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A Self-Priming Microfluidic Chip with Cushion Chambers for Easy Digital PCR

A polydimethylsiloxane (PDMS)-based self-priming microfluidic chip with cushion chambers is presented in this study for robust and easy-operation digital polymerase chain reaction (dPCR). The chip has only one inlet and can partition samples autonomously through negative pressure, provided by a de-g...

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Detalles Bibliográficos
Autores principales: Xu, Gangwei, Si, Huaqing, Jing, Fengxiang, Sun, Peng, Wu, Dongping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155915/
https://www.ncbi.nlm.nih.gov/pubmed/34069758
http://dx.doi.org/10.3390/bios11050158
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author Xu, Gangwei
Si, Huaqing
Jing, Fengxiang
Sun, Peng
Wu, Dongping
author_facet Xu, Gangwei
Si, Huaqing
Jing, Fengxiang
Sun, Peng
Wu, Dongping
author_sort Xu, Gangwei
collection PubMed
description A polydimethylsiloxane (PDMS)-based self-priming microfluidic chip with cushion chambers is presented in this study for robust and easy-operation digital polymerase chain reaction (dPCR). The chip has only one inlet and can partition samples autonomously through negative pressure, provided by a de-gassed PDMS layer with a multi-level vertical branching microchannel design. Meanwhile, cushion chambers make the chip capable of very robust use for sample partitioning. Finally, the proposed microfluidic chip showed excellent performance in the absolute quantification of a target gene by performing quantitative detection of a 10-fold serial dilution DNA template. Owing to its characteristics of easy operation, low cost, and high robustness, the proposed dPCR chip is expected to further promote the extensive application of digital PCR, especially in resource-limited settings.
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spelling pubmed-81559152021-05-28 A Self-Priming Microfluidic Chip with Cushion Chambers for Easy Digital PCR Xu, Gangwei Si, Huaqing Jing, Fengxiang Sun, Peng Wu, Dongping Biosensors (Basel) Article A polydimethylsiloxane (PDMS)-based self-priming microfluidic chip with cushion chambers is presented in this study for robust and easy-operation digital polymerase chain reaction (dPCR). The chip has only one inlet and can partition samples autonomously through negative pressure, provided by a de-gassed PDMS layer with a multi-level vertical branching microchannel design. Meanwhile, cushion chambers make the chip capable of very robust use for sample partitioning. Finally, the proposed microfluidic chip showed excellent performance in the absolute quantification of a target gene by performing quantitative detection of a 10-fold serial dilution DNA template. Owing to its characteristics of easy operation, low cost, and high robustness, the proposed dPCR chip is expected to further promote the extensive application of digital PCR, especially in resource-limited settings. MDPI 2021-05-18 /pmc/articles/PMC8155915/ /pubmed/34069758 http://dx.doi.org/10.3390/bios11050158 Text en © 2021 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
Xu, Gangwei
Si, Huaqing
Jing, Fengxiang
Sun, Peng
Wu, Dongping
A Self-Priming Microfluidic Chip with Cushion Chambers for Easy Digital PCR
title A Self-Priming Microfluidic Chip with Cushion Chambers for Easy Digital PCR
title_full A Self-Priming Microfluidic Chip with Cushion Chambers for Easy Digital PCR
title_fullStr A Self-Priming Microfluidic Chip with Cushion Chambers for Easy Digital PCR
title_full_unstemmed A Self-Priming Microfluidic Chip with Cushion Chambers for Easy Digital PCR
title_short A Self-Priming Microfluidic Chip with Cushion Chambers for Easy Digital PCR
title_sort self-priming microfluidic chip with cushion chambers for easy digital pcr
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155915/
https://www.ncbi.nlm.nih.gov/pubmed/34069758
http://dx.doi.org/10.3390/bios11050158
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