LC-MS/MS assay of fluoropezil and its two major metabolites in human plasma: an application to pharmacokinetic studies

Bioanalysis. 2022 Jun;14(11):817-829. doi: 10.4155/bio-2022-0045. Epub 2022 Jun 23.

Abstract

Background: LC-MS/MS methods were developed for pharmacokinetic analysis and verified to measure fluoropezil, a new AchE inhibitor for Alzheimer's disease treatment, and its two primary metabolites (N-debenzyl fluoride fluoropezil [M1] and N-oxidized fluoropezil [M11]) in human plasma. Methods & results: Analytes were extracted from 50 μl plasma using protein precipitation and separated by HPLC using a bridged ethyl hybrid column and gradient elution procedure. Analytical detection was performed with a triple quadrupole mass spectrometer and electrospray ionization source in multiple reaction monitoring mode. The LC-MS/MS method was fully validated. The quantification linear ranges were 0.100-50.0 ng/ml (fluoropezil), 0.0500-25.0 ng/ml (M1) and 0.0500-25.0 ng/ml (M11). Conclusion: A sensitive, reliable LC-MS/MS method was established and used successfully to explore the pharmacokinetics of fluoropezil.

Keywords: DC20; LC–MS/MS; assay; bioanalysis; fluoropezil; metabolites; pharmacokinetics.

MeSH terms

  • Chromatography, High Pressure Liquid / methods
  • Chromatography, Liquid / methods
  • Humans
  • Linear Models
  • Reproducibility of Results
  • Tandem Mass Spectrometry* / methods