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Published on: May 7, 2018
An LC/MS/MS method for quantifying testosterone and dehydroepiandrosterone sulfate in four different serum samples
Shunsuke Fujimura1, Takenori Ito1, Shoujiro Ogawa1,2
1Faculty of Pharmaceutical Sciences, Tokyo University of Science, 2641 Yamazaki, Noda, 278-8510, Japan.
This study introduces a novel LC/ESI-MS/MS method using Girard reagents for simultaneous testosterone (TS) and dehydroepiandrosterone sulfate (DHEAS) quantification. The approach significantly enhances analysis throughput for men's health assessments.
Area of Science:
- Clinical Chemistry
- Analytical Chemistry
- Mass Spectrometry
Background:
- Simultaneous measurement of circulating testosterone (TS) and dehydroepiandrosterone sulfate (DHEAS) is crucial for men's health assessment.
- Liquid chromatography/electrospray ionization-tandem mass spectrometry (LC/ESI-MS/MS) is a reliable method but requires improved analysis throughput.
Purpose of the Study:
- To develop an LC/ESI-MS/MS method for parallel quantification of TS and DHEAS in multiple serum samples.
- To enhance the analysis throughput for androgen measurements.
Main Methods:
- Utilized a quadruplicate of Girard reagents for derivatization.
- Developed a method to pretreat, derivatize, and combine four serum samples for single-run LC/ESI-MS/MS analysis.
- Quantified TS and DHEAS in parallel across four samples.
Main Results:
- The developed method demonstrated practical measuring ranges with good precision, accuracy, and negligible matrix effects.
- Analysis of 40 serum samples showed a 60% reduction in post-pretreatment analysis time compared to non-derivatization methods.
- Achieved parallel quantification of androgens from four serum samples in a single run.
Conclusions:
- The novel Girard reagent-based LC/ESI-MS/MS method significantly improves efficiency for TS and DHEAS measurements.
- This method offers a valuable tool for high-throughput clinical assessment of men's health.
- The technique provides a faster and reliable alternative for routine androgen analysis.
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