dc.creatorSANTORO, Maria Ines Rocha Miritello
dc.creatorTSUBONE, Camila
dc.creatorGOMES, Fabio Pereira
dc.creatorKEDOR-HACKMANN, Erika Rosa Maria
dc.creatorGARCIA, Pedro Lopez
dc.date.accessioned2012-10-19T03:19:16Z
dc.date.accessioned2018-07-04T14:56:59Z
dc.date.available2012-10-19T03:19:16Z
dc.date.available2018-07-04T14:56:59Z
dc.date.created2012-10-19T03:19:16Z
dc.date.issued2008
dc.identifierANALYTICAL LETTERS, v.41, n.11, p.2044-2057, 2008
dc.identifier0003-2719
dc.identifierhttp://producao.usp.br/handle/BDPI/19901
dc.identifier10.1080/00032710802209342
dc.identifierhttp://dx.doi.org/10.1080/00032710802209342
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1616686
dc.description.abstractHigh performance liquid chromatographic (HPLC) and UV derivative spectrophotometric (UVDS) methods were developed and validated for the quantitative determination of sotalol hydrochloride in tablets. The HPLC method was performed on a C18 column with fluorescence detection. The excitation and emission wavelengths were 235 and 310nm, respectively. The mobile phase was composed of acetonitrile-water containing 0.1% trietylamine (7:93v/v) and pH adjusted to 4.6 with formic acid. The UVDS method was performed taking a signal at 239.1nm in the first derivative. The correlation coefficients (r) obtained were 0.9998 and 0.9997 for HPLC and UVDS methods, respectively. The proposed methods are simple and adaptable to routine analysis.
dc.languageeng
dc.publisherTAYLOR & FRANCIS INC
dc.relationAnalytical Letters
dc.rightsCopyright TAYLOR & FRANCIS INC
dc.rightsrestrictedAccess
dc.subjectbeta-blockers
dc.subjecthigh performance liquid chromatography
dc.subjectpharmaceutical formulations
dc.subjectsotalol hydrochloride
dc.subjectUV derivative spectrophotometry
dc.titleDevelopment and validation of high performance liquid chromatographic and UV-derivative spectrophotometric methods for the determination of sotalol hydrochloride in tablets
dc.typeArtículos de revistas


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