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Targeted glucocorticoid analysis using ion mobility-mass spectrometry (IM-MS)

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ELSEVIER
DOI: 10.1016/j.jmsacl.2022.03.003

关键词

Glucocorticoids; Ion mobility spectrometry; Ion mobility-mass spectrometry

资金

  1. Agilent Technologies (Global Academic Research Support Program) [2624930]
  2. Florida Institute of Technology startup funds
  3. Partnership for Clean Competition Research Collaborative

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LC-IM-MS is a multidimensional separation technique that allows for the analysis and separation of 16 glucocorticoids in three dimensions (retention time, CCS, and m/z). Despite modest resolution of isomer pairs under standard conditions, improvements were observed with alternative alkali, alkaline earth, and transition metals, as well as in carbon dioxide drift gas.
Introduction: Ion mobility-mass spectrometry (IM-MS) is an emerging technique in the -omics fields that has broad potential applicability to the clinical lab. As a rapid, gas-phase structure-based separation technique, IMMS offers promise in isomer separations and can be easily combined with existing LC-MS methods (i.e., LC-IMMS). Several experimental conditions, including analyte cation adducts and drift composition further provide a means to tune separations for global and/or targeted applications. Objectives: The primary objective of this study was to demonstrate the utility of IM-MS under a range of experimental conditions for detection of glucocorticoids, and specifically for the separation of several isomeric pairs. Methods: LC-IM-MS was used to characterize 16 glucocorticoids including three isomer pairs: cortisone/prednisolone, betamethasone/dexamethasone, and flunisolide/triamcinolone acetonide. Collision cross section (CCS) values were measured for all common adducts (e.g., protonated and sodiated) using both step-field and singlefield methods. Alternative alkali, alkaline earth, and transition metals were introduced, such that their adducts could also be measured. Finally, four different drift gases (helium, nitrogen, argon, and carbon dioxide) were compared for their relative separation capability. Results: LC-IM-MS offered a robust, multidimensional separation technique that allowed for the 16 glucocorticoids to be analyzed and separated in three-dimensions (retention time, CCS, and m/z). Despite the relatively modest resolution of isomer pairs under standard conditions (i.e., nitrogen drift gas, sodiated ions, etc.), improvements were observed for alkaline earth and transition metals (notable barium adducts) and in carbon dioxide drift gas. Conclusion: In summary, LC-IM-MS offers potential as a clinical method due to its ease of coupling with traditional LC-MS methods and its promise for tuning separations to better resolve targeted and/or global isomers in complex biological samples.

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