can be measur ...
... with Hodgkin’s disease. To establish the efficacy of such immunotoxins the most conventional method documented is by treating nude mice bearing engrafts of human tumors. The disadvantage of this system is that those tumors do not metastasize and hence only reduction in local tumor size can be measur ...
CHAPTER 17
... (a) “Anteroom” means an area where personnel perform hand hygiene and garbing procedures, staging of components, order entry, CSP labeling, and other high-particulate generating activities. It is also a transition area that provides assurance that pressure relationships are constantly maintained so ...
... (a) “Anteroom” means an area where personnel perform hand hygiene and garbing procedures, staging of components, order entry, CSP labeling, and other high-particulate generating activities. It is also a transition area that provides assurance that pressure relationships are constantly maintained so ...
Applications of nanoparticles in Chemistry
... cross-resistance to structurally unrelated drugs, emphasize the need for a new therapeutic targets. Raising the immunocompetence of individuals in malaria endemic areas by vaccination could significantly lower the death tolls due to clinically severe malaria. A viable malaria vaccine could be regard ...
... cross-resistance to structurally unrelated drugs, emphasize the need for a new therapeutic targets. Raising the immunocompetence of individuals in malaria endemic areas by vaccination could significantly lower the death tolls due to clinically severe malaria. A viable malaria vaccine could be regard ...
study
... test organisms as a check on the effect of media and inherent sensitivity of isolates on zones of inhibition produced by the antibacterial substances. The fungal isolate (Candida albicans) was treated in a slightly different manner. It was first grown on Sabouraud Dextrose broth (oxoid cm 41) and as ...
... test organisms as a check on the effect of media and inherent sensitivity of isolates on zones of inhibition produced by the antibacterial substances. The fungal isolate (Candida albicans) was treated in a slightly different manner. It was first grown on Sabouraud Dextrose broth (oxoid cm 41) and as ...
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.