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Simultaneously ultrasensitive and quantitative detection of influenza A virus, SARS-CoV-2, and respiratory syncytial virus via multichannel magnetic SERS-based lateral flow immunoassay

Respiratory viruses usually induced similar clinical symptoms at early infection. Herein, we presented a multichannel surface-enhanced Raman scattering-based lateral flow immunoassay (SERS-based LFA) using high-performance magnetic SERS tags for the simultaneous ultrasensitive detection of respirato...

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Autores principales: Liu, Zhenzhen, Wang, Chongwen, Zheng, Shuai, Yang, Xingsheng, Han, Han, Dai, Yuwei, Xiao, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622431/
https://www.ncbi.nlm.nih.gov/pubmed/36328340
http://dx.doi.org/10.1016/j.nano.2022.102624
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author Liu, Zhenzhen
Wang, Chongwen
Zheng, Shuai
Yang, Xingsheng
Han, Han
Dai, Yuwei
Xiao, Rui
author_facet Liu, Zhenzhen
Wang, Chongwen
Zheng, Shuai
Yang, Xingsheng
Han, Han
Dai, Yuwei
Xiao, Rui
author_sort Liu, Zhenzhen
collection PubMed
description Respiratory viruses usually induced similar clinical symptoms at early infection. Herein, we presented a multichannel surface-enhanced Raman scattering-based lateral flow immunoassay (SERS-based LFA) using high-performance magnetic SERS tags for the simultaneous ultrasensitive detection of respiratory viruses, namely influenza A virus (H1N1), severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and respiratory syncytial virus (RSV) in biological samples. As-prepared magnetic SERS tags can directly enrich and capture target viruses without pretreatment of samples, avoiding the interference of impurities in the samples as well as improving the sensitivity. With the capture-detection method, the detection limits of the proposed assay reached 85 copies mL(−1), 8 pg mL(−1), and 8 pg mL(−1) for H1N1, SARS-CoV-2 and RSV, respectively. Moreover, the detection properties of the proposed method for target viruses in throat swab samples were verified, suggesting its remarkable potential for the early and rapid differential diagnosis of respiratory viruses.
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spelling pubmed-96224312022-11-01 Simultaneously ultrasensitive and quantitative detection of influenza A virus, SARS-CoV-2, and respiratory syncytial virus via multichannel magnetic SERS-based lateral flow immunoassay Liu, Zhenzhen Wang, Chongwen Zheng, Shuai Yang, Xingsheng Han, Han Dai, Yuwei Xiao, Rui Nanomedicine Original Article Respiratory viruses usually induced similar clinical symptoms at early infection. Herein, we presented a multichannel surface-enhanced Raman scattering-based lateral flow immunoassay (SERS-based LFA) using high-performance magnetic SERS tags for the simultaneous ultrasensitive detection of respiratory viruses, namely influenza A virus (H1N1), severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and respiratory syncytial virus (RSV) in biological samples. As-prepared magnetic SERS tags can directly enrich and capture target viruses without pretreatment of samples, avoiding the interference of impurities in the samples as well as improving the sensitivity. With the capture-detection method, the detection limits of the proposed assay reached 85 copies mL(−1), 8 pg mL(−1), and 8 pg mL(−1) for H1N1, SARS-CoV-2 and RSV, respectively. Moreover, the detection properties of the proposed method for target viruses in throat swab samples were verified, suggesting its remarkable potential for the early and rapid differential diagnosis of respiratory viruses. Published by Elsevier Inc. 2023-01 2022-11-01 /pmc/articles/PMC9622431/ /pubmed/36328340 http://dx.doi.org/10.1016/j.nano.2022.102624 Text en © 2022 Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Original Article
Liu, Zhenzhen
Wang, Chongwen
Zheng, Shuai
Yang, Xingsheng
Han, Han
Dai, Yuwei
Xiao, Rui
Simultaneously ultrasensitive and quantitative detection of influenza A virus, SARS-CoV-2, and respiratory syncytial virus via multichannel magnetic SERS-based lateral flow immunoassay
title Simultaneously ultrasensitive and quantitative detection of influenza A virus, SARS-CoV-2, and respiratory syncytial virus via multichannel magnetic SERS-based lateral flow immunoassay
title_full Simultaneously ultrasensitive and quantitative detection of influenza A virus, SARS-CoV-2, and respiratory syncytial virus via multichannel magnetic SERS-based lateral flow immunoassay
title_fullStr Simultaneously ultrasensitive and quantitative detection of influenza A virus, SARS-CoV-2, and respiratory syncytial virus via multichannel magnetic SERS-based lateral flow immunoassay
title_full_unstemmed Simultaneously ultrasensitive and quantitative detection of influenza A virus, SARS-CoV-2, and respiratory syncytial virus via multichannel magnetic SERS-based lateral flow immunoassay
title_short Simultaneously ultrasensitive and quantitative detection of influenza A virus, SARS-CoV-2, and respiratory syncytial virus via multichannel magnetic SERS-based lateral flow immunoassay
title_sort simultaneously ultrasensitive and quantitative detection of influenza a virus, sars-cov-2, and respiratory syncytial virus via multichannel magnetic sers-based lateral flow immunoassay
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622431/
https://www.ncbi.nlm.nih.gov/pubmed/36328340
http://dx.doi.org/10.1016/j.nano.2022.102624
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