High-performance liquid chromatographic determination of new 2,3-benzodiazepines

J Chromatogr B Biomed Sci Appl. 1998 Jan 23;705(1):149-53. doi: 10.1016/s0378-4347(97)00463-5.

Abstract

A simple high-performance liquid chromatographic assay with ultraviolet detection at 254 nm for simultaneous determination of 2,3-benzodiazepine derivatives (2,3-BZ2 and 2,3-BZ2Me) and their metabolites in rat plasma is described. The procedure involves a fast extraction of the drugs from the buffered sample using methanol. The extract is evaporated to dryness at 45 degrees C and the residue is redissolved in methanol (twice). A 20-microl aliquot is injected into the liquid chromatograph and eluted with methanol-water (65:35, v/v) on a C18 reversed-phase column. At a flow-rate of 1.5 ml/min the detection time was 3.1 min for 2,3-BZ2, 5.06 min for 2,3-BZ2Me and 10.9 min for prazepam, used as internal standard for the quantification of the studied compounds. The method has been used to investigate the steady-state concentrations of two 2,3-benzodiazepine derivatives in Sprague-Dawley rat plasma.

MeSH terms

  • Animals
  • Anticonvulsants / administration & dosage
  • Anticonvulsants / blood*
  • Anticonvulsants / pharmacokinetics
  • Benzodiazepines / administration & dosage
  • Benzodiazepines / blood*
  • Benzodiazepines / pharmacokinetics
  • Chromatography, High Pressure Liquid
  • Gas Chromatography-Mass Spectrometry
  • Injections, Intraperitoneal
  • Rats
  • Rats, Sprague-Dawley
  • Sensitivity and Specificity

Substances

  • Anticonvulsants
  • Benzodiazepines