Determination of ebrotidine and its metabolites by capillary electrophoresis with UV and mass spectrometry detection

J Chromatogr A. 2000 Aug 4;888(1-2):281-92. doi: 10.1016/s0021-9673(00)00536-7.

Abstract

This study describes the application of capillary electrophoresis (CE) to the analysis of ebrotidine and its metabolites as an alternative analytical technique to liquid chromatography. Comparison between UV-diode array spectroscopy and mass spectrometry (MS) using an ion-trap system with electrospray ionization as detection systems has been performed. The quality parameters of the UV detection method were established, obtaining linear calibration curves over the range studied (8-200 mg ml(-1)), limits of detection between 3.4 and 4.3 microg ml(-1), and run-to-run and day-to-day precision lower than 14%. For these compounds the protonated species [M+H]+ and, in some cases, sodium adducts were observed in the MS spectra. Using MS coupled to CE, limits of detection were between 0.5 and 2.6 microg ml(-1).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benzenesulfonates / metabolism*
  • Buffers
  • Cations
  • Electrolytes
  • Electrophoresis, Capillary / methods*
  • Histamine H2 Antagonists / metabolism*
  • Mass Spectrometry
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Solvents
  • Spectrophotometry, Ultraviolet
  • Thiazoles / metabolism*

Substances

  • Benzenesulfonates
  • Buffers
  • Cations
  • Electrolytes
  • Histamine H2 Antagonists
  • Solvents
  • Thiazoles
  • ebrotidine