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A novel delayed lateral flow immunoassay for enhanced detection of SARS-CoV-2 spike antigen
A new detection strategy was developed to improve the sensitivity of a lateral flow immunoassay platform utilizing a delayed hydrophobic barrier fabricated with trimethylsilyl cellulose (TMSC). The SARS-CoV-2 spike receptor-binding domain (SARS-CoV-2 SP RBD) antigen was chosen as a model analyte to...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486763/ https://www.ncbi.nlm.nih.gov/pubmed/36125616 http://dx.doi.org/10.1007/s00604-022-05467-3 |
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author | Srithong, Pawanrat Chaiyo, Sudkate Pasomsub, Ekawat Rengpipat, Sirirat Chailapakul, Orawon Praphairaksit, Narong |
author_facet | Srithong, Pawanrat Chaiyo, Sudkate Pasomsub, Ekawat Rengpipat, Sirirat Chailapakul, Orawon Praphairaksit, Narong |
author_sort | Srithong, Pawanrat |
collection | PubMed |
description | A new detection strategy was developed to improve the sensitivity of a lateral flow immunoassay platform utilizing a delayed hydrophobic barrier fabricated with trimethylsilyl cellulose (TMSC). The SARS-CoV-2 spike receptor-binding domain (SARS-CoV-2 SP RBD) antigen was chosen as a model analyte to demonstrate the superior detectability of this scheme. The novel device consists of 2 separate layers, so-called delayed lateral flow immunoassay (d-LFIA). The upper layer is intended for the analyte or sample flow path, where the test solution flows freely straight to the detection zone to bind with the primary antibody. The lower layer, located just underneath, is designed for the SARS-CoV-2 spike receptor-binding domain-conjugated gold nanoparticles (SARS-CoV-2 SP RBD-AuNPs) used for producing a colorimetric signal. This layer is fabricated with a TMSC barrier to time-delay the movement of SARS-CoV-2 SP RBD-AuNPs, thus allowing the antigen to bind with the primary antibody more efficiently. This platform exhibited a 2.6-fold enhancement in the sensitivity and 9.1-fold improvement in the limit of detection (LOD) as compared with the conventional LFIA. In addition, this d-LFIA device was satisfactorily applied to accurate screening of COVID-19 patients. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00604-022-05467-3. |
format | Online Article Text |
id | pubmed-9486763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-94867632022-09-21 A novel delayed lateral flow immunoassay for enhanced detection of SARS-CoV-2 spike antigen Srithong, Pawanrat Chaiyo, Sudkate Pasomsub, Ekawat Rengpipat, Sirirat Chailapakul, Orawon Praphairaksit, Narong Mikrochim Acta Original Paper A new detection strategy was developed to improve the sensitivity of a lateral flow immunoassay platform utilizing a delayed hydrophobic barrier fabricated with trimethylsilyl cellulose (TMSC). The SARS-CoV-2 spike receptor-binding domain (SARS-CoV-2 SP RBD) antigen was chosen as a model analyte to demonstrate the superior detectability of this scheme. The novel device consists of 2 separate layers, so-called delayed lateral flow immunoassay (d-LFIA). The upper layer is intended for the analyte or sample flow path, where the test solution flows freely straight to the detection zone to bind with the primary antibody. The lower layer, located just underneath, is designed for the SARS-CoV-2 spike receptor-binding domain-conjugated gold nanoparticles (SARS-CoV-2 SP RBD-AuNPs) used for producing a colorimetric signal. This layer is fabricated with a TMSC barrier to time-delay the movement of SARS-CoV-2 SP RBD-AuNPs, thus allowing the antigen to bind with the primary antibody more efficiently. This platform exhibited a 2.6-fold enhancement in the sensitivity and 9.1-fold improvement in the limit of detection (LOD) as compared with the conventional LFIA. In addition, this d-LFIA device was satisfactorily applied to accurate screening of COVID-19 patients. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00604-022-05467-3. Springer Vienna 2022-09-20 2022 /pmc/articles/PMC9486763/ /pubmed/36125616 http://dx.doi.org/10.1007/s00604-022-05467-3 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Paper Srithong, Pawanrat Chaiyo, Sudkate Pasomsub, Ekawat Rengpipat, Sirirat Chailapakul, Orawon Praphairaksit, Narong A novel delayed lateral flow immunoassay for enhanced detection of SARS-CoV-2 spike antigen |
title | A novel delayed lateral flow immunoassay for enhanced detection of SARS-CoV-2 spike antigen |
title_full | A novel delayed lateral flow immunoassay for enhanced detection of SARS-CoV-2 spike antigen |
title_fullStr | A novel delayed lateral flow immunoassay for enhanced detection of SARS-CoV-2 spike antigen |
title_full_unstemmed | A novel delayed lateral flow immunoassay for enhanced detection of SARS-CoV-2 spike antigen |
title_short | A novel delayed lateral flow immunoassay for enhanced detection of SARS-CoV-2 spike antigen |
title_sort | novel delayed lateral flow immunoassay for enhanced detection of sars-cov-2 spike antigen |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486763/ https://www.ncbi.nlm.nih.gov/pubmed/36125616 http://dx.doi.org/10.1007/s00604-022-05467-3 |
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