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dc.contributor.authorTunçel, Muzaffer
dc.contributor.authorAk, Dilek
dc.contributor.authorYeniceli, Duygu
dc.contributor.authorUslu, B.
dc.contributor.authorDoğan, B.
dc.date.accessioned2019-10-19T14:02:44Z
dc.date.available2019-10-19T14:02:44Z
dc.date.issued2006
dc.identifier.issn0009-5893
dc.identifier.issn1612-1112
dc.identifier.urihttps://dx.doi.org/10.1365/s10337-006-0775-0
dc.identifier.urihttps://hdl.handle.net/11421/12365
dc.descriptionWOS: 000237841500017en_US
dc.description.abstractA capillary electrophoretic method was described for the determination of droperidol in pharmaceutical tablets and human serum. Droperidol and internal standard, lansoprazole, were separated on an uncoated fused-silica capillary using a run buffer containing borate (10 mM; pH 9.3) and aqueous methanol (20%, v/v). The signals were detected at 210 nm. The migration times for droperidol and internal standard were 2.1 and 2.9 min, respectively. The method has been validated in the range of 2.2 x 10(-5) - 7.8 x 10(-5) M and applied to both tablets and human serum with good repeatability and no interference.en_US
dc.language.isoengen_US
dc.publisherSpringer Heidelbergen_US
dc.relation.isversionof10.1365/s10337-006-0775-0en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCapillary Electrophoresisen_US
dc.subjectHuman Serumen_US
dc.subjectDroperidolen_US
dc.titleCE determination of droperidol in tablets and human serumen_US
dc.typearticleen_US
dc.relation.journalChromatographiaen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesi, Analitik Kimya Anabilim Dalıen_US
dc.identifier.volume63en_US
dc.identifier.issue9.Ekien_US
dc.identifier.startpage507en_US
dc.identifier.endpage511en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorTunçel, Muzaffer
dc.contributor.institutionauthorAk, Dilek


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