Culturing neuron cells on electrode with self-assembly monolayer

被引:17
|
作者
Palyvoda, Olena [1 ]
Chen, Chung-Chu
Auner, Gregory W.
机构
[1] Wayne State Univ, Dept Elect & Comp Engn, SSIM, Detroit, MI 48202 USA
[2] Wayne State Univ, Dept Biomed Engn, Detroit, MI USA
来源
BIOSENSORS & BIOELECTRONICS | 2007年 / 22卷 / 9-10期
关键词
neural interface; cortical neuron; self-assembly monolayer; cell culturing; micro-electrode array;
D O I
10.1016/j.bios.2006.08.021
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The success of neuronal implantable microsystems relies on the quality of the interface with neuronal cells. Depending on the application, specifically engineered surfaces may either prevent or enhance cell/tissue growth with an appropriate host response. The surface chemistry and topography have major effects on the cell adherence and the interaction between the tissue and devices. We report on a simple technique to precisely explant cortical neurons in a serum-free medium on 2D electrode arrays and investigated the pad size effect on neuron cell culture and immobilization. We produced gold patterns on glass substrates using microfabrication processes. 11-Amino-1-undecanethiol self-assembled monolayer was coated only on the gold surface. Cortical neurons were cultured on the arrays to examine the dependence of neuron growth and cells distribution on pad size. We found that the terminal functional groups of the highly oriented 11-amino-1-undecanethiol thin film are essential for generating cell-adhesive areas for the rat cortical neurons. A 50 mu m x 50 mu m SAM pad size was found to be suitable for single cortical neuron immobilization, while the larger pads provide excellent neuron coverage. This technology may enable precise and localized neuron stimulation and surveillance for both biological research and medical applications. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:2346 / 2350
页数:5
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