High-performance liquid-chromatographic determination of warfarin enantiomers in plasma with automated on-line sample enrichment

被引:36
作者
Boppana, VK [1 ]
Schaefer, WH [1 ]
Cyronak, MJ [1 ]
机构
[1] GlaxoSmithKline, Drug Metab & Pharmacokinet, King Of Prussia, PA 19406 USA
来源
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS | 2002年 / 54卷 / 1-3期
关键词
semipermeable surface; R- and S-warfarins; fluorescence detection; column-switching valves;
D O I
10.1016/S0165-022X(02)00122-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A sensitive and selective chiral high performance liquid chromatographic method was developed for the direct determination of R- and S-warfarin enantiomers in human plasma. The method involved direct injection of human plasma onto a semipermeable surface (SPS) guard column, washing the proteins from the column with aqueous acetonitrile and back flushing the analytes onto a reversed phase ovomucoid silica HPLC column using switching valves. After separation, the analytes were simultaneously detected and quantitated with a fluorometer. The recoveries of R-warfarin from human plasma at 25 and 2500 ng/ml were 98.9% and 88.1%, respectively. The recoveries of S-warfarin at 25 and 2500 ng/ml were 105.4% and 93.9%, respectively. Using 100 mul of human plasma, the lower limit of quantification for both R- and S-warfarins was 25 ng/ml. Linear responses in analyte/intemal standard peak height ratios were observed for analyte concentrations ranging from 25 to 2500 ng/ml for both enantiomers. Fluorescence chromatograms of drug-free human plasma showed no interfering peaks with retention times similar to those for R- and S-warthrins and the internal standard. Results from a 3-day validation study for both enantiomers demonstrated excellent precision (1.7-9.0%) and accuracy (97-109%) across the calibration range. (C) 2002 Elsevier Science B.V. All rights reserved.
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页码:315 / 326
页数:12
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