检验医学 ›› 2026, Vol. 41 ›› Issue (4): 369-373.DOI: 10.3969/j.issn.1673-8640.2026.04.009

• 论著 • 上一篇    下一篇

醛固酮冰冻人血清国家标准品的建立

于婷1, 沈宣辛2, 沈敏3(), 胡泽斌1()   

  1. 1 中国食品药品检定研究院体外诊断试剂所非传染病诊断试剂室北京 100050
    2 吉林省医疗器械检验研究院化学室吉林 长春 130062
    3 美康生物参考实验室浙江 宁波 315104
  • 收稿日期:2024-09-05 修回日期:2025-02-14 出版日期:2026-04-30 发布日期:2026-05-07
  • 通讯作者: 沈 敏,E-mail:min.shen@nbmedicalsystem.com。胡泽斌,E-mail:huzebin@nifdc.org.cn
  • 作者简介:于 婷,女,1978年生,博士,研究员,主要从事体外诊断试剂检定和标准物质研制工作;
    沈宣辛,女,1988年生,工程师,主要从事体外诊断试剂类医疗器械产品检验工作。第一联系人:于婷和沈宣辛对本研究具有同等贡献,并列为第一作者。
  • 基金资助:
    广东省社会发展科技协同创新项目(2023A1111120024)

Establishment of the national standard reference material of aldosterone in frozen human serum

YU Ting1, SHEN Xuanxin2, SHEN Min3(), HU Zebin1()   

  1. 1 Division of In Vitro Diagnostics for Non-infectious Diseasesthe National Institutes for Food and Drug ControlBeijing 100050, China
    2 Chemistry DepartmentJilin Institute of Medical Device InspectionChangchun 130062,Jilin, China
    3 Reference LaboratoryMedicalsystem Biotechnology Co.,Ltd.Ningbo 315104,Zhejiang, China
  • Received:2024-09-05 Revised:2025-02-14 Online:2026-04-30 Published:2026-05-07

摘要:

目的 建立醛固酮冰冻人血清国家标准品,用于醛固酮检测的量值传递和正确度评价。方法 收集外观清亮,无明显黄疸、溶血和乳糜,且传染病四项检测均为阴性的临床血清样本,经多级过滤、除菌后,制备成高、低2个水平的候选品,-70 ℃及以下保存。评价候选品的均匀性、稳定性、互通性。选择5家实验室,采用参考方法(同位素稀释液相色谱-串联质谱法)进行联合赋值。结果 均匀性评估结果显示,高水平和低水平候选品的F值分别为1.355 3、1.473 3,均<F0.05(1.511 7);稳定性评估结果显示,2个水平候选品室温条件均可稳定5 h,(2~8)℃均可稳定20 d,-20 ℃均至少可稳定30 d。高水平、低水平候选品定值结果分别为(0.239±0.018)nmol·L-1k=2)、(0.845±0.052)nmol·L-1k=2),或(86.22±6.31)pg·mL-1k=2)、(304.74±18.80)pg·mL-1k=2)。2个水平候选品在5种主流常规检测系统中的互通性均良好。结论 建立的醛固酮候选品均匀、稳定,且互通性良好,定值准确可靠,可作为国家标准品使用。该国家标准品的建立,对于促进醛固酮检测结果的标准化具有重要意义。

关键词: 醛固酮, 冰冻人血清, 国家标准品

Abstract:

Objective To establish a national standard reference material of aldosterone in frozen human serum for the transfer of measurement values and the evaluation of accuracy in aldosterone determination. Methods Clinical serum samples with clear appearance,no obvious jaundice,hemolysis or lipemia,and negative results for 4 infectious disease determinations were collected. After multi-level filtration and sterilization,the samples were classified into high- and low- level candidate reference materials and stored at -70 ℃ or below. The homogeneity,stability and intercommunity of the candidate reference materials were evaluated. Totally,5 laboratories were selected to jointly assign values using the reference method(isotope dilution liquid chromatography-tandem mass spectrometry). Results The results of homogeneity test showed that the F values of the high- and low- level candidate reference materials were 1.355 3 and 1.473 3,respectively,both <F0.05(1.511 7). The results of stability test showed that the candidate reference materials were stable for 5 h at room temperature,20 d at 2-8 ℃,and at least 30 d at -20 ℃. The assigned values of the high- and low- level candidate reference materials were(0.239±0.018)nmol·L-1k=2) and(0.845±0.052)nmol·L-1k=2),or(86.22±6.31)pg·mL-1k=2) and(304.74±18.80)pg·mL-1k=2),respectively. The intercommunity of the 2 levels of candidate reference materials was good in 5 mainstream routine determination systems. Conclusions The established aldosterone candidate reference materials are homogeneous and stable and have good intercommunity,with accurate and reliable assigned values,and can be used as national standard reference materials. The establishment of this national standard reference material is of significance for promoting the standardization of aldosterone determination results.

Key words: Aldosterone, Frozen human serum, National standard reference material

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