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pubmed-article:7633602pubmed:abstractTextSensitive 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.lld:pubmed
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pubmed-article:7633602pubmed:authorpubmed-author:SunY LYLlld:pubmed
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pubmed-article:7633602pubmed:pagination259-67lld:pubmed
pubmed-article:7633602pubmed:dateRevised2007-10-16lld:pubmed
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pubmed-article:7633602pubmed:year1995lld:pubmed
pubmed-article:7633602pubmed:articleTitleDetermination of felodipine, its enantiomers, and a pyridine metabolite in human plasma by capillary gas chromatography with mass spectrometric detection.lld:pubmed
pubmed-article:7633602pubmed:affiliationDepartment of Drug Metabolism, Merck Research Laboratories, West Point, PA 19486, USA.lld:pubmed
pubmed-article:7633602pubmed:publicationTypeJournal Articlelld:pubmed