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干血斑样品中维生素 D 测定的候选参考方法。

Candidate reference method for determination of vitamin D from dried blood spot samples.

机构信息

School of Health and Biomedical Sciences, RMIT University, Bundoora, Victoria, Australia.

Murdoch Children's Research Institute, Parkville, Victoria, Australia.

出版信息

Clin Chem Lab Med. 2020 Apr 28;58(5):817-827. doi: 10.1515/cclm-2019-0397.

Abstract

Background The current millennium has seen an explosion in vitamin D testing with the overarching aim of requests to clinically stratify patients as replete or deficient in vitamin D. At a population level, dried blood spot (DBS) sampling offers a less invasive and more practical application for assessment of vitamin D status. We have therefore aimed to develop a sensitive and robust DBS vitamin D method that is traceable to serum for use in population-based studies. Methods Blood spots, calibrators and controls were prepared by punching a 3.2 mm DBS from filter paper and placed into a 96-well micro-plate. The DBS disk was eluted with a combination of water-methanol and internal standard (ISTD) solution followed by supported-liquid extraction and derivatisation. The extract was analysed by liquid-chromatography tandem-mass spectrometry in positive electrospray-ionisation mode with 732.5 > 673.4 and 738.4 > 679.4 m/z ion-transitions for derivatised vitamin D and the ISTD, respectively. Vitamin D results were made traceable to the National Institute of Standards and Technology reference material through the inclusion of Chromsystems vitamin D calibrators. Results 25-Hydroxy-vitamin D3 and its related ISTD were detected at a retention time of 7 min. The seven-point calibration-curve consistently demonstrated a coefficient of determination of 0.99 with an experimentally determined reportable range of 0.5-376 nmol/L. Method validation studies using DBS samples demonstrated 12.9% between-assay imprecision at 45 nmol/L, 84% average recovery and high correlation with plasma vitamin D (correlation coefficient = 0.86). Conclusions We have successfully developed an analytical method for vitamin D quantitation from DBSs which will be applied to our population-based vitamin D research study. This approach improves traceability of DBS results and potentially could be used broadly for other DBS measurands that require comparison to serum/plasma for their interpretation.

摘要

背景 当前的千年见证了维生素 D 检测的爆炸式增长,其主要目的是请求将患者按照维生素 D 充足或缺乏进行临床分层。在人群水平上,干血斑 (DBS) 采样提供了一种更具侵入性和实用性的方法来评估维生素 D 状态。因此,我们旨在开发一种灵敏且稳健的 DBS 维生素 D 方法,该方法可溯源至血清,用于基于人群的研究。

方法 通过从滤纸打孔制备 3.2mm 的 DBS 血斑、校准品和质控品,并将其放入 96 孔微孔板中。DBS 圆盘用水-甲醇和内标 (ISTD) 溶液洗脱,然后进行支持液-液萃取和衍生化。提取物通过正电喷雾电离模式下的液相色谱串联质谱分析,衍生化的维生素 D 和 ISTD 的离子转移分别为 732.5 > 673.4 和 738.4 > 679.4 m/z。通过包含 Chromsystems 维生素 D 校准品,使维生素 D 结果可溯源至国家标准与技术研究院参考物质。

结果 25-羟维生素 D3 及其相关的 ISTD 在 7 分钟的保留时间处被检测到。七点校准曲线始终显示出 0.99 的决定系数,实验确定的报告范围为 0.5-376 nmol/L。使用 DBS 样本进行的方法验证研究表明,在 45 nmol/L 时,批内精密度为 12.9%,平均回收率为 84%,与血浆维生素 D 高度相关(相关系数= 0.86)。

结论 我们成功开发了一种从 DBS 定量测定维生素 D 的分析方法,该方法将应用于我们的基于人群的维生素 D 研究。这种方法提高了 DBS 结果的可追溯性,并且可能广泛用于其他需要与血清/血浆进行比较以进行解释的 DBS 测定物。

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