MCU based real-time temperature control system for universal microfluidic PCR chip

被引:12
作者
Han, Dawoon [1 ]
Jang, You-Cheol [2 ]
Oh, Sung-Nam [3 ]
Chand, Rohit [1 ]
Lim, Ki-Tae [1 ]
Kim, Kab-Il [3 ]
Kim, Yong-Sang [1 ]
机构
[1] Sungkyunkwan Univ, Sch Elect & Elect Engn, Suwon 440746, Gyeonggi, South Korea
[2] STATSChipPac, Dept Res & Dev, Inchon 467734, Gyeonggi, South Korea
[3] Myongji Univ, Dept Elect Engn, Yongin 449728, Gyeonggi, South Korea
来源
MICROSYSTEM TECHNOLOGIES-MICRO-AND NANOSYSTEMS-INFORMATION STORAGE AND PROCESSING SYSTEMS | 2014年 / 20卷 / 03期
关键词
DIAGNOSTICS; FABRICATION; GLASS;
D O I
10.1007/s00542-013-1970-1
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
The analysis of genetic materials in the post-human genome project era has become an ever-expanding branch of research and thus routinely employed in majority of biochemical laboratories. Most of the diagnostic research area emphasizes on polymerase chain reaction for detecting pathogenic organisms. However, the conventional polymerase chain reaction requires expensive and sophisticated thermal cycler and is not handy owing to its large dimensions. Therefore, we fabricated a continuous-flow polymerase chain reaction chip on a PDMS based microfluidic platform to ease the hardship of the conventional system. Temperature being the most crucial factor in polymerase chain reaction, was monitored and regulated by thermostatic action using an on-line computer system. Indium tin oxide coated glass platform was used for heating as it is transparent and has good thermal conductivity under the influence of DC bias. The heating circuit used an ATMega 128 MCU to control the temperature. As a result, a precise and quick heating environment was maintained on the microfluidic chip to amplify the target DNA. We successfully amplified Lambda phage and Escherichia coli DNA on our chip to prove the practicality of the device.
引用
收藏
页码:471 / 476
页数:6
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