School of Health and Biomedical Sciences, RMIT University, Bundoora, Victoria, Australia.
Murdoch Children's Research Institute, Parkville, Victoria, Australia.
Clin Chem Lab Med. 2020 Apr 28;58(5):817-827. doi: 10.1515/cclm-2019-0397.
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.
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。