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On-Chip Nucleic Acid Purification Followed by ddPCR for SARS-CoV-2 Detection
We developed a microfluidic chip integrated with nucleic acid purification and droplet-based digital polymerase chain reaction (ddPCR) modules to realize a ‘sample-in, result-out’ infectious virus diagnosis. The whole process involved pulling magnetic beads through drops in an oil-enclosed environme...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216157/ https://www.ncbi.nlm.nih.gov/pubmed/37232879 http://dx.doi.org/10.3390/bios13050517 |
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author | Ma, Cong Sun, Yimeng Huang, Yuhang Gao, Zehang Huang, Yaru Pandey, Ikshu Jia, Chunping Feng, Shilun Zhao, Jianlong |
author_facet | Ma, Cong Sun, Yimeng Huang, Yuhang Gao, Zehang Huang, Yaru Pandey, Ikshu Jia, Chunping Feng, Shilun Zhao, Jianlong |
author_sort | Ma, Cong |
collection | PubMed |
description | We developed a microfluidic chip integrated with nucleic acid purification and droplet-based digital polymerase chain reaction (ddPCR) modules to realize a ‘sample-in, result-out’ infectious virus diagnosis. The whole process involved pulling magnetic beads through drops in an oil-enclosed environment. The purified nucleic acids were dispensed into microdroplets by a concentric-ring, oil–water-mixing, flow-focusing droplets generator driven under negative pressure conditions. Microdroplets were generated with good uniformity (CV = 5.8%), adjustable diameters (50–200 μm), and controllable flow rates (0–0.3 μL/s). Further verification was provided by quantitative detection of plasmids. We observed a linear correlation of R(2) = 0.9998 in the concentration range from 10 to 10(5) copies/μL. Finally, this chip was applied to quantify the nucleic acid concentrations of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The measured nucleic acid recovery rate of 75 ± 8.8% and detection limit of 10 copies/μL proved its on-chip purification and accurate detection abilities. This chip can potentially be a valuable tool in point-of-care testing. |
format | Online Article Text |
id | pubmed-10216157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102161572023-05-27 On-Chip Nucleic Acid Purification Followed by ddPCR for SARS-CoV-2 Detection Ma, Cong Sun, Yimeng Huang, Yuhang Gao, Zehang Huang, Yaru Pandey, Ikshu Jia, Chunping Feng, Shilun Zhao, Jianlong Biosensors (Basel) Article We developed a microfluidic chip integrated with nucleic acid purification and droplet-based digital polymerase chain reaction (ddPCR) modules to realize a ‘sample-in, result-out’ infectious virus diagnosis. The whole process involved pulling magnetic beads through drops in an oil-enclosed environment. The purified nucleic acids were dispensed into microdroplets by a concentric-ring, oil–water-mixing, flow-focusing droplets generator driven under negative pressure conditions. Microdroplets were generated with good uniformity (CV = 5.8%), adjustable diameters (50–200 μm), and controllable flow rates (0–0.3 μL/s). Further verification was provided by quantitative detection of plasmids. We observed a linear correlation of R(2) = 0.9998 in the concentration range from 10 to 10(5) copies/μL. Finally, this chip was applied to quantify the nucleic acid concentrations of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The measured nucleic acid recovery rate of 75 ± 8.8% and detection limit of 10 copies/μL proved its on-chip purification and accurate detection abilities. This chip can potentially be a valuable tool in point-of-care testing. MDPI 2023-05-05 /pmc/articles/PMC10216157/ /pubmed/37232879 http://dx.doi.org/10.3390/bios13050517 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ma, Cong Sun, Yimeng Huang, Yuhang Gao, Zehang Huang, Yaru Pandey, Ikshu Jia, Chunping Feng, Shilun Zhao, Jianlong On-Chip Nucleic Acid Purification Followed by ddPCR for SARS-CoV-2 Detection |
title | On-Chip Nucleic Acid Purification Followed by ddPCR for SARS-CoV-2 Detection |
title_full | On-Chip Nucleic Acid Purification Followed by ddPCR for SARS-CoV-2 Detection |
title_fullStr | On-Chip Nucleic Acid Purification Followed by ddPCR for SARS-CoV-2 Detection |
title_full_unstemmed | On-Chip Nucleic Acid Purification Followed by ddPCR for SARS-CoV-2 Detection |
title_short | On-Chip Nucleic Acid Purification Followed by ddPCR for SARS-CoV-2 Detection |
title_sort | on-chip nucleic acid purification followed by ddpcr for sars-cov-2 detection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216157/ https://www.ncbi.nlm.nih.gov/pubmed/37232879 http://dx.doi.org/10.3390/bios13050517 |
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