A validated UPLC-MS/MS method for flibanserin in plasma and its pharmacokinetic interaction with bosentan in rats

Bioanalysis. 2018 Jul;10(14):1087-1097. doi: 10.4155/bio-2018-0065. Epub 2018 Apr 25.

Abstract

Aim: The purpose of this study was development, validation and application of ultra-performance liquid chromatography (UPLC)-ESI-MS/MS method for quantitation of flibanserin in plasma samples.

Method & results: After extraction of analyte from plasma by diethyl ether, separation was performed on UPLC C18 column using mobile phase composition of 10 mM ammonium formate-acetonitrile (30:70, v/v) by isocratic elution of 0.3 ml/min. The multiple reaction monitoring transitions of m/z 391.13 → 161.04 and 384.20 → 253.06 were used for detection of analyte and internal standard (quetiapine), respectively. The calibration curves were linear (r ≥ 0.995) between 0.22 and 555 ng/ml concentration and all validation results were within the acceptable range as per US FDA guidelines.

Conclusion: The assay procedure was fully validated and successfully applied in pharmacokinetic interaction study of flibanserin with bosentan in rats.

Keywords: UPLC–tandem mass spectrometry; bosentan; flibanserin; pharmacokinetics; plasma; rats.

MeSH terms

  • Animals
  • Benzimidazoles / blood*
  • Benzimidazoles / pharmacokinetics*
  • Bosentan
  • Chromatography, High Pressure Liquid
  • Female
  • Rats
  • Rats, Wistar
  • Sulfonamides / blood
  • Sulfonamides / chemistry*
  • Tandem Mass Spectrometry

Substances

  • Benzimidazoles
  • Sulfonamides
  • flibanserin
  • Bosentan