Simultaneous determination of selenomethionine enantiomers in biological fluids by stable isotope dilution gas chromatography-mass spectrometry

J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Nov 1;879(29):3253-8. doi: 10.1016/j.jchromb.2011.03.057. Epub 2011 Apr 7.

Abstract

A method for the stereoselective determination of D- and L-enantiomers of selenomethionine in mouse plasma was developed using gas chromatography-mass spectrometry with selected-ion monitoring (GC-MS-SIM). DL-[(2)H(3,)(82)Se]selenomethionine was used as analytical internal standard to account for losses associated with the extraction, derivatization and chromatography. Selenomethionine enantiomers in mouse plasma were purified by cation-exchange chromatography using BondElut SCX cartridge and derivatized with HCl in methanol to form methyl ester followed by subsequent N-acylation with optically active (+)-α-methoxy-α-trifluoromethylphenylacetyl chloride to form diastereomeric amide. Quantification was performed by SIM of the molecular-related ions of the diastereomers on the chemical ionization mode. The intra- and inter-day precision for D- and L-selenomethionine spiked to mouse plasma gave good reproducibility with relative standard deviation of 3% and 3% for D-selenomethionine and 6% and 3% for L-selenomethionine, respectively. The estimated amounts were in good agreement with the actual amounts spiked, the intra- and inter-day relative error being 5% and 2% for D-selenomethionine and 2% and 1% for L-selenomethionine, respectively. The present method is sensitive enough to determine pharmacokinetics of selenomethionine enantiomers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Gas Chromatography-Mass Spectrometry / methods*
  • Least-Squares Analysis
  • Mice
  • Reproducibility of Results
  • Selenomethionine / blood*
  • Selenomethionine / chemistry
  • Sensitivity and Specificity
  • Stereoisomerism

Substances

  • Selenomethionine