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Electrospun nanofibrous scaffolds for controlled release of adeno-associated viral vectors

Authors
Lee, SlgirimKim, Jung-SukChu, Hun SuKim, Go-WoonWon, Jong-InJang, Jae-Hyung
Issue Date
Nov-2011
Publisher
ELSEVIER SCI LTD
Keywords
Elastin-like polypeptide; Polycaprolactone; Adeno-associated virus; Gene delivery; Tissue engineering
Citation
ACTA BIOMATERIALIA, v.7, no.11, pp.3868 - 3876
Journal Title
ACTA BIOMATERIALIA
Volume
7
Number
11
Start Page
3868
End Page
3876
URI
https://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/19795
DOI
10.1016/j.actbio.2011.06.035
ISSN
1742-7061
Abstract
The integration of viral gene delivery with key features of biomaterial scaffolds that modulate viral delivery in a controlled manner offers a promising strategy for numerous tissue engineering applications. In this study adeno-associated virus (AAV), which is widely utilized in human gene therapy as a gene carrier due to its safety and efficient gene delivery capability, was encapsulated within electrospun nanofibrous scaffolds composed of blended mixtures of elastin-like polypeptides (ELP) and poly (epsilon-caprolactone) (PCL) and was employed to transduce fibroblasts adherent on the scaffolds. Combinatorial interactions between ELP and PCL chains upon physical blending significantly altered the mechanical properties (i.e. wettability, elastic modulus, strain, etc.) of the ELP/PCL composites, thus providing key tools to mediate controlled release of AAV vectors and robust cellular transduction on the fibrous scaffolds. The ability of ELP/PCL composites to manipulate the controlled release of AAV-mediated gene delivery for subsequent high-efficiency cellular transduction will provide tremendous opportunities for a variety of tissue engineering applications. (C) 2011 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
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