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A portable system for economical nucleic acid amplification testing
Introduction: Regular and rapid large-scale screening for pathogens is crucial for controlling pandemics like Coronavirus Disease 2019 (COVID-19). In this study, we present the development of a digital point-of-care testing (POCT) system utilizing microfluidic paper-based analytical devices (μPADs)...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436208/ https://www.ncbi.nlm.nih.gov/pubmed/37600301 http://dx.doi.org/10.3389/fbioe.2023.1214624 |
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author | Dong, Hui Mo, Jin Yu, Yongjian Xie, Wantao Zheng, Jianping Jia, Chao |
author_facet | Dong, Hui Mo, Jin Yu, Yongjian Xie, Wantao Zheng, Jianping Jia, Chao |
author_sort | Dong, Hui |
collection | PubMed |
description | Introduction: Regular and rapid large-scale screening for pathogens is crucial for controlling pandemics like Coronavirus Disease 2019 (COVID-19). In this study, we present the development of a digital point-of-care testing (POCT) system utilizing microfluidic paper-based analytical devices (μPADs) for the detection of SARS-CoV-2 gene fragments. The system incorporates temperature tuning and fluorescent detection components, along with intelligent and autonomous image acquisition and self-recognition programs. Methods: The developed POCT system is based on the nucleic acid amplification test (NAAT), a well-established molecular biology technique for detecting and amplifying nucleic acids. We successfully detected artificially synthesized SARS-CoV-2 gene fragments, namely ORF1ab gene, N gene, and E gene, with minimal reagent consumption of only 2.2 μL per readout, representing a mere 11% of the requirements of conventional in-tube methods. The power dissipation of the system was low, at 6.4 W. Results: Our testing results demonstrated that the proposed approach achieved a limit of detection of 1000 copies/mL, which is equivalent to detecting 1 copy or a single RNA template per reaction. By employing standard curve analysis, the quantity of the target templates can be accurately determined. Conclusion: The developed digital POCT system shows great promise for rapid and reliable detection of SARS-CoV-2 gene fragments, offering a cost-effective and efficient solution for controlling pandemics. Its compatibility with other diagnostic techniques and low reagent consumption make it a viable option to enhance healthcare in resource-limited areas. |
format | Online Article Text |
id | pubmed-10436208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104362082023-08-19 A portable system for economical nucleic acid amplification testing Dong, Hui Mo, Jin Yu, Yongjian Xie, Wantao Zheng, Jianping Jia, Chao Front Bioeng Biotechnol Bioengineering and Biotechnology Introduction: Regular and rapid large-scale screening for pathogens is crucial for controlling pandemics like Coronavirus Disease 2019 (COVID-19). In this study, we present the development of a digital point-of-care testing (POCT) system utilizing microfluidic paper-based analytical devices (μPADs) for the detection of SARS-CoV-2 gene fragments. The system incorporates temperature tuning and fluorescent detection components, along with intelligent and autonomous image acquisition and self-recognition programs. Methods: The developed POCT system is based on the nucleic acid amplification test (NAAT), a well-established molecular biology technique for detecting and amplifying nucleic acids. We successfully detected artificially synthesized SARS-CoV-2 gene fragments, namely ORF1ab gene, N gene, and E gene, with minimal reagent consumption of only 2.2 μL per readout, representing a mere 11% of the requirements of conventional in-tube methods. The power dissipation of the system was low, at 6.4 W. Results: Our testing results demonstrated that the proposed approach achieved a limit of detection of 1000 copies/mL, which is equivalent to detecting 1 copy or a single RNA template per reaction. By employing standard curve analysis, the quantity of the target templates can be accurately determined. Conclusion: The developed digital POCT system shows great promise for rapid and reliable detection of SARS-CoV-2 gene fragments, offering a cost-effective and efficient solution for controlling pandemics. Its compatibility with other diagnostic techniques and low reagent consumption make it a viable option to enhance healthcare in resource-limited areas. Frontiers Media S.A. 2023-08-02 /pmc/articles/PMC10436208/ /pubmed/37600301 http://dx.doi.org/10.3389/fbioe.2023.1214624 Text en Copyright © 2023 Dong, Mo, Yu, Xie, Zheng and Jia. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Dong, Hui Mo, Jin Yu, Yongjian Xie, Wantao Zheng, Jianping Jia, Chao A portable system for economical nucleic acid amplification testing |
title | A portable system for economical nucleic acid amplification testing |
title_full | A portable system for economical nucleic acid amplification testing |
title_fullStr | A portable system for economical nucleic acid amplification testing |
title_full_unstemmed | A portable system for economical nucleic acid amplification testing |
title_short | A portable system for economical nucleic acid amplification testing |
title_sort | portable system for economical nucleic acid amplification testing |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436208/ https://www.ncbi.nlm.nih.gov/pubmed/37600301 http://dx.doi.org/10.3389/fbioe.2023.1214624 |
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