Measurement of the (R)- and (S)-isomers of warfarin in patients undergoing anticoagulant therapy

• Published in: Chirality (New York, N.Y.) Vol. 4; no. 8; p. 488
• Main Authors: McAleer, S D, Chrystyn, H, Foondun, A S
• Format: Journal Article
• Language: English
• Published: United States 1992
• Subjects: Chromatography, High Pressure Liquid - instrumentation; Chromatography, High Pressure Liquid - methods; Evaluation Studies as Topic; Female; Humans; Male; Stereoisomerism; Warfarin - blood; Warfarin - chemistry; Warfarin - therapeutic use
• ISSN: 0899-0042
• DOI: 10.1002/chir.530040806

An achiral/chiral high-performance liquid chromatographic system for the analysis of total warfarin together with the (R)- and (S)-enantiomers in clinical samples has been developed. The achiral analysis is achieved using a C8 column, which is coupled to a chiral stationary phase, alpha 1-acid glycoprotein (AGP), thereby allowing for analysis of warfarin isomers without interfering serum peaks. A 0.015 M phosphate buffer mobile phase with 15% v/v propan-2-ol (pH 7.0) was used on the C8/AGP system. UV analysis at 308 nm was used for quantitation of total warfarin on the C8 column and fluorescence (excitation 300 nm, emission 390 nm) detection was employed for isomer quantitation on the AGP. Retention time of total warfarin on the C8 column was 5.95 min, while that of the (S)- and (R)-warfarin on the AGP column was 10.38 and 12.69 min, respectively. Peak resolution of the warfarin isomers was 1.64. All serum samples were subjected to solid-phase extraction. Data from two patients in a single dose study indicate that a two-compartmental model could represent the warfarin concentration-time data with enterohepatic circulation. In some patients studied during steady state therapy, concentrations of (S)-warfarin were greater than (R)-warfarin indicating that the clearance of the former is slower in these patients.