<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xu L</submitter><funding>“Blue Ocean Talent Plan” Innovation and Entrepreneurship Team</funding><funding>National Natural Science Foundation of China</funding><funding>Beijing Technology and Business University</funding><pagination>560-569</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7112149</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>61(4)</volume><pubmed_abstract>This article focuses on the establishment of an accurate and sensitive quantitation method for the analysis of furan fatty acids. In particular, the sensitivity of GC/MS and UPLC/ESI/MS/MS was compared for the identification and quantification of furan fatty acids. Different methylation methods were tested with respect to GC/MS analysis. Special attention needs to be paid to the methylation of furan fatty acids, as acidic catalysts might lead to the degradation of the furan ring. GC/MS analysis in full-scan mode demonstrated that the limit of quantitation was 10 μM. UPLC/ESI/MS/MS in multiple reaction monitoring mode displayed a higher detection sensitivity than GC/MS. Moreover, the identification of furan fatty acids with charge-reversal derivatization was tested in the positive mode with</pubmed_abstract><journal>Journal of lipid research</journal><pubmed_title>Development of a sensitive and quantitative method for the identification of two major furan fatty acids in human plasma.</pubmed_title><pmcid>PMC7112149</pmcid><funding_grant_id>201811070001</funding_grant_id><funding_grant_id>31601398</funding_grant_id><funding_grant_id>20171049</funding_grant_id><pubmed_authors>Xu L</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Yin H</pubmed_authors><pubmed_authors>Hu C</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Vetter W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of a sensitive and quantitative method for the identification of two major furan fatty acids in human plasma.</name><description>This article focuses on the establishment of an accurate and sensitive quantitation method for the analysis of furan fatty acids. In particular, the sensitivity of GC/MS and UPLC/ESI/MS/MS was compared for the identification and quantification of furan fatty acids. Different methylation methods were tested with respect to GC/MS analysis. Special attention needs to be paid to the methylation of furan fatty acids, as acidic catalysts might lead to the degradation of the furan ring. GC/MS analysis in full-scan mode demonstrated that the limit of quantitation was 10 μM. UPLC/ESI/MS/MS in multiple reaction monitoring mode displayed a higher detection sensitivity than GC/MS. Moreover, the identification of furan fatty acids with charge-reversal derivatization was tested in the positive mode with</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Apr</publication><modification>2026-05-07T10:54:21.248Z</modification><creation>2026-04-07T22:47:11.953Z</creation></dates><accession>S-EPMC7112149</accession><cross_references><pubmed>32029512</pubmed><doi>10.1194/jlr.d119000514</doi><doi>10.1194/jlr.D119000514</doi></cross_references></HashMap>