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Anti-inflammatory polymer electrodes for glial scar treatment: bringing the conceptual idea to future results
Conducting polymer films offer a convenient route for the functionalization of implantable microelectrodes without compromising their performance as excellent recording units. A micron thick coating, deposited on the surface of a regular metallic electrode, can elute anti-inflammatory drugs for the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026681/ https://www.ncbi.nlm.nih.gov/pubmed/24860493 http://dx.doi.org/10.3389/fneng.2014.00009 |
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author | Asplund, Maria Boehler, Christian Stieglitz, Thomas |
author_facet | Asplund, Maria Boehler, Christian Stieglitz, Thomas |
author_sort | Asplund, Maria |
collection | PubMed |
description | Conducting polymer films offer a convenient route for the functionalization of implantable microelectrodes without compromising their performance as excellent recording units. A micron thick coating, deposited on the surface of a regular metallic electrode, can elute anti-inflammatory drugs for the treatment of glial scarring as well as growth factors for the support of surrounding neurons. Electro-activation of the polymer drives the release of the substance and should ideally provide a reliable method for controlling quantity and timing of release. Driving signals in the form of a constant potential (CP), a slow redox sweep or a fast pulse are all represented in literature. Few studies present such release in vivo from actual recording and stimulating microelectronic devices. It is essential to bridge the gap between studies based on release in vitro, and the intended application, which would mean release into living and highly delicate tissue. In the biological setting, signals are limited both by available electronics and by the biological safety. Driving signals must not be harmful to tissue and also not activate the tissue in an uncontrolled manner. This review aims at shedding more light on how to select appropriate driving parameters for the polymer electrodes for the in vivo setting. It brings together information regarding activation thresholds for neurons, as well as injury thresholds, and puts this into context with what is known about efficient driving of release from conducting polymer films. |
format | Online Article Text |
id | pubmed-4026681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-40266812014-05-23 Anti-inflammatory polymer electrodes for glial scar treatment: bringing the conceptual idea to future results Asplund, Maria Boehler, Christian Stieglitz, Thomas Front Neuroeng Neuroscience Conducting polymer films offer a convenient route for the functionalization of implantable microelectrodes without compromising their performance as excellent recording units. A micron thick coating, deposited on the surface of a regular metallic electrode, can elute anti-inflammatory drugs for the treatment of glial scarring as well as growth factors for the support of surrounding neurons. Electro-activation of the polymer drives the release of the substance and should ideally provide a reliable method for controlling quantity and timing of release. Driving signals in the form of a constant potential (CP), a slow redox sweep or a fast pulse are all represented in literature. Few studies present such release in vivo from actual recording and stimulating microelectronic devices. It is essential to bridge the gap between studies based on release in vitro, and the intended application, which would mean release into living and highly delicate tissue. In the biological setting, signals are limited both by available electronics and by the biological safety. Driving signals must not be harmful to tissue and also not activate the tissue in an uncontrolled manner. This review aims at shedding more light on how to select appropriate driving parameters for the polymer electrodes for the in vivo setting. It brings together information regarding activation thresholds for neurons, as well as injury thresholds, and puts this into context with what is known about efficient driving of release from conducting polymer films. Frontiers Media S.A. 2014-05-13 /pmc/articles/PMC4026681/ /pubmed/24860493 http://dx.doi.org/10.3389/fneng.2014.00009 Text en Copyright © 2014 Asplund, Boehler and Stieglitz. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Asplund, Maria Boehler, Christian Stieglitz, Thomas Anti-inflammatory polymer electrodes for glial scar treatment: bringing the conceptual idea to future results |
title | Anti-inflammatory polymer electrodes for glial scar treatment: bringing the conceptual idea to future results |
title_full | Anti-inflammatory polymer electrodes for glial scar treatment: bringing the conceptual idea to future results |
title_fullStr | Anti-inflammatory polymer electrodes for glial scar treatment: bringing the conceptual idea to future results |
title_full_unstemmed | Anti-inflammatory polymer electrodes for glial scar treatment: bringing the conceptual idea to future results |
title_short | Anti-inflammatory polymer electrodes for glial scar treatment: bringing the conceptual idea to future results |
title_sort | anti-inflammatory polymer electrodes for glial scar treatment: bringing the conceptual idea to future results |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026681/ https://www.ncbi.nlm.nih.gov/pubmed/24860493 http://dx.doi.org/10.3389/fneng.2014.00009 |
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