dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorCorrêa, Josilene Chaves Ruela
dc.creatorSoares, Cristina Duarte Vianna
dc.creatorSalgado, Hérida Regina Nunes
dc.date2016-01-28T16:56:28Z
dc.date2016-10-25T21:28:48Z
dc.date2016-01-28T16:56:28Z
dc.date2016-10-25T21:28:48Z
dc.date2012
dc.date.accessioned2017-04-06T09:50:06Z
dc.date.available2017-04-06T09:50:06Z
dc.identifierChromatography Research International, v. 2012, p. 1-8, 2012.
dc.identifier2090-3510
dc.identifierhttp://hdl.handle.net/11449/133751
dc.identifierhttp://acervodigital.unesp.br/handle/11449/133751
dc.identifierISSN2090-3510-2012-2012-01-08.pdf
dc.identifier9881720291571774
dc.identifier6036218587648028
dc.identifierhttp://dx.doi.org/10.1155/2012/610427
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/944280
dc.descriptionThe purpose of this study is to develop and validate a dissolution test for fluconazole, an antifungal used for the treatment of superficial, cutaneous, and cutaneomucous infections caused by Candida species, in capsules dosage form. Techniques by HPLC and UV first derivative spectrophotometry (UV-FDS) were selected for quantitative evaluation. In the development of release profile, several conditions were evaluated. Dissolution test parameters were considered appropriate when a most discriminative release profile for fluconazole capsules was yielded. Dissolution test conditions for fluconazole capsules were 900 mL of HCl 0.1 M, 37 ± 0.5 °C using baskets with 50 rpm for 30 min of test. The developed HPLC and UV-FDS methods for the antifungal evaluation were selective and met requirements for an appropriate and validated method, according to ICH and USP requirements. Both methods can be useful in the registration process of new drugs or their renewal. For routine analysis application cost, simplicity, equipment, solvents, speed, and application to large or small workloads should be observed.
dc.languageeng
dc.relationChromatography Research International
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleDevelopment and validation of dissolution test for fluconazole capsules by HPLC and derivative UV spectrophotometry
dc.typeOtro


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