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SARS‐CoV‐2 Virus Detection Via a Polymeric Nanochannel‐Based Electrochemical Biosensor
The development of simple, cost‐effective, rapid, and quantitative diagnostic tools remains critical to monitor infectious COVID‐19 disease. Although numerous diagnostic platforms, including rapid antigen tests, are developed and used, they suffer from limited accuracy, especially when tested with a...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9880620/ https://www.ncbi.nlm.nih.gov/pubmed/36585382 http://dx.doi.org/10.1002/smll.202205281 |
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author | Shiohara, Amane Wojnilowicz, Marcin Lyu, Quanxia Pei, Yi Easton, Christopher D. Chen, Yu White, Jacinta F McAuley, Alexander Prieto‐Simon, Beatriz Thissen, Helmut Voelcker, Nicolas H |
author_facet | Shiohara, Amane Wojnilowicz, Marcin Lyu, Quanxia Pei, Yi Easton, Christopher D. Chen, Yu White, Jacinta F McAuley, Alexander Prieto‐Simon, Beatriz Thissen, Helmut Voelcker, Nicolas H |
author_sort | Shiohara, Amane |
collection | PubMed |
description | The development of simple, cost‐effective, rapid, and quantitative diagnostic tools remains critical to monitor infectious COVID‐19 disease. Although numerous diagnostic platforms, including rapid antigen tests, are developed and used, they suffer from limited accuracy, especially when tested with asymptomatic patients. Here, a unique approach to fabricate a nanochannel‐based electrochemical biosensor that can detect the entire virion instead of virus fragments, is demonstrated. The sensing platform has uniform nanoscale channels created by the convective assembly of polystyrene (PS) beads on gold electrodes. The PS beads are then functionalized with bioreceptors while the gold surface is endowed with anti‐fouling properties. When added to the biosensor, SARS‐CoV‐2 virus particles block the nanochannels by specific binding to the bioreceptors. The nanochannel blockage hinders the diffusion of a redox probe; and thus, allows quantification of the viral load by measuring the changes in the oxidation current before and after virus incubation. The biosensor shows a low limit of detection of ≈1.0 viral particle mL(−1) with a wide detection range up to 10(8) particles mL(−1) in cell culture media. Moreover, the biosensor is able to differentiate saliva samples with SARS‐CoV‐2 from those without, demonstrating the potential of this technology for translation into a point‐of‐care biosensor product. |
format | Online Article Text |
id | pubmed-9880620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98806202023-01-27 SARS‐CoV‐2 Virus Detection Via a Polymeric Nanochannel‐Based Electrochemical Biosensor Shiohara, Amane Wojnilowicz, Marcin Lyu, Quanxia Pei, Yi Easton, Christopher D. Chen, Yu White, Jacinta F McAuley, Alexander Prieto‐Simon, Beatriz Thissen, Helmut Voelcker, Nicolas H Small Research Articles The development of simple, cost‐effective, rapid, and quantitative diagnostic tools remains critical to monitor infectious COVID‐19 disease. Although numerous diagnostic platforms, including rapid antigen tests, are developed and used, they suffer from limited accuracy, especially when tested with asymptomatic patients. Here, a unique approach to fabricate a nanochannel‐based electrochemical biosensor that can detect the entire virion instead of virus fragments, is demonstrated. The sensing platform has uniform nanoscale channels created by the convective assembly of polystyrene (PS) beads on gold electrodes. The PS beads are then functionalized with bioreceptors while the gold surface is endowed with anti‐fouling properties. When added to the biosensor, SARS‐CoV‐2 virus particles block the nanochannels by specific binding to the bioreceptors. The nanochannel blockage hinders the diffusion of a redox probe; and thus, allows quantification of the viral load by measuring the changes in the oxidation current before and after virus incubation. The biosensor shows a low limit of detection of ≈1.0 viral particle mL(−1) with a wide detection range up to 10(8) particles mL(−1) in cell culture media. Moreover, the biosensor is able to differentiate saliva samples with SARS‐CoV‐2 from those without, demonstrating the potential of this technology for translation into a point‐of‐care biosensor product. John Wiley and Sons Inc. 2022-12-30 /pmc/articles/PMC9880620/ /pubmed/36585382 http://dx.doi.org/10.1002/smll.202205281 Text en © 2022 The Authors. Small published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Shiohara, Amane Wojnilowicz, Marcin Lyu, Quanxia Pei, Yi Easton, Christopher D. Chen, Yu White, Jacinta F McAuley, Alexander Prieto‐Simon, Beatriz Thissen, Helmut Voelcker, Nicolas H SARS‐CoV‐2 Virus Detection Via a Polymeric Nanochannel‐Based Electrochemical Biosensor |
title | SARS‐CoV‐2 Virus Detection Via a Polymeric Nanochannel‐Based Electrochemical Biosensor |
title_full | SARS‐CoV‐2 Virus Detection Via a Polymeric Nanochannel‐Based Electrochemical Biosensor |
title_fullStr | SARS‐CoV‐2 Virus Detection Via a Polymeric Nanochannel‐Based Electrochemical Biosensor |
title_full_unstemmed | SARS‐CoV‐2 Virus Detection Via a Polymeric Nanochannel‐Based Electrochemical Biosensor |
title_short | SARS‐CoV‐2 Virus Detection Via a Polymeric Nanochannel‐Based Electrochemical Biosensor |
title_sort | sars‐cov‐2 virus detection via a polymeric nanochannel‐based electrochemical biosensor |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9880620/ https://www.ncbi.nlm.nih.gov/pubmed/36585382 http://dx.doi.org/10.1002/smll.202205281 |
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