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Loop-Mediated Isothermal Amplification–Based Microfluidic Platforms for the Detection of Viral Infections
PURPOSE OF REVIEW: Easy-to-use, fast, and accurate virus detection method is essential for patient management and epidemic surveillance, especially during severe pandemics. Loop-mediated isothermal amplification (LAMP) on a microfluidic platform is suitable for detecting infectious viruses, regardle...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9628606/ https://www.ncbi.nlm.nih.gov/pubmed/36341307 http://dx.doi.org/10.1007/s11908-022-00790-5 |
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author | Zeng, Yuanyuan Wu, Chuan He, Yang |
author_facet | Zeng, Yuanyuan Wu, Chuan He, Yang |
author_sort | Zeng, Yuanyuan |
collection | PubMed |
description | PURPOSE OF REVIEW: Easy-to-use, fast, and accurate virus detection method is essential for patient management and epidemic surveillance, especially during severe pandemics. Loop-mediated isothermal amplification (LAMP) on a microfluidic platform is suitable for detecting infectious viruses, regardless of the availability of medical resources. The purpose of this review is to introduce LAMP-based microfluidic devices for virus detection, including their detection principles, methods, and application. RECENT FINDINGS: Facing the uncontrolled spread of viruses, the large-scale deployment of LAMP-based microfluidic platforms at the grassroots level can help expand the coverage of nucleic acid testing and shorten the time to obtain test reports. Microfluidic chip technology is highly integrated and miniaturized, enabling precise fluid control for effective virus detection. Performing LAMP on miniaturized systems can reduce analysis time, reagent consumption and risk of sample contamination, and improve analytical performance. SUMMARY: Compared to traditional benchtop protocols, LAMP-based microfluidic devices reduce the testing time, reagent consumption, and the risk of sample contamination. In addition to simultaneous detection of multiple target genes by special channel design, microfluidic chips can also integrate digital LAMP to achieve absolute quantification of target genes. |
format | Online Article Text |
id | pubmed-9628606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-96286062022-11-02 Loop-Mediated Isothermal Amplification–Based Microfluidic Platforms for the Detection of Viral Infections Zeng, Yuanyuan Wu, Chuan He, Yang Curr Infect Dis Rep Technology and Infectious Disease (C Hebert, Section Editor) PURPOSE OF REVIEW: Easy-to-use, fast, and accurate virus detection method is essential for patient management and epidemic surveillance, especially during severe pandemics. Loop-mediated isothermal amplification (LAMP) on a microfluidic platform is suitable for detecting infectious viruses, regardless of the availability of medical resources. The purpose of this review is to introduce LAMP-based microfluidic devices for virus detection, including their detection principles, methods, and application. RECENT FINDINGS: Facing the uncontrolled spread of viruses, the large-scale deployment of LAMP-based microfluidic platforms at the grassroots level can help expand the coverage of nucleic acid testing and shorten the time to obtain test reports. Microfluidic chip technology is highly integrated and miniaturized, enabling precise fluid control for effective virus detection. Performing LAMP on miniaturized systems can reduce analysis time, reagent consumption and risk of sample contamination, and improve analytical performance. SUMMARY: Compared to traditional benchtop protocols, LAMP-based microfluidic devices reduce the testing time, reagent consumption, and the risk of sample contamination. In addition to simultaneous detection of multiple target genes by special channel design, microfluidic chips can also integrate digital LAMP to achieve absolute quantification of target genes. Springer US 2022-11-02 2022 /pmc/articles/PMC9628606/ /pubmed/36341307 http://dx.doi.org/10.1007/s11908-022-00790-5 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022, Springer Nature or its licensor (e.g. a society or other partner) 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 | Technology and Infectious Disease (C Hebert, Section Editor) Zeng, Yuanyuan Wu, Chuan He, Yang Loop-Mediated Isothermal Amplification–Based Microfluidic Platforms for the Detection of Viral Infections |
title | Loop-Mediated Isothermal Amplification–Based Microfluidic Platforms for the Detection of Viral Infections |
title_full | Loop-Mediated Isothermal Amplification–Based Microfluidic Platforms for the Detection of Viral Infections |
title_fullStr | Loop-Mediated Isothermal Amplification–Based Microfluidic Platforms for the Detection of Viral Infections |
title_full_unstemmed | Loop-Mediated Isothermal Amplification–Based Microfluidic Platforms for the Detection of Viral Infections |
title_short | Loop-Mediated Isothermal Amplification–Based Microfluidic Platforms for the Detection of Viral Infections |
title_sort | loop-mediated isothermal amplification–based microfluidic platforms for the detection of viral infections |
topic | Technology and Infectious Disease (C Hebert, Section Editor) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9628606/ https://www.ncbi.nlm.nih.gov/pubmed/36341307 http://dx.doi.org/10.1007/s11908-022-00790-5 |
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