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dc.contributor.authorSoltani, S
dc.contributor.authorRamezani, AM
dc.contributor.authorSoltani, N
dc.contributor.authorJouyban, A
dc.date.accessioned2018-08-26T08:04:12Z
dc.date.available2018-08-26T08:04:12Z
dc.date.issued2012
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/49493
dc.description.abstractBackground: A simple, precise and sensitive HPLC method has been developed for simultaneous determination of carvedilol and losartan in human plasma and urine samples. The analytes were extracted by a dispersive liquid-liquid microextraction method. A mobile phase of 15 mM sodium dihydrogen phosphate buffer (pH 4.0)/acetonitrile/2-propanol (70/27.5/2.5, v/v/v) was used to separate the drugs using a Waters (R) ODS column (250 X 4.6 mm) and detected by a UV detector at 222 nm. Results: The developed method is selective for studied drugs possessing a linearity range of 0.1-1.0 and 0.05-0.75 mu g/ml, respectively, for losartan and carvedilol with precision <15%. The accuracy is better than 15% and the mean recovery of carvedilol and losartan was 98.9 and 100.2% for plasma and 100.7 and 100.5% for urine samples, respectively. Conclusion: The developed method is applicable for therapeutic drug monitoring and PK analyses.
dc.language.isoEnglish
dc.relation.ispartofBIOANALYSIS
dc.titleAnalysis of losartan and carvedilol in urine and plasma samples using a dispersive liquid-liquid microextraction isocratic HPLC-UV method
dc.typeArticle
dc.citation.volume4
dc.citation.issue23
dc.citation.spage2805
dc.citation.epage2821
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.4155/BIO.12.261


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