Simultaneous determination of venlafaxine and its main active metabolite O-desmethyl venlafaxine in rat plasma by LC-MS/MS

Anal Sci. 2009 Oct;25(10):1207-10. doi: 10.2116/analsci.25.1207.

Abstract

A simple, sensitive and selective liquid chromatography tandem mass spectrometry (LC-MS/MS) method was developed and validated for the analysis of venlafaxine (VX) and its major active metabolite O-desmethyl venlafaxine (ODV) in rat plasma using carbamazepine as an internal standard (IS). The analytes from the biological matrix were extracted by liquid-liquid extraction using tert-butyl methyl ether (TBME). The HPLC separation of the analytes was performed on a water symmetry C18 (150 x 4.6 mm i.d., 5 microm) column, using a 10 mM ammonium formate:methanol (20:80 v/v) as mobile phase. The calibration curve concentration range was 10.10 to 8000.00 ng/mL for VX and ODV with coefficient of determination above 0.9970. The lower limit of quantification (LLOQ) of VX and ODV were 3.35 and 3.86 ng/mL, respectively. The intra- and inter-day coefficients of variation were within 15%.

MeSH terms

  • Animals
  • Blood Chemical Analysis / methods*
  • Blood Chemical Analysis / standards
  • Calibration
  • Carbamazepine / blood
  • Chromatography, Liquid
  • Cyclohexanols / blood*
  • Cyclohexanols / chemistry
  • Cyclohexanols / isolation & purification
  • Cyclohexanols / metabolism*
  • Desvenlafaxine Succinate
  • Limit of Detection
  • Linear Models
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Reference Standards
  • Solid Phase Extraction
  • Solvents / chemistry
  • Tandem Mass Spectrometry
  • Time Factors
  • Venlafaxine Hydrochloride

Substances

  • Cyclohexanols
  • Solvents
  • Carbamazepine
  • Venlafaxine Hydrochloride
  • Desvenlafaxine Succinate