Study of a Liquid Plug-Flow Thermal Cycling Technique Using a Temperature Gradient-Based Actuator

被引:10
作者
Fuchiwaki, Yusuke [1 ,2 ]
Nagai, Hidenori [3 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Hlth Res Inst, Takamatsu, Kagawa 7610395, Japan
[2] CEA LETI, F-38054 Grenoble 9, France
[3] Natl Inst Adv Ind Sci & Technol, Hlth Res Inst, Ikeda, Osaka 5638577, Japan
关键词
thermal cycling; DNA amplification; PCR; microfluidics; DNA AMPLIFICATION;
D O I
10.3390/s141120235
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Easy-to-use thermal cycling for performing rapid and small-volume DNA amplification on a single chip has attracted great interest in the area of rapid field detection of biological agents. For this purpose, as a more practical alternative to conventional continuous flow thermal cycling, liquid plug-flow thermal cycling utilizes a thermal gradient generated in a serpentine rectangular flow microchannel as an actuator. The transit time and flow speed of the plug flow varied drastically in each temperature zone due to the difference in the tension at the interface between temperature gradients. According to thermal distribution analyses in microfluidics, the plug flow allowed for a slow heating process, but a fast cooling process. The thermal cycle of the microfluid was consistent with the recommended temperature gradient for PCR. Indeed, amplification efficiency of the plug flow was superior to continuous flow PCR, and provided an impressive improvement over previously-reported flow microchannel thermal cycling techniques.
引用
收藏
页码:20235 / 20244
页数:10
相关论文
共 9 条
[1]   A reusable flow-through polymerase chain reaction instrument for the continuous monitoring of infectious biological agents [J].
Belgrader, P ;
Elkin, CJ ;
Brown, SB ;
Nasarabadi, SN ;
Langlois, RG ;
Milanovich, FP ;
Colston, BW ;
Marshall, GD .
ANALYTICAL CHEMISTRY, 2003, 75 (14) :3446-3450
[2]   Developments toward a complete micro-total analysis system for Duchenne muscular dystrophy diagnosis [J].
Ferrance, JP ;
Wu, QR ;
Giordano, B ;
Hernandez, C ;
Kwok, Y ;
Snow, K ;
Thibodeau, S ;
Landers, JP .
ANALYTICA CHIMICA ACTA, 2003, 500 (1-2) :223-236
[3]   Microfabricated flow-through device for DNA amplification - towards in situ gene analysis [J].
Fukuba, T ;
Yamamoto, T ;
Naganuma, T ;
Fujii, T .
CHEMICAL ENGINEERING JOURNAL, 2004, 101 (1-3) :151-156
[4]   Chemical amplification: Continuous-flow PCR on a chip [J].
Kopp, MU ;
de Mello, AJ ;
Manz, A .
SCIENCE, 1998, 280 (5366) :1046-1048
[5]   Monolithic integrated microfluidic DNA amplification and capillary electrophoresis analysis system [J].
Lagally, ET ;
Simpson, PC ;
Mathies, RA .
SENSORS AND ACTUATORS B-CHEMICAL, 2000, 63 (03) :138-146
[6]   An optimal design method for preventing air bubbles in high-temperature microfluidic devices [J].
Nakayama, Tsuyoshi ;
Hiep, Ha Minh ;
Furui, Satoshi ;
Yonezawa, Yuji ;
Saito, Masato ;
Takamura, Yuzuru ;
Tamiya, Eiichi .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2010, 396 (01) :457-464
[7]   Continuous-flow DNA and RNA amplification chip combined with laser-induced fluorescence detection [J].
Obeid, PJ ;
Christopoulos, TK .
ANALYTICA CHIMICA ACTA, 2003, 494 (1-2) :1-9
[8]  
Schneegass I, 2001, J Biotechnol, V82, P101, DOI 10.1016/S1389-0352(01)00033-2
[9]   Miniaturized PCR chips for nucleic acid amplification and analysis: latest advances and future trends [J].
Zhang, Chunsun ;
Xing, Da .
NUCLEIC ACIDS RESEARCH, 2007, 35 (13) :4223-4237