Assay method for the carboxylic acid metabolite of clopidogrel in human plasma by gas chromatography-mass spectrometry

J Chromatogr B Biomed Sci Appl. 1998 Dec 11;720(1-2):107-17. doi: 10.1016/s0378-4347(98)00452-6.

Abstract

This paper describes a GC-MS method for the analysis of the carboxylic acid metabolite (SR26334, II) of methyl (+)-(S)-alpha-(o-chlorophenyl)-6,7-dihydrothieno[3,2-c]pyridine-5( 4H)-acetate hydrogensulfate (clopidogrel, SR 25990, I) in plasma and serum. The analytical procedure involves a robotic liquid-liquid extraction with diethyl ether followed by a solid-liquid extraction on C18 cartridges. The derivatization process was performed using n-ethyl diisopropylethylamine and alpha-bromo-2,3,4,5,6-pentafluoro toluene. A structural analogue (III) of II, was used as internal standard. The 1/X2; weighted calibration curve obtained in the range 5-250 ng/ml was well described by a quadratic equation. The extraction efficiency was better than 48% over the range studied; for the internal standard it averaged 51% at 50 ng/ml. Precision ranged from 3.6 to 15.8%, and accuracy was between 92 and 114%. Dilution has no influence on the performance of the method which could then be used to quantitate plasma samples containing up to 25000 ng/ml. The limit of quantification was 5 ng/ml. The method validation results indicate that the performance characteristics of the method fulfilled the requirements for assay methods for use in pharmacokinetic studies.

MeSH terms

  • Calibration
  • Carboxylic Acids / blood
  • Clopidogrel
  • Gas Chromatography-Mass Spectrometry / methods*
  • Humans
  • Platelet Aggregation Inhibitors / blood*
  • Reference Standards
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Ticlopidine / analogs & derivatives*
  • Ticlopidine / blood

Substances

  • Carboxylic Acids
  • Platelet Aggregation Inhibitors
  • Clopidogrel
  • Ticlopidine