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Cocaine - Computer Science
Cocaine - Computer Science

... model keeps the false positive rate to 0.87/day in the lab, even though 10+ candidate windows (due to significant physical activity) are found during 9+ hours/day of sensor wearing in the lab. On 922 days of the field data, we find 27 episodes of cocaine use with good quality sensor data from 13 par ...
PREPARATION AND CHARACTERIZATION OF LORNOXICAM LOADED SOLID LIPID
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... physiochemical characteristics and stability of drug-loaded SLNs depend on the properties of drug and ingredients [2]. Suitable choice of lipids, surfactants, and their composition affect the particle size, entrapment efficiency, zeta potential, stability during storage, and release behavior [3]. Lo ...
physiological and pharmacological effect of somina
physiological and pharmacological effect of somina

... by 46% and 20% respectively than their control (Fig. 3a & 3b). On the other hand the use of Ach and Somina on Atr pre-treatment heart did not show such decline in heart rate as shown earlier without Atropine pre-treatment. It means that Atr has occupied the cholinergic receptor and Somina and Ach ha ...
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... Aprotinin is freely soluble in water (5 mg/ml) and in ...
MATRICARIA EXTRACT IN MICE RECUTITA
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... relaxant effects at doses similar to those used for classical benzodiazepines[24,25]. Meanwhile, others revealed that flavonoid as quercetin has neuroprotective effect against electrical kindling in rats [26]. Based on these observations it is possible that the anticonvulsant effect of Matricaria re ...
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... GlobalData’s pharmaceuticals report, “Zicronapine – Analysis and Forecasts from 2014 to 2020” provides Zicronapine sales estimates for US and EU5. In addition, it covers detailed clinical assessment of the drug, factors impacting drug sales, competitive landscape, and analysis of sales performance d ...
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... prepared by the injection method. MLVs have the size ranging from 400 nanometers to 3.5 ...
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... the diphenyl ether derivatives as InhA inhibitors [35]. The analog 5-octyl-2-phenoxyphenol (8PP) showed the best activity with Ki and IC50 values of 1.1 and 5 nM, respectively. As the alkyl substituent is lengthened from two to eight carbons, a corresponding decrease in IC50 values is observed. Howe ...
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kashaya and ksheerpaka - International Journal of Pharmacy and
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... uses. The medicinal value of the plant is mainly due to the active metabolites and is generally used in the form of an extract where the active constituents are concentrated. This helps to reduce dose of drug, potentiates action and facilitates palatability. Extraction involves separation of medicin ...
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Linköping University Post Print Transdermal iontophoresis as an in-vivo
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... various ways (Figure 5). Some investigators have used the absolute increase in perfusion, with or without subtraction of baseline perfusion values. Others have expressed the responses as change with respect to baseline. Besides maximum responses (Abou-Elenin et al., 2002; Newton et al., 2001), the p ...
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... feed addictive, etc. shall be governed by the relevant laws and regulations. However, the environmental management of the activities related to new chemical substances used as raw materials and intermediates of the aforesaid products shall be governed by these Measures. ...
Cytisine, the world`s oldest smoking cessation aid
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... in eastern and central Europe to help people quit smoking. An alkaloid with high affinity for the α4β2 nicotinic acetylcholine receptor subtype, cytisine is derived from the plant Cytisus laburnum. It was discovered in 1818, first isolated in 1865,1 and its actions were documented as “qualitatively ...
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... The Chemical Equation and the Information It Conveys In a chemical equation, the identity of reactants and products must be specified. Reactants are written to the left of the reaction arrow () and products to the right. The physical states of reactants and products are shown in parentheses. The sy ...
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... studies on adverse health effects of environmental contaminants have focused mainly on agricultural or industrial pesticides [2], heavy metals [3], and toxic industrial wastes and residues [2]. One large class of chemicals that has received little attention in this context comprises residues of phar ...
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... when the nerve terminal is activated. Therefore, drugs that target membrane ion channels to influence release of classic neurotransmitters, e.g., bretylium, will also influence neuropeptide release as well. D. Binding of neurotransmitter – peptide neurotransmitters travel much farther distances to r ...
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ISOLATION AND IDENTIFICATION OF NAPHTHOQUINONES EUCLEA NATALENSIS WITH ACTIVITY AGAINST

... suggests that the number of new cases world-wide will rise from the current 7 million a year to 10 million by 2015. It is estimated that between 2000 and 2020, nearly I-billion more people will be newly infected, 200-million people will get sick and 70 million will die from TB if control of the dise ...
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... in pregnant women may be acceptable despite the risk (e.g., if the drug is needed in a life-threatening situation or for a serious disease for which safer drugs cannot be used or are ineffective). ...
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B. Braun Needles, Syringes and Accessories

... Introducing B. Braun’s full line of needles and syringes—a unique value that gives you the confidence of using world-leading products at more sensible prices that save your organization money. B. Braun’s heritage of expertise and innovation means you can trust B. Braun’s needles and syringes to be o ...
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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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