A simple device using magnetic transportation for droplet-based PCR

被引:87
作者
Ohashi, Tetsuo [1 ]
Kuyama, Hiroki
Hanafusa, Nobuhiro
Togawa, Yoshiyuki
机构
[1] Shimadzu Co Ltd, Analyt & Measuring Instruments, Life Sci Lab, Kyoto 6048511, Japan
[2] Osaka Univ, Inst Prot Res, Suita, Osaka 5650871, Japan
关键词
magnetic beads; droplets; polymerase chain reaction; microfluidic technology;
D O I
10.1007/s10544-007-9078-y
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The Polymerase chain reaction (PCR) was successfully and rapidly performed in a simple reaction device devoid of channels, pumps, valves, or other control elements used in conventional lab-on-a-chip technology. The basic concept of this device is the transportation of aqueous droplets containing hydrophilic magnetic beads in a flat-bottomed, tray-type reactor filled with silicone oil. The whole droplets sink to the bottom of the reactor because their specific gravity is greater than that of the silicone oil used here. The droplets follow the movement of a magnet located underneath the reactor. The notable advantage of the droplet-based PCR is the ability to switch rapidly the proposed reaction temperature by moving the droplets to the required temperature zones in the temperature gradient. The droplet-based reciprocative thermal cycling was performed by moving the droplets composed of PCR reaction mixture to the designated temperature zones on a linear temperature gradient from 50 degrees C to 94 degrees C generated on the flat bottom plate of the tray reactor. Using human-derived DNA containing the mitochondria genes as the amplification targets, the droplet-based PCR with magnetic reciprocative thermal cycling successfully provided the five PCR products ranging from 126 to 1,219 bp in 11 min with 30 cycles. More remarkably, the human genomic gene amplification targeting glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene was accomplished rapidly in 3.6 min with 40 cycles.
引用
收藏
页码:695 / 702
页数:8
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