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Amplifying Lateral Flow Assay Signals for Rapid Detection of COVID‐19 Specific Antibodies

Rapid lateral flow immune‐assays are point‐of‐care diagnostic tools that are easy to use, cheap, and do not need centralized infrastructure. Therefore, these devices are appealing for rapid detection of the humoral immune responses to infections, particularly severe acute respiratory syndrome corona...

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Autores principales: Alhabbab, Rowa Y., Alfaleh, Mohamed A., Alsulaiman, Reem M., Alamri, Sawsan S., Eyouni, Mais S., ElAssouli, M‐Zaki, Abuzenadah, Adel M., Hashem, Anwar M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284640/
https://www.ncbi.nlm.nih.gov/pubmed/35860397
http://dx.doi.org/10.1002/gch2.202200008
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author Alhabbab, Rowa Y.
Alfaleh, Mohamed A.
Alsulaiman, Reem M.
Alamri, Sawsan S.
Eyouni, Mais S.
ElAssouli, M‐Zaki
Abuzenadah, Adel M.
Hashem, Anwar M.
author_facet Alhabbab, Rowa Y.
Alfaleh, Mohamed A.
Alsulaiman, Reem M.
Alamri, Sawsan S.
Eyouni, Mais S.
ElAssouli, M‐Zaki
Abuzenadah, Adel M.
Hashem, Anwar M.
author_sort Alhabbab, Rowa Y.
collection PubMed
description Rapid lateral flow immune‐assays are point‐of‐care diagnostic tools that are easy to use, cheap, and do not need centralized infrastructure. Therefore, these devices are appealing for rapid detection of the humoral immune responses to infections, particularly severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2). The novel technique introduced here uses a complex of anti‐SARS‐CoV‐2 N‐protein antibodies conjugated to gold nanoparticles that are bound to five SARS‐CoV‐2 N protein conjugated to gold nanoparticles to amplify the signals obtained from the conjugated SARS‐CoV‐2 N protein and to enhance the assay detection limit. To validate the performance of the adopted lateral flow, serum from SARS‐CoV‐2 seropositive individuals and prepandamic negative samples are tested and compared to a validated enzyme‐linked immunosorbent assay (ELISA) for the detection of SARS‐CoV‐2 N protein specific IgG and IgM antibodies. The data shows that the designed lateral flow assay has an excellent sensitivity and specificity upon detecting IgM and IgG antibodies by applying only 2 µL from the serum sample to the adopted strips. Taken together, the developed lateral flow immunoassay assay provides a rapid, specific, and highly sensitive means to detect the immune responses against SARS‐CoV‐2 with only 2 µL from the serum sample.
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spelling pubmed-92846402022-07-19 Amplifying Lateral Flow Assay Signals for Rapid Detection of COVID‐19 Specific Antibodies Alhabbab, Rowa Y. Alfaleh, Mohamed A. Alsulaiman, Reem M. Alamri, Sawsan S. Eyouni, Mais S. ElAssouli, M‐Zaki Abuzenadah, Adel M. Hashem, Anwar M. Glob Chall Research Articles Rapid lateral flow immune‐assays are point‐of‐care diagnostic tools that are easy to use, cheap, and do not need centralized infrastructure. Therefore, these devices are appealing for rapid detection of the humoral immune responses to infections, particularly severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2). The novel technique introduced here uses a complex of anti‐SARS‐CoV‐2 N‐protein antibodies conjugated to gold nanoparticles that are bound to five SARS‐CoV‐2 N protein conjugated to gold nanoparticles to amplify the signals obtained from the conjugated SARS‐CoV‐2 N protein and to enhance the assay detection limit. To validate the performance of the adopted lateral flow, serum from SARS‐CoV‐2 seropositive individuals and prepandamic negative samples are tested and compared to a validated enzyme‐linked immunosorbent assay (ELISA) for the detection of SARS‐CoV‐2 N protein specific IgG and IgM antibodies. The data shows that the designed lateral flow assay has an excellent sensitivity and specificity upon detecting IgM and IgG antibodies by applying only 2 µL from the serum sample to the adopted strips. Taken together, the developed lateral flow immunoassay assay provides a rapid, specific, and highly sensitive means to detect the immune responses against SARS‐CoV‐2 with only 2 µL from the serum sample. John Wiley and Sons Inc. 2022-05-11 /pmc/articles/PMC9284640/ /pubmed/35860397 http://dx.doi.org/10.1002/gch2.202200008 Text en © 2022 The Authors. Global Challenges published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Alhabbab, Rowa Y.
Alfaleh, Mohamed A.
Alsulaiman, Reem M.
Alamri, Sawsan S.
Eyouni, Mais S.
ElAssouli, M‐Zaki
Abuzenadah, Adel M.
Hashem, Anwar M.
Amplifying Lateral Flow Assay Signals for Rapid Detection of COVID‐19 Specific Antibodies
title Amplifying Lateral Flow Assay Signals for Rapid Detection of COVID‐19 Specific Antibodies
title_full Amplifying Lateral Flow Assay Signals for Rapid Detection of COVID‐19 Specific Antibodies
title_fullStr Amplifying Lateral Flow Assay Signals for Rapid Detection of COVID‐19 Specific Antibodies
title_full_unstemmed Amplifying Lateral Flow Assay Signals for Rapid Detection of COVID‐19 Specific Antibodies
title_short Amplifying Lateral Flow Assay Signals for Rapid Detection of COVID‐19 Specific Antibodies
title_sort amplifying lateral flow assay signals for rapid detection of covid‐19 specific antibodies
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284640/
https://www.ncbi.nlm.nih.gov/pubmed/35860397
http://dx.doi.org/10.1002/gch2.202200008
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