Poster Abstract
Steroid analysis for clinical research can require very low limits of detection which demand high recoveries and very clean
extracted samples. Supported Liquid Extraction (SLE) can provide very clean extracted samples with less method
development and a streamlined workflow compared to solid phase extraction (SPE). Laboratories desire high-throughput
methods which consolidate analytes into one panel with fast chromatographic run times. Chromatographic separation of
steroid isomers with the same m/z is necessary for accurate quantitation by LC-MS/MS. Meeting these criteria can be
challenging in a single LC-MS/MS method.