Numerical Simulation and Experimental Verification of Droplet Generation in Microfluidic Digital PCR Chip

被引:13
|
作者
Meng, Xiangkai [1 ,2 ]
Yu, Yuanhua [1 ,3 ]
Jin, Guangyong [1 ,2 ]
机构
[1] Changchun Univ Sci & Technol, Sch Life Sci & Technol, Changchun 130022, Peoples R China
[2] Changchun Univ Sci & Technol, Sch Sci, Changchun 130022, Peoples R China
[3] Key Lab Biol Detect Engn, Changchun 130022, Peoples R China
关键词
droplet digital PCR; droplet generation; microfluidic; COMSOL Multiphysics; POLYMERASE-CHAIN-REACTION; FLOW; DYNAMICS;
D O I
10.3390/mi12040409
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The generation of droplets is one of the most critical steps in the droplet digital polymerase chain reaction (ddPCR) procedure. In this study, the mechanism of droplet formation in microchannel structure and factors affecting droplet formation were studied. The physical field of laminar two-phase flow level was used to simulate the process of droplet generation through microfluidic technology. The effect of the parameters including flow rate, surface tension, and viscosity on the generated droplet size were evaluated by the simulation. After that, the microfluidic chip that has the same dimension as the simulation was then, fabricated and evaluated. The chip was made by conventional SU-8 photolithography and injection molding. The accuracy of the simulation was validated by comparing the generated droplets in the real scenario with the simulation result. The relative error (RE) between experimentally measured droplet diameter and simulation results under different flow rate, viscosity, surface tension and contact angle was found less than 3.5%, 1.8%, 1.4%, and 1.2%, respectively. Besides, the coefficient of variation (CV) of the droplet diameter was less than 1%, which indicates the experimental droplet generation was of high stability and reliability. This study provides not only fundamental information for the design and experiment of droplet generation by microfluidic technology but also a reliable and efficient investigation method in the ddPCR field.
引用
收藏
页数:12
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