4.5 Article

Resolution, quantification, and reliable determination of enantiomeric excess of proteinogenic and non-proteinogenic amino acids by comprehensive two-dimensional gas chromatography

期刊

JOURNAL OF SEPARATION SCIENCE
卷 45, 期 24, 页码 4416-4426

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/jssc.202200606

关键词

amino acid; chirality; enantioseparation; N-trifluoroacetyl-O-methyl ester; two-dimensional gas chromatography

资金

  1. European Research Council under the European Union [804144]
  2. French Ministry of Science and Education
  3. European Research Council (ERC) [804144] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

This work proposes a comprehensive two-dimensional gas chromatography method for the resolution and quantification of 27 amino acids. The method combines derivatization and enantioselective gas chromatography to accurately determine enantiomeric excess.
This work proposes a comprehensive two-dimensional gas chromatography method for the resolution and quantification of 27 amino acids, including 17 enantiomeric pairs, as stable N-trifluoroacetyl-O-methyl ester derivatives. The derivatization approach in combination with enantioselective two-dimensional gas chromatography has proven to be highly responsive with a method detection limit of 1-7 pg even for sterically hindered amino acids such as alpha,alpha-dialkylated, and N-alkylated amino acids. Accurate determination of the enantiomeric excess was achieved with errors in the range of +/- 0.5%-2.5% (1 sigma) at concentrations >= 10(-6) M. A thorough study of the mass spectra of the amino acid derivatives allowed the fragmentation pathways to be distinguished, enabling chromatographic peaks to be unambiguously assigned. The proposed method is particularly suited for applications that require the precise determination of enantiomeric excesses such as those concerning the role of d-amino acid enantiomers in humans, animals, and the environment, as well as for analyses of extraterrestrial samples aimed at understanding the selection of amino acids in stereochemical l-configuration.

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