Abstract
Steroids are one of the important indicators of health and disease. However, due to the high similarity of steroid structures, there are several potential obstacles in the differentiation of steroids, especially for their isomers. Herein, we described a trapped ion mobility spectrometry-mass spectrometry (TIMS-MS) approach based on the steroid analogue adduction for isomer-specific identification of steroids. The application of dexamethasone (DEX) to form heterodimers with steroids enhanced the separation of their isomers in TIMS. Two isomer pairs including 17-hydroxyprogesterone/11-deoxycorticosterone and androsterone/epiandrosterone were successfully separated as the heterodimers with DEX by TIMS. The stability of DEX-adducted heterodimers is comparable with steroid dimers. Owing to the high separation efficiency and stability, the relative quantification of steroid isomers was demonstrated with the proposed method.
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The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
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Funding
This work was financially supported by the National Natural Science Foundation of China (22204085) and the Zhejiang Provincial Natural Science Foundation of China under Grant No. LQ23B050005.
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Yang Li: data curation; visualization; investigation; methodology; writing original draft. Yujiao Qin: methodology; investigation. Songchang Wei: methodology; investigation. Ling Ling: resources; funding acquisition; supervision; conceptualization; writing—review and editing. Chuan-Fan Ding: supervision; resources; funding acquisition; writing—review and editing.
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Li, Y., Qin, Y., Wei, S. et al. Differentiation of steroid isomers by steroid analogues adducted trapped ion mobility spectrometry-mass spectrometry. Anal Bioanal Chem 416, 313–319 (2024). https://doi.org/10.1007/s00216-023-05019-5
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DOI: https://doi.org/10.1007/s00216-023-05019-5