Neural probe design for reduced tissue encapsulation in CNS

被引:358
作者
Seymour, John P. [1 ]
Kipke, Daryl R. [1 ]
机构
[1] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
关键词
biosensor; cell encapsulation; foreign body response; neural prosthesis;
D O I
10.1016/j.biomaterials.2007.03.024
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This study investigated relationships between a microscale neural probe's size and shape and its chronic reactive tissue response. Parylene-based probes were microfabricated with a thick shank (48 mu m by 68 mu m) and an integrated thin lateral platform (5 mu m by 100 pm, either solid or one of three lattice sizes). Devices were implanted in rat cerebral cortex for 4 weeks before immunostaining for neurons, astrocytes, microglia, fibronectin, laminin, and neurofilament. While nonneuronal density (NND) generally increased and neuronal density decreased within 75 mu m of a probe interface compared to unimplanted control regions, there were significant differential tissue responses within 25 mu m of the platform's lateral edge compared to the shank. The NND in this region of the lateral edge was less than one-third of the corresponding region of the shank (129% and 425% increase, respectively). Moreover, neuronal density around the platform lateral edge was about one-third higher than at the shank (0.70 and 0.52 relative to control, respectively). Also, microglia reactivity and extracellular protein deposition was reduced at the lateral edge. There were no significant differences among platform designs. These results suggest that neural probe geometry is an important parameter for reducing chronic tissue encapsulation. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3594 / 3607
页数:14
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