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Engineering light-initiated afterglow lateral flow immunoassay for infectious disease diagnostics
The pandemic of highly contagious diseases has put forward urgent requirements for high sensitivity and adaptive capacity of point-of-care testing (POCT). Herein, for the first time, we report an aggregation-induced emission (AIE) dye-energized light-initiated afterglow nanoprobes (named LiAGNPs), i...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9119864/ https://www.ncbi.nlm.nih.gov/pubmed/35623251 http://dx.doi.org/10.1016/j.bios.2022.114411 |
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author | Hao, Liangwen Yang, Weitao Xu, Yan Cui, Tianming Zhu, Guoqi Zeng, Weiwei Bian, Kexin Liang, Hongying Zhang, Pengfei Zhang, Bingbo |
author_facet | Hao, Liangwen Yang, Weitao Xu, Yan Cui, Tianming Zhu, Guoqi Zeng, Weiwei Bian, Kexin Liang, Hongying Zhang, Pengfei Zhang, Bingbo |
author_sort | Hao, Liangwen |
collection | PubMed |
description | The pandemic of highly contagious diseases has put forward urgent requirements for high sensitivity and adaptive capacity of point-of-care testing (POCT). Herein, for the first time, we report an aggregation-induced emission (AIE) dye-energized light-initiated afterglow nanoprobes (named LiAGNPs), implemented onto a lateral flow immunoassay (LFIA) test strip, for diagnosis of two highly contagious diseases, human immunodeficiency virus (HIV) and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) as model validation. The primary working mechanism relies on the cyclically generated singlet oxygen ((1)O(2))-triggered time-resolved luminescent signals of LiAGNPs in which AIE dyes (TTMN) and chemiluminescent substrates (SO) are loaded. The designed LiAGNPs were found 2-fold and 32-fold sensitive than the currently used Eu(III)-based time-resolved fluorescent nanoparticles and gold nanoparticles in lateral flow immunoassay (LFIA), respectively. In addition, the extra optical behaviors of nude color and fluorescence of LiAGNPs enable the LFIA platform with the capability of the naked eye and fluorescent detection to satisfy the applications under varying scenarios. In short, the versatile LiAGNPs have great potential as a novel time-resolved reporter in enhancing detection sensitivity and application flexibility with LFIA platform for rapid but sensitive infectious disease diagnostics. |
format | Online Article Text |
id | pubmed-9119864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91198642022-05-20 Engineering light-initiated afterglow lateral flow immunoassay for infectious disease diagnostics Hao, Liangwen Yang, Weitao Xu, Yan Cui, Tianming Zhu, Guoqi Zeng, Weiwei Bian, Kexin Liang, Hongying Zhang, Pengfei Zhang, Bingbo Biosens Bioelectron Article The pandemic of highly contagious diseases has put forward urgent requirements for high sensitivity and adaptive capacity of point-of-care testing (POCT). Herein, for the first time, we report an aggregation-induced emission (AIE) dye-energized light-initiated afterglow nanoprobes (named LiAGNPs), implemented onto a lateral flow immunoassay (LFIA) test strip, for diagnosis of two highly contagious diseases, human immunodeficiency virus (HIV) and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) as model validation. The primary working mechanism relies on the cyclically generated singlet oxygen ((1)O(2))-triggered time-resolved luminescent signals of LiAGNPs in which AIE dyes (TTMN) and chemiluminescent substrates (SO) are loaded. The designed LiAGNPs were found 2-fold and 32-fold sensitive than the currently used Eu(III)-based time-resolved fluorescent nanoparticles and gold nanoparticles in lateral flow immunoassay (LFIA), respectively. In addition, the extra optical behaviors of nude color and fluorescence of LiAGNPs enable the LFIA platform with the capability of the naked eye and fluorescent detection to satisfy the applications under varying scenarios. In short, the versatile LiAGNPs have great potential as a novel time-resolved reporter in enhancing detection sensitivity and application flexibility with LFIA platform for rapid but sensitive infectious disease diagnostics. Elsevier B.V. 2022-09-15 2022-05-20 /pmc/articles/PMC9119864/ /pubmed/35623251 http://dx.doi.org/10.1016/j.bios.2022.114411 Text en © 2022 Elsevier B.V. All rights reserved. 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 | Article Hao, Liangwen Yang, Weitao Xu, Yan Cui, Tianming Zhu, Guoqi Zeng, Weiwei Bian, Kexin Liang, Hongying Zhang, Pengfei Zhang, Bingbo Engineering light-initiated afterglow lateral flow immunoassay for infectious disease diagnostics |
title | Engineering light-initiated afterglow lateral flow immunoassay for infectious disease diagnostics |
title_full | Engineering light-initiated afterglow lateral flow immunoassay for infectious disease diagnostics |
title_fullStr | Engineering light-initiated afterglow lateral flow immunoassay for infectious disease diagnostics |
title_full_unstemmed | Engineering light-initiated afterglow lateral flow immunoassay for infectious disease diagnostics |
title_short | Engineering light-initiated afterglow lateral flow immunoassay for infectious disease diagnostics |
title_sort | engineering light-initiated afterglow lateral flow immunoassay for infectious disease diagnostics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9119864/ https://www.ncbi.nlm.nih.gov/pubmed/35623251 http://dx.doi.org/10.1016/j.bios.2022.114411 |
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