Quantitative reagent monitoring in paper-based electrochemical rapid diagnostic tests

被引:1
|
作者
Bezinge, Leonard [1 ]
deMello, Andrew J. [1 ]
Shih, Chih-Jen [1 ]
Richards, Daniel A. [1 ]
机构
[1] Swiss Fed Inst Technol, Dept Chem & Appl Biosci, Inst Chem & Bioengn, Vladimir Prelog Weg 1, CH-8093 Zurich, Switzerland
关键词
GOLD NANOPARTICLES; FLOW; POINT;
D O I
10.1039/d4lc00390j
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Paper-based rapid diagnostic tests (RDTs) are an essential component of modern healthcare, particularly for the management of infectious diseases. Despite their utility, these capillary-driven RDTs are compromised by high failure rates, primarily caused by user error. This limits their utility in complex assays that require multiple user operations. Here, we demonstrate how this issue can be directly addressed through continuous electrochemical monitoring of reagent flow inside an RDT using embedded graphenized electrodes. Our method relies on applying short voltage pulses and measuring variations in capacitive discharge currents to precisely determine the flow times of injected samples and reagents. This information is reported to the user, guiding them through the testing process, highlighting failure cases and ultimately decreasing errors. Significantly, the same electrodes can be used to quantify electrochemical signals from immunoassays, providing an integrated solution for both monitoring assays and reporting results. We demonstrate the applicability of this approach in a serology test for the detection of anti-SARS-CoV-2 IgG in clinical serum samples. This method paves the way towards "smart" RDTs able to continuously monitor the testing process and improve the robustness of point-of-care diagnostics. Exploiting non-faradaic signals from electrochemical sensors to track reagent flow in rapid diagnostic tests: towards smart tests with reduced user errors.
引用
收藏
页码:3651 / 3657
页数:7
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