Toward a self-deploying shape memory polymer neuronal electrode

被引:82
作者
Sharp, Andrew A. [1 ]
Panchawagh, Hrishikesh V.
Ortega, Alicia
Artale, Ryan
Richardson-Burns, Sarah
Finch, Dudley S.
Gall, Ken
Mahajan, Roop L.
Restrepo, Diego
机构
[1] Univ Colorado, Rocky Mt Taste & Smell Ctr, Neurosci Program, Aurora, CO 80045 USA
[2] Univ Colorado, Dept Cell & Dev Biol, Aurora, CO 80045 USA
[3] Hlth Sci Ctr, Aurora, CO 80045 USA
[4] Univ Colorado, Dept Mech Engn, Boulder, CO 80309 USA
[5] Georgia Inst Technol, Sch Mat Sci & Engn, Atlanta, GA 30332 USA
[6] Georgia Inst Technol, Woodruff Sch Mech Engn, Atlanta, GA 30332 USA
关键词
D O I
10.1088/1741-2560/3/4/L02
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The widespread application of neuronal probes for chronic recording of brain activity and functional stimulation has been slow to develop partially due to long-term biocompatibility problems with existing metallic and ceramic probes and the tissue damage caused during probe insertion. Stiff probes are easily inserted into soft brain tissue but cause astrocytic scars that become insulating sheaths between electrodes and neurons. In this communication, we explore the feasibility of a new approach to the composition and implantation of chronic electrode arrays. We demonstrate that softer polymer-based probes can be inserted into the olfactory bulb of a mouse and that slow insertion of the probes reduces astrocytic scarring. We further present the development of a micromachined shape memory polymer probe, which provides a vehicle to self-deploy an electrode at suitably slow rates and which can provide sufficient force to penetrate the brain. The deployment rate and composition of shape memory polymer probes can be tailored by polymer chemistry and actuator design. We conclude that it is feasible to fabricate shape memory polymer-based electrodes that would slowly self-implant compliant conductors into the brain, and both decrease initial trauma resulting from implantation and enhance long-term biocompatibility for long-term neuronal measurement and stimulation.
引用
收藏
页码:L23 / L30
页数:8
相关论文
共 51 条
[1]   A high-yield microassembly structure for three-dimensional microelectrode arrays [J].
Bai, Q ;
Wise, KD ;
Anderson, DJ .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 2000, 47 (03) :281-289
[2]   Review of current evidence for apoptosis after spinal cord injury [J].
Beattie, MS ;
Farooqui, AA ;
Bresnahan, JC .
JOURNAL OF NEUROTRAUMA, 2000, 17 (10) :915-925
[3]   Neuronal cell loss accompanies the brain tissue response to chronically implanted silicon microelectrode arrays [J].
Biran, R ;
Martin, DC ;
Tresco, PA .
EXPERIMENTAL NEUROLOGY, 2005, 195 (01) :115-126
[4]   Effects of insertion conditions on tissue strain and vascular damage during neuroprosthetic device insertion [J].
Bjornsson, C. S. ;
Oh, S. J. ;
Al-Kofahi, Y. A. ;
Lim, Y. J. ;
Smith, K. L. ;
Turner, J. N. ;
De, S. ;
Roysam, B. ;
Shain, W. ;
Kim, S. J. .
JOURNAL OF NEURAL ENGINEERING, 2006, 3 (03) :196-207
[5]   Polytrodes: High-density silicon electrode arrays for large-scale multiunit recording [J].
Blanche, TJ ;
Spacek, MA ;
Hetke, JF ;
Swindale, NV .
JOURNAL OF NEUROPHYSIOLOGY, 2005, 93 (05) :2987-3000
[6]   Migration of perilesional microglia after focal brain injury and modulation by CC chemokine receptor 5:: An in situ time-lapse confocal imaging study [J].
Carbonell, WS ;
Murase, SI ;
Horwitz, AF ;
Mandell, JW .
JOURNAL OF NEUROSCIENCE, 2005, 25 (30) :7040-7047
[7]   Massively parallel recording of unit and local field potentials with silicon-based electrodes [J].
Csicsvari, J ;
Henze, DA ;
Jamieson, B ;
Harris, KD ;
Sirota, A ;
Barthó, P ;
Wise, KD ;
Buzsáki, G .
JOURNAL OF NEUROPHYSIOLOGY, 2003, 90 (02) :1314-1323
[8]   In vivo imaging of migrating neurons in the mammalian forebrain [J].
Davenne, M ;
Custody, C ;
Charneau, P ;
Lledo, PM .
CHEMICAL SENSES, 2005, 30 :I115-i116
[9]   Reactive astrocytes protect tissue and preserve function after spinal cord injury [J].
Faulkner, JR ;
Herrmann, JE ;
Woo, MJ ;
Tansey, KE ;
Doan, NB ;
Sofroniew, MV .
JOURNAL OF NEUROSCIENCE, 2004, 24 (09) :2143-2155
[10]  
Feninat FEL, 2002, ADV ENG MATER, V4, P91, DOI DOI 10.1002/1527-2648(200203)4:3<91::AID-ADEM91>3.0.CO