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Honeycomb-shaped electro-neural interface enables cellular-scale pixels in subretinal prosthesis
High-resolution visual prostheses require small, densely packed pixels, but limited penetration depth of the electric field formed by a planar electrode array constrains such miniaturization. We present a novel honeycomb configuration of an electrode array with vertically separated active and return...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6650428/ https://www.ncbi.nlm.nih.gov/pubmed/31337815 http://dx.doi.org/10.1038/s41598-019-47082-y |
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author | Flores, Thomas Huang, Tiffany Bhuckory, Mohajeet Ho, Elton Chen, Zhijie Dalal, Roopa Galambos, Ludwig Kamins, Theodore Mathieson, Keith Palanker, Daniel |
author_facet | Flores, Thomas Huang, Tiffany Bhuckory, Mohajeet Ho, Elton Chen, Zhijie Dalal, Roopa Galambos, Ludwig Kamins, Theodore Mathieson, Keith Palanker, Daniel |
author_sort | Flores, Thomas |
collection | PubMed |
description | High-resolution visual prostheses require small, densely packed pixels, but limited penetration depth of the electric field formed by a planar electrode array constrains such miniaturization. We present a novel honeycomb configuration of an electrode array with vertically separated active and return electrodes designed to leverage migration of retinal cells into voids in the subretinal space. Insulating walls surrounding each pixel decouple the field penetration depth from the pixel width by aligning the electric field vertically, enabling a decrease of the pixel size down to cellular dimensions. We demonstrate that inner retinal cells migrate into the 25 μm deep honeycomb wells as narrow as 18 μm, resulting in more than half of these cells residing within the electrode cavities. Immune response to honeycombs is comparable to that with planar arrays. Modeled stimulation threshold current density with honeycombs does not increase substantially with reduced pixel size, unlike quadratic increase with planar arrays. This 3-D electrode configuration may enable functional restoration of central vision with acuity better than 20/100 for millions of patients suffering from age-related macular degeneration. |
format | Online Article Text |
id | pubmed-6650428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66504282019-07-29 Honeycomb-shaped electro-neural interface enables cellular-scale pixels in subretinal prosthesis Flores, Thomas Huang, Tiffany Bhuckory, Mohajeet Ho, Elton Chen, Zhijie Dalal, Roopa Galambos, Ludwig Kamins, Theodore Mathieson, Keith Palanker, Daniel Sci Rep Article High-resolution visual prostheses require small, densely packed pixels, but limited penetration depth of the electric field formed by a planar electrode array constrains such miniaturization. We present a novel honeycomb configuration of an electrode array with vertically separated active and return electrodes designed to leverage migration of retinal cells into voids in the subretinal space. Insulating walls surrounding each pixel decouple the field penetration depth from the pixel width by aligning the electric field vertically, enabling a decrease of the pixel size down to cellular dimensions. We demonstrate that inner retinal cells migrate into the 25 μm deep honeycomb wells as narrow as 18 μm, resulting in more than half of these cells residing within the electrode cavities. Immune response to honeycombs is comparable to that with planar arrays. Modeled stimulation threshold current density with honeycombs does not increase substantially with reduced pixel size, unlike quadratic increase with planar arrays. This 3-D electrode configuration may enable functional restoration of central vision with acuity better than 20/100 for millions of patients suffering from age-related macular degeneration. Nature Publishing Group UK 2019-07-23 /pmc/articles/PMC6650428/ /pubmed/31337815 http://dx.doi.org/10.1038/s41598-019-47082-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Flores, Thomas Huang, Tiffany Bhuckory, Mohajeet Ho, Elton Chen, Zhijie Dalal, Roopa Galambos, Ludwig Kamins, Theodore Mathieson, Keith Palanker, Daniel Honeycomb-shaped electro-neural interface enables cellular-scale pixels in subretinal prosthesis |
title | Honeycomb-shaped electro-neural interface enables cellular-scale pixels in subretinal prosthesis |
title_full | Honeycomb-shaped electro-neural interface enables cellular-scale pixels in subretinal prosthesis |
title_fullStr | Honeycomb-shaped electro-neural interface enables cellular-scale pixels in subretinal prosthesis |
title_full_unstemmed | Honeycomb-shaped electro-neural interface enables cellular-scale pixels in subretinal prosthesis |
title_short | Honeycomb-shaped electro-neural interface enables cellular-scale pixels in subretinal prosthesis |
title_sort | honeycomb-shaped electro-neural interface enables cellular-scale pixels in subretinal prosthesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6650428/ https://www.ncbi.nlm.nih.gov/pubmed/31337815 http://dx.doi.org/10.1038/s41598-019-47082-y |
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