Department of Laboratory Medicine, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine (Guangdong Provincial Hospital of Chinese Medicine), Guangzhou, 510120, China.
State Key Laboratory of Dampness Syndrome of Chinese Medicine, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, 510120, China.
Anal Bioanal Chem. 2022 Mar;414(7):2523-2531. doi: 10.1007/s00216-022-03896-w. Epub 2022 Feb 25.
To solve long-term lack of traceability of commercial calibrator kits and standardize clinical routine assays, we developed a human serum matrix-based unconjugated estriol (uE3) reference material (RM) with five concentration gradients. The RMs of uE3 were certified by the National Institute of Metrology (NIM) with the codes of GBW (E) 091048, GBW (E) 091049, GBW (E) 091050, GBW (E) 091051, and GBW (E) 091052. The RMs were determined by isotope dilution liquid chromatography-tandem mass spectrometry (ID-LC-MS/MS) reference method which was developed in our group and recommended by the Joint Committee on Traceability on Laboratory Medicine (JCTLM). GBW09224 is intended for use as a primary reference material to enable the SI-traceable measurement of uE3. This study describes the development process of these certified RMs. The candidate material was prepared by collecting from the remaining serum samples after routine clinical testing. Satisfactory homogeneity and stability were shown in these RMs. They are also commutable between the reference method and the three routine clinical immunoassay systems. To improve the accuracy of value assignment, a collaborative study in nine reference laboratories was conducted which was performed according to ISO/WD 15725-1 and all of the reference laboratories have been confirmed by China National Accreditation Service for Conformity Assessment (CNAS). The raw results were statistically analyzed and processed, coupled with uncertainty evaluation, to obtain the certified value: GBW (E) 091048 is 22.1 ± 1.3 nmol/L, GBW (E) 091049 is 33.6 ± 1.6 nmol/L, GBW (E) 091050 is 10.4 ± 0.8 nmol/L, GBW (E) 091051 is 15.5 ± 1.0 nmol/L, GBW (E) 091052 is 47.0 ± 2.0 nmol/L. The preparation process of human serum matrix-based reference material and the lack of these type of secondary (commutable) reference material of unconjugated estriol lead to the interruption of its traceability chain, which is a problem to be solved in its standardization as mentioned in the metrological traceability in ISO 17511, 2020.
为了解决商业校准试剂盒长期缺乏可追溯性以及规范临床常规检测的问题,我们开发了一种基于人血清基质的未结合雌三醇(uE3)参考物质(RM),具有五个浓度梯度。这些 uE3 的 RM 已由中国计量科学研究院(NIM)通过代码 GBW(E)091048、GBW(E)091049、GBW(E)091050、GBW(E)091051 和 GBW(E)091052 进行了认证。这些 RM 是通过我们小组开发并由实验室医学溯源联合委员会(JCTLM)推荐的同位素稀释液相色谱-串联质谱法(ID-LC-MS/MS)参考方法来确定的。GBW09224 旨在用作主要参考物质,以实现 uE3 的 SI 可溯源测量。本研究描述了这些经认证的 RM 的开发过程。候选材料是通过收集常规临床检测后的剩余血清样本制备的。这些 RM 表现出良好的均一性和稳定性。它们在参考方法和三种常规临床免疫分析系统之间也是可互换的。为了提高赋值准确性,在中国合格评定国家认可委员会(CNAS)的确认下,在 9 个参考实验室进行了协作研究,该研究按照 ISO/WD 15725-1 进行。对原始结果进行了统计分析和处理,并结合不确定度评估,以获得认证值:GBW(E)091048 为 22.1±1.3nmol/L,GBW(E)091049 为 33.6±1.6nmol/L,GBW(E)091050 为 10.4±0.8nmol/L,GBW(E)091051 为 15.5±1.0nmol/L,GBW(E)091052 为 47.0±2.0nmol/L。人血清基质参考物质的制备过程以及缺乏这种未结合雌三醇的二级(可互换)参考物质,导致其溯源链中断,这是 ISO 17511、2020 中提到的标准化过程中需要解决的问题。