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HPLC method for simultaneous determination of cefprozil diastereomers in human plasma

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dc.contributor.authorTae-Hwan Park-
dc.contributor.authorJin-Ki Kim-
dc.contributor.authorJun-Pil Jee-
dc.contributor.authorJeong-Sook Park-
dc.contributor.authorChong-Kook Kim-
dc.date.accessioned2021-06-24T00:39:16Z-
dc.date.available2021-06-24T00:39:16Z-
dc.date.created2021-01-21-
dc.date.issued2004-09-
dc.identifier.issn0731-7085-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/46557-
dc.description.abstractA high-performance liquid chromatography method was developed for the determination of cefprozil diastereomers in human plasma. Cefprozil exists as cis and trans isomer at the ratio of 90:10. Plasma samples were prepared by protein precipitation using acetonitrile, trichloroacetic acid and methylene chloride. After the mixtures were vortexed and centrifuged, the aqueous supernatant was injected into a reversed-phase C-8 column. The mobile phase consisted of acetonitrile, glacial acetic acid and distilled water at the volume ratio of 5.5:1.75:92.75 (pH 2.7). The signals were monitored with UV detection at 280 nm. The calibration curves of cis and trans isomer were linear in concentration ranges of 0.1-25 and 0.02-2.5 mug/mL with the correlation coefficient of 0.9999 and 0.9989, respectively. After oral administration of cefprozil in humans, C-max and T-max of total cefprozil were 18.80 +/- 2.14 mug/mL and 2.06 +/- 0.62 h. This method was sensitive with excellent selectivity and reproducibility, and successfully applied to a bioavailability study of cefprozil in healthy subjects. (C) 2004 Elsevier B.V. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE BV-
dc.titleHPLC method for simultaneous determination of cefprozil diastereomers in human plasma-
dc.typeArticle-
dc.contributor.affiliatedAuthorJin-Ki Kim-
dc.identifier.doi10.1016/j.jpba.2004.06.001-
dc.identifier.scopusid2-s2.0-4444302855-
dc.identifier.wosid000224328000033-
dc.identifier.bibliographicCitationJOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, v.36, no.1, pp.243 - 248-
dc.relation.isPartOfJOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS-
dc.citation.titleJOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS-
dc.citation.volume36-
dc.citation.number1-
dc.citation.startPage243-
dc.citation.endPage248-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusORAL CEPHALOSPORIN-
dc.subject.keywordPlusINVITRO ACTIVITY-
dc.subject.keywordPlusBMY-28100-
dc.subject.keywordPlusCEFACLOR-
dc.subject.keywordPlusPHARMACOKINETICS-
dc.subject.keywordAuthorcefprozil-
dc.subject.keywordAuthorstereoisomer-
dc.subject.keywordAuthorcis-
dc.subject.keywordAuthortrans-
dc.subject.keywordAuthorHPLC-
dc.subject.keywordAuthorpharmacokinetic studies in human-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0731708504002523?via%3Dihub-
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