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Determination of beraprost in human plasma by a high-performance liquid chromatography-tandem mass spectrometry

Authors
Lee, J.Kim, H.Jeong, J. C.Park, E. S.Hwang, K. W.Yang, S. J.Jeong, J. H.
Issue Date
Nov-2007
Publisher
ELSEVIER SCIENCE BV
Keywords
beraprost; prostacyclin; tandem mass spectrometry; pharmacokinetics
Citation
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, v.859, no.2, pp 229 - 233
Pages
5
Journal Title
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES
Volume
859
Number
2
Start Page
229
End Page
233
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/23911
DOI
10.1016/j.jchromb.2007.09.034
ISSN
1570-0232
1873-376X
Abstract
A simple, rapid, sensitive and specific liquid chromatography-tandem mass spectrometry method was developed and validated for quantification of beraprost, a stable, orally active prostacyclin analogue with vasodilatory, antiplatelet and cytoprotective effects. The analyte and internal standard, indomethacin, were extracted by solid-phase extraction using OASIS HLB cartridge. The chromatographic separation was performed on a C-18 column with a mobile of 0.1% formic acid-methanol (30:70, v/v). The highest daughter ion of deprotonated analyte was quantitated in negative ionization by multiple reactions monitoring with a mass spectrometer. The mass transitions m/z 397>269 and m/z 356>312 were used to measure beraprost and internal standard, respectively. The assay exhibited a linear range from 0.02 to 2 ng/mL for beraprost in human plasma. The lower limit of quantitation was 20 pg/mL with a relative standard deviation of less than 20%. The method was validated with respect to linearity, sensitivity, specificity, recovery, accuracy and precision. The validated method has been successfully used to analyze human plasma samples for application in pharmacokinetic study. (c) 2007 Elsevier B.V. All rights reserved.
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