dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:24:54Z
dc.date.available2014-05-20T13:24:54Z
dc.date.created2014-05-20T13:24:54Z
dc.date.issued2009-06-01
dc.identifierChromatographia. Wiesbaden: Vieweg, v. 69, p. 207-211, 2009.
dc.identifier0009-5893
dc.identifierhttp://hdl.handle.net/11449/7849
dc.identifier10.1365/s10337-009-1015-1
dc.identifierWOS:000267330400016
dc.identifier9129780536724256
dc.description.abstractA reversed phase LC method was developed and validated to analyze the in vitro release of AZT from microemulsions. A mobile phase of acetonitrile:water (15:85) was used. The method validation showed good selectivity and linearity (r = 0.9993) for sample concentrations ranging from 0.6 to 100.0 mu g mL(-1). The RSD values (0.7-4.3%) and percentage recovery (88.1-109.8%) were within acceptable limits. The limit of detection (LOD) and limit of quantitation (LOQ) were found to be 0.012 and 0.041 mu g mL(-1). Quantitative analysis of the values obtained in the drug release assay indicates that the microemulsions used promote sustained release of AZT, which follows a Fickian diffusion mechanism.
dc.languageeng
dc.publisherVieweg
dc.relationChromatographia
dc.relation1.401
dc.relation0,514
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectColumn liquid chromatography
dc.subjectIn vitro drug release
dc.subjectDrug delivery system
dc.subjectZidovudine
dc.titleLC Evaluation of In Vitro Release of AZT from Microemulsions
dc.typeArtículos de revistas


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