Kato Megumi, Kinumi Tomoya, Yoshioka Mariko, Goto Mari, Fujii Shin-Ichiro, Takatsu Akiko
Organic Analytical Chemistry Division, Bio-Medical Standards Section, National Metrology Institute of Japan, National Institute of Advanced Industrial Science and Technology, 1-1-1 Umezono, Tsukuba, Ibaraki, 305-8563, Japan,
Anal Bioanal Chem. 2015 Apr;407(11):3137-46. doi: 10.1007/s00216-014-8190-0. Epub 2014 Oct 11.
To standardize C-reactive protein (CRP) assays, the National Metrology Institute of Japan (NMIJ) has developed a C-reactive protein solution certified reference material, CRM 6201-b, which is intended for use as a primary reference material to enable the SI-traceable measurement of CRP. This study describes the development process of CRM 6201-b. As a candidate material of the CRM, recombinant human CRP solution was selected because of its higher purity and homogeneity than the purified material from human serum. Gel filtration chromatography was used to examine the homogeneity and stability of the present CRM. The total protein concentration of CRP in the present CRM was determined by amino acid analysis coupled to isotope-dilution mass spectrometry (IDMS-AAA). To improve the accuracy of IDMS-AAA, we optimized the hydrolysis process by examining the effect of parameters such as the volume of protein samples taken for hydrolysis, the procedure of sample preparation prior to the hydrolysis, hydrolysis temperature, and hydrolysis time. Under optimized conditions, we conducted two independent approaches in which the following independent hydrolysis and liquid chromatography-isotope dilution mass spectrometry (LC-IDMS) were combined: one was vapor-phase acid hydrolysis (130 °C, 24 h) and hydrophilic interaction liquid chromatography-mass spectrometry (HILIC-MS) method, and the other was microwave-assisted liquid-phase acid hydrolysis (150 °C, 3 h) and pre-column derivatization liquid chromatography-tandem mass spectrometry (LC-MS/MS) method. The quantitative values of the two different amino acid analyses were in agreement within their uncertainties. The certified value was the weighted mean of the results of the two methods. Uncertainties from the value-assignment method, between-method variance, homogeneity, long-term stability, and short-term stability were taken into account in evaluating the uncertainty for a certified value. The certified value and the expanded uncertainty (k = 2) of CRM 6201-b are (40.0 ± 1.6) μmol kg(-1).
为规范C反应蛋白(CRP)检测方法,日本国家计量院(NMIJ)研制了一种C反应蛋白溶液标准物质CRM 6201-b,旨在用作一级标准物质,以实现CRP的SI可溯源测量。本研究描述了CRM 6201-b的研制过程。作为CRM的候选物质,选择重组人CRP溶液是因为其纯度和均一性高于从人血清中纯化得到的物质。采用凝胶过滤色谱法检测了本标准物质的均一性和稳定性。本标准物质中CRP的总蛋白浓度通过氨基酸分析结合同位素稀释质谱法(IDMS-AAA)测定。为提高IDMS-AAA的准确性,我们通过考察水解所用蛋白质样品体积、水解前样品制备程序、水解温度和水解时间等参数的影响,优化了水解过程。在优化条件下,我们进行了两种独立的方法,将以下独立水解和液相色谱-同位素稀释质谱法(LC-IDMS)相结合:一种是气相酸水解(130℃,24小时)和亲水作用液相色谱-质谱法(HILIC-MS),另一种是微波辅助液相酸水解(150℃,3小时)和柱前衍生化液相色谱-串联质谱法(LC-MS/MS)。两种不同氨基酸分析的定量值在其不确定度范围内一致。认定值为两种方法结果的加权平均值。在评估认定值的不确定度时,考虑了赋值方法、方法间方差、均一性、长期稳定性和短期稳定性的不确定度。CRM 6201-b的认定值和扩展不确定度(k = 2)为(40.0±1.6)μmol kg-1。