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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
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.
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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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