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Ultra-Rapid and Ultra-Sensitive Detection of SARS-CoV-2 Antibodies in COVID-19 Patients via A 3D-Printed Nanomaterial-Based Biosensing Platform

Rapid detection of antibodies during infection and after vaccination is critical for the control of infectious outbreaks, understanding immune response, and evaluating vaccine efficacy. In this manuscript, we evaluate a simple ultra-rapid test for SARS-CoV-2 antibodies in COVID-19 patients, which gi...

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Autores principales: Ali, Azahar, Zhang, George Fei, Hu, Chunshan, Yuan, Bin, Jahan, Sanjida, Kitsios, Georgios D., Morris, Alison, Gao, Shou-Jiang, Panat, Rahul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9538259/
https://www.ncbi.nlm.nih.gov/pubmed/35981973
http://dx.doi.org/10.1002/jmv.28075
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author Ali, Azahar
Zhang, George Fei
Hu, Chunshan
Yuan, Bin
Jahan, Sanjida
Kitsios, Georgios D.
Morris, Alison
Gao, Shou-Jiang
Panat, Rahul
author_facet Ali, Azahar
Zhang, George Fei
Hu, Chunshan
Yuan, Bin
Jahan, Sanjida
Kitsios, Georgios D.
Morris, Alison
Gao, Shou-Jiang
Panat, Rahul
author_sort Ali, Azahar
collection PubMed
description Rapid detection of antibodies during infection and after vaccination is critical for the control of infectious outbreaks, understanding immune response, and evaluating vaccine efficacy. In this manuscript, we evaluate a simple ultra-rapid test for SARS-CoV-2 antibodies in COVID-19 patients, which gives quantitative results (i.e., antibody concentration) in 10–15 seconds using a previously reported nanomaterial-based 3D-printed biosensing platform. This platform consists of a micropillar array electrode fabricated via 3D printing of aerosolized gold nanoparticles and coated with nanoflakes of graphene and specific SARS-CoV-2 antigens, including spike S1, S1 receptor-binding domain (RBD) and nucleocapsid (N). The sensor works on the principle of electrochemical transduction where the change of sensor impedance is realized by the interactions between the viral proteins attached to the sensor electrode surface and the antibodies. The three sensors were used to test samples from 17 COVID-19 patients and 3 patients without COVID-19. Unlike other serological tests, the 3D sensors quantitatively detected antibodies at concentration as low as picomole within 10–12 seconds in human plasma samples. We found that the studied COVID-19 patients had higher concentrations of antibodies to spike proteins (RBD and S1) than to the N protein. These results demonstrate the enormous potential of the rapid antibody test platform for understanding patients’ immunity, disease epidemiology and vaccine efficacy, and facilitating control and prevention of infectious epidemics.
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spelling pubmed-95382592023-12-01 Ultra-Rapid and Ultra-Sensitive Detection of SARS-CoV-2 Antibodies in COVID-19 Patients via A 3D-Printed Nanomaterial-Based Biosensing Platform Ali, Azahar Zhang, George Fei Hu, Chunshan Yuan, Bin Jahan, Sanjida Kitsios, Georgios D. Morris, Alison Gao, Shou-Jiang Panat, Rahul J Med Virol Article Rapid detection of antibodies during infection and after vaccination is critical for the control of infectious outbreaks, understanding immune response, and evaluating vaccine efficacy. In this manuscript, we evaluate a simple ultra-rapid test for SARS-CoV-2 antibodies in COVID-19 patients, which gives quantitative results (i.e., antibody concentration) in 10–15 seconds using a previously reported nanomaterial-based 3D-printed biosensing platform. This platform consists of a micropillar array electrode fabricated via 3D printing of aerosolized gold nanoparticles and coated with nanoflakes of graphene and specific SARS-CoV-2 antigens, including spike S1, S1 receptor-binding domain (RBD) and nucleocapsid (N). The sensor works on the principle of electrochemical transduction where the change of sensor impedance is realized by the interactions between the viral proteins attached to the sensor electrode surface and the antibodies. The three sensors were used to test samples from 17 COVID-19 patients and 3 patients without COVID-19. Unlike other serological tests, the 3D sensors quantitatively detected antibodies at concentration as low as picomole within 10–12 seconds in human plasma samples. We found that the studied COVID-19 patients had higher concentrations of antibodies to spike proteins (RBD and S1) than to the N protein. These results demonstrate the enormous potential of the rapid antibody test platform for understanding patients’ immunity, disease epidemiology and vaccine efficacy, and facilitating control and prevention of infectious epidemics. 2022-12 2022-08-30 /pmc/articles/PMC9538259/ /pubmed/35981973 http://dx.doi.org/10.1002/jmv.28075 Text en
spellingShingle Article
Ali, Azahar
Zhang, George Fei
Hu, Chunshan
Yuan, Bin
Jahan, Sanjida
Kitsios, Georgios D.
Morris, Alison
Gao, Shou-Jiang
Panat, Rahul
Ultra-Rapid and Ultra-Sensitive Detection of SARS-CoV-2 Antibodies in COVID-19 Patients via A 3D-Printed Nanomaterial-Based Biosensing Platform
title Ultra-Rapid and Ultra-Sensitive Detection of SARS-CoV-2 Antibodies in COVID-19 Patients via A 3D-Printed Nanomaterial-Based Biosensing Platform
title_full Ultra-Rapid and Ultra-Sensitive Detection of SARS-CoV-2 Antibodies in COVID-19 Patients via A 3D-Printed Nanomaterial-Based Biosensing Platform
title_fullStr Ultra-Rapid and Ultra-Sensitive Detection of SARS-CoV-2 Antibodies in COVID-19 Patients via A 3D-Printed Nanomaterial-Based Biosensing Platform
title_full_unstemmed Ultra-Rapid and Ultra-Sensitive Detection of SARS-CoV-2 Antibodies in COVID-19 Patients via A 3D-Printed Nanomaterial-Based Biosensing Platform
title_short Ultra-Rapid and Ultra-Sensitive Detection of SARS-CoV-2 Antibodies in COVID-19 Patients via A 3D-Printed Nanomaterial-Based Biosensing Platform
title_sort ultra-rapid and ultra-sensitive detection of sars-cov-2 antibodies in covid-19 patients via a 3d-printed nanomaterial-based biosensing platform
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9538259/
https://www.ncbi.nlm.nih.gov/pubmed/35981973
http://dx.doi.org/10.1002/jmv.28075
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