Numerical modeling of transport and accumulation of DNA on electronically active biochips

被引:35
作者
Kassegne, SK
Reese, H
Hodko, D
Yang, JM
Sarkar, K
Smolko, D
Swanson, P
Raymond, DE
Heller, MJ
Madou, MJ
机构
[1] Nanogen Inc, San Diego, CA 92121 USA
[2] Genoptix, San Diego, CA 92121 USA
[3] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[4] Univ Calif Irvine, Dept Mech & Aerosp Engn, Irvine, CA 92697 USA
基金
美国国家卫生研究院;
关键词
electrophoresis; active electronic chip; DNA transport; hybridization; finite element analysis; micro-electrodes;
D O I
10.1016/S0925-4005(03)00322-8
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Transport and accumulation of biomolecules, particularly DNA, in active electronic chips are investigated through numerical modeling and experimental verification. Various geometric and design configurations of electronically active DNA chips are considered. Further, we investigate the effect of electric field distribution on practical design of flow cells and chips. Particular attention is focused on the geometric effects on current and electric field distribution which are well captured by a finite element method-based model. We demonstrate that these geometric effects are observed only in buffers of very low conductivity. We also demonstrate that numerical models which do not include the charge transfer mechanism between electrodes and the buffer solution will fail to predict the reduction of these geometric effects with increased buffer conductivity. The review of the technology is based on computer simulation using a finite element-based computational model and experimental results of electric field distribution, DNA transport and accumulation. Comparison of theoretical results for electrophoretic DNA accumulation with those obtained from experiments and a simple analytical model is presented. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:81 / 98
页数:18
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