Seo Hee Won, Cha Seongkwang, Jeong Yurim, Ahn Jungryul, Lee Kyeong Jae, Kim Sohee, Goo Yong Sook
Department of Robotics and Mechatronics Engineering, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, Republic of Korea.
Department of Physiology, Chungbuk National University School of Medicine, Cheongju, Republic of Korea.
Biomed Eng Lett. 2023 Dec 26;14(2):355-365. doi: 10.1007/s13534-023-00342-3. eCollection 2024 Mar.
Subretinal prostheses have been developed to stimulate survived retinal ganglion cells (RGCs), indirectly following the physiological visual pathways. However, current spreading from the prosthesis electrode causes the activation of unintended RGCs, thereby limiting the spatial resolution of artificial vision. This study proposes a strategy for focal stimulation of RGCs using a subretinal electrode array, in which six hexagonally arranged peripheral electrodes surround a stimulating electrode. RGCs in an in-vitro condition were subretinally stimulated using a fabricated electrode array coated with iridium oxide, following the three different stimulation configurations (with no peripheral, six electrodes of opposite current, and six ground). In-vitro experiments showed that the stimulation with six electrodes of opposite current was most effective in controlling RGC responses with a high spatial resolution. The results suggest that the effective utilization of return electrodes, such as by applying an opposite current to them, could help reduce current spreading beyond the local area targeted for stimulation and elicit RGC responses only in the vicinity of the stimulating electrode.
The online version contains supplementary material available at 10.1007/s13534-023-00342-3.
视网膜下假体已被开发出来,用于刺激存活的视网膜神经节细胞(RGCs),间接遵循生理视觉通路。然而,目前来自假体电极的电流扩散会导致非预期的RGCs激活,从而限制了人工视觉的空间分辨率。本研究提出了一种使用视网膜下电极阵列对RGCs进行局部刺激的策略,其中六个六边形排列的周边电极围绕着一个刺激电极。使用涂有氧化铱的预制电极阵列,按照三种不同的刺激配置(无周边电极、六个反向电流电极和六个接地电极),在体外条件下对RGCs进行视网膜下刺激。体外实验表明,六个反向电流电极的刺激在以高空间分辨率控制RGC反应方面最有效。结果表明,有效利用返回电极,例如通过向它们施加反向电流,有助于减少电流扩散到目标刺激局部区域之外,并仅在刺激电极附近引发RGC反应。
在线版本包含可在10.1007/s13534-023-00342-3获取的补充材料。