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dc.contributor.authorMalesuik, Marcelo Donadelpt_BR
dc.contributor.authorPaim, Clésio Soldatelipt_BR
dc.contributor.authorSteppe, Martinpt_BR
dc.contributor.authorSchapoval, Elfrides Eva Schermanpt_BR
dc.date.accessioned2013-07-02T01:43:22Zpt_BR
dc.date.issued2010pt_BR
dc.identifier.issn0100-4042pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/72886pt_BR
dc.description.abstractA rapid, economical, reproducible, and simple direct spectrophotometric method was developed and validated for the assay of nitazoxanide in pharmaceutical formulations. Nitazoxanide concentration was estimated in water at 345 nm and pH 4.5. The method was suitable and validated for specificity, linearity, precision, and accuracy. There was no interference of the excipients in the determination of the active pharmaceutical ingredient. The proposed method was successfully applied in the determination of nitazoxanide in coated tablets and in powders for oral suspension. This method was compared to a previously developed and validated method for liquid chromatography to the same drug. There was no significative difference between these methods for nitazoxanide quantitation.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofQuímica nova. São Paulo. Vol. 33, n. 3 (2010), p. 739-742pt_BR
dc.rightsOpen Accessen
dc.subjectNitazoxanideen
dc.subjectNitazoxanidapt_BR
dc.subjectValidação : Métodos de análise de fármacospt_BR
dc.subjectUV-spectrophotometryen
dc.subjectMethod validationen
dc.titleDevelopment of a simple, rapid and validated spectrophotometric method for nitazoxanide in pharmaceutical formulations and comparison with hplcpt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb000753027pt_BR
dc.type.originNacionalpt_BR


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