Enantioselective determination of pazinaclone, a new isoindoline anxiolytic, and its active metabolite in rat plasma by high-performance liquid chromatography

J Chromatogr B Biomed Appl. 1995 Apr 21;666(2):291-7. doi: 10.1016/0378-4347(94)00574-o.

Abstract

A sensitive and specific high-performance liquid chromatographic method has been developed for the simultaneous determination of the enantiomers of pazinaclone (DN-2327), a new anxiolytic agent, and those of its active metabolite, M-II, in rat plasma. Organic solvent extraction of pazinaclone, M-II, and internal standard (I.S.) in plasma was followed by separation of the analytes from other metabolites using an achiral reversed-phase column. Fluorescence detection was employed with excitation and emission wavelengths of 328 and 367 nm, respectively. Separation of all the enantiomers and I.S. was then accomplished with normal- and chiral-phase columns connected in series. For each analyte, the lower quantitation limit was 0.5 ng/ml. The assay has been applied to a chiral inversion study in rats. Chiral conversion from one enantiomer of pazinaclone to the other hardly occurred. This method is suitable for enantioselective pharmacokinetic and toxicokinetic studies in animals.

MeSH terms

  • Animals
  • Anti-Anxiety Agents / blood*
  • Chromatography, High Pressure Liquid / methods*
  • Isoindoles
  • Male
  • Naphthyridines / blood*
  • Rats
  • Rats, Wistar
  • Reproducibility of Results
  • Spiro Compounds / blood*
  • Stereoisomerism

Substances

  • Anti-Anxiety Agents
  • Isoindoles
  • Naphthyridines
  • Spiro Compounds
  • pazinaclone