Multifunctional hydrogel coatings on the surface of neural cuff electrode for improving electrode-nerve tissue interfaces

被引:69
作者
Heo, Dong Nyoung [1 ,2 ]
Song, Su-Jin [1 ]
Kim, Han-Jun [3 ]
Lee, Yi Jae [4 ]
Ko, Wan-Kyu [1 ]
Lee, Sang Jin [5 ]
Lee, Donghyun [5 ]
Park, Sung Jin [4 ]
Zhang, Lijie Grace [2 ]
Kang, Ji Yoon [4 ]
Do, Sun Hee [3 ]
Lee, Soo Hyun [4 ]
Kwon, Il Keun [1 ]
机构
[1] Kyung Hee Univ, Sch Dent, Dept Dent Mat, Seoul 02447, South Korea
[2] George Washington Univ, Dept Mech & Aerosp Engn, Washington, DC 20052 USA
[3] Konkuk Univ, Coll Vet Med, Dept Clin Pathol, Seoul 05029, South Korea
[4] Korea Inst Sci & Technol, Ctr BioMicroSyst, Seoul 02455, South Korea
[5] Kyung Hee Univ, Grad Sch, Dept Dent, Seoul 02447, South Korea
基金
新加坡国家研究基金会;
关键词
Cuff electrode; Cyclosporine A; Sciatic nerve; Hydrogel coating; Drug delivery; Neural signal recording; CONTROLLED DRUG-RELEASE; CONDUCTING POLYMERS; SCIATIC-NERVE; CYCLOSPORINE; RAT; SYSTEM; IMMUNOSUPPRESSION; DEXAMETHASONE; REGENERATION; NANOFIBERS;
D O I
10.1016/j.actbio.2016.05.009
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Recently, implantable neural electrodes have been developed for recording and stimulation of the nervous system. However, when the electrode is implanted onto the nerve trunk, the rigid polyimide has a risk of damaging the nerve and can also cause inflammation due to a mechanical mismatch between the stiff polyimide and the soft biological tissue. These processes can interrupt the transmission of nerve signaling. In this paper, we have developed a nerve electrode coated with PEG hydrogel that contains poly (lactic-co-glycolic) acid (PLGA) microspheres (MS) loaded with anti-inflammatory cyclosporin A (CsA). Micro-wells were introduced onto the electrode in order to increase their surface area. This allows for loading a high-dose of the drug. Additionally, chemically treating the surface with aminopropylmethacry-lamide can improve the adhesive interface between the electrode and the hydrogel. The surface of the micro-well cuff electrode (MCE) coated with polyethylene glycol (PEG) hydrogel and drug loaded PLGA microspheres (MS) were characterized by SEM and optical microscopy. Additionally, the conductive polymers, poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT/PSS), were formed on the hydrogel layer for improving the nerve signal quality, and then characterized for their electrochemical properties. The loading efficiencies and release profiles were investigated by High Performance Liquid Chromatography (HPLC). The drug loaded electrode resulted in a sustained release of CsA. Moreover, the surface coated electrode with PEG hydrogel and CsA loaded MP showed a significantly decreased fibrous tissue deposition and increased axonal density in animal tests. We expect that the developed nerve electrode will minimize the tissue damage during regeneration of the nervous system. Statement of Significance The nerve electrodes are used for interfacing with the central nervous system (CNS) or with the peripheral nervous system (PNS). The interface electrodes should facilitate a closed interconnection with the nerve tissue and provide for selective stimulation and recording from multiple, independent, neurons of the neural system. In this case, an extraneural electrodes such as cuff and perineural electrodes are widely investigated because they can completely cover the nerve trunk and provide for a wide interface area. In this study, we have designed and prepared a functionalized nerve cuff electrode coated with PEG hydrogel containing Poly lactic-co-glycol acid (PLGA) microspheres (MS) loaded with cyclosporine A (CsA). To our knowledge, our findings suggest that surface coating a soft-hydrogel along with an anti-inflammatory drug loaded MS can be a useful strategy for improving the long-term biocompatibility of electrodes. (C) 2016 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:25 / 33
页数:9
相关论文
共 38 条
[11]   Sustained release of proteins from electrospun biodegradable fibers [J].
Chew, SY ;
Wen, J ;
Yim, EKF ;
Leong, KW .
BIOMACROMOLECULES, 2005, 6 (04) :2017-2024
[12]   Improvement of signal-to-interference ratio and signal-to-noise ratio in nerve cuff electrode systems [J].
Chu, Jun-Uk ;
Song, Kang-Il ;
Han, Sungmin ;
Lee, Soo Hyun ;
Kim, Jinseok ;
Kang, Ji Yoon ;
Hwang, Dosik ;
Suh, Jun-Kyo Francis ;
Choi, Kuiwon ;
Youn, Inchan .
PHYSIOLOGICAL MEASUREMENT, 2012, 33 (06) :943-967
[13]   Effects of the novel cyclosporine derivative PSC833 on glucose metabolism in rat primary cultures of neuronal and glial cells [J].
Cruz, F ;
Wolf, A .
BIOCHEMICAL PHARMACOLOGY, 2001, 62 (01) :129-139
[14]   Polymer microspheres for controlled drug release [J].
Freiberg, S ;
Zhu, X .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 282 (1-2) :1-18
[15]   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
[16]   Implanted Neural Interfaces: Biochallenges and Engineered Solutions [J].
Grill, Warren M. ;
Norman, Sharon E. ;
Bellamkonda, Ravi V. .
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2009, 11 :1-24
[17]   Stretchable Polymeric Multielectrode Array for Conformal Neural Interfacing [J].
Guo, Liang ;
Ma, Mingming ;
Zhang, Ning ;
Langer, Robert ;
Anderson, Daniel G. .
ADVANCED MATERIALS, 2014, 26 (09) :1427-1433
[18]   Improving Cochlear Implant Properties Through Conductive Hydrogel Coatings [J].
Hassarati, Rachelle T. ;
Dueck, Wolfram F. ;
Tasche, Claudia ;
Carter, Paul M. ;
Poole-Warren, Laura A. ;
Green, Rylie A. .
IEEE TRANSACTIONS ON NEURAL SYSTEMS AND REHABILITATION ENGINEERING, 2014, 22 (02) :411-418
[19]   Implantable bioelectronic interfaces for lost nerve functions [J].
Heiduschka, P ;
Thanos, S .
PROGRESS IN NEUROBIOLOGY, 1998, 55 (05) :433-461
[20]  
Heo D.N., 2012, P SPIE, V84099