Novel Isotope Dilution High-Performance Liquid Chromatography Quadrupole–Linear Ion Trap Tandem Mass Spectrometry Method for the Determination of Five Steroid Hormones in Human Serum

化学 色谱法 同位素稀释 四极离子阱 质谱法 离子阱 串联质谱法 类固醇 检出限 三级四极质谱仪 选择性反应监测 分析化学(期刊) 激素 生物化学
作者
Jie Xie,Wei Wan,Keke Yi,Ziyu Qu,Di Zhang,Zejian Huang,Zihong Ye,Xinhua Dai,You Jiang,Xiang Fang
出处
期刊:Analytical Letters [Informa]
卷期号:57 (8): 1257-1270 被引量:1
标识
DOI:10.1080/00032719.2023.2245078
摘要

AbstractAccurate measurement of endogenous steroid hormones in serum is a powerful tool for understanding the status of human adrenal diseases. Isotope dilution–liquid chromatography–tandem mass spectrometry is the most commonly used method for determination of steroids in serum. In this study, we used a laboratory-constructed quadrupole-linear ion trap (Q-LIT) tandem mass spectrometer to develop a new method for the quantification of five steroid hormones in serum. A simple and efficient pretreatment was improved, wherein the serum was extracted once by a mixed solvent of 1.0 mL of ethyl acetate and n-hexane. Using the optimized method, the regression coefficients of the calibration curves were all higher than 0.99, the limits of detection were from 0.31 to 1.25 ng mL−1, and the limits of quantification were between 1.00 and 2.50 ng mL−1. The intra-day (n = 3) relative standard deviations ranged from 4.24% to 13.79%, and the inter-day (n = 3) relative standard deviations from 3.99% to 11.43%. After internal standard correction, the relative recoveries of all steroids were from 86.08% to 106.60%. Twenty-two serum samples were analyzed by Q-LIT, which was compared with commercial triple quadrupole mass spectrometer. The results of the instruments had high consistency. Therefore, Q-LIT accurately quantified steroid hormones in human samples and may be used for clinical diagnosis and monitoring of hormone-dependent diseases.Keywords: High-performance liquid chromatography quadrupole–tandem mass spectrometryquadrupole–linear ion trapserumsteroid hormones Disclosure statementThere are no conflicts of interest to declare.Additional informationFundingThis work was financially supported by the National Key Research and Development Program of China (2020YFF01014600, 2022YFF0607900, 2021YFC2401100), the National Natural Science Foundation of China (21927812), and the Research Project of the National Institute of Metrology (AKY1934, AKYZZ2122). We sincerely thank Xiaoting Qiao for help with the experiments.
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