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一种新型的、无损的、基于干血斑的红细胞压积预测方法,采用非接触漫反射光谱技术。

A Novel, Nondestructive, Dried Blood Spot-Based Hematocrit Prediction Method Using Noncontact Diffuse Reflectance Spectroscopy.

机构信息

Laboratory of Toxicology, Faculty of Pharmaceutical Sciences, Ghent University , Ottergemsesteenweg 460, 9000 Ghent, Belgium.

Department of Biomedical Engineering and Physics, Academic Medical Center, University of Amsterdam , Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands.

出版信息

Anal Chem. 2016 Jun 21;88(12):6538-46. doi: 10.1021/acs.analchem.6b01321. Epub 2016 Jun 3.

Abstract

Dried blood spot (DBS) sampling is recognized as a valuable alternative sampling strategy both in research and in clinical routine. Although many advantages are associated with DBS sampling, its more widespread use is hampered by several issues, of which the hematocrit effect on DBS-based quantitation remains undoubtedly the most widely discussed one. Previously, we developed a method to derive the approximate hematocrit from a nonvolumetrically applied DBS based on its potassium content. Although this method yielded good results and was straightforward to perform, it was also destructive and required sample preparation. Therefore, we now developed a nondestructive method which allows to predict the hematocrit of a DBS based on its hemoglobin content, measured via noncontact diffuse reflectance spectroscopy. The developed method was thoroughly validated. A linear calibration curve was established after log/log transformation. The bias, intraday and interday imprecision of quality controls at three hematocrit levels and at the lower and upper limit of quantitation (0.20 and 0.67, respectively) were less than 11%. In addition, the influence of storage and the volume spotted was evaluated, as well as DBS homogeneity. Application of the method to venous DBSs prepared from whole blood patient samples (n = 233) revealed a good correlation between the actual and the predicted hematocrit. Limits of agreement obtained after Bland and Altman analysis were -0.076 and +0.018. Incurred sample reanalysis demonstrated good method reproducibility. In conclusion, mere scanning of a DBS suffices to derive its approximate hematocrit, one of the most important variables in DBS analysis.

摘要

干血斑 (DBS) 采样在研究和临床常规中被认为是一种有价值的替代采样策略。尽管 DBS 采样有许多优点,但由于几个问题,其更广泛的应用受到了阻碍,其中 DBS 定量分析中的血细胞比容效应无疑是讨论最多的一个。此前,我们开发了一种方法,根据 DBS 中的钾含量,从非体积应用的 DBS 中得出近似的血细胞比容。虽然该方法得到了很好的结果,并且执行起来也很简单,但它也是破坏性的,需要进行样本制备。因此,我们现在开发了一种非破坏性的方法,可以根据 DBS 中的血红蛋白含量来预测其血细胞比容,该方法通过非接触漫反射光谱法进行测量。所开发的方法经过了彻底的验证。经过对数/对数转换后,建立了线性校准曲线。在三个血细胞比容水平和定量下限(分别为 0.20 和 0.67)下的质控品的偏差、日内和日间精密度小于 11%。此外,还评估了储存和斑点体积的影响以及 DBS 的均匀性。将该方法应用于从全血患者样本制备的静脉 DBS(n=233),实际血细胞比容与预测血细胞比容之间显示出良好的相关性。 Bland 和 Altman 分析得到的一致性界限为-0.076 和+0.018。经 incurred 样品再分析证明了该方法具有良好的重现性。总之,只需扫描 DBS 即可得出其近似的血细胞比容,这是 DBS 分析中最重要的变量之一。

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