Numeric simulation of heat transfer and electrokinetic flow in an electroosmosis-based continuous flow PCR chip

被引:33
作者
Gui, Lin [1 ]
Ren, Carolyn L. [1 ]
机构
[1] Univ Waterloo, Dept Mech Engn, Waterloo, ON N2L 3G1, Canada
关键词
D O I
10.1021/ac060553d
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学]; 081704 [应用化学];
摘要
Precise design and operational control of the polymerase chain reaction process is key to the performance of on-chip DNA analysis. This research is dedicated to understanding the fluid flow and heat transfer mechanisms occurring in continuous flow PCR chips from the engineering point of view. In this work, a 3-dimensional model was developed to simulate the electrical potential field, the flow field, and the temperature field in an electroosmosis-based continuous flow PCR chip. On the basis of the simultaneous solution to this model, the effects of the channel/chip size, the chip material, and the applied voltage difference on the temperature distribution and control are discussed in detail. The importance of each heat transfer mechanism for different situations is also discussed. It was found that if a larger chip thickness or a material with a lower heat conductivity was used, the temperature in the microfluidic PCR chip would decrease dramatically. The effects of the applied electrical field strength and flow velocity on the temperature distribution, however, are negligible for microchannels with a small cross-sectional area. With bigger channels, the flow direction will affect the temperature distribution in the channel because heat convection will dominate heat transfer.
引用
收藏
页码:6215 / 6222
页数:8
相关论文
共 37 条
[1]
Miniaturised nucleic acid analysis [J].
Auroux, PA ;
Koc, Y ;
deMello, A ;
Manz, A ;
Day, PJR .
LAB ON A CHIP, 2004, 4 (06) :534-546
[2]
A magneto-hydrodynamically controlled fluidic network [J].
Bau, HH ;
Zhu, JZ ;
Qian, SZ ;
Xiang, Y .
SENSORS AND ACTUATORS B-CHEMICAL, 2003, 88 (02) :205-216
[3]
BAU HH, 2001, IMECE 2001 MEMS 2388
[4]
Micromanipulation of single cells from tissue imprints is an alternative to laser-assisted microdissection [J].
Brauns, TC ;
Goos, M .
JOURNAL OF CUTANEOUS PATHOLOGY, 2005, 32 (07) :461-466
[5]
Design and theoretical evaluation of a novel microfluidic device to be used for PCR [J].
Bu, MQ ;
Melvin, T ;
Ensell, G ;
Wilkinson, JS ;
Evans, AGR .
JOURNAL OF MICROMECHANICS AND MICROENGINEERING, 2003, 13 (04) :S125-S130
[6]
Rapid identification of yeasts in positive blood cultures by a multiplex PCR method [J].
Chang, HC ;
Leaw, SN ;
Huang, AH ;
Wuk, TL ;
Chang, TC .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (10) :3466-3471
[7]
Thermosiphon-based PCR reactor: Experiment and modeling [J].
Chen, ZY ;
Qian, SZ ;
Abrams, WR ;
Malamud, D ;
Bau, HH .
ANALYTICAL CHEMISTRY, 2004, 76 (13) :3707-3715
[8]
A miniaturized cyclic PCR device - modeling and experiments [J].
Chou, CF ;
Changrani, R ;
Roberts, P ;
Sadler, D ;
Burdon, J ;
Zenhausern, F ;
Lin, S ;
Mulholland, A ;
Swami, N ;
Terbrueggen, R .
MICROELECTRONIC ENGINEERING, 2002, 61-2 :921-925
[9]
Continuous segmented-flow polymerase chain reaction for high-throughput miniaturized DNA amplification [J].
Curcio, M ;
Roeraade, J .
ANALYTICAL CHEMISTRY, 2003, 75 (01) :1-7
[10]
Silicon microchambers for DNA amplification [J].
Daniel, JH ;
Iqbal, S ;
Millington, RB ;
Moore, DF ;
Lowe, CR ;
Leslie, DL ;
Lee, MA ;
Pearce, MJ .
SENSORS AND ACTUATORS A-PHYSICAL, 1998, 71 (1-2) :81-88