Multisite recording of extracellular potentials produced by microchannel-confined neurons in-vitro

被引:30
作者
Claverol-Tinture, E. [1 ]
Cabestany, J.
Rosell, X.
机构
[1] Tech Univ Catalonia, Dept Elect, Barcelona 08028, Spain
[2] Biomed Engn Res Ctr, Barcelona 08028, Spain
关键词
cell patterning; current source density analysis; Helix aspersa; microfluidics; multichannel electrophysiology; neural interfaces; neuronal culture; PDMS; snail neurons;
D O I
10.1109/TBME.2006.880903
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Towards establishing electrical interfaces with patterned in vitro neurons, we have previously described the fabrication of hybrid elastomer-glass devices polymer-on-multielectrode array technology and obtained single-electrode recordings of extracellular potentials from confined neurons (Claverol-Tinture et al, 2005). Here, we demonstrate the feasibility of spatially localized multisite recordings from individual microcharmel-guided neurites extending from microwell-confined somas with good signal-to-noise ratios (20 dB) and spike magnitudes of up to 300 mu V. Single-cell current source density (scCSD) analysis of the spatio-temporal patterns of membrane currents along individual processes is illustrated.
引用
收藏
页码:331 / 335
页数:5
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