gms | German Medical Science

Artificial Vision 2019

The International Symposium on Visual Prosthetics

13.12. - 14.12.2019, Aachen

Transparent 3D microelectrodes with high resolution for sub-retinal stimulation

Meeting Abstract

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  • Sohee Kim - Department of Robotics Engineering, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu/ROK
  • H. W. Seo - Department of Robotics Engineering, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu/ROK
  • N. Kim - Department of Robotics Engineering, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu/ROK

Artificial Vision 2019. Aachen, 13.-14.12.2019. Düsseldorf: German Medical Science GMS Publishing House; 2019. Doc19artvis12

doi: 10.3205/19artvis12, urn:nbn:de:0183-19artvis123

Veröffentlicht: 10. Dezember 2019

© 2019 Kim et al.
Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung). Lizenz-Angaben siehe http://creativecommons.org/licenses/by/4.0/.


Gliederung

Text

Objective: Various microelectrodes included in retinal prosthetic devices have been developed to replace damaged retinal cells. To stimulate remaining retinal cells more effectively, we present 3D microelectrode arrays for a subretinal device.

Methods: The 3D microelectrodes were fabricated using micro-electro-mechanical system technologies. Polydimethylsiloxane (PDMS) was used as a substrate of electrodes to realize the flexible and transparent electrode array. To obtain a 3D electrode shape with high resolution, dry and wet etching processes were performed such as deep reactive ion etching and HNA etching in addition to dicing.

Results: The microelectrodes consisting of 16 pixels to 64 pixels were fabricated, supported by 150 μm-thick PDMS. The fabricated 3D microelectrodes were further assembled with an integrated circuit (IC) to stimulate retinal cells.

Discussion: Transparent 3D microelectrode arrays have been developed and 16-pixel microelectrodes have been tested to demonstrate the stimulation capacity in in-vitro subretinal setup. To evaluate the stimulation performance and biocompatibility, more experiments in in-vitro and in-vivo environments will be performed as a further study.

Acknowledgement: This work was supported by the Bio & Medical Technology Development Program of the National Research Foundation funded by the Korean government (No. NRF-2017M3A9E2056463).