Analysis of tofisopam in human serum by column-switching semi-micro high-performance liquid chromatography and evaluation of tofisopam bioequivalency

Biomed Chromatogr. 2002 Jun;16(4):277-81. doi: 10.1002/bmc.142.

Abstract

A rapid and sensitive column-switching semi-micro HPLC method is described for the direct analysis of tofisopam in human serum. The sample (100 microL) was directly injected onto the precolumn (Capcell Pak MF Ph-1), where unretained proteins were eluted to waste. Tofisopam was then eluted into an enrichment column using 13% acetonitrile in 50 mM phosphate buffer (pH 7.0) containing 5 mM sodium octanesulfonate and subsequently into the analytical column using 43% acetonitrile in 0.1% phosphoric acid containing 5 mM sodium octanesulfonate. The detection limit (2 ng/mL), good precision (CV < or = 4.2%) and speed (total analysis time 24 min) of the present method were sufficient for drug monitoring. This method was successfully applied to a bioequivalence test of two commercial tofisopam tablets.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Anti-Anxiety Agents / blood*
  • Anti-Anxiety Agents / pharmacokinetics
  • Benzodiazepines*
  • Chromatography, High Pressure Liquid / methods*
  • Drug Evaluation, Preclinical
  • Humans
  • Male
  • Reproducibility of Results

Substances

  • Anti-Anxiety Agents
  • Benzodiazepines
  • tofisopam