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dc.date.accessioned2020-09-08T17:53:17Z
dc.date.available2020-09-08T17:53:17Z
dc.date.created2020-08-24T08:40:51Z
dc.date.issued2020
dc.identifier.citationVyas, Cian Zhang, Jun Øvrebø, Øystein Huang, Boyang Roberts, Iwan Setty, Mohan Allardyce, Benjamin J Haugen, Håvard Jostein Rajkhowa, Rangam Bàrtolo, Paulo Jorge da Silva . 3D printing of silk microparticle reinforced polycaprolactone scaffolds for tissue engineering applications. Materials Science and Engineering C: Materials for Biological Applications. 2020
dc.identifier.urihttp://hdl.handle.net/10852/79228
dc.description.abstractPolycaprolactone (PCL) scaffolds have been widely investigated for tissue engineering applications, however, they exhibit poor cell adhesion and mechanical properties. Subsequently, PCL composites have been produced to improve the material properties. This study utilises a natural material, Bombyx mori silk microparticles (SMP) prepared by milling silk fibre, to produce a composite to enhance the scaffolds properties. Silk is biocompatible and biodegradable with excellent mechanical properties. However, there are no studies using SMPs as a reinforcing agent in a 3D printed thermoplastic polymer scaffold. PCL/SMP (10, 20, 30 wt%) composites were prepared by melt blending. Rheological analysis showed that SMP loading increased the shear thinning and storage modulus of the material. Scaffolds were fabricated using a screw-assisted extrusion-based additive manufacturing system. Scanning electron microscopy and X-ray microtomography was used to determine scaffold morphology. The scaffolds had high interconnectivity with regular printed fibres and pore morphologies within the designed parameters. Compressive mechanical testing showed that the addition of SMP significantly improved the compressive Young's modulus of the scaffolds. The scaffolds were more hydrophobic with the inclusion of SMP which was linked to a decrease in total protein adsorption. Cell behaviour was assessed using human adipose derived mesenchymal stem cells. A cytotoxic effect was observed at higher particle loading (30 wt%) after 7 days of culture. By day 21, 10 wt% loading showed significantly higher cell metabolic activity and proliferation, high cell viability, and cell migration throughout the scaffold. Calcium mineral deposition was observed on the scaffolds during cell culture. Large calcium mineral deposits were observed at 30 wt% and smaller calcium deposits were observed at 10 wt%. This study demonstrates that SMPs incorporated into a PCL scaffold provided effective mechanical reinforcement, improved the rate of degradation, and increased cell proliferation, demonstrating potential suitability for bone tissue engineering applications.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.title3D printing of silk microparticle reinforced polycaprolactone scaffolds for tissue engineering applications
dc.typeJournal article
dc.creator.authorVyas, Cian
dc.creator.authorZhang, Jun
dc.creator.authorØvrebø, Øystein
dc.creator.authorHuang, Boyang
dc.creator.authorRoberts, Iwan
dc.creator.authorSetty, Mohan
dc.creator.authorAllardyce, Benjamin J
dc.creator.authorHaugen, Håvard Jostein
dc.creator.authorRajkhowa, Rangam
dc.creator.authorBàrtolo, Paulo Jorge da Silva
cristin.unitcode185,16,17,62
cristin.unitnameBiomaterialer
cristin.ispublishedtrue
cristin.fulltextpreprint
cristin.qualitycode1
dc.identifier.cristin1824688
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Materials Science and Engineering C: Materials for Biological Applications&rft.volume=&rft.spage=&rft.date=2020
dc.identifier.jtitleMaterials Science and Engineering C: Materials for Biological Applications
dc.identifier.doihttps://doi.org/10.1016/j.msec.2020.111433
dc.identifier.urnURN:NBN:no-82336
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn0928-4931
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/79228/4/1-s2.0-S0928493120333518-main.pdf
dc.type.versionPublishedVersion
cristin.articleid111433
dc.relation.projectEU/EP/L014904/1


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