Multifunctional Nanobiomaterials for Neural Interfaces

被引:322
作者
Abidian, Mohammad Reza [1 ]
Martin, David C. [1 ,2 ,3 ]
机构
[1] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Mat Sci & Engn, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Macromol Sci & Engn, Ann Arbor, MI 48109 USA
关键词
STRUCTURE-PROPERTY RELATIONSHIPS; MASSIVE POLY(ALPHA-HYDROXY ACIDS); MICROELECTRODE ARRAYS; CONDUCTING POLYMERS; AQUEOUS-MEDIA; CORTICOSTEROID-THERAPY; DRUG-RELEASE; DEGRADATION; MORPHOLOGY; POLY(3,4-ETHYLENEDIOXYTHIOPHENE);
D O I
10.1002/adfm.200801473
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Neural electrodes are designed to interface with the nervous system and provide control signals for neural prostheses. However, robust and reliable chronic recording and stimulation remains a challenge for neural electrodes. Here, a novel method for the fabrication of soft, low impedance, high charge density, and controlled releasing nanobiomaterials that can be used for the surface modification of neural microelectrodes to stabilize the electrode/tissue interface is reported. The fabrication process includes electrospinning of anti-inflammatory drug-incorporated biodegradable nanofibers, encapsulation of these nanofibers; by an alginate hydrogel layer, followed by electrochemical polymerization of conducting polymers around the electrospun drug-loaded nanofibers to form nanotubes and within the alginate hydrogel scaffold to form cloud-like nanostructures. The three-dimensional conducting polymer nanostructures significantly decrease the electrode impedance and increase the charge capacity density. Dexamethasone release profiles show that the alginate hydrogel coating slows down the release of the drug, significantly reducing the burst effect. These multifunctional materials are expected to be of interest for a variety of electrode/tissue interfaces in biomedical devices.
引用
收藏
页码:573 / 585
页数:13
相关论文
共 80 条
[21]   Conducting polymers for neural interfaces: Challenges in developing an effective long-term implant [J].
Green, Rylie A. ;
Lovell, Nigel H. ;
Wallace, Gordon G. ;
Poole-Warren, Laura A. .
BIOMATERIALS, 2008, 29 (24-25) :3393-3399
[22]  
Groenendaal BL, 2000, ADV MATER, V12, P481, DOI 10.1002/(SICI)1521-4095(200004)12:7<481::AID-ADMA481>3.0.CO
[23]  
2-C
[24]   Electrochemistry of poly(3,4-alkylenedioxythiophene) derivatives [J].
Groenendaal, L ;
Zotti, G ;
Aubert, PH ;
Waybright, SM ;
Reynolds, JR .
ADVANCED MATERIALS, 2003, 15 (11) :855-879
[25]   Conducting polymers in biomedical engineering [J].
Guimard, Nathalie K. ;
Gomez, Natalia ;
Schmidt, Christine E. .
PROGRESS IN POLYMER SCIENCE, 2007, 32 (8-9) :876-921
[26]   POLY(ALKYLENEDIOXYTHIOPHENE)S - NEW, VERY STABLE CONDUCTING POLYMERS [J].
HEYWANG, G ;
JONAS, F .
ADVANCED MATERIALS, 1992, 4 (02) :116-118
[27]   CRYSTAL-STRUCTURE, CONFORMATION, AND MORPHOLOGY OF SOLUTION-SPUN POLY(L-LACTIDE) FIBERS [J].
HOOGSTEEN, W ;
POSTEMA, AR ;
PENNINGS, AJ ;
TENBRINKE, G ;
ZUGENMAIER, P .
MACROMOLECULES, 1990, 23 (02) :634-642
[28]   The effect of initial polymer morphology on the degradation and drug release from polyglycolide [J].
Hurrell, S ;
Cameron, RE .
BIOMATERIALS, 2002, 23 (11) :2401-2409
[29]   Scaffolds in tissue engineering bone and cartilage [J].
Hutmacher, DW .
BIOMATERIALS, 2000, 21 (24) :2529-2543
[30]   Electronic control of Ca2+ signalling in neuronal cells using an organic electronic ion pump [J].
Isaksson, Joakim ;
Kjaell, Peter ;
Nilsson, David ;
Robinson, Nathaniel D. ;
Berggren, Magnus ;
Richter-Dahlfors, Agneta .
NATURE MATERIALS, 2007, 6 (09) :673-679