Determination of doxazosin and verapamil in human serum by fast LC-MS/MS: application to document non-compliance of patients

J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Nov 15;878(30):3167-73. doi: 10.1016/j.jchromb.2010.09.032. Epub 2010 Oct 23.

Abstract

A rapid and sensitive method using liquid chromatography-tandem mass spectrometry (LC-MS/MS) for simultaneous determination of doxazosin and verapamil in human serum has been developed. Trimipramine-d₃ as an isotopic labelled internal standard was used for quantification. Serum samples were prepared by simple liquid-liquid extraction with mixture of tert butyl methyl ether and ethyl acetate (1:1, v:v). The analytes and internal standard were separated on C18 column using an isocratic elution with 5 mM ammonium formate with 0.02% formic acid and 0.02% formic acid in acetonitrile (55:45, v:v) at a flow rate of 1.1 mL/min. Positive TurboIonSpray mass spectrometry was used with multiple reaction monitoring of the transitions at: m/z 455.3→165.2 and 150.2 for verapamil, m/z 452.2→344.4 and 247.4 for doxazosin, m/z 298.2→103.1 for trimipramine-d₃. Linearity was achieved between 1 and 500 ng/mL (R² ≥ 0.997) for both analytes. An extensive pre-study method validation was carried out in accordance with FDA guidelines. This assay was successfully applied to determine the serum concentrations of doxazosin and verapamil in suspect non-compliance patients.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antihypertensive Agents / blood*
  • Chromatography, Liquid / methods*
  • Doxazosin / blood*
  • Humans
  • Hypertension / blood*
  • Hypertension / drug therapy
  • Patient Compliance*
  • Tandem Mass Spectrometry / methods*
  • Verapamil / blood*

Substances

  • Antihypertensive Agents
  • Verapamil
  • Doxazosin