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Soft Capsules: A Versatile Drug Delivery System
Soft Capsules: A Versatile Drug Delivery System

... properties of the “vehicle”, allowing for enhanced solubilization of the second species • Optimum solubility and improved stability is achieved at mole ratios in the region 0.5 - 0.7 • However, for gelatin shell softgels, basic vehicles (pHapp  7.6) can lead to time-dependent destabilization of the ...
Crime Bulletin No. 4: The illicit market for ADHD prescription drugs
Crime Bulletin No. 4: The illicit market for ADHD prescription drugs

... intravenous means. The user may vary the administration from oral to snorting to intravenous injection in order to intensify the effects of the drug. Parran and Jasinski (1991) estimated the mean daily methylphenidate dose during a binge session to be 200 mg. Oral consumption is not the preferred me ...
2 The Nature of Matter
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... interactions between different forms of matter. They include a chemical’s stability, its reactivity with other chemicals, its toxicity, and its flammability. Most physical properties describe relationships or interactions between matter and energy. A material’s electrical properties, magnetic proper ...
Relationship between the Serotonergic Activity and Reinforcing
Relationship between the Serotonergic Activity and Reinforcing

... Vanover et al., 1992; Howell and Byrd, 1995). Among amphetamine-like drugs that are not as selective for 5-HT activity, Ritz and Kuhar (1989) reported a negative correlation between potency as a reinforcer and binding affinity at the 5-HT transporter (SERT). The depletion of 5-HT by medial forebrain ...
Chapter 13 Spectroscopy
Chapter 13 Spectroscopy

... Both give us information about the number of chemically nonequivalent nuclei (nonequivalent hydrogens or nonequivalent carbons). Both give us information about the environment of the nuclei (hybridization state, attached atoms, etc.). It is convenient to use FT-NMR techniques for 1H; it is standard ...
Review the published MAY03-1-BIO manuscript.
Review the published MAY03-1-BIO manuscript.

... sulindac among familial adenomatous polyposis patients was reported over two decades ago (1), numerous cell culture, animal model, and human observational studies have shown consistent anticancer effects from several different NSAIDs (2). Although the mechanisms of action remain incompletely defined ...
Vitamins, Supplements and Medication Safety
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Thermogenesis in human skeletal muscle as
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Determination of ceftriaxone, ceftizoxime, paracetamol, and
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Chapter 7 – Chemical Formulas and Chemical
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Consumer Updates > Antibacterial Soap? You Can Skip It -
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... Many liquid soaps labeled antibacterial contain triclosan, an ingredient of concern to many environmental, academic and regulatory groups. Animal studies have shown that triclosan alters the way some hormones work in the body and raises potential concerns for the effects of use in humans. We don’t y ...
Formulation, Development and Evaluation of delayed release
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... Delayed release dosage forms1 are designed to release the drug at a time rather than promptly after administration. The delay may be time based or ...
Radiocontrast media and breastfeeding
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... “Although most package inserts for these products suggest that nursing mothers postpone breastfeeding their babies for 24 hours after use, research indicates that this is not necessary (Kubik-Huch 2000; Rofsky 1993; Nielson 1987; Fitz-John 1982). In Medications and Mothers' Milk (2002), Dr. Thomas H ...
International Journal of Pharmaceutical Science and Health Care
International Journal of Pharmaceutical Science and Health Care

... products during and after manufacturing and at various intervals during the shelf life of the product. [4] As such the need to ensure that the generic and branded drugs products are pharmaceutically equivalent cannot be overemphasized and the necessity to select one product from several generic drug ...
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CARBOXYMETHYL ETHERS OF LOCUST BEAN GUM­ A REVIEW    Review Article  PARAMITA DEY
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... Finely  powdered  Locust  bean  gum  and  sodium  bicarbonate  are  mixed  well  manually  in  a  pestle  mortar.  To  this  1%  v/v  of  ethanol  and solid monochloro‐acetic acid is added. The reaction was carried  out  at  ambient  or  elevated  temperature  (60,  80,  98°C)  for  2  hours  with  ...
Memorandum
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... were able to be marketed as a dietary supplement. We have significant concerns about the evidence on which you rely to support your conclusion that a dietary supplement containing AHYP will reasonably be expected to be safe. Your submission indicates that use of AHYP may result in adverse effects. Y ...
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full public report: ltd/1397

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KATHLEEN A. WAGNER, Plaintiff, v. Defendants
KATHLEEN A. WAGNER, Plaintiff, v. Defendants

... Wagner’s amended complaint alleges many different Wisconsin state law claims, including: varieties of negligence; strict products liability; misrepresentation; breach of warranty; consumer fraud; assault and battery; and infliction of emotional distress. The factual allegations underlying each of Wa ...
From Molecule to Dose Form – Accelerated Bioavailability
From Molecule to Dose Form – Accelerated Bioavailability

... drug in the surrounding bulk fluid low, e.g. by facilitating the subsequent drug transport away from its site of dissolution. On the other hand, the thickness of the liquid, unstirred boundary layer as well as the diffusion coefficient of the drug in this layer are generally very difficult to alter ...
STRESS DEGRADATION STUDIES AND DEVELOPMENT AND VALIDATION OF RP-HPLC
STRESS DEGRADATION STUDIES AND DEVELOPMENT AND VALIDATION OF RP-HPLC

... control of the final dosage form, the use of analytical technology covers an immense range of techniques and disciplines. Analytical methods are developed according to ICH guidelines. Forced degradation or accelerated degradation is a process whereby the natural degradation rate of a product or mate ...
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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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