LampPort: a handheld digital microfluidic device for loop-mediated isothermal amplification (LAMP)

被引:46
|
作者
Wan, Liang [1 ,2 ]
Gao, Jie [1 ]
Chen, Tianlan [1 ]
Dong, Cheng [1 ]
Li, Haoran [1 ,2 ]
Wen, Yan-Zi [3 ]
Lun, Zhao-Rong [3 ]
Jia, Yanwei [1 ]
Mak, Pui-In [1 ,2 ]
Martins, Rui P. [1 ,2 ]
机构
[1] Univ Macau, State Key Lab Analog & Mixed Signal VLSI, Macau, Peoples R China
[2] Univ Macau, Dept ECE, Fac Sci & Technol, Macau, Peoples R China
[3] Sun Yat Sen Univ, Sch Life Sci, State Key Lab Biocontrol, Ctr Parasit Organisms, Guangzhou 510275, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Digital microfluidic system; Handheld device; Loop-mediated isothermal amplification (LAMP); Naked-eye visualisation; ASSAY;
D O I
10.1007/s10544-018-0354-9
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A major goal in the development of point-of-care (POC) devices is to build them as portable to provide a rapid and effective determination for disease pathogens. In nucleic acid testing, an optical detection system used to monitor the product of nucleic acid amplification has always been a bulky accessory. In this work, we developed a handheld, automatic and detection system-free thermal digital microfluidic (DMF) device for DNA detection by loop-mediated isothermal amplification (LAMP). Droplet manipulation and real-time temperature control systems were integrated into a handheld device. The control software could be installed into any tablet and communicate with the device via Bluetooth. In the experimentation, we loaded 2-l samples with an electrowetting force into sandwich-structured DMF chips, thereby considerably reducing reagent consumptions. After an on-chip LAMP reaction, we added a highly concentrated SYBR Green I droplet and mixed it with a reaction droplet to enable product detection with the naked eye. This step prevented aerosol contamination by avoiding the exposure of the reaction droplet to the air. Using a blood parasite Trypanosoma brucei as a model system, this system showed similar results as a commercial thermal cycler and could detect 40 copies per reaction of the DNA target. This low-cost, compact device removed the bulky optical system for DNA detection, thus enabling it to be well suited for POC testing.
引用
收藏
页数:8
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