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基于干血斑的全自动血细胞比容光学测量

Fully Automated Optical Hematocrit Measurement From Dried Blood Spots.

作者信息

Luginbühl Marc, Fischer Yannick, Gaugler Stefan

机构信息

CAMAG DBS Laboratory, Sonnenmattstrasse 11, 4132 Muttenz, Switzerland.

University of Applied Sciences and Arts Northwestern Switzerland, Institute for Chemistry and Bioanalytics.

出版信息

J Anal Toxicol. 2020 Dec 5. doi: 10.1093/jat/bkaa189.

DOI:10.1093/jat/bkaa189
PMID:33277901
Abstract

The impact of the hematocrit (HCT) on the dried blood spot's (DBS) spreading area is one of the most important hurdles which prevents the full acceptance of quantitative microsampling strategies. Several destructive- and non-destructive strategies to assess the HCT from a DBS post-sampling have been presented. Unfortunately, the current methods are either labor-intensive, require a complicated algorithm, or are not automatable. Here, we present a novel setup that permits the fully automated reflectance analysis to measure the HCT from a DBS. The underlying principle is based on the concept presented by Capiau et al. for the non-destructive single-wavelength measurement of the HCT. The novel module was embedded within the DBS-MS 500 platform to enable high-throughput analysis of hematocrit values in combination with automated DBS extraction. The novel setup was assessed and optimized for the probe to card distance, stability, anti-coagulant, spotting volume, scan number, calibration variability, accuracy, and precision. It showed excellent inter-day (≤3.7%) and intra-day (≤1.16%) precision, as well as high accuracy when analyzing authentic samples 101%±7% (range:87%-127%). Besides, the simple and straightforward application of an HCT correction for DBS was demonstrated during a pharmacokinetic study with diclofenac involving three subjects. Thereby, the sample's HCT and the HCT impact on the analyte was assessed and compensated. In conclusion, the novel setup enables quantitative analysis of non-volumetric samples in an automated fashion without compromising the concept of cost-effective, minimally invasive sampling.

摘要

血细胞比容(HCT)对干血斑(DBS)扩散面积的影响是阻碍定量微量采样策略被全面接受的最重要障碍之一。已经提出了几种在采样后从DBS评估HCT的破坏性和非破坏性策略。不幸的是,目前的方法要么劳动强度大,需要复杂的算法,要么无法自动化。在此,我们提出了一种新颖的装置,它允许通过全自动化反射率分析来测量DBS中的HCT。其基本原理基于Capiau等人提出的用于HCT无损单波长测量的概念。这个新颖的模块被嵌入到DBS-MS 500平台中,以便结合自动DBS提取实现血细胞比容值的高通量分析。对该新颖装置的探针与卡片距离、稳定性、抗凝剂、点样体积、扫描次数、校准变异性、准确性和精密度进行了评估和优化。它在分析真实样品时显示出出色的日间(≤3.7%)和日内(≤1.16%)精密度,以及较高的准确性,为101%±7%(范围:87%-127%)。此外,在一项涉及三名受试者的双氯芬酸药代动力学研究中,展示了对DBS进行HCT校正的简单直接应用。由此,评估并补偿了样品的HCT及其对分析物的影响。总之,这种新颖的装置能够以自动化方式对非体积样品进行定量分析,而不会损害具有成本效益的微创采样概念。

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