Epoxy-amine synthesised hydrogel scaffolds for soft-tissue engineering
| dc.contributor.author | Hamid, Z.A.A. | |
| dc.contributor.author | Blencowe, A. | |
| dc.contributor.author | Ozcelik, B. | |
| dc.contributor.author | Palmer, J.A. | |
| dc.contributor.author | Stevens, G.W. | |
| dc.contributor.author | Abberton, K.M. | |
| dc.contributor.author | Morrison, W.A. | |
| dc.contributor.author | Penington, A.J. | |
| dc.contributor.author | Qiao, G.G. | |
| dc.date.issued | 2010 | |
| dc.description | Data source: Supplementary data, https://doi.org/10.1016/j.biomaterials.2010.05.008 | |
| dc.description.abstract | Highly porous and biodegradable hydrogels based on poly(ethylene glycol) (PEG) and cystamine (Cys) were fabricated using epoxy-amine chemistry and investigated as scaffolds for soft-tissue engineering. Whereas the application of fused-salt templates provided a comprehensive interconnecting pore morphology, the incorporation of a specially designed poly(epsilon-caprolactone) (PCL) cross-linker provided enhanced mechanical function without adversely effecting the scaffolds positive biological interactions. The addition of only 1.2 wt% of the PCL cross-linker was sufficient to provide improvements in the ultimate stress of 30-40%. In vitro studies not only confirmed the non-cytotoxic nature of the scaffolds, but also their degradation products, which were isolated and characterised by nuclear magnetic resonance (NMR) and matrix-assisted laser desorption/ionisation time-of-flight mass spectroscopy (MALDI ToF MS). In vivo trials were conducted over a period of 8 weeks through implantation of the scaffolds into the dorsal region of rats. At both 2 and 8 week time points the explants revealed complete infiltration by the surrounding tissue and the development of a vascular network to support the newly generated tissue, without an excessive foreign-body response. | |
| dc.identifier.citation | Biomaterials, 2010; 31(25):6454-6467 | |
| dc.identifier.doi | 10.1016/j.biomaterials.2010.05.008 | |
| dc.identifier.issn | 0142-9612 | |
| dc.identifier.issn | 1878-5905 | |
| dc.identifier.orcid | Blencowe, A. [0000-0002-7630-4874] | |
| dc.identifier.uri | https://hdl.handle.net/1959.8/153064 | |
| dc.language.iso | en | |
| dc.publisher | ELSEVIER SCI LTD | |
| dc.relation.funding | ARC LE0882576 | |
| dc.relation.grant | http://purl.org/au-research/grants/arc/LE0882576 | |
| dc.rights | Copyright 2010 Elsevier | |
| dc.source.uri | https://doi.org/10.1016/j.biomaterials.2010.05.008 | |
| dc.subject | 3T3 Cells | |
| dc.subject | Animals | |
| dc.subject | Mice | |
| dc.subject | Rats | |
| dc.subject | Rats, Sprague-Dawley | |
| dc.subject | Polyethylene Glycols | |
| dc.subject | Amines | |
| dc.subject | Cystamine | |
| dc.subject | Epoxy Compounds | |
| dc.subject | Biocompatible Materials | |
| dc.subject | Hydrogels | |
| dc.subject | Tissue Engineering | |
| dc.subject | Materials Testing | |
| dc.subject | Absorbable Implants | |
| dc.subject | Cell Survival | |
| dc.subject | Porosity | |
| dc.subject | Male | |
| dc.subject | Tissue Scaffolds | |
| dc.title | Epoxy-amine synthesised hydrogel scaffolds for soft-tissue engineering | |
| dc.type | Journal article | |
| pubs.publication-status | Published | |
| ror.mmsid | 9915910472001831 |