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dc.contributor.authorWang, Y.
dc.contributor.authorMiao, Y.
dc.contributor.authorZhang, J.
dc.contributor.authorWu, J.
dc.contributor.authorKirk, Brett
dc.contributor.authorXu, J.
dc.contributor.authorMa, D.
dc.contributor.authorXue, W.
dc.date.accessioned2018-04-30T02:40:35Z
dc.date.available2018-04-30T02:40:35Z
dc.date.created2018-04-16T07:41:31Z
dc.date.issued2017
dc.identifier.citationWang, Y. and Miao, Y. and Zhang, J. and Wu, J. and Kirk, B. and Xu, J. and Ma, D. et al. 2017. Three-dimensional printing of shape memory hydrogels with internal structure for drug delivery. Materials Science and Engineering C. 84: pp. 44-51.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/66437
dc.identifier.doi10.1016/j.msec.2017.11.025
dc.description.abstract

© 2017 Elsevier B.V. Hydrogels with shape memory behavior and internal structure have wide applications in fields ranging from tissue engineering and medical instruments to drug delivery; however, creating the hydrogels has proven to be extremely challenging. This study presents a three-dimensional (3D) printing technology to fabricate the shape memory hydrogels with internal structure (SMHs) by combining sodium alginate (alginate) and pluronic F127 diacrylate macromer (F127DA). SMHs were constituted by a dual network structure. One is a stable network which is formed by F127DA photo-crosslinking; the other one is a reversible network which is formed by Ca 2 + cross-linked alginate. SMHs recovery ratio was 98.15% in 10 min after Ca 2 + was removed in the Na 2 CO 3 solution, and the elastic modulus remains essentially stable after the shape memory cycle. It showed that the drug releasing rate is more rapid compared with traditional drug-loaded hydrogels in in vitro experiments. The viability of 3T3 fibroblasts remained intact which revealed its excellent biocompatibility. Therefore, SMHs have a huge prospect for application in drug carriers and tissue engineering scaffold.

dc.publisherElsevier
dc.titleThree-dimensional printing of shape memory hydrogels with internal structure for drug delivery
dc.typeJournal Article
dcterms.source.volume84
dcterms.source.startPage44
dcterms.source.endPage51
dcterms.source.issn0928-4931
dcterms.source.titleMaterials Science and Engineering C
curtin.departmentSchool of Civil and Mechanical Engineering (CME)
curtin.accessStatusFulltext not available


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