Analysis of acylcarnitines as their N-demethylated ester derivatives by gas chromatography-chemical ionization mass spectrometry

Anal Biochem. 1991 Nov 15;199(1):98-105. doi: 10.1016/0003-2697(91)90275-x.

Abstract

A novel approach to the analysis of acylcarnitines has been developed. It involves a direct esterification using propyl chloroformate in aqueous propanol followed by ion-pair extraction with potassium iodide into chloroform and subsequent on-column N-demethylation of the resulting acylcarnitine propyl ester iodides. The products, acyl N-demethylcarnitine propyl esters, are volatile and are easily analyzed by gas chromatography-chemical ionization mass spectrometry. For medium-chain-length (C4-C12) acylcarnitine standards, detection limits are demonstrated to be well below 1 ng starting material using selected ion monitoring. Well-separated gas chromatographic peaks and structure-specific mass spectra are obtained with samples of synthetic and biological origin. Seven acylcarnitines have been characterized in the urine of a patient suffering from medium-chain acyl-CoA dehydrogenase deficiency.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acyl-CoA Dehydrogenase
  • Acyl-CoA Dehydrogenases / deficiency
  • Acylation
  • Carnitine / analogs & derivatives*
  • Carnitine / analysis*
  • Carnitine / urine
  • Humans
  • Lipid Metabolism, Inborn Errors / urine
  • Molecular Structure
  • Spectrometry, Mass, Fast Atom Bombardment / methods

Substances

  • Acyl-CoA Dehydrogenases
  • Acyl-CoA Dehydrogenase
  • Carnitine