DETERMINATION OF FELODIPINE, ITS ENANTIOMERS, AND A PYRIDINE METABOLITE IN HUMAN PLASMA BY CAPILLARY GAS-CHROMATOGRAPHY WITH MASS-SPECTROMETRIC DETECTION

被引:36
作者
DRU, JDY
HSIEH, JYK
MATUSZEWSKI, BK
DOBRINSKA, MR
机构
[1] Department of Drug Metabolism, Merck Research Laboratories, West Point
来源
JOURNAL OF CHROMATOGRAPHY B-BIOMEDICAL APPLICATIONS | 1995年 / 666卷 / 02期
关键词
D O I
10.1016/0378-4347(94)00579-T
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Sensitive methods based on capillary gas chromatography (GC) with mass spectrometric (MS) detection in a selected-ion monitoring mode (SIM) for the determination of racemic felodipine, its enantiomers, and a pyridine metabolite in human plasma are described. Following liquid-liquid extraction from plasma, enantiomers of felodipine were separated on a chiral HPLC column (Chiralcel OJ) and fractions containing each isomer were collected on a continuous basis using a fraction collector. These fractions were later analyzed by GC-MS-SIM. A similar method based on GC-MS-SIM detection was developed for the determination of racemic felodipine and its pyridine metabolite with a minor modification of sample preparation. The limits of quantitation in plasma were 0.1 ng/ml for both the R(+)- and S(-)-enantiomers of felodipine and 0.5 ng/ml for both racemic felodipine and its pyridine metabolite. The stereoselective assay was used to support a clinical study with racemic felodipine, and was capable of analyzing more than 30 plasma samples per day.
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收藏
页码:259 / 267
页数:9
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