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dc.contributor.authorTalar, R
dc.contributor.authorArshosaz, J
dc.contributor.authorMostafavi, A
dc.contributor.authorNokhodchi, A
dc.date.accessioned2018-08-26T08:08:17Z
dc.date.available2018-08-26T08:08:17Z
dc.date.issued2011
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/50309
dc.description.abstractA sensitive, simple and accurate reverse phase HPLC method was developed to determine plasma levels of gliclazide (GL) in rat. The method uses liquid-liquid extraction that is not expensive and ibuprofen as internal standard, that is easily available. Mean recovery for GL and internal standard was 80% and 82% respectively. Relative standard errors and CV% ranged from 0.47 to 8.99 and from 0.72 to 12.54% for intraday and interday HPLC injections, respectively. The limit of quantitation (LOQ) and the limit of detection (LOD) for GL in serum were 0.12 mu g/mL and 0.06 mu g/mL respectively. The developed HPLC method is a suitable and rapid method to be adopted for pharmacokinetic studies in rat and human.
dc.language.isoEnglish
dc.relation.ispartofFARMACIA
dc.subjectreverse-phase HPLC
dc.subjectgliclazide
dc.subjectpharmacokinetics
dc.subjectrat
dc.titleDEVELOPMENT AND VALIDATION OF A NOVEL RP-HPLC METHOD FOR PHARMACOKINETIC STUDIES OF GLICLAZIDE IN RAT
dc.typeArticle
dc.citation.volume59
dc.citation.issue3
dc.citation.spage388
dc.citation.epage395
dc.citation.indexWeb of science


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