Simple method for determination of the active metabolite of the inotropic drug pimobendan in rat liver microsomes

J Chromatogr B Biomed Sci Appl. 2000 Jul 7;744(1):189-93. doi: 10.1016/s0378-4347(00)00224-3.

Abstract

A rapid and sensitive high-performance liquid chromatographic method for quantitation of the O-demethylated active metabolite formed in a liver microsomal assay system has been developed. The metabolite was separated on an Inertsil ODS-2 column and quantitated by fluorescence detection (excitation at 338 nm, emission at 405 nm). The retention times for pimobendan and its metabolite were 5.6 and 2.8 min, respectively. The intra- and inter-assay relative standard deviations in the measurement of pimobendan O-demethylase activity at the substrate concentrations of 1 microM and 500 microM were 2.0%, 6.8%, 2.1% and 5.6%, respectively, and the limit of detection was 0.1 ng for the demethylated metabolite.

Publication types

  • Evaluation Study

MeSH terms

  • Animals
  • Calibration
  • Cardiotonic Agents / analysis
  • Cardiotonic Agents / metabolism
  • Chromatography, High Pressure Liquid / methods
  • Male
  • Microsomes, Liver / metabolism*
  • Pyridazines / analysis*
  • Pyridazines / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reproducibility of Results

Substances

  • Cardiotonic Agents
  • Pyridazines
  • pimobendan