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Impact of degradable nanowires on long-term brain tissue responses
BACKGROUND: A promising approach to improve the performance of neural implants consists of adding nanomaterials, such as nanowires, to the surface of the implant. Nanostructured interfaces could improve the integration and communication stability, partly through the reduction of the cell-to-electrod...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979107/ https://www.ncbi.nlm.nih.gov/pubmed/27507159 http://dx.doi.org/10.1186/s12951-016-0216-7 |
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author | Gällentoft, Lina Pettersson, Lina M. E. Danielsen, Nils Schouenborg, Jens Prinz, Christelle N. Linsmeier, Cecilia Eriksson |
author_facet | Gällentoft, Lina Pettersson, Lina M. E. Danielsen, Nils Schouenborg, Jens Prinz, Christelle N. Linsmeier, Cecilia Eriksson |
author_sort | Gällentoft, Lina |
collection | PubMed |
description | BACKGROUND: A promising approach to improve the performance of neural implants consists of adding nanomaterials, such as nanowires, to the surface of the implant. Nanostructured interfaces could improve the integration and communication stability, partly through the reduction of the cell-to-electrode distance. However, the safety issues of implanted nanowires in the brain need to be evaluated and understood before nanowires can be used on the surface of implants for long periods of time. To this end we here investigate whether implanted degradable nanowires offer any advantage over non-degradable nanowires in a long-term in vivo study (1 year) with respect to brain tissue responses. RESULTS: The tissue response after injection of degradable silicon oxide (SiOx)-coated gallium phosphide nanowires and biostable hafnium oxide-coated GaP nanowires into the rat striatum was compared. One year after nanowire injection, no significant difference in microglial or astrocytic response, as measured by staining for ED1 and glial fibrillary acidic protein, respectively, or in neuronal density, as measured by staining for NeuN, was found between degradable and biostable nanowires. Of the cells investigated, only microglia cells had engulfed the nanowires. The SiOx-coated nanowire residues were primarily seen in aggregated hypertrophic ED1-positive cells, possibly microglial cells that have fused to create multinucleated giant cells. Occasionally, degradable nanowires with an apparently intact shape were found inside single, small ED1-positive cells. The biostable nanowires were found intact in microglia cells of both phenotypes described. CONCLUSION: The present study shows that the degradable nanowires remain at least partly in the brain over long time periods, i.e. 1 year; however, no obvious bio-safety issues for this degradable nanomaterial could be detected. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12951-016-0216-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4979107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49791072016-08-11 Impact of degradable nanowires on long-term brain tissue responses Gällentoft, Lina Pettersson, Lina M. E. Danielsen, Nils Schouenborg, Jens Prinz, Christelle N. Linsmeier, Cecilia Eriksson J Nanobiotechnology Research BACKGROUND: A promising approach to improve the performance of neural implants consists of adding nanomaterials, such as nanowires, to the surface of the implant. Nanostructured interfaces could improve the integration and communication stability, partly through the reduction of the cell-to-electrode distance. However, the safety issues of implanted nanowires in the brain need to be evaluated and understood before nanowires can be used on the surface of implants for long periods of time. To this end we here investigate whether implanted degradable nanowires offer any advantage over non-degradable nanowires in a long-term in vivo study (1 year) with respect to brain tissue responses. RESULTS: The tissue response after injection of degradable silicon oxide (SiOx)-coated gallium phosphide nanowires and biostable hafnium oxide-coated GaP nanowires into the rat striatum was compared. One year after nanowire injection, no significant difference in microglial or astrocytic response, as measured by staining for ED1 and glial fibrillary acidic protein, respectively, or in neuronal density, as measured by staining for NeuN, was found between degradable and biostable nanowires. Of the cells investigated, only microglia cells had engulfed the nanowires. The SiOx-coated nanowire residues were primarily seen in aggregated hypertrophic ED1-positive cells, possibly microglial cells that have fused to create multinucleated giant cells. Occasionally, degradable nanowires with an apparently intact shape were found inside single, small ED1-positive cells. The biostable nanowires were found intact in microglia cells of both phenotypes described. CONCLUSION: The present study shows that the degradable nanowires remain at least partly in the brain over long time periods, i.e. 1 year; however, no obvious bio-safety issues for this degradable nanomaterial could be detected. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12951-016-0216-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-09 /pmc/articles/PMC4979107/ /pubmed/27507159 http://dx.doi.org/10.1186/s12951-016-0216-7 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Gällentoft, Lina Pettersson, Lina M. E. Danielsen, Nils Schouenborg, Jens Prinz, Christelle N. Linsmeier, Cecilia Eriksson Impact of degradable nanowires on long-term brain tissue responses |
title | Impact of degradable nanowires on long-term brain tissue responses |
title_full | Impact of degradable nanowires on long-term brain tissue responses |
title_fullStr | Impact of degradable nanowires on long-term brain tissue responses |
title_full_unstemmed | Impact of degradable nanowires on long-term brain tissue responses |
title_short | Impact of degradable nanowires on long-term brain tissue responses |
title_sort | impact of degradable nanowires on long-term brain tissue responses |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979107/ https://www.ncbi.nlm.nih.gov/pubmed/27507159 http://dx.doi.org/10.1186/s12951-016-0216-7 |
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