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Targeted delivery of Tet1 peptide functionalized polymersomes to the rat cochlear nerve

Polymersomes are nanosized vesicles formed from amphiphilic block copolymers, and have been identified as potential drug delivery vehicles to the inner ear. The aim of this study was to provide targeting to specific cells within the inner ear by functionalizing the polymersome surface with Tet1 pept...

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Detalles Bibliográficos
Autores principales: Zhang, Ya, Zhang, Weikai, Johnston, Alexander H, Newman, Tracey A, Pyykkö, Ilmari, Zou, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292415/
https://www.ncbi.nlm.nih.gov/pubmed/22403485
http://dx.doi.org/10.2147/IJN.S28185
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author Zhang, Ya
Zhang, Weikai
Johnston, Alexander H
Newman, Tracey A
Pyykkö, Ilmari
Zou, Jing
author_facet Zhang, Ya
Zhang, Weikai
Johnston, Alexander H
Newman, Tracey A
Pyykkö, Ilmari
Zou, Jing
author_sort Zhang, Ya
collection PubMed
description Polymersomes are nanosized vesicles formed from amphiphilic block copolymers, and have been identified as potential drug delivery vehicles to the inner ear. The aim of this study was to provide targeting to specific cells within the inner ear by functionalizing the polymersome surface with Tet1 peptide sequence. Tet1 peptide specifically binds to the trisialoganglioside clostridial toxin receptor on neurons and was expected to target the polymersomes toward the cochlear nerve. The Tet1 functionalized PEG-b-PCL polymersomes were administered using routine drug delivery routes: transtympanic injection and cochleostomy. Delivery via cochleostomy of Tet1 functionalized polymersomes resulted in cochlear nerve targeting; in contrast this was not seen after transtympanic injection.
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spelling pubmed-32924152012-03-08 Targeted delivery of Tet1 peptide functionalized polymersomes to the rat cochlear nerve Zhang, Ya Zhang, Weikai Johnston, Alexander H Newman, Tracey A Pyykkö, Ilmari Zou, Jing Int J Nanomedicine Original Research Polymersomes are nanosized vesicles formed from amphiphilic block copolymers, and have been identified as potential drug delivery vehicles to the inner ear. The aim of this study was to provide targeting to specific cells within the inner ear by functionalizing the polymersome surface with Tet1 peptide sequence. Tet1 peptide specifically binds to the trisialoganglioside clostridial toxin receptor on neurons and was expected to target the polymersomes toward the cochlear nerve. The Tet1 functionalized PEG-b-PCL polymersomes were administered using routine drug delivery routes: transtympanic injection and cochleostomy. Delivery via cochleostomy of Tet1 functionalized polymersomes resulted in cochlear nerve targeting; in contrast this was not seen after transtympanic injection. Dove Medical Press 2012 2012-02-23 /pmc/articles/PMC3292415/ /pubmed/22403485 http://dx.doi.org/10.2147/IJN.S28185 Text en © 2012 Zhang et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Zhang, Ya
Zhang, Weikai
Johnston, Alexander H
Newman, Tracey A
Pyykkö, Ilmari
Zou, Jing
Targeted delivery of Tet1 peptide functionalized polymersomes to the rat cochlear nerve
title Targeted delivery of Tet1 peptide functionalized polymersomes to the rat cochlear nerve
title_full Targeted delivery of Tet1 peptide functionalized polymersomes to the rat cochlear nerve
title_fullStr Targeted delivery of Tet1 peptide functionalized polymersomes to the rat cochlear nerve
title_full_unstemmed Targeted delivery of Tet1 peptide functionalized polymersomes to the rat cochlear nerve
title_short Targeted delivery of Tet1 peptide functionalized polymersomes to the rat cochlear nerve
title_sort targeted delivery of tet1 peptide functionalized polymersomes to the rat cochlear nerve
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292415/
https://www.ncbi.nlm.nih.gov/pubmed/22403485
http://dx.doi.org/10.2147/IJN.S28185
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