检验医学 ›› 2015, Vol. 30 ›› Issue (5): 416-420.DOI: 10.3969/j.issn.1673-8640.2015.05.003

• 质谱技术在临床生化检验中的应用专题 • 上一篇    下一篇

液相色谱-串联质谱法检测血清25-羟基维生素D的方法建立和性能评价

宋斌斌, 秦嘉倩, 彭颖斐, 张春燕, 吴炯, 王蓓丽, 郭玮, 潘柏申   

  1. 复旦大学附属中山医院检验科,上海 200032
  • 收稿日期:2014-04-03 出版日期:2015-05-30 发布日期:2015-06-17
  • 作者简介:null

    作者简介:宋斌斌,男,1975年生,硕士,主管技师,主要从事临床免疫检验工作。

    作者简介:潘柏申,联系电话:021-64041990-2376。

  • 基金资助:
    “十二五”国家科技支撑计划课题资助项目(2012BAI37B01);国家临床重点检验专科建设项目资助项目

Establishment on a LC-MS/MS and its performance characteristic evaluation for the determination of serum 25-hydroxyvitamin D

SONG Binbin, QIN Jiaqian, PENG Yingfei, ZHANG Chunyan, WU Jiong, WANG Beili, GUO Wei, PAN Baishen   

  1. Department of Clinical Laboratory, Zhongshan Hospital, Fudan University, Shanghai 200032, China
  • Received:2014-04-03 Online:2015-05-30 Published:2015-06-17

摘要: 目的 建立定量检测血清25-羟基维生素D[25(OH)D]的液相色谱-串联质谱(LC-MS/MS)方法,并对此方法进行基本分析性能验证。方法 使用Waters® XevoTM TQ MS ACQUITY UPLC®液质联用仪(LC-MS/MS)同时定量检测血清中的25(OH)D2和25(OH)D3含量。参照美国食品和药品管理局(FDA)的生物分析方法验证导则标准对所建方法进行线性、检出限、精密度和准确性等基本性能的验证。结果 LC-MS/MS检测25(OH)D2和25(OH)D3的线性范围为6.25~500.00 nmol/L;25(OH)D2和25(OH)D3的定量检出限分别为2.50和1.25 nmol/L;批内、批间变异系数(CV)分别为<4%、<6%;回收率为93.26%~112.16%;维生素D国际室间质量评价计划(DEQAS)室间质评结果偏倚<10%。结论 建立的LC-MS/MS基本性能符合评价标准,能够灵敏且准确的检测出血清中25(OH)D2和25(OH)D3 的浓度。

关键词: 25羟基维生素D, 液相串联质谱, 性能验证

Abstract: Objective To establish a liquid chromatography-tandem mass spectrometry (LC-MS/MS) for the quantitation determination of serum 25-hydroxyvitamin D [25(OH)D] and perform the general method performance verification. Methods The LC-MS/MS was used for the quantitation determination of 25(OH)D2 and 25(OH)D3 in serum by Waters® XevoTM TQ MS ACQUITY UPLC® mass spectrometry instrument. According to US Food and Drug Administration (FDA)'s guideline (Guidance for Industry Bioanalytical Method Validation), the general method performance verification was performed for linearity, determination limit, precision and accuracy. Results The linear ranges of 25(OH)D2 and 25(OH)D3 were 6.25-500.00 nmol/L. The LC-MS/MS had quantitation determination limits of 2.50 nmol/L for 25(OH)D2 and 1.25 nmol/L for 25(OH)D3. The within-run and between-run coefficients of variation (CV) of 25(OH)D2 and 25(OH)D3 were <4% and <6%, respectively. The recovery rates were 93.26%-112.16%. The result of the Vitamin D External Quality Assessment Scheme (DEQAS) interlaboratory quality assessment had a bias <10%. Conclusions The basic performance of LC-MS/MS meets the evaluation standards, and LC-MS/MS is sensitive and accurate for detecting the concentrations of 25(OH)D2 and 25(OH)D3 in serum.

Key words: 25-hydroxyvitamin D, Liquid chromatography-tandem mass spectrometry, Performance verification

中图分类号: