一种便携式、低成本的酶联免疫吸附法检测炭疽芽孢杆菌孢子

IF 2.3 Q3 ELECTROCHEMISTRY
G. D. Peckham, Brian E. Hew, D. Waller, Charles R. Holdaway, Michael Jen
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引用次数: 12

摘要

基于抗体的检测分析通常是稳健的,这是现场使用的理想特性。然而,为了量化比色或荧光信号,这些分析需要昂贵和脆弱的仪器,不适合在现场使用。横向流动装置(lfd)规避了这些可移植性障碍,但其灵敏度和主观解释较差。本文将一种基于抗体的检测方法与ELISA和lfd进行比较,该方法通过安培信号产生检测炭疽芽孢杆菌孢子。这种安培免疫分析法使用抗体偶联到磁珠和葡萄糖氧化酶(GOX)以及电子介质2,6 -二氯酚吲哚酚(DCPIP),从0.4 V偏置电压产生可测量的电流。具有与ELISA相似的灵敏度,在笔记本电脑上完全供电和操作的情况下,该分析可在约75分钟内完成。免疫测定安培法有望将低成本、定量的危险试剂检测带到现场。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Amperometric Detection of Bacillus anthracis Spores: A Portable, Low-Cost Approach to the ELISA
Antibody-based detection assays are generally robust, a desirable characteristic for in-the-field use. However, to quantify the colorimetric or fluorescent signal, these assays require expensive and fragile instruments which are ill-suited to in-the-field use. Lateral flow devices (LFDs) circumvent these barriers to portability but suffer from poor sensitivity and subjective interpretation. Here, an antibody-based method for detecting Bacillus anthracis spores via amperometric signal generation is compared to ELISA and LFDs. This amperometric immunoassay uses antibody conjugated to magnetic beads and glucose oxidase (GOX) along with the electron mediator 2, 6-dichlorophenolindophenol (DCPIP) for production of a measurable current from a 0.4 V bias voltage. With similar sensitivity to ELISA, the assay can be completed in about 75 minutes while being completely powered and operated from a laptop computer. Immunoassay amperometry holds promise for bringing low-cost, quantitative detection of hazardous agents to the field.
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