Analysis of Aldosterone in Plasma for Clinical Research using the ACQUITY UPLC I-Class/Xevo TQ-S micro System
Applications | 2018 | WatersInstrumentation
Aldosterone is an essential mineralocorticoid steroid hormone investigated in clinical research to elucidate the pharmacological action of aldosterone synthase inhibitors. Circulating levels are typically below 100 pmol/L, making precise measurement challenging. High analytical sensitivity and selectivity are therefore critical to reliably detect and quantify these low concentrations.
This study demonstrates the capability of the ACQUITY UPLC I-Class System paired with the Xevo TQ-S micro Mass Spectrometer to accurately measure aldosterone in human plasma. A fully automated sample preparation workflow and optimized UPLC-MS/MS method were employed to achieve reliable quantitative performance across a broad concentration range.
Sample preparation was automated on a Tecan Freedom EVO100/4 workstation using 96-well Oasis MAX µElution SPE plates. Plasma samples were diluted with internal standard (aldosterone-2H4), zinc sulfate, methanol, and phosphoric acid, then centrifuged and loaded onto conditioned SPE plates. Following acid and organic washes, analytes were eluted with 70% aqueous methanol. Chromatographic separation was performed on an ACQUITY UPLC I-Class System with a CORTECS UPLC C18 column under a water/methanol gradient. Detection utilized a Xevo TQ-S micro Mass Spectrometer with StepWave ion source technology, operating in MRM mode with quantifier and qualifier transitions (m/z 359.2 > 189.2 and 359.2 > 297.2) and aldosterone-2H4 as internal standard (m/z 363.2 > 190.2).
Calibration curves over 42–4161 pmol/L showed excellent linearity (r² = 0.9988) and low variability (%RSD slope = 1.3%). The lowest calibrator (42 pmol/L) achieved signal-to-noise ratios >25:1 across five days. Method precision assessed at low (128 pmol/L), mid (1011 pmol/L), and high (2926 pmol/L) levels yielded total %RSD ≤7.2% and repeatability ≤7.0%. The use of Oasis MAX chemistry delivered clean extracts with minimal background noise, ensuring selective ESI-MS/MS detection of aldosterone at low concentrations.
Advancements may include further miniaturization of analytical platforms, integration of multiplexed steroid panels for comprehensive endocrine profiling, and incorporation of machine learning algorithms for automated data processing. Expanded automation and novel ion-source designs could enhance throughput and detection limits, facilitating broader applications in pharmacokinetic and biomarker studies.
The developed UPLC-MS/MS workflow combining automated SPE on a Freedom EVO100/4 and the Xevo TQ-S micro system provides a robust, sensitive, and precise approach for aldosterone quantification in plasma. Its performance meets the stringent requirements of clinical research on aldosterone synthase inhibitors, delivering reproducible results with minimal manual intervention.
1. Schumacher CD et al. Aldosterone synthase inhibition for the treatment of hypertension and the derived mechanistic requirements for a new therapeutic strategy. Journal of Hypertension. 2013;31(10):2085–2093.
LC/MS, LC/MS/MS, LC/QQQ
IndustriesClinical Research
ManufacturerWaters
Summary
Význam tématu
Aldosterone is an essential mineralocorticoid steroid hormone investigated in clinical research to elucidate the pharmacological action of aldosterone synthase inhibitors. Circulating levels are typically below 100 pmol/L, making precise measurement challenging. High analytical sensitivity and selectivity are therefore critical to reliably detect and quantify these low concentrations.
Cíle a přehled studie / článku
This study demonstrates the capability of the ACQUITY UPLC I-Class System paired with the Xevo TQ-S micro Mass Spectrometer to accurately measure aldosterone in human plasma. A fully automated sample preparation workflow and optimized UPLC-MS/MS method were employed to achieve reliable quantitative performance across a broad concentration range.
Použitá metodika a instrumentace
Sample preparation was automated on a Tecan Freedom EVO100/4 workstation using 96-well Oasis MAX µElution SPE plates. Plasma samples were diluted with internal standard (aldosterone-2H4), zinc sulfate, methanol, and phosphoric acid, then centrifuged and loaded onto conditioned SPE plates. Following acid and organic washes, analytes were eluted with 70% aqueous methanol. Chromatographic separation was performed on an ACQUITY UPLC I-Class System with a CORTECS UPLC C18 column under a water/methanol gradient. Detection utilized a Xevo TQ-S micro Mass Spectrometer with StepWave ion source technology, operating in MRM mode with quantifier and qualifier transitions (m/z 359.2 > 189.2 and 359.2 > 297.2) and aldosterone-2H4 as internal standard (m/z 363.2 > 190.2).
Hlavní výsledky a diskuse
Calibration curves over 42–4161 pmol/L showed excellent linearity (r² = 0.9988) and low variability (%RSD slope = 1.3%). The lowest calibrator (42 pmol/L) achieved signal-to-noise ratios >25:1 across five days. Method precision assessed at low (128 pmol/L), mid (1011 pmol/L), and high (2926 pmol/L) levels yielded total %RSD ≤7.2% and repeatability ≤7.0%. The use of Oasis MAX chemistry delivered clean extracts with minimal background noise, ensuring selective ESI-MS/MS detection of aldosterone at low concentrations.
Přínosy a praktické využití metody
- High sensitivity: reliable quantification down to 42 pmol/L in plasma.
- Automated sample preparation: reduced manual handling, lower risk of errors, and increased throughput.
- Robust performance: total precision ≤7.2% over five days, supporting reproducible clinical research analyses.
Budoucí trendy a možnosti využití
Advancements may include further miniaturization of analytical platforms, integration of multiplexed steroid panels for comprehensive endocrine profiling, and incorporation of machine learning algorithms for automated data processing. Expanded automation and novel ion-source designs could enhance throughput and detection limits, facilitating broader applications in pharmacokinetic and biomarker studies.
Závěr
The developed UPLC-MS/MS workflow combining automated SPE on a Freedom EVO100/4 and the Xevo TQ-S micro system provides a robust, sensitive, and precise approach for aldosterone quantification in plasma. Its performance meets the stringent requirements of clinical research on aldosterone synthase inhibitors, delivering reproducible results with minimal manual intervention.
Reference
1. Schumacher CD et al. Aldosterone synthase inhibition for the treatment of hypertension and the derived mechanistic requirements for a new therapeutic strategy. Journal of Hypertension. 2013;31(10):2085–2093.
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