Thermoresponsive hyperbranched copolymer with multi acrylate functionality for in situ cross-linkable hyaluronic acid composite semi-IPN hydrogel

Dong, Yixiao, Hassan, Waqar, Zheng, Yu, Saeed, Aram Omer, Cao, Hongliang, Tai, Hongyun, Pandit, Abhay and Wang, Wenxin (2012) Thermoresponsive hyperbranched copolymer with multi acrylate functionality for in situ cross-linkable hyaluronic acid composite semi-IPN hydrogel. Journal of Materials Science-Materials in Medicine, 23 (1). pp. 25-35. ISSN 0957-4530

Full text not available from this repository. (Request a copy)

Abstract

Thermoresponsive polymers have been widely used for in situ formed hydrogels in drug delivery and tissue engineering as they are easy to handle and their shape can easily conform to tissue defects. However, non-covalent bonding and mechanical weakness of these hydrogels limit their applications. In this study, a physically and chemically in situ cross-linkable hydrogel system was developed from a novel thermoresponsive hyperbranched PEG based copolymer with multi acrylate functionality, which was synthesized via an ‘one pot and one step’ in situ deactivation enhanced atom transfer radical co-polymerization of poly(ethylene glycol) diacrylate (PEGDA, Mn = 258 g mol-1), poly(ethylene glycol) methyl ether methacrylate (PEGMEMA, Mn = 475 g mol-1) and (2-methoxyethoxy) ethyl methacrylate (MEO2MA). This hyperbranched copolymer was tailored to have the lower critical solution temperature to form physical gelation around 37°C. Meanwhile, with high level of acrylate functionalities, a chemically cross-linked gel was formed from this copolymer using thiol functional cross-linker of pentaerythritol tetrakis (3-mercaptopropionate) (QT) via thiol-ene Michael addition reaction. Furthermore, a semi-interpenetrated polymer networks (semi-IPN) structure was developed by combining this polymer with hyaluronic acid (HA), leading to an in situ cross-linkable hydrogel with significantly increased porosity, enhanced swelling behavior and improved cell adhesion and viability both in 2D and 3D cell culture models.

Item Type: Article
Faculty \ School: Faculty of Science > School of Pharmacy
Depositing User: Pure Connector
Date Deposited: 23 Oct 2013 11:58
Last Modified: 17 Mar 2020 18:45
URI: https://ueaeprints.uea.ac.uk/id/eprint/43814
DOI: 10.1007/s10856-011-4496-z

Actions (login required)

View Item View Item