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dc.contributor.authorBajerski, Lisianept_BR
dc.contributor.authorPaim, Clésio Soldatelipt_BR
dc.contributor.authorPereira, Andréa Garciapt_BR
dc.contributor.authorDias, Carolina Lupipt_BR
dc.contributor.authorRossi, Rochele Cassantapt_BR
dc.contributor.authorTodeschini, Vítorpt_BR
dc.contributor.authorSteppe, Martinpt_BR
dc.contributor.authorBergold, Ana Mariapt_BR
dc.contributor.authorFroehlich, Pedro Eduardopt_BR
dc.date.accessioned2013-07-03T01:43:53Zpt_BR
dc.date.issued2013pt_BR
dc.identifier.issn0100-4042pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/73025pt_BR
dc.description.abstractA stability-indicating method using MEKC was validated for the analysis of olmesartan medoxomil in tablets. Successful separation was achieved using a fused silica capillary (40 cm x 50 μm i.d.); background electrolyte consisted of a combination of 10 mmol L-1 borate buffer and 5 mmol L-1 anionic detergent sodium dodecyl sulfate (95:5; v/v) pH 6.5; hydrodynamic mode at 50 mBar for 5 s; 25 kV separation voltage at 25 ºC; and column temperature 25 ºC with detection at 257 nm. The proposed method, validated following ICH guidelines, was applied to the determination of this antihypertensive with good results compared with an LC method.en
dc.format.mimetypeapplication/pdf
dc.language.isoengpt_BR
dc.relation.ispartofQuímica nova. São Paulo: Sociedade Brasileira de Química, 1978-. Vol. 36, n. 1, (2013), p. 34-39pt_BR
dc.rightsOpen Accessen
dc.subjectOlmesartan medoxomilen
dc.subjectCromatografia capilar eletrocinética micelarpt_BR
dc.subjectMEKCen
dc.subjectCromatografia liquidapt_BR
dc.subjectOlmesartana medoxomilapt_BR
dc.subjectLCen
dc.titleStability-indicating comparative methods using mekc and lc for determination of olmesartan medoxomilpt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb000881771pt_BR
dc.type.originNacionalpt_BR


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