Detection of reactive metabolites using isotope-labeled glutathione trapping and simultaneous neutral loss and precursor ion scanning with ultra-high-pressure liquid chromatography triple quadruple mass spectrometry.

Metabolic activation of drugs to electrophilic species is responsible for over 60% of black box warnings and drug withdrawals from the market place in the United States. Reactive metabolite trapping using glutathione (GSH) and analysis using high-performance liquid chromatography-tandem Mass spectrometry (HPLC-MS/MS) or HPLC with high resolution' mass. spectrometry (mass defect filtering) have enabled screening for metabolic activation to become routine during drug development. However, current MS-based approaches cannot detect all,GSH conjugates present in complex mixtures, especially those present in extracts of botanical dietary supplements. To Overcome these limitations, a fast triple quadrupole mass spectrometer-based approach was developed that can detect positively and negatively charged GSH conjugates in a single analysis without the need for advanced knowledge Of the elemental compositions of. potential Conjugates and while avoiding false positives This approach utilized UHPLC instead of HPLC to shorten separation time and enhance sensitivity, incorporated stable-isotope labeled,GSH to avoid false polarity, and used fast polarity switching electrospray MS/MS to detect: GSH conjugates that form positive and/or negative ions The general new method was then used to test the licorice dietary supplement Glycyrrhiza glabra, which was found to form Multiple GSH conjugates upon Metabolic activation. Among the GSH conjugates found in the licorice assay Were conjugates with isoliquiritigenin and glabridin, which 18,an irreversible inhibitor of cytochrome p450 enzymes.