| Autor: |
Hellhake S; School of Mathematics and Natural Sciences, University of Wuppertal, Gauss-Str. 20, 42119, Wuppertal, Germany., Meckelmann SW; Applied Analytical Chemistry & Teaching and Research Center for Separation, University of Duisburg-Essen, Universitätsstr. 5-7, 45141, Essen, Germany., Empl MT; Institute for Food Toxicology, University of Veterinary Medicine Hannover, Bünteweg 2, 30559, Hannover, Germany., Rentmeister K; Applied Analytical Chemistry & Teaching and Research Center for Separation, University of Duisburg-Essen, Universitätsstr. 5-7, 45141, Essen, Germany., Wißdorf W; School of Mathematics and Natural Sciences, University of Wuppertal, Gauss-Str. 20, 42119, Wuppertal, Germany., Steinberg P; Institute for Food Toxicology, University of Veterinary Medicine Hannover, Bünteweg 2, 30559, Hannover, Germany., Schmitz OJ; Applied Analytical Chemistry & Teaching and Research Center for Separation, University of Duisburg-Essen, Universitätsstr. 5-7, 45141, Essen, Germany., Benter T; School of Mathematics and Natural Sciences, University of Wuppertal, Gauss-Str. 20, 42119, Wuppertal, Germany., Schebb NH; School of Mathematics and Natural Sciences, University of Wuppertal, Gauss-Str. 20, 42119, Wuppertal, Germany. nils@schebb-web.de. |
| Abstrakt: |
Eicosanoids and other oxylipins play an important role in mediating inflammation as well as other biological processes. For the investigation of their biological role(s), comprehensive analytical methods are necessary, which are able to provide reliable identification and quantification of these compounds in biological matrices. Using charge-switch derivatization with AMPP (N-(4-aminomethylphenyl)pyridinium chloride) in combination with liquid chromatography ion mobility quadrupole time-of-flight mass spectrometry (LC-IM-QTOF-MS), we developed a non-target approach to analyze oxylipins in plasma, serum, and cells. The developed workflow makes use of an ion mobility resolved fragmentation to pinpoint derivatized molecules based on the cleavage of AMPP, which yields two specific fragment ions. This allows a reliable identification of known and unknown eicosanoids and other oxylipins. We characterized the workflow using 52 different oxylipins and investigated their fragmentation patterns and ion mobilities. Limits of detection ranged between 0.2 and 10.0 nM (1.0-50 pg on column), which is comparable with other state-of-the-art methods using LC triple quadrupole (QqQ) MS. Moreover, we applied this strategy to analyze oxylipins in different biologically relevant matrices, as cultured cells, human plasma, and serum. Graphical abstract. |
