Determination of an arylether antiarrhythmic and its N-dealkyl metabolite in rat plasma and hepatic microsomal incubates using liquid chromatography-tandem mass spectrometry

J Chromatogr B Biomed Sci Appl. 2001 Aug 15;759(2):259-66. doi: 10.1016/s0378-4347(01)00230-4.

Abstract

A method was developed and validated for the quantification of (+/-)-trans-[2-morpholino-1-(1-naphthalene-ethyloxy]cyclohexane monohydrochloride (RSD1070) and its N-dealkyl metabolite in rat plasma and hepatic microsomal incubates. Chromatographic separations were achieved using reversed-phase high-performance liquid chromatography coupled with positive ion electrospray ionization and detection by tandem mass spectrometry. The assay was linear from 2.5 to 100 ng/ml and this range was used for validation. Inter- and intra-assay variability (n=6), extraction recovery, and stability in plasma were assessed. The estimated limit of quantitation was in the range 2.5-3 ng/ml for both analytes in rat plasma. The analytical method was used in a pharmacokinetic study of RSD1070 in rats after a single i.v. bolus of 12 mg/kg.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Arrhythmia Agents / blood
  • Anti-Arrhythmia Agents / metabolism*
  • Anti-Arrhythmia Agents / pharmacokinetics
  • Calibration
  • Chromatography, High Pressure Liquid / methods*
  • Male
  • Microsomes, Liver / metabolism*
  • Morpholines / blood
  • Morpholines / metabolism*
  • Morpholines / pharmacokinetics
  • Naphthalenes / blood
  • Naphthalenes / metabolism*
  • Naphthalenes / pharmacokinetics
  • Rats
  • Rats, Sprague-Dawley
  • Sensitivity and Specificity
  • Spectrometry, Mass, Electrospray Ionization / methods*

Substances

  • Anti-Arrhythmia Agents
  • Morpholines
  • Naphthalenes
  • RSD1070