Transcription of Developing methods to compare tablet …
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*Correspondence: M. A. Oliveira. Centro Universit rio Norte do Esp rito Santo, Universidade Federal Espirito Santo. Rodovia BR 101 Norte, km 60, 29932-540 - S o Mateus - ES, Brasil. E-mail: Journal of Pharmaceutical Sciencesvol. 48, n. 4, , 2012 Developing methods to compare tablet formulations of atorvastatinMarcelo Antonio de Oliveira*, Caroline Dutra Lacerda, Andr Faz lo BonellaUniversity Center of the North of Espirito Santo, Federal University of Espirito SantoAtorvastatin (ATV) is an antilipemic drug of great interest to the pharmaceutical industry. ATV does not appear in the monographs of Brazilian pharmacopoeia, and analytical methodologies for its determination have been validated. The chromatographic conditions used included: RP-18 column-octadecylsilane (250 x mm, 5 mm), detection at 238 nm, mobile phase containing phosphoric acid and acetonitrile (35:65% v/v), flow at mL min-1, oven temperature at 30oC, and injection volume of 10 mL.
Developing methods to compare tablet formulations of atorvastatin 803 mization of pharmaceutical formulations, to monitor manufacturing processes, to minimize the risk of a …
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Physicochemical Properties of Various, Dissolution, Intrinsic dissolution rate, Paper on the dissolution specification, Dispersions as a formulation strategy, Dispersions as a formulation strategy for poorly soluble, Dissolution Testing for Poorly Soluble, Dissolution Testing for Poorly Soluble Drugs: A Continuing Perspective, Relationships between Lipophilicity and Solubility, Chapter 2 - WATER QUALITY, World Health, Transport and Fate of Contaminants in the, Transport and Fate of Contaminants in the Subsurface