PNNL

Abstract

Bile acids (BAs) constitute an important class of steroid metabolites with changes implicated in disease states and other health conditions. Current analyses for these structurally similar compounds are limited by a lack of sensitivity, and long separation times with often poor isomeric resolution. To overcome these challenges and provide rapid analyses for the BA isomers, we utilized cyclodextrin adducts and ion mobility (IM) separations in structures for lossless ion manipulations (SLIM). Cyclodextrin was found to interact with both the tauro- and glyco-conjugated BA isomers studied, forming rigid noncovalent host-guest inclusion complexes. SLIM capabilities for the accumulation of large ion populations and peak compression, enabled both the sensitive detection and high-resolution separation of all the isomers studied.