A lab-on-a-chip for the concurrent electrochemical detection of SARS-CoV-2 RNA and anti-SARS-CoV-2 antibodies in saliva and plasma

被引:0
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作者
Devora Najjar
Joshua Rainbow
Sanjay Sharma Timilsina
Pawan Jolly
Helena de Puig
Mohamed Yafia
Nolan Durr
Hani Sallum
Galit Alter
Jonathan Z. Li
Xu G. Yu
David R. Walt
Joseph A. Paradiso
Pedro Estrela
James J. Collins
Donald E. Ingber
机构
[1] Harvard University,Wyss Institute for Biologically Inspired Engineering
[2] Massachusetts Institute of Technology,Institute for Medical Engineering and Science and Department of Biological Engineering
[3] Massachusetts Institute of Technology,MIT Media Lab
[4] University of Bath,Centre for Biosensors, Bioelectronics and Biodevices (C3Bio) and Department of Electronic and Electrical Engineering
[5] Ragon Institute of MGH,Division of Infectious Diseases
[6] MIT and Harvard,Department of Pathology
[7] Brigham and Women’s Hospital,Infectious Disease and Microbiome Program
[8] Harvard Medical School,Vascular Biology Program and Department of Surgery
[9] Brigham and Women’s Hospital,Harvard John A. Paulson School of Engineering and Applied Sciences
[10] Broad Institute of MIT and Harvard,undefined
[11] Boston Children’s Hospital,undefined
[12] Harvard University,undefined
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摘要
Rapid, accurate and frequent detection of the RNA of SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) and of serological host antibodies to the virus would facilitate the determination of the immune status of individuals who have Coronavirus disease 2019 (COVID-19), were previously infected by the virus, or were vaccinated against the disease. Here we describe the development and application of a 3D-printed lab-on-a-chip that concurrently detects, via multiplexed electrochemical outputs and within 2 h, SARS-CoV-2 RNA in saliva as well as anti-SARS-CoV-2 immunoglobulins in saliva spiked with blood plasma. The device automatedly extracts, concentrates and amplifies SARS-CoV-2 RNA from unprocessed saliva, and integrates the Cas12a-based enzymatic detection of SARS-CoV-2 RNA via isothermal nucleic acid amplification with a sandwich-based enzyme-linked immunosorbent assay on electrodes functionalized with the Spike S1, nucleocapsid and receptor-binding-domain antigens of SARS-CoV-2. Inexpensive microfluidic electrochemical sensors for performing multiplexed diagnostics at the point of care may facilitate the widespread monitoring of COVID-19 infection and immunity.
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页码:968 / 978
页数:10
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