Hydrolytically Stable Thiol-ene Networks for Flexible Bioelectronics

被引:17
|
作者
Reit, Radu [1 ]
Zamorano, Daniel [2 ]
Parker, Shelbi [1 ]
Simon, Dustin [3 ]
Lund, Benjamin [3 ]
Voit, Walter [1 ,2 ,3 ,4 ]
Ware, Taylor H. [1 ]
机构
[1] Univ Texas Dallas, Dept Bioengn, 800 West Campbell Rd,Mailstop RL 10, Richardson, TX 75080 USA
[2] Univ Texas Dallas, Dept Chem, Richardson, TX 75080 USA
[3] Univ Texas Dallas, Dept Mat Sci & Engn, Richardson, TX 75080 USA
[4] Univ Texas Dallas, Dept Mech Engn, Richardson, TX 75080 USA
基金
美国国家科学基金会;
关键词
PERIPHERAL-NERVE STIMULATION; NEURAL INTERFACES; PHYSICAL-PROPERTIES; PHOTOPOLYMERIZATION; ELECTRONICS; POLYMER;
D O I
10.1021/acsami.5b10593
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Hydrolytically stable, tunable modulus polymer networks are demonstrated to survive harsh alkaline environments and offer promise for use in long-term implantable bioelectronic medicines known as electroceuticals. Todays polymer networks (such as polyimides or polysiloxanes) succeed in providing either stiff or soft substrates for bioelectronics devices; however, the capability to significantly tune the modulus of such materials is lacking. Within the space of materials with easily modified elastic moduli, thiolene copolymers are a subset of materials that offer a promising solution to build next generation flexible bioelectronics but have typically been susceptible to hydrolytic degradation chronically. In this inquiry, we demonstrate a materials space capable of tuning the substrate modulus and explore the mechanical behavior of such networks. Furthermore, we fabricate an array of microelectrodes that can withstand accelerated aging environments shown to destroy conventional flexible bioelectronics.
引用
收藏
页码:28673 / 28681
页数:9
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