Electrokinetic generation of temporally and spatially stable concentration gradients in microchannels

被引:12
作者
Biddiss, E [1 ]
Li, DQ [1 ]
机构
[1] Univ Toronto, Dept Mech & Ind Engn, Toronto, ON M5S 3G8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
electrokinetic; microfluidics; concentration gradient;
D O I
10.1016/j.jcis.2005.03.037
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Generating stable microscale concentration gradients is key to numerous biological and chemical analyses, Microfluidic systems offer the ability to maintain laminar fluid diffusion interfaces ideal for the production of temporally stable concentration gradients. Previous efforts have focused on pressure driven flows and have relied on networks of branching channels to create streams of varying concentration which can subsequently be combined to form the desired gradients, In this Study, we numerically and experimentally demonstrate a novel electrokinetic technique which utilizes applied voltages and surface charge heterogeneity in simpler channel geometries to control and manipulate microscale concentration gradients without the need for parallel lamination, Flow rates ranged from 30 to 460 nl min(-1) for Peclet numbers between 70 and 1100. Spatial stability of 0.6 mm or greater was obtained for a wide range of gradient shape and magnitudes over lateral dimensions of 400-450 mu m. Sensitivity analysis determined that this technique is, largely independent of channel depth and species electrophoretic mobility, however channel width and the diffusion coefficient of the analyte are critical. It was concluded that by adjusting applied voltages and/or channel width, this approach to concentration gradient generation can be adapted to a wide range of applications. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:606 / 615
页数:10
相关论文
共 38 条
[11]   Gradients of substrate-bound laminin orient axonal specification of neurons [J].
Dertinger, SKW ;
Jiang, XY ;
Li, ZY ;
Murthy, VN ;
Whitesides, GM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :12542-12547
[12]   Rapid prototyping of microfluidic systems in poly(dimethylsiloxane) [J].
Duffy, DC ;
McDonald, JC ;
Schueller, OJA ;
Whitesides, GM .
ANALYTICAL CHEMISTRY, 1998, 70 (23) :4974-4984
[13]   Neutrophil chemotaxis in moving gradients of fMLP [J].
Ebrahimzadeh, PR ;
Högfors, C ;
Braide, M .
JOURNAL OF LEUKOCYTE BIOLOGY, 2000, 67 (05) :651-661
[14]   Electrokinetically controlled DNA hybridization microfluidic chip enabling rapid target analysis [J].
Erickson, D ;
Liu, XZ ;
Krull, U ;
Li, DQ .
ANALYTICAL CHEMISTRY, 2004, 76 (24) :7269-7277
[15]   Modeling of DNA hybridization kinetics for spatially resolved biochips [J].
Erickson, D ;
Li, DQ ;
Krull, UJ .
ANALYTICAL BIOCHEMISTRY, 2003, 317 (02) :186-200
[16]   Joule heating and heat transfer in poly(dimethylsiloxane) microfluidic systems [J].
Erickson, D ;
Sinton, D ;
Li, DQ .
LAB ON A CHIP, 2003, 3 (03) :141-149
[17]   Influence of surface heterogeneity on electrokinetically driven microfluidic mixing [J].
Erickson, D ;
Li, DQ .
LANGMUIR, 2002, 18 (05) :1883-1892
[18]   LOCOMOTION AND CHEMOTAXIS OF LEUKOCYTES - GRADIENT PERCEPTION AND LOCOMOTOR CAPACITY [J].
HASTON, WS ;
WILKINSON, PC .
CURRENT OPINION IN IMMUNOLOGY, 1988, 1 (01) :5-9
[19]   Surface-chemistry technology for microfluidics [J].
Hau, WLW ;
Trau, DW ;
Sucher, NJ ;
Wong, M ;
Zohar, Y .
JOURNAL OF MICROMECHANICS AND MICROENGINEERING, 2003, 13 (02) :272-278
[20]   The potential of micromixers for contacting of disperse liquid phases [J].
Haverkamp, V ;
Ehrfeld, W ;
Gebauer, K ;
Hessel, V ;
Löwe, H ;
Richter, T ;
Wille, C .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1999, 364 (07) :617-624