Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14169
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dc.contributor.authorRukthong P.
dc.contributor.authorSangvanich P.
dc.contributor.authorKitchaiya S.
dc.contributor.authorJantratid E.
dc.contributor.authorSathirakul K.
dc.date.accessioned2021-04-05T03:33:25Z-
dc.date.available2021-04-05T03:33:25Z-
dc.date.issued2013
dc.identifier.issn1253395
dc.identifier.other2-s2.0-84874720510
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14169-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84874720510&partnerID=40&md5=f6a4d43745eaa95f179842315162cda0
dc.description.abstractDetermination of atorvastatin in human plasma using LC-MS/MS has been widely accepted as an effective method owing to its practical applicability in routine drug analysis in pharmacokinetic and pharmacogenetic study. Nevertheless, the method sensitivity can be compromised when limited sample volume is available. This problem is typically encountered in pharmacokinetics studies for which only a small volume of plasma sample can be obtained. Drug extraction from human plasma was performed with the aid of reversed-phase C18 solid phase micro-extraction. The detection was accomplished by LC-MS/MS. The need of plasma volume of less than 250 μl for each sample made it possible to decrease the sample preparation time. The method was successfully validated and proved appropriate for the analysis of atorvastatin in human plasma and can be applied to pharmacokinetics and pharmacogenetics study.
dc.titleThe quantitation of atorvastatin in human plasma by solid phase micro-extraction followed by LC-MS/MS and its application to pharmacokinetics study
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationSongklanakarin Journal of Science and Technology. Vol 35, No.1 (2013), p.41-50
Appears in Collections:Scopus 1983-2021

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