A micro circulating PCR chip using a suction-type membrane for fluidic transport

被引:19
作者
Chien, Liang-Ju [1 ]
Wang, Jung-Hao [1 ]
Hsieh, Tsung-Min [2 ]
Chen, Ping-Hei [4 ]
Chen, Pei-Jer [5 ]
Lee, Da-Sheng [6 ]
Luo, Ching-Hsing [2 ]
Lee, Gwo-Bin [1 ,3 ]
机构
[1] Natl Cheng Kung Univ, Dept Engn Sci, Tainan 701, Taiwan
[2] Natl Cheng Kung Univ, Dept Elect Engn, Tainan 701, Taiwan
[3] Ind Technol Res Inst, Med Elect & Device Technol Ctr, Hsinchu 310, Taiwan
[4] Natl Taiwan Univ, Dept Mech Engn, Taipei 100, Taiwan
[5] Natl Taiwan Univ, Natl Taiwan Univ Hosp, Taipei 100, Taiwan
[6] Natl Taipei Univ Technol, Dept Energy & Refrigerating Air Conditioning Engn, Taipei 106, Taiwan
关键词
PCR; Molecular diagnosis; Microfluidics; Microheaters; MEMS; POLYMERASE-CHAIN-REACTION; CONTINUOUS-FLOW PCR; CAPILLARY-ELECTROPHORESIS; ENZYMATIC AMPLIFICATION; REACTION SYSTEM; INTEGRATION; SEPARATION; ACTUATION; DEVICE; CELL;
D O I
10.1007/s10544-008-9242-z
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A new micromachined circulating polymerase chain reaction (PCR) chip is reported in this study. A novel liquid transportation mechanism utilizing a suction-type membrane and three microvalves were used to create a new microfluidic control module to rapidly transport the DNA samples and PCR reagents around three bio-reactors operating at three different temperatures. When operating at a membrane actuation frequency of 14.29 Hz and a pressure of 5 psi, the sample flow rate in the microfluidic control module can be as high as 18 mu L/s. In addition, an array-type microheater was adopted to improve the temperature uniformity in the reaction chambers. Open-type reaction chambers were designed to facilitate temperature calibration. Experimental data from infrared images showed that the percentage of area inside the reaction chamber with a thermal variation of less than 1A degrees C was over 90% for a denaturing temperature of 94A degrees C. Three array-type heaters and temperature sensors were integrated into this new circulating PCR chip to modulate three specific operating temperatures for the denaturing, annealing, and extension steps of a PCR process. With this approach, the cycle numbers and reaction times of the three separate reaction steps can be individually adjusted. To verify the performance of this circulating PCR chip, a PCR process to amplify a detection gene (150 base pairs) associated with the hepatitis C virus was performed. Experimental results showed that DNA samples with concentrations ranging from 10(5) to 10(2)copies/mu L can be successfully amplified. Therefore, this new circulating PCR chip may provide a useful platform for genetic identification and molecular diagnosis.
引用
收藏
页码:359 / 367
页数:9
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