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. 2022 Jul 30;78(2):373–379. doi: 10.1007/s12020-022-03140-6

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© The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

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Fig. 1 — LC-MS/MS chromatogram for steroid hormones in mix solution. Numbers indicate the following metabolites. 1: Aldosterone; 2: Cortisol; 3: 21-deoxycortisol, 4: Corticosterone, 5: 11-deoxycortisol, 6: Androstenedione, 7: Estrone, 8: 11-deoxycorticosterone, 9: Testosterone 10: Estradiol, 11: Dehydroepiandrosterone, 12: 17-hydroxyprogesterone, 13: 17-hydroxypPregnenolone, 14: Dihydrotestosterone, 15: Progesterone, 16: Androsterone, 17: Pregnenolone