Design of a Digital LAMP Detection Platform Based on Droplet Microfluidic Technology

被引:4
|
作者
Jiang, Liying [1 ,2 ]
Lan, Xianghao [1 ]
Ren, Linjiao [1 ]
Yang, Mingzhu [3 ]
Wei, Bo [4 ]
Wang, Yang [5 ]
机构
[1] Zhengzhou Univ Light Ind, Sch Elect & Informat Engn, Zhengzhou 450002, Peoples R China
[2] Zhengzhou Univ Light Ind, Acad Quantum Sci & Technol, Zhengzhou 450002, Peoples R China
[3] Beijing Res Inst Mech Equipment, Beijing 100143, Peoples R China
[4] Capital Med Univ, Beijing Tiantan Hosp, Dept Thorac Surg, Beijing 100070, Peoples R China
[5] Beihang Univ, Sch Engn Med, Beijing Adv Innovat Ctr Biomed Engn, Key Lab Biomech & Mechanobiol, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
microfluidic; droplet generation; digital-LAMP; high sensitivity; ISOTHERMAL AMPLIFICATION LAMP; DIAGNOSIS; CHIP; PCR;
D O I
10.3390/mi14051077
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Loop-mediated isothermal amplification (LAMP) is a rapid and high-yield amplification technology for specific DNA or RNA molecules. In this study, we designed a digital loop-mediated isothermal amplification (digital-LAMP)-functioning microfluidic chip to achieve higher sensitivity for detection of nucleic acids. The chip could generate droplets and collect them, based on which we could perform Digital-LAMP. The reaction only took 40 min at a constant temperature of 63 degrees C. The chip enabled highly accurate quantitative detection, with the limit of detection (LOD) down to 10(2) copies mu L-1. For better performance while reducing the investment of money and time in chip structure iterations, we used COMSOL Multiphysics to simulate different droplet generation ways by including flow-focusing structure and T-junction structure. Moreover, the linear structure, serpentine structure, and spiral structure in the microfluidic chip were compared to study the fluid velocity and pressure distribution. The simulations provided a basis for chip structure design while facilitating chip structure optimization. The digital-LAMP-functioning chip proposed in the work provides a universal platform for analysis of viruses.
引用
收藏
页数:13
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