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Distribution of nanoparticles throughout the cerebral cortex of rodents and non-human primates: Implications for gene and drug therapy
When nanoparticles/proteins are infused into the brain, they are often transported to distal sites in a manner that is dependent both on the characteristics of the infusate and the region targeted. We have previously shown that adeno-associated virus (AAV) is disseminated within the brain by perivas...
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/PMC3956368/ https://www.ncbi.nlm.nih.gov/pubmed/24672434 http://dx.doi.org/10.3389/fnana.2014.00009 |
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author | Salegio, Ernesto A. Streeter, Hillary Dube, Nikhil Hadaczek, Piotr Samaranch, Lluis Kells, Adrian P. San Sebastian, Waldy Zhai, Yuying Bringas, John Xu, Ting Forsayeth, John Bankiewicz, Krystof S. |
author_facet | Salegio, Ernesto A. Streeter, Hillary Dube, Nikhil Hadaczek, Piotr Samaranch, Lluis Kells, Adrian P. San Sebastian, Waldy Zhai, Yuying Bringas, John Xu, Ting Forsayeth, John Bankiewicz, Krystof S. |
author_sort | Salegio, Ernesto A. |
collection | PubMed |
description | When nanoparticles/proteins are infused into the brain, they are often transported to distal sites in a manner that is dependent both on the characteristics of the infusate and the region targeted. We have previously shown that adeno-associated virus (AAV) is disseminated within the brain by perivascular flow and also by axonal transport. Perivascular distribution usually does not depend strongly on the nature of the infusate. Many proteins, neutral liposomes and AAV particles distribute equally well by this route when infused under pressure into various parenchymal locations. In contrast, axonal transport requires receptor-mediated uptake of AAV by neurons and engagement with specific transport mechanisms previously demonstrated for other neurotropic viruses. Cerebrospinal fluid (CSF) represents yet another way in which brain anatomy may be exploited to distribute nanoparticles broadly in the central nervous system. In this study, we assessed the distribution and perivascular transport of nanoparticles of different sizes delivered into the parenchyma of rodents and CSF in non-human primates. |
format | Online Article Text |
id | pubmed-3956368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-39563682014-03-26 Distribution of nanoparticles throughout the cerebral cortex of rodents and non-human primates: Implications for gene and drug therapy Salegio, Ernesto A. Streeter, Hillary Dube, Nikhil Hadaczek, Piotr Samaranch, Lluis Kells, Adrian P. San Sebastian, Waldy Zhai, Yuying Bringas, John Xu, Ting Forsayeth, John Bankiewicz, Krystof S. Front Neuroanat Neuroscience When nanoparticles/proteins are infused into the brain, they are often transported to distal sites in a manner that is dependent both on the characteristics of the infusate and the region targeted. We have previously shown that adeno-associated virus (AAV) is disseminated within the brain by perivascular flow and also by axonal transport. Perivascular distribution usually does not depend strongly on the nature of the infusate. Many proteins, neutral liposomes and AAV particles distribute equally well by this route when infused under pressure into various parenchymal locations. In contrast, axonal transport requires receptor-mediated uptake of AAV by neurons and engagement with specific transport mechanisms previously demonstrated for other neurotropic viruses. Cerebrospinal fluid (CSF) represents yet another way in which brain anatomy may be exploited to distribute nanoparticles broadly in the central nervous system. In this study, we assessed the distribution and perivascular transport of nanoparticles of different sizes delivered into the parenchyma of rodents and CSF in non-human primates. Frontiers Media S.A. 2014-03-17 /pmc/articles/PMC3956368/ /pubmed/24672434 http://dx.doi.org/10.3389/fnana.2014.00009 Text en Copyright © 2014 Salegio, Streeter, Dube, Hadaczek, Samaranch, Kells, San Sebastian, Zhai, Bringas, Xu, Forsayeth and Bankiewicz. 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 Salegio, Ernesto A. Streeter, Hillary Dube, Nikhil Hadaczek, Piotr Samaranch, Lluis Kells, Adrian P. San Sebastian, Waldy Zhai, Yuying Bringas, John Xu, Ting Forsayeth, John Bankiewicz, Krystof S. Distribution of nanoparticles throughout the cerebral cortex of rodents and non-human primates: Implications for gene and drug therapy |
title | Distribution of nanoparticles throughout the cerebral cortex of rodents and non-human primates: Implications for gene and drug therapy |
title_full | Distribution of nanoparticles throughout the cerebral cortex of rodents and non-human primates: Implications for gene and drug therapy |
title_fullStr | Distribution of nanoparticles throughout the cerebral cortex of rodents and non-human primates: Implications for gene and drug therapy |
title_full_unstemmed | Distribution of nanoparticles throughout the cerebral cortex of rodents and non-human primates: Implications for gene and drug therapy |
title_short | Distribution of nanoparticles throughout the cerebral cortex of rodents and non-human primates: Implications for gene and drug therapy |
title_sort | distribution of nanoparticles throughout the cerebral cortex of rodents and non-human primates: implications for gene and drug therapy |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3956368/ https://www.ncbi.nlm.nih.gov/pubmed/24672434 http://dx.doi.org/10.3389/fnana.2014.00009 |
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