Back to Journals » International Journal of Nanomedicine » Volume 7

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

Authors Zhang Y, Zhang W, Johnston, Newman, Pyykko I, Zou JZ

Received 12 November 2011

Accepted for publication 6 December 2011

Published 23 February 2012 Volume 2012:7 Pages 1015—1022

DOI https://doi.org/10.2147/IJN.S28185

Review by Single-blind

Peer reviewer comments 3


Ya Zhang1, Weikai Zhang1*, Alexander H Johnston2*, Tracey A Newman3, Ilmari Pyykkö1, Jing Zou1

1Department of Otolaryngology, University of Tampere, Medical School, Tampere, Finland; 2Centre for Biological Sciences, 3Clinical Neurosciences, University of Southampton, Southampton, UK

*These authors are co-contributors

Abstract: 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.

Keywords: nanoparticles, peptide, round window membrane, nerve fibers, spiral ganglion cell, drug delivery

Creative Commons License This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License. By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms.

Download Article [PDF]  View Full Text [HTML][Machine readable]