An isotope dilution liquid chromatography-tandem mass spectrometry candidate reference measurement procedure for aldosterone measurement in human plasma

被引:7
作者
Zhang, Qiaoxuan [1 ,2 ]
Han, Liqiao [1 ]
Zheng, Songbai [3 ]
Ouyang, Fen [1 ]
Wu, Xiaobin [1 ]
Yan, Jun [1 ]
Zhan, Min [1 ]
Ke, Peifeng [1 ]
Zhuang, Junhua [1 ]
Huang, Xianzhang [1 ]
机构
[1] Guangzhou Univ Chinese Med, Affiliated Hosp 2, Dept Lab Med, Guangzhou 510120, Guangdong, Peoples R China
[2] Guangzhou Univ Chinese Med, Clin Med Coll 2, Guangzhou 510120, Guangdong, Peoples R China
[3] Fujian Huayin Med Lab Ctr, Xiamen 361101, Fujian, Peoples R China
关键词
Aldosterone; Reference measurement procedure; Tandem mass spectrometry; Clinical laboratory measurements;
D O I
10.1007/s00216-021-03405-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Accurate quantitation of aldosterone is clinically important in standardized testing for primary aldosteronism. The results are often variable when performed by clinical immunoassays. To standardize and ensure the accuracy of clinical systems, reference measurement procedures (RMPs) with higher metrological order are required. A simple and reliable isotope dilution LC-IDMS/MS-based measurement procedure for human plasma aldosterone has been developed. This method involved plasma spiked with a deuterium-labelled internal standard, equilibrated for 0.5 h, and extracted by liquid-liquid extraction (LLE) without derivatization. Aldosterone and its structural analogues were baseline separated with a C18-packed UHPLC column with gradient elution within 7 min. The signal intensity variability and measurement imprecision were reduced by bracketing calibration during plasma aldosterone value assignment. The limit of detection (LoD) was 19.4 pmol/L with a signal-to-noise ratio (S/N) > 3. The lowest limit of quantification (LLoQ) was 27.7 pmol/L (S/N > 10 and CV < 10.0%). LLE was performed with 1 mL of n-hexane/ethyl acetate (3:2, v/v), and the extraction recovery was determined to be 92.15 +/- 3.54%. The imprecisions were <= 3.18% for samples at 124.8, 867.0, and 2628.5 pmol/L. The recoveries were 98.11-101.61%. The relative bias between this candidate RMP and the established RMP was 2.76-1.89%. The linearity response ranged from 27.7 to 2774.4 pmol/L with R-2 = 0.999. The method performance met the requirements of RMPs (<= 5% total CV and <= 3% bias). Furthermore, the developed method was applied to evaluate immunoassays through 41 patient sample comparisons. The calibration and measurement capability (CMC) of this method were also evaluated by measuring these samples. The candidate RMP can serve as an accurate reference baseline for routine methods and can be used for value assignment for reference materials.
引用
收藏
页码:4471 / 4481
页数:11
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