Gas chromatography–mass spectrometry determination of metabolites of conjugated cis-9, trans-11, cis-15 18:3 fatty acid

Abstract

Structural determination of polyunsaturated fatty acids by gas chromatography–mass spectrometry (GC–MS) requires currently the use of nitrogen containing derivatives such as picolinyl esters, 4,4-dimethyloxazoline or pyrrolidides derivatives. The derivatization is required in most cases to obtain low energy fragmentation that allows accurate location of the double bonds. In the present work, the following metabolites of rumelenic ( cis-9, trans-11, cis-15 18:3) acid, from rat livers, were identified: cis-8, cis-11, trans-13, cis-17 20:4, cis-5, cis-8, cis-11, trans-13, cis-17 20:5, cis-7, cis-10, cis-13, trans-15, cis-19 22:5, and cis-4, cis-7, cis-10, cis-13, trans-15, cis-19 22:6 acids by GC–MS as their 4,4-dimethyloxazoline and methyl esters derivatives. Specific fragmentation of the methyl ester derivatives revealed some similarity with their corresponding DMOX derivatives. Indeed, intense ion fragments at m/ z = M + − 69, corresponding to a cleavage at the center of a bis-methylene interrupted double bond system were observed for all identified metabolites. Moreover, intense ion fragments at m/ z = M + − 136, corresponding to allylic cleavage of the n-12 double bonds were observed for the C20:5, C22:5, C22:6 acid metabolites. For the long chain polyunsaturated fatty acids from the rumelenic metabolism, we showed that single methyl esters derivatives might be used for both usual quantification by GC–FID and identification by GC–MS.