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Targeted LC–MS derivatization for aldehydes and carboxylic acids with a new derivatization agent 4-APEBA

M. Eggink,M. Wijtmans,A. Kretschmer,J. Kool,H. Lingeman,I. D. de Esch,W. Niessen,H. Irth

Published 2010 in Analytical and Bioanalytical Chemistry

ABSTRACT

AbstractBased on the template of a recently introduced derivatization reagent for aldehydes, 4-(2-(trimethylammonio)ethoxy)benzeneaminium dibromide (4-APC), a new derivatization agent was designed with additional features for the analysis and screening of biomarkers of lipid peroxidation. The new derivatization reagent, 4-(2-((4-bromophenethyl)dimethylammonio)ethoxy)benzenaminium dibromide (4-APEBA) contains a bromophenethyl group to incorporate an isotopic signature to the derivatives and to add additional fragmentation identifiers, collectively enhancing the abilities for detection and screening of unknown aldehydes. Derivatization can be achieved under mild conditions (pH 5.7, 10 °C). By changing the secondary reagent (1-ethyl-3-(3-dimethylaminopropyl) carbodiimide instead of sodium cyanoborohydride), 4-APEBA is also applicable to the selective derivatization of carboxylic acids. Synthesis of the new label, exploration of the derivatization conditions, characterization of the fragmentation of the aldehyde and carboxylic acid derivatives in MS/MS, and preliminary applications of the labeling strategy for the analysis of aldehydes in urine and plasma are described. FigureStructure and MS/MS fragmentation spectrum of 4-APEBA reagents derivatized with octanoic acid

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