Abstract
Simultaneous measurements of the circulating testosterone (TS) and dehydroepiandrosterone sulfate (DHEAS) are deemed to be helpful for the assessment of men’s health. Liquid chromatography/electrospray ionization–tandem mass spectrometry (LC/ESI–MS/MS) is the most reliable methodology for this purpose; however, it has room for improvement in analysis throughput. In this study, a quadruplicate of the Girard reagents was used to develop an LC/ESI–MS/MS method capable of quantifying TS and DHEAS in four different serum samples in a single run. The four serum samples were separately pretreated, derivatized with one of four Girard reagents, and then combined. The LC/ESI–MS/MS analysis of the combined sample provided the androgen concentrations of four serum samples in parallel. The method had practical measuring ranges, in which good precision and accuracy, as well as negligible matrix effects were verified. The speed-up capability of the developed method was evaluated through the analysis of ten batches of serum samples (total 40 samples); the method saved a 60% post-pretreatment analysis time compared to the non-derivatization method for 40 samples.
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This study was supported in part by the Japan Society for the Promotion of Science (JSPS) KAKENHI Grant Number 20K06990.
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Supplementary file1 The ESI–MS/MS parameters, method validation procedures and data, and non-derivatization method are available free of charge on the Web at http://www.jasc.or.jp/analsci/. (DOCX 82 KB)
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Fujimura, S., Ito, T., Ogawa, S. et al. An LC/MS/MS method for quantifying testosterone and dehydroepiandrosterone sulfate in four different serum samples during a single run. ANAL. SCI. 38, 167–173 (2022). https://doi.org/10.2116/analsci.21P268
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DOI: https://doi.org/10.2116/analsci.21P268