Engineered 3D printed poly(ɛ-caprolactone)/graphene scaffolds for bone tissue engineering.

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dc.contributor.author Wang, Weiguang en
dc.contributor.author Junior, José Roberto Passarini en
dc.contributor.author Nalesso, Paulo Roberto Lopes en
dc.contributor.author Musson, David en
dc.contributor.author Cornish, Jillian en
dc.contributor.author Mendonça, Fernanda en
dc.contributor.author Caetano, Guilherme Ferreira en
dc.contributor.author Bártolo, Paulo en
dc.date.accessioned 2019-05-28T21:32:57Z en
dc.date.issued 2019-07 en
dc.identifier.issn 0928-4931 en
dc.identifier.uri http://hdl.handle.net/2292/46825 en
dc.description.abstract Scaffolds are important physical substrates for cell attachment, proliferation and differentiation. Multiple factors could influence the optimal design of scaffolds for a specific tissue, such as the geometry, the materials used to modulate cell proliferation and differentiation, its biodegradability and biocompatibility. The optimal design of a scaffold for a specific tissue strongly depends on both materials and manufacturing processes. Previous studies of human adipose-derived stem cells (hADSCs) seeded on poly(ε-caprolactone) (PCL)/graphene scaffolds have proved that the addition of small concentrations of graphene to PCL scaffolds improves cell proliferation. Based on such results, this paper further investigates, for the first time, both in vitro and in vivo characteristics of 3D printed PCL/graphene scaffolds. Scaffolds were evaluated from morphological, biological and short term immune response points of view. Results show that the produced scaffolds induce an acceptable level of immune response, suggesting high potential for in vivo applications. Finally, the scaffolds were used to treat a rat calvaria critical size defect with and without applying micro electrical stimulation (10 μA). Quantification of connective and new bone tissue formation and the levels of ALP, RANK, RANKL, OPG were considered. Results show that the use of scaffolds containing graphene and electrical stimulation seems to increase cell migration and cell influx, leading to new tissue formation, well-organized tissue deposition and bone remodelling. en
dc.format.medium Print-Electronic en
dc.language eng en
dc.relation.ispartofseries Materials science & engineering. C, Materials for biological applications en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.subject Bone and Bones en
dc.subject Skull en
dc.subject Cell Line en
dc.subject Animals en
dc.subject Humans en
dc.subject Mice en
dc.subject Rats, Wistar en
dc.subject Graphite en
dc.subject Alkaline Phosphatase en
dc.subject Tissue Engineering en
dc.subject Cell Proliferation en
dc.subject Cell Survival en
dc.subject Adsorption en
dc.subject Male en
dc.subject RANK Ligand en
dc.subject Receptor Activator of Nuclear Factor-kappa B en
dc.subject Osteoprotegerin en
dc.subject Tissue Scaffolds en
dc.subject Printing, Three-Dimensional en
dc.title Engineered 3D printed poly(ɛ-caprolactone)/graphene scaffolds for bone tissue engineering. en
dc.type Journal Article en
dc.identifier.doi 10.1016/j.msec.2019.03.047 en
pubs.begin-page 759 en
pubs.volume 100 en
dc.rights.holder Copyright: The author en
pubs.end-page 770 en
pubs.publication-status Published en
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Journal Article en
pubs.elements-id 766871 en
pubs.org-id Medical and Health Sciences en
pubs.org-id School of Medicine en
pubs.org-id Medicine Department en
pubs.org-id Science en
pubs.org-id Science Research en
pubs.org-id Maurice Wilkins Centre (2010-2014) en
dc.identifier.eissn 1873-0191 en
pubs.record-created-at-source-date 2019-04-06 en
pubs.dimensions-id 30948113 en


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