Department of Mechanical Engineering, The University of Texas at Dallas, Richardson, TX 75080, United States of America.
J Neural Eng. 2018 Aug;15(4):045002. doi: 10.1088/1741-2552/aab90d. Epub 2018 Mar 23.
We sought to develop a cervical spinal cord stimulator for the rat that is durable, stable, and does not perturb the underlying spinal cord.
We created a softening spinal cord stimulation (SCS) array made from shape memory polymer (SMP)-based flexible electronics. We developed a new photolithographic process to pattern high surface area titanium nitride (TiN) electrodes onto gold (Au) interconnects. The thiol-ene acrylate polymers are stiff at room temperature and soften following implantation into the body. Durability was measured by the duration the devices produced effective stimulation and by accelerated aging in vitro. Stability was measured by the threshold to provoke an electromyogram (EMG) muscle response and by measuring impedance using electrochemical impedance spectroscopy (EIS). In addition, spinal cord modulation of motor cortex potentials was measured. The spinal column and implanted arrays were imaged with MRI ex vivo, and histology for astrogliosis and immune reaction was performed.
For durability, the design of the arrays was modified over three generations to create an array that demonstrated activity up to 29 weeks. SCS arrays showed no significant degradation over a simulated 29 week period of accelerated aging. For stability, the threshold for provoking an EMG rose in the first few weeks and then remained stable out to 16 weeks; the impedance showed a similar rise early with stability thereafter. Spinal cord stimulation strongly enhanced motor cortex potentials throughout. Upon explantation, device performance returned to pre-implant levels, indicating that biotic rather than abiotic processes were the cause of changing metrics. MRI and histology showed that softening SCS produced less tissue deformation than Parylene-C arrays. There was no significant astrogliosis or immune reaction to either type of array.
Softening SCS arrays meet the needs for research-grade devices in rats and could be developed into human devices in the future.
我们旨在开发一种用于大鼠的耐用、稳定且不会干扰脊髓的脊髓刺激器。
我们创建了一个由基于形状记忆聚合物 (SMP) 的柔性电子产品制成的软化脊髓刺激 (SCS) 阵列。我们开发了一种新的光刻工艺,将高表面积氮化钛 (TiN) 电极图案化到金 (Au) 互连上。硫醇-烯丙烯酸酯聚合物在室温下坚硬,在植入体内后会软化。耐用性通过设备产生有效刺激的持续时间和体外加速老化来衡量。稳定性通过引发肌电图 (EMG) 肌肉反应的阈值以及使用电化学阻抗谱 (EIS) 测量阻抗来衡量。此外,还测量了脊髓对运动皮层电位的调制。在体外用 MRI 对脊柱和植入的阵列进行成像,并进行星形胶质细胞增生和免疫反应的组织学检查。
对于耐用性,通过三代的阵列设计修改,创建了一个可以证明活动长达 29 周的阵列。在模拟的 29 周加速老化期间,SCS 阵列没有显示出明显的降解。对于稳定性,引发 EMG 的阈值在最初几周内上升,然后在 16 周内保持稳定;阻抗在此早期也显示出类似的上升,此后保持稳定。脊髓刺激强烈增强了整个运动皮层的电位。在取出时,设备性能恢复到植入前的水平,这表明变化的指标是由生物因素而不是非生物因素引起的。MRI 和组织学显示,与 Parylene-C 阵列相比,软化 SCS 产生的组织变形更小。两种类型的阵列都没有明显的星形胶质细胞增生或免疫反应。
软化 SCS 阵列满足了大鼠研究级设备的需求,将来可能会开发出用于人类的设备。