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

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机构: [1]Department of Laboratory Medicine, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou 510120, Guangdong, China [2]Second Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou 510120, Guangdong, China [3]Fujian Huayin Medical Laboratory Center, Xiamen 361101, Fujian, China
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关键词: Aldosterone Clinical laboratory measurements Reference measurement procedure Tandem mass spectrometry

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 R2 = 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. Graphical abstract: [Figure not available: see fulltext.] © 2021, Springer-Verlag GmbH Germany, part of Springer Nature.

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基金编号: 2020A1515010668

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出版当年[2020]版:
大类 | 3 区 化学
小类 | 2 区 分析化学 3 区 生化研究方法
最新[2025]版:
大类 | 2 区 化学
小类 | 3 区 生化研究方法 3 区 分析化学
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出版当年[2019]版:
Q1 BIOCHEMICAL RESEARCH METHODS Q1 CHEMISTRY, ANALYTICAL
最新[2023]版:
Q1 BIOCHEMICAL RESEARCH METHODS Q1 CHEMISTRY, ANALYTICAL

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第一作者机构: [1]Department of Laboratory Medicine, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou 510120, Guangdong, China [2]Second Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou 510120, Guangdong, China
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