Development of UME CRM 1008: certified reference material for C-reactive protein

IF 0.8 4区 工程技术 Q4 CHEMISTRY, ANALYTICAL Accreditation and Quality Assurance Pub Date : 2024-01-12 DOI:10.1007/s00769-023-01563-w
Merve Oztug, Evren Saban, Meltem Asicioglu, Alper Isleyen, Muslum Akgoz
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Abstract

A certified reference material (CRM) specifically designed for C-reactive protein (CRP) measurement in clinical laboratories was produced in this study. CRP, a protein synthesized by the liver, serves as an indicator of inflammation when present in elevated concentrations in the bloodstream. The primary goal is to ensure accurate measurement and quality control in accredited clinical laboratories. To achieve this, a recombinant CRP solution was selected as the most suitable candidate material for the CRM due to its exceptional purity. The homogeneity and stability of the developed CRM were thoroughly examined using size exclusion chromatography coupled with ultraviolet detection and high-performance liquid chromatography, (SEC-UV-HPLC). Additionally, traceable amino acid analysis coupled with isotope dilution mass spectrometry (ID-LC/MS-AAA) was employed to determine the protein concentration of CRP in the CRM solution. The evaluation of uncertainties originating from factors such as characterization, homogeneity, long-term stability, and short-term stability data was incorporated to assess the uncertainty associated with the certified CRP value. Consequently, the certified value of the CRM, denoted as UME CRM 1008, was determined to be 43.2 ± 2.2 μmol kg−1, with an expanded uncertainty at a coverage factor of k = 2. The CRP-certified reference material resulting from this study is intended to be used as a primary reference material to enable SI traceable measurement of CRP.

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开发 UME CRM 1008:C 反应蛋白认证标准物质
在这项研究中,生产出了一种专用于临床实验室测量 C 反应蛋白 (CRP) 的有证标准物质 (CRM)。CRP 是一种由肝脏合成的蛋白质,在血液中浓度升高时可作为炎症指标。其主要目的是确保认可临床实验室的准确测量和质量控制。为实现这一目标,重组 CRP 溶液因其卓越的纯度而被选为 CRM 的最合适候选材料。使用尺寸排阻色谱-紫外检测和高效液相色谱法(SEC-UV-HPLC)对所开发的 CRM 的均匀性和稳定性进行了全面检测。此外,还采用了可追溯氨基酸分析和同位素稀释质谱法(ID-LC/MS-AAA)来测定 CRM 溶液中 CRP 的蛋白质浓度。对表征、均匀性、长期稳定性和短期稳定性数据等因素产生的不确定性进行了评估,以评估与 CRP 认证值相关的不确定性。因此,有证标准物质的认证值(UME CRM 1008)被确定为 43.2 ± 2.2 μmol kg-1,覆盖因子 k = 2 时的不确定性有所扩大。这项研究产生的有证标准物质将用作主要标准物质,以实现有证标准物质的 SI 可追溯测量。
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来源期刊
Accreditation and Quality Assurance
Accreditation and Quality Assurance 工程技术-分析化学
CiteScore
1.80
自引率
22.20%
发文量
39
审稿时长
6-12 weeks
期刊介绍: Accreditation and Quality Assurance has established itself as the leading information and discussion forum for all aspects relevant to quality, transparency and reliability of measurement results in chemical and biological sciences. The journal serves the information needs of researchers, practitioners and decision makers dealing with quality assurance and quality management, including the development and application of metrological principles and concepts such as traceability or measurement uncertainty in the following fields: environment, nutrition, consumer protection, geology, metallurgy, pharmacy, forensics, clinical chemistry and laboratory medicine, and microbiology.
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