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Self-enhancement lateral flow immunoassay for COVID-19 diagnosis
Equipment-free colorimetric-based lateral flow immunoassay (LFIA) is the most convenient and popular tool for various applications, including diagnostic tools requiring high sensitivity for the detection of pathogens. Thus, improvements and developments of LFIA are constantly being reported. Herein,...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147571/ https://www.ncbi.nlm.nih.gov/pubmed/37151731 http://dx.doi.org/10.1016/j.snb.2023.133898 |
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author | Ruantip, Sirowan Pimpitak, Umaporn Rengpipat, Sirirat Pasomsub, Ekawat Seepiban, Channarong Gajanandana, Oraprapai Torvorapanit, Pattama Hirankarn, Nattiya Jaru-ampornpan, Peera Siwamogsatham, Siwaruk Pongpaibool, Pornanong Siwamogsatham, Sarawut Thongchul, Nuttha Chaiyo, Sudkate |
author_facet | Ruantip, Sirowan Pimpitak, Umaporn Rengpipat, Sirirat Pasomsub, Ekawat Seepiban, Channarong Gajanandana, Oraprapai Torvorapanit, Pattama Hirankarn, Nattiya Jaru-ampornpan, Peera Siwamogsatham, Siwaruk Pongpaibool, Pornanong Siwamogsatham, Sarawut Thongchul, Nuttha Chaiyo, Sudkate |
author_sort | Ruantip, Sirowan |
collection | PubMed |
description | Equipment-free colorimetric-based lateral flow immunoassay (LFIA) is the most convenient and popular tool for various applications, including diagnostic tools requiring high sensitivity for the detection of pathogens. Thus, improvements and developments of LFIA are constantly being reported. Herein, we enriched the sensitivity of LFIA using the gold enhancement principle, emphasizing needlessly complicated apparatus, only one step for the strip test operation, and typical time incubation (15 min) process. Self-enhanced LFIA was then executed for subsequent flows by overlapping the additionally enhanced pad composed of gold ions and reducing agent on the conjugate pad and the sample pad. Self-enhanced LFIA was performed to detect SARS-CoV-2 antigens in saliva. The obtained result depicted that the achieved sensitivity was up to tenfold compared with that of conventional LFIA by visual measurements. The detection limits of self-enhanced LFIA detecting nucleocapsid protein antigens in the saliva sample was 0.50 and 0.10 ng/mL employed by naked eye detection and calibration curve-based calculation, respectively. When the proposed device was applied to 207 human saliva samples, the diagnostic performance presented a 96.10 % sensitivity and 99.23 % specificity. This self-enhanced LFIA could be implemented in large-scale production and demonstrates higher sensitivity with effortless use, which meets the requirements for point-of-care testing and on-field mass screening. |
format | Online Article Text |
id | pubmed-10147571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101475712023-05-01 Self-enhancement lateral flow immunoassay for COVID-19 diagnosis Ruantip, Sirowan Pimpitak, Umaporn Rengpipat, Sirirat Pasomsub, Ekawat Seepiban, Channarong Gajanandana, Oraprapai Torvorapanit, Pattama Hirankarn, Nattiya Jaru-ampornpan, Peera Siwamogsatham, Siwaruk Pongpaibool, Pornanong Siwamogsatham, Sarawut Thongchul, Nuttha Chaiyo, Sudkate Sens Actuators B Chem Article Equipment-free colorimetric-based lateral flow immunoassay (LFIA) is the most convenient and popular tool for various applications, including diagnostic tools requiring high sensitivity for the detection of pathogens. Thus, improvements and developments of LFIA are constantly being reported. Herein, we enriched the sensitivity of LFIA using the gold enhancement principle, emphasizing needlessly complicated apparatus, only one step for the strip test operation, and typical time incubation (15 min) process. Self-enhanced LFIA was then executed for subsequent flows by overlapping the additionally enhanced pad composed of gold ions and reducing agent on the conjugate pad and the sample pad. Self-enhanced LFIA was performed to detect SARS-CoV-2 antigens in saliva. The obtained result depicted that the achieved sensitivity was up to tenfold compared with that of conventional LFIA by visual measurements. The detection limits of self-enhanced LFIA detecting nucleocapsid protein antigens in the saliva sample was 0.50 and 0.10 ng/mL employed by naked eye detection and calibration curve-based calculation, respectively. When the proposed device was applied to 207 human saliva samples, the diagnostic performance presented a 96.10 % sensitivity and 99.23 % specificity. This self-enhanced LFIA could be implemented in large-scale production and demonstrates higher sensitivity with effortless use, which meets the requirements for point-of-care testing and on-field mass screening. Elsevier B.V. 2023-08-15 2023-04-29 /pmc/articles/PMC10147571/ /pubmed/37151731 http://dx.doi.org/10.1016/j.snb.2023.133898 Text en © 2023 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 Ruantip, Sirowan Pimpitak, Umaporn Rengpipat, Sirirat Pasomsub, Ekawat Seepiban, Channarong Gajanandana, Oraprapai Torvorapanit, Pattama Hirankarn, Nattiya Jaru-ampornpan, Peera Siwamogsatham, Siwaruk Pongpaibool, Pornanong Siwamogsatham, Sarawut Thongchul, Nuttha Chaiyo, Sudkate Self-enhancement lateral flow immunoassay for COVID-19 diagnosis |
title | Self-enhancement lateral flow immunoassay for COVID-19 diagnosis |
title_full | Self-enhancement lateral flow immunoassay for COVID-19 diagnosis |
title_fullStr | Self-enhancement lateral flow immunoassay for COVID-19 diagnosis |
title_full_unstemmed | Self-enhancement lateral flow immunoassay for COVID-19 diagnosis |
title_short | Self-enhancement lateral flow immunoassay for COVID-19 diagnosis |
title_sort | self-enhancement lateral flow immunoassay for covid-19 diagnosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147571/ https://www.ncbi.nlm.nih.gov/pubmed/37151731 http://dx.doi.org/10.1016/j.snb.2023.133898 |
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