Identification of natural diacylglycerols as the 3,5-dinitrophenylurethanes by chiral phase liquid chromatography with mass spectrometry |
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Authors: | Y. Itabashi L. Marai A. Kuksis |
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Affiliation: | (1) Banting and Best Department of Medical Research, University of Toronto, C.H. Best Institute, 112 College Street, M5G 1L6 Toronto, Canada;(2) Present address: Department of Chemistry, Faculty of Fisheries, Hokkaido University, Hakodate, Japan |
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Abstract: | This study reports a facile identification of the molecular species of enantiomeric diacylglycerols by combining chiral phase
high-performance liquid chromatography with positive chemical ionization mass spectrometry. For this purpose the 3,5-dinitrophenylurethane
(DNPU) derivatives ofsn-1,2(2,3)-diacylglycerols are separated on an (R+)-naphthylethylamine polymer column (25 cm × 0.46 cm ID) using an isocratic
solvent system made up of hexane/dichloroethane/acetonitrile (85∶10∶5, by vol) or isooctane/tert-butyl methyl ether/acetonitrile/isopropanol (80∶10∶5∶5, by vol). About 1% of the column effluent (1 mL/min) was admitted
to a quadrupole mass spectrometer (Hewlett-Packard, Palo Alto, CA)via direct liquid inlet interface, and positive chemical ionization spectra were recorded over the range of 200–900 mass units.
The DNPU derivatives of diacylglycerols yield characteristic [M-DNPU]+ and [RCO+74]+ ions for each diacylglycerol species from which the molecular weight and exact pairing of fatty acids can be unequivocally
obtained. The characteristic ions appear to be generated in nearly correct mass proportions as indicated by preliminary quantitative
comparisons.
The abbreviations 14∶0, 16∶1, 18∶2, etc. represent normal chain fatty acids of 14, 16, 18, etc. acyl carbons and 0, 1, 2,
etc. double bonds, respectively; 16∶0–18∶1, etc. represent diacylglycerols containing 16∶0 and 18∶1 fatty acids of unspecified
positional distribution;sn indicates stereospecific numbering of glycerol carbons;sn-1,2-diacylglycerols andsn-2,3-diacylglycerols are enantiomeric diacylglycerols of unspecified fatty acid composition;rac-1,2-diacylglycerols are racemic diacylglycerols representing equal amounts ofsn-1,2-andsn-2,3-enantiomers;sn-1,2(2,3)-diacylglycerols are a mixture ofsn-1,2-andsn-2,3-diacylglycerols of unspecified proportion of enantiomers and unspecified fatty acid compisition and positional distribution;
X-1,3-diacylglycerols are diacylglycerols of unspecified fatty acid composition and reverse isomer content. |
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