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와파린의 HPLC 분석법 및 한국인에서의 약동학적 특징

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dc.contributor.author배정우-
dc.contributor.author김현경-
dc.contributor.author양상인-
dc.contributor.author김지홍-
dc.contributor.author김경혜-
dc.contributor.author장춘곤-
dc.contributor.author박영서-
dc.contributor.author손의동-
dc.contributor.author이석용-
dc.date.available2019-07-16T03:59:15Z-
dc.date.issued2005-
dc.identifier.issn0377-9556-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/28211-
dc.description.abstractWarfarin is a widely used oral anticoagulant agent used to treat thromboembolic disease. The purpose of this study was to develop the efficient assay method of warfarin sodium in human plasma and to assess the pharmacokinetic profile of the warfarin in healthy Korean volunteers. The pharmacokinetics of warfarin administered orally was evaluated after a dose of 10 mg. Warfarin in plasma was assayed using a specific HPLC method with UV absorbance at 304 nm. AUC was 46.33±9.95㎍/ml·hr, Cmax 1.22±0.22㎍/ml , Tmax 2.50±1.41 hr and half-life 43.49±4.33 hr. Tmax was slightly shorter than that in Caucasian (3~9 hr), whereas the half-life was longer than that in Caucasian (10~45 hr, mean: 36 hr). These results suggest that warfarin may have a longer duration in Korea than in Caucasian.-
dc.format.extent6-
dc.publisher대한약학회-
dc.title와파린의 HPLC 분석법 및 한국인에서의 약동학적 특징-
dc.title.alternativeHPLC Determination and Pharmacokinetic Profile of Warfarin in Korean Subjects-
dc.typeArticle-
dc.identifier.bibliographicCitation약 학 회 지, v.49, no.2, pp 134 - 139-
dc.identifier.kciidART001114903-
dc.description.isOpenAccessN-
dc.citation.endPage139-
dc.citation.number2-
dc.citation.startPage134-
dc.citation.title약 학 회 지-
dc.citation.volume49-
dc.publisher.location대한민국-
dc.subject.keywordAuthorwarfarin sodium-
dc.subject.keywordAuthorcoumadin tablets-
dc.subject.keywordAuthorHPLC-
dc.description.journalRegisteredClasskci-
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