Identification of monoacylglycerol regio-isomers by gas chromatography-mass spectrometry

J Chromatogr A. 2010 Feb 26;1217(9):1543-8. doi: 10.1016/j.chroma.2010.01.016. Epub 2010 Jan 14.

Abstract

Monoacylglycerols (MAGs) are lipids found in trace amounts in plants and animal tissues. While they are widely used in various industrial applications, accurate determination of the regio-specific distribution is hindered by the lack of stable, commercially available standards. Indeed, unsaturated beta-MAG (or Sn-2 MAG) readily undergoes isomerization into alpha-MAG (acyl chain is attached to the Sn-1 or the Sn-3 position). In the present study, we describe structural elucidation of alpha- and beta-regio-isomers of monopalmitoyl-glycerol (MAG C16:0) as model compounds in their silylated forms using gas chromatography-mass spectrometry (GC-MS) with electronic impact (EI) ionization. MS fragmentation of alpha-MAG C16:0 is characterized by the loss of methylene(trimethylsilyl)oxonium (103 amu) and the consecutive loss of acyl chain yielding a fragment ion at m/z 205. The fragmentation pattern of beta-MAG C16:0 shows a series of diagnostic fragments at m/z 218, 203, 191 and 103 that are not formed from the alpha-isomer and hereby enable reliable distinction of these regio-isomers. Possible fragmentation scenarios are postulated to explain the formation of these marker ions, which were also applied to characterize the regio-isomer composition of a complex mixture of MAG sample containing n-3 long-chain polyunsaturated fatty acids.

MeSH terms

  • Gas Chromatography-Mass Spectrometry / methods*
  • Monoglycerides / analysis*
  • Monoglycerides / chemistry*
  • Spectrometry, Mass, Electrospray Ionization
  • Stereoisomerism

Substances

  • Monoglycerides