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基于 HPAEC-PAD 的候选参考测量程序,用于开发血清中单糖的有证参考物质。

Candidate reference measurement procedure based on HPAEC-PAD for the development of certified reference materials for monosaccharides in serum.

机构信息

Biometrology Group, Division of Chemical and Biological Metrology, Korea Research Institute of Standards and Science, 267 Gajeong-ro, Yuseong-Gu, Daejeon, 34113, Republic of Korea.

Department of Chemistry, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul, 02841, Republic of Korea.

出版信息

Anal Bioanal Chem. 2021 Sep;413(21):5517-5527. doi: 10.1007/s00216-021-03537-8. Epub 2021 Jul 20.

Abstract

To achieve the measurement reliability of monosaccharides used as diagnostic markers in clinical fields, it is essential to establish certified reference materials (CRMs). The purpose of this study is to develop a serum CRM by adopting high-performance anion-exchange chromatography with pulsed amperometric detection (HPAEC-PAD) as a new candidate reference measurement procedure for the measurement of glucose and galactose, common diagnostic markers of diabetes and galactosemia, respectively. Using various monosaccharides as internal standards, the accuracy of the HPAEC-PAD method was tested by measuring glucose CRM following treatment with three different deproteinization methods: ultrafiltration, protein precipitation by trichloroacetic acid (TCA), and protein precipitation by acetonitrile. Results showed that ultrafiltration and 5% TCA provided good accuracy with every tested monosaccharide as the internal standard. Accordingly, serum samples in this study were treated by ultrafiltration after adding 2-deoxy-D-glucose and arabinose, which were selected as internal standards for galactose and glucose, respectively. Both intra- and inter-day recovery tests showed good precision and accuracy within 2%. From the serum CRM batches prepared at two levels, 11 units were analyzed by exact-matched calibration methods, and the mass fractions of galactose and glucose were determined via HPAEC-PAD. The between-unit relative standard deviations were not more than 1.5%, showing homogeneity. The expanded uncertainties (%) of galactose and glucose for both levels were less than 3.6% and 2.3% at 95% confidence. The HPAEC-PAD method presented in this study can significantly improve the accuracy and precision of simultaneous monosaccharide analysis, allowing for the development of further serum CRMs for monosaccharides. Graphical abstract.

摘要

为了实现临床领域中作为诊断标志物的单糖的测量可靠性,建立经过认证的参考物质(CRM)是至关重要的。本研究的目的是采用高效阴离子交换色谱-脉冲安培检测法(HPAEC-PAD)作为葡萄糖和半乳糖的新候选参考测量程序,建立血清 CRM。葡萄糖和半乳糖分别是糖尿病和半乳糖血症的常见诊断标志物。通过用三种不同的蛋白质沉淀方法(超滤、三氯乙酸(TCA)沉淀和乙腈沉淀)处理葡萄糖 CRM,用各种单糖作为内标测试 HPAEC-PAD 方法的准确性。结果表明,超滤和 5%TCA 与每种测试的内标物一起提供了良好的准确性。因此,本研究在添加 2-脱氧-D-葡萄糖和阿拉伯糖作为半乳糖和葡萄糖的内标后,通过超滤处理血清样品。这两种内标物分别用于半乳糖和葡萄糖。日内和日间回收测试均显示出 2%以内的良好精密度和准确性。从两个水平制备的血清 CRM 批次中,通过精确匹配的校准方法分析了 11 个单位,通过 HPAEC-PAD 测定半乳糖和葡萄糖的质量分数。单位间相对标准偏差不超过 1.5%,表现出均匀性。两个水平的半乳糖和葡萄糖的扩展不确定度(%)均小于 3.6%和 2.3%,置信度为 95%。本研究中提出的 HPAEC-PAD 方法可显著提高单糖分析的准确性和精密度,从而进一步开发单糖的血清 CRM。

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