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A multi-volume microfluidic device with no reagent loss for low-cost digital PCR application

•A multi-volume multi-level vertical branching microchannel dPCR chip was presented and verified.•The dPCR chip achieved a dynamic range of over 104 for nucleic acid quantification with only 1792 chambers.•The dPCR chip can partition samples autonomously and realized 100 % sample compartmentalizatio...

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Bibliographic Details
Published in:Sensors and actuators. B, Chemical Chemical, 2020-09, Vol.318, p.128197, Article 128197
Main Authors: Si, Huaqing, Xu, Gangwei, Jing, Fengxiang, Sun, Peng, Zhao, Dan, Wu, Dongping
Format: Article
Language:English
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Summary:•A multi-volume multi-level vertical branching microchannel dPCR chip was presented and verified.•The dPCR chip achieved a dynamic range of over 104 for nucleic acid quantification with only 1792 chambers.•The dPCR chip can partition samples autonomously and realized 100 % sample compartmentalization without any loss. A multi-volume multi-level vertical branching microchannel microfludic chip is presented in this study for low-cost and easy-operation digital PCR (dPCR). The chip with multi-volume design can achieve a dynamic range of over 104 for nucleic acid quantification with only 1792 chambers, which consist of two types of chambers with different volumes and quantities. Meanwhile, the dPCR chip realizes 100 % sample compartmentalization without any loss. In addition, the chip can partition samples autonomously in a simple way through negative pressure provided by a degassed PDMS layer. Furthermore, a glass-PDMS-glass “sandwich” structure was employed in the chip to form a robust support. The quantitative capability of the digital PCR chip is evaluated by measuring a 10-fold serial dilution of the KRAS plasmid template. Owing to its characteristics of easy operation process, low cost, relative wide dynamic range, and no sample loss, the proposed dPCR chip is expected to further promote the extensive application of digital PCR, especially in the POCT field.
ISSN:0925-4005
1873-3077
DOI:10.1016/j.snb.2020.128197