DEVELOPMENT AND VALIDATION OF A NOVEL RP-HPLC METHOD FOR PHARMACOKINETIC STUDIES OF GLICLAZIDE IN RAT
dc.contributor.author | Talar, R | |
dc.contributor.author | Arshosaz, J | |
dc.contributor.author | Mostafavi, A | |
dc.contributor.author | Nokhodchi, A | |
dc.date.accessioned | 2018-08-26T08:08:17Z | |
dc.date.available | 2018-08-26T08:08:17Z | |
dc.date.issued | 2011 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/50309 | |
dc.description.abstract | A 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.iso | English | |
dc.relation.ispartof | FARMACIA | |
dc.subject | reverse-phase HPLC | |
dc.subject | gliclazide | |
dc.subject | pharmacokinetics | |
dc.subject | rat | |
dc.title | DEVELOPMENT AND VALIDATION OF A NOVEL RP-HPLC METHOD FOR PHARMACOKINETIC STUDIES OF GLICLAZIDE IN RAT | |
dc.type | Article | |
dc.citation.volume | 59 | |
dc.citation.issue | 3 | |
dc.citation.spage | 388 | |
dc.citation.epage | 395 | |
dc.citation.index | Web of science |
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