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基于微管尖端的免疫测定,结合电化学检测抗组织转谷氨酰胺酶,使用订书钉和基于纸的平台诊断乳糜泻。

Micropipette Tip-Based Immunoassay with Electrochemical Detection of Antitissue Transglutaminase to Diagnose Celiac Disease Using Staples and a Paper-Based Platform.

机构信息

Department of Physical and Analytical Chemistry , University of Oviedo , 33006 Oviedo , Spain.

出版信息

ACS Sens. 2019 Oct 25;4(10):2679-2687. doi: 10.1021/acssensors.9b01096. Epub 2019 Sep 20.

DOI:10.1021/acssensors.9b01096
PMID:31497948
Abstract

In this work, 1-200 μL polypropylene micropipette tips were used as platforms for performing immunoassays after converting their inner surfaces on a capture zone for the analyte of interest. We have used a micropipette-tip immunoelectroanalytical platform for the detection of antitissue transglutaminase (IgA), the main biomarker for celiac disease. Modification of the tip wall with poly-l-lysine allowed adsorption of tissue transglutaminase (tTG), which will capture later anti-tTG (IgA) antibodies developed in celiac-affected people. A sandwich-type format was followed, incubating simultaneously the analyte and the detection antibody, labeled with horseradish peroxidase. With this new application for an extremely common lab material, we can perform quantitative analysis by dispensing the liquid into a low-cost and miniaturized staple-based paper electrochemical platform. The analytical signal was the reduction of the enzymatically oxidized substrate, recorded chronoamperometrically (- curve). The intensity of the current obtained at a fixed time after the application of the cathodic potential followed a linear relationship with anti-tTG (IgA) concentration. The relative standard deviation obtained for immunoassays performed in different tips indicates the adequate precision of this new methodology, which is very promising for decentralized analysis. Negative and positive controls produced results that were in accordance with those obtained with spectrophotometric enzyme linked-immunosorbent assays.

摘要

在这项工作中,我们使用了 1-200μL 的聚丙烯微量移液器吸头,将其内壁转换为感兴趣分析物的捕获区域,从而将其用作进行免疫测定的平台。我们已经使用了一种微量吸头免疫电化学分析平台来检测抗组织转谷氨酰胺酶(IgA),这是乳糜泻的主要生物标志物。修饰吸头壁上的聚赖氨酸允许组织转谷氨酰胺酶(tTG)吸附,该酶将捕获后来自乳糜泻患者的抗 tTG(IgA)抗体。采用夹心型格式,同时孵育分析物和检测抗体,标记辣根过氧化物酶。通过这种对极其常见的实验室材料的新应用,我们可以通过将液体分配到低成本和微型化的基于订书钉的纸电化学平台上来进行定量分析。分析信号是酶氧化底物的还原,通过计时安培法(-曲线)记录。在施加阴极电势后的固定时间获得的电流强度与抗 tTG(IgA)浓度呈线性关系。在不同吸头中进行免疫测定的相对标准偏差表明该新方法具有足够的精度,非常适合分散式分析。阴性和阳性对照的结果与分光光度酶联免疫吸附测定法获得的结果一致。

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