检验医学 ›› 2020, Vol. 35 ›› Issue (8): 811-817.DOI: 10.3969/j.issn.1673-8640.2020.08.016

• 技术研究与评价·论著 • 上一篇    下一篇

血清醛固酮候选参考测量程序的建立及性能评估

邹继华1, 李全乐1, 沈敏1, 张曼2, 杨晓东1, 屠敏敏1, 冯东方3, 孙宏娜1   

  1. 1. 美康生物参考实验室,浙江 宁波 315104
    2. 首都医科大学附属北京世纪坛医院检验科,北京 100038
    3. 西藏军区总医院检验科,西藏 拉萨 850007
  • 收稿日期:2020-02-13 出版日期:2020-08-30 发布日期:2020-09-24
  • 作者简介:null

    作者简介:邹继华,男,1979年生,硕士,高级工程师,主要从事体外诊断试剂量值溯源及研发。李全乐,女,1989年生,硕士,工程师,主要从事体外诊断试剂量值溯源及研发。

  • 基金资助:
    国家重点研发计划(2019YFF0216504)

Establishment and performance evaluation of candidate reference measurement procedure for serum aldosterone by liquid chromatography-tandem mass spectrometry

ZOU Jihua1, LI Quanle1, SHEN Min1, ZHANG Man2, YANG Xiaodong1, TU Minmin1, FENG Dongfang3, SUN Hongna1   

  1. 1. Reference Laboratory,Medical System Biotechnology Co.,Ltd.,Ningbo 315104,Zhejiang,China
    2. Department of Clinical Laboratory,Beijing Shijitan Hospital,Capital Medical University,Beijing 100038,China
    3. Department of Clinical Laboratory,General Hospital of Tibet Military Region,Lhasa 850007,Tibet,China
  • Received:2020-02-13 Online:2020-08-30 Published:2020-09-24

摘要:

目的 建立基于同位素稀释液相色谱-串联质谱(ID-LC-MS/MS)的血清醛固酮候选参考方法。方法 以甲基叔丁基醚为萃取剂,采用液液萃取方式进行样本前处理。以醛固酮-2H7为内标,采用电喷雾离子源(ESI)负离子模式建立检测血清醛固酮的ID-LC-MS/MS方法,并对方法的准确度、精密度、灵敏度、线性等基本分析性能进行验证。结果 ID-LC-MS/MS测定血清醛固酮的线性范围为0.08~3.55 nmol/L,检测限和定量限(LOQ)分别为0.012 nmol/L和0.045 nmol/L。批内和批间变异系数(CV)分别为<5.0%和<4.1%。平均加标回收率为98.52%~100.14%。测定国际临床化学和检验医学联合会参考实验室外部质量评价计划(RELA)样本的结果偏移<1.6%。结论 建立的测定血清醛固酮的ID-LC-MS/MS方法准确、精密,有望作为测定血清醛固酮的参考方法。

关键词: 醛固酮, 同位素稀释液相色谱-串联质谱, 参考方法

Abstract:

Objective To establish a candidate reference measurement procedure for serum aldosterone by isotope dilution liquid chromatography-tandem mass spectrometry(ID-LC-MS/MS). Methods The sample was prepared by liquid-liquid extraction with methyltert-bytylether as extractant. The aldosterone-2H7 was selected as internal standard. Samples were prepared by liquid-liquid extraction,and aldosterone was detected by ID-LC-MS/MS in negative ion mode. The basic analysis performance of the established candidate reference measurement procedure,including accuracy,precision,sensitivity and linearity,was evaluated. Results The linear range of aldosterone was 0.08-3.55 nmol/L. The limit of detection and the limit of quantitation were (LOQ)0.012 nmol/L and 0.045 nmol/L,respectively. The within-run coefficients of variation(CV) was <5.0%,and the between-run CV was <4.1%. The average recovery rates were 98.52%-100.14%. The bias of the International Federation of Clinical Chemistry and Laboratory Medicine External Quality Assessment Scheme for Reference Laboratories in Laboratory Medicine(RELA) was <1.6%. Conclusions The established ID-LC-MS/MS for detecting aldosterone in serum is accuracy and precise,and may be used as a candidate reference measurement procedure.

Key words: Aldosterone, Isotope dilution liquid chromatography-tandem mass spectrometry, Reference method

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