High-Throughput Screening and Characterization of Reactive Metabolites Using Polarity Switching of Hybrid Triple Quadrupole Linear Ion Trap Mass Spectrometry

• Published in: Analytical chemistry (Washington) 2008-03, Vol.80 (5), p.1788-1799
• Main Authors: Wen, Bo, Ma, Li, Nelson, Sidney D, Zhu, Mingshe
• Format: Article
• Language: English
• Subjects: Analytical chemistry; Anti-Inflammatory Agents, Non-Steroidal - chemistry; Antidepressive Agents, Tricyclic - chemistry; Antipsychotic Agents - chemistry; Chemistry; Chromatographic methods and physical methods associated with chromatography; Chromatography; Clozapine - chemistry; Comparative analysis; Electrochemistry; Exact sciences and technology; Glutathione - chemistry; Glutathione - metabolism; Imipramine - chemistry; Liver; Mass spectrometry; Mass Spectrometry - methods; Other chromatographic methods; Peptides; Platelet Aggregation Inhibitors - chemistry; Reproducibility of Results; Sensitivity and Specificity; Spectrometric and optical methods; Ticlopidine - chemistry
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/ac702232r

A highly sensitive and efficient method has been developed for detection and characterization of glutathione (γ-glutamyl-cysteinylglycine, GSH)-trapped reactive metabolites using a negative precursor ion (PI) as the survey scan to trigger the acquisition of positive enhanced product ion (EPI) spectra on a triple quadrupole linear ion trap mass spectrometer. The negative precursor ion scan step was carried out monitoring the anion at m/z 272, corresponding to deprotonated γ-glutamyl-dehydroalanyl-glycine originating from the glutathionyl moiety. Because of the uniqueness and abundance of the anion at m/z 272, this single survey scan exhibited broad utility in the detection of unknown GSH conjugates. Further structural characterization was achieved by analyzing positive MS2 spectra that featured rich fragments without mass cutoff and were acquired in the same liquid chromatography/tandem mass spectrometry (LC/MS/MS) analysis. The effectiveness and reliability of this approach was evaluated using a number of model compounds in human liver microsomal incubations, including acetaminophen, clozapine, diclofenac, imipramine, meclofenamic acid, and ticlopidine. As a result, the PI-EPI approach revealed the presence of known adducts and, in many instances, identified additional conjugates that had not been reported previously. In comparison to the widely used neutral loss (NL) scanning analysis, this approach provided superior sensitivity and selectivity for different types of GSH conjugates. More importantly, the PI-EPI approach is suitable for high-throughput screening of reactive metabolites in the drug discovery process.