ENANTIOSELECTIVE DETERMINATION OF ISRADIPINE IN HUMAN SERUM USING CHIRAL STATIONARY-PHASE LIQUID-CHROMATOGRAPHY AND GAS-CHROMATOGRAPHY WITHNITROGEN-SELECTIVE DETECTION

Citation
Hs. Rask et al., ENANTIOSELECTIVE DETERMINATION OF ISRADIPINE IN HUMAN SERUM USING CHIRAL STATIONARY-PHASE LIQUID-CHROMATOGRAPHY AND GAS-CHROMATOGRAPHY WITHNITROGEN-SELECTIVE DETECTION, Chirality, 10(9), 1998, pp. 808-812
Citations number
9
Categorie Soggetti
Chemistry Medicinal","Chemistry Analytical","Chemistry Inorganic & Nuclear","Pharmacology & Pharmacy
Journal title
ISSN journal
08990042
Volume
10
Issue
9
Year of publication
1998
Pages
808 - 812
Database
ISI
SICI code
0899-0042(1998)10:9<808:EDOIIH>2.0.ZU;2-Z
Abstract
rac-Isradipine is a dihydropyridine type calcium antagonist. Its calci um entry blocking effect is due primarily to the (+)-(S)-enantiomer. T his study describes a sensitive enantioselective method for the determ ination of isradipine in human serum. Following alkaline extraction in to hexane, the enantiomers of isradipine are separated quantitatively by high-performance liquid chromatography on a Chiralcel OJ column at 39 degrees C. The collected fractions were evaporated and assayed usin g capillary gas chromatography on a HP 50+ column with nitrogen select ive detection. Using 2.0 ml of serum, 0.7 nmol/l (0.26 ng/ml) of each enantiomer could be determined with acceptable precision. The method h as successfully been used to measure (+)-(S)- and (-)-(R)-isradipine c oncentrations in samples from volunteers after intravenous and oral ad ministration of isradipine. (C) 1998 Wiley-Liss, Inc.