Chiral analysis of carvedilol and its metabolites hydroxyphenyl carvedilol and O-desmethyl carvedilol in human plasma by liquid chromatography-tandem mass spectrometry: Application to a clinical pharmacokinetic study

J Chromatogr B Analyt Technol Biomed Life Sci. 2016 Mar 15:1015-1016:173-180. doi: 10.1016/j.jchromb.2016.02.028. Epub 2016 Feb 23.

Abstract

Carvedilol is an antihypertensive drug, which is available in clinical practice as a racemic mixture. (S)-(-)-carvedilol is a β- and α1-adrenergic antagonist, while (R)-(+)-carvedilol only acts as an α1-adrenergic antagonist. Carvedilol is metabolized mainly by glucuronidation and, to a lesser extent, by CYP2D6 to hydroxyphenyl carvedilol (OHC) and by CYP2C9 to O-desmethyl carvedilol (DMC). This study describes the development and validation of a method for the sequential analysis of the enantiomers of carvedilol, OHC and DMC in plasma using a Chirobiotic(®) V chiral-phase column coupled to an LC-MS/MS system. The method was linear in the range of 0.05-100, 0.05-10 and 0.02-10 ng/mL for the carvedilol, OHC and DMC enantiomers, respectively. Application of the method to the investigation of a patient with type 2 diabetes mellitus treated with a single oral dose of 25mg racemic carvedilol showed plasma accumulation of the (R)-(+)-carvedilol, (R)-(+)-DMC and (R)-(+)-OHC enantiomers. These results suggest that plasma accumulation of (R)-(+)-carvedilol cannot be explained by its oxidative metabolism.

Keywords: Carvedilol; Diabetes; Enantiomers; Metabolism; Pharmacokinetics; Plasma.

MeSH terms

  • Adrenergic beta-Antagonists / blood
  • Adrenergic beta-Antagonists / chemistry
  • Adrenergic beta-Antagonists / metabolism
  • Adrenergic beta-Antagonists / pharmacokinetics
  • Carbazoles / blood*
  • Carbazoles / chemistry
  • Carbazoles / metabolism
  • Carbazoles / pharmacokinetics*
  • Carvedilol
  • Chromatography, Liquid / methods*
  • Diabetes Mellitus, Type 2 / metabolism
  • Humans
  • Linear Models
  • Middle Aged
  • Propanolamines / blood*
  • Propanolamines / chemistry
  • Propanolamines / metabolism
  • Propanolamines / pharmacokinetics*
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Stereoisomerism
  • Tandem Mass Spectrometry / methods*

Substances

  • Adrenergic beta-Antagonists
  • Carbazoles
  • Propanolamines
  • Carvedilol