Aerosol-jet-printed graphene electrochemical immunosensors for rapid and label-free detection of SARS-CoV-2 in saliva

被引:34
|
作者
Pola, Cicero C. [1 ]
Rangnekar, Sonal, V [2 ]
Sheets, Robert [1 ]
Downing, Julia R. [2 ]
Parate, Kshama W. [2 ]
Wallace, Shay G. [1 ]
Tsai, Daphne [2 ]
Hersam, Mark C. [2 ]
Gomes, Carmen L. [2 ,3 ,4 ]
Claussen, Jonathan C. [1 ]
机构
[1] Iowa State Univ, Dept Mech Engn, Ames, IA 50011 USA
[2] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
[3] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[4] Northwestern Univ, Dept Elect & Comp Engn, Evanston, IL 60208 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
graphene; biosensor; electrochemical impedance spectroscopy; COVID-19; aerosol jet printing; POINT-OF-CARE; IMPEDANCE SPECTROSCOPY; HIGH-RESOLUTION; NASOPHARYNGEAL SWAB; CONDUCTIVITY; CHALLENGES; ANTIBODIES; BIOSENSOR; GRAPHITE;
D O I
10.1088/2053-1583/ac7339
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Rapid, inexpensive, and easy-to-use coronavirus disease 2019 (COVID-19) home tests are key tools in addition to vaccines in the world wide fight to eliminate national and local shutdowns. However, currently available tests for SARS-CoV-2, the virus that causes COVID-19, are too expensive, painful, and irritating, or not sufficiently sensitive for routine, accurate home testing. Herein, we employ custom-formulated graphene inks and aerosol jet printing to create a rapid electrochemical immunosensor for direct detection of SARS-CoV-2 spike receptor-binding domain (RBD) in saliva samples acquired noninvasively. This sensor demonstrated limits of detection that are considerably lower than most commercial SARS-CoV-2 antigen tests (22.91 +/- 4.72 pg ml(-1) for spike RBD and 110.38 +/- 9.00 pg ml(-1) for spike S1) as well as fast response time (similar to 30 min), which was facilitated by the functionalization of printed graphene electrodes in a single-step with SARS-CoV-2 polyclonal antibody through the carbodiimide reaction without the need for nanoparticle functionalization or secondary antibody or metallic nanoparticle labels. This immunosensor presents a wide linear sensing range from 1 to 1000 ng ml(-1) and does not react with other coexisting influenza viruses such as H1N1 hemagglutinin. By combining high-yield graphene ink synthesis, automated printing, high antigen selectivity, and rapid testing capability, this work offers a promising alternative to current SARS-CoV-2 antigen tests.
引用
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页数:17
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