Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/145279
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dc.creatorCoelho, CC
dc.creatorPadrão, T
dc.creatorCosta, L
dc.creatorPinto, MT
dc.creatorCosta, PC
dc.creatorDomingues, VF
dc.creatorQuadros, PA
dc.creatorMonteiro, FJ
dc.creatorSousa, SR
dc.date.accessioned2022-11-17T11:33:17Z-
dc.date.available2022-11-17T11:33:17Z-
dc.date.issued2020
dc.identifier.issn2045-2322
dc.identifier.urihttps://hdl.handle.net/10216/145279-
dc.description.abstractBone graft infections are serious complications in orthopaedics and the growing resistance to antibiotics is increasing the need for antibacterial strategies. The use of magnesium oxide (MgO) is an interesting alternative since it possesses broad-spectrum antibacterial activity. Additionally, magnesium ions also play a role in bone regeneration, which makes MgO more appealing than other metal oxides. Therefore, a bone substitute composed of hydroxyapatite and MgO (HAp/MgO) spherical granules was developed using different sintering heat-treatment cycles to optimize its features. Depending on the sintering temperature, HAp/MgO spherical granules exhibited distinct surface topographies, mechanical strength and degradation profiles, that influenced the in vitro antibacterial activity and cytocompatibility. A proper balance between antibacterial activity and cytocompatibility was achieved with HAp/MgO spherical granules sintered at 1100 ºC. The presence of MgO in these granules was able to significantly reduce bacterial proliferation and simultaneously provide a suitable environment for osteoblasts growth. The angiogenic and inflammation potentials were also assessed using the in vivo chicken embryo chorioallantoic membrane (CAM) model and the spherical granules containing MgO stimulated angiogenesis without increasing inflammation. The outcomes of this study evidence a dual effect of MgO for bone regenerative applications making this material a promising antibacterial bone substitute.
dc.description.sponsorshipThis work was financed by the project NoMIC2Bone (NORTE-01-0247-FEDER-017905) and project Biotherapies (NORTE-01-0145-FEDER-000012) supported by Norte Portugal Regional Operational Program (NORTE2020), under the PORTUGAL 2020 Partnership Agreement through the European Regional Development Fund (ERDF). Financial supported was also obtained from FEDER—Fundo Europeu de Desenvolvimento Regional funds through the COMPETE 2020—Operacional Programme for Competitiveness and Internationalization (POCI), PORTUGAL 2020, and by Portuguese funds through FCT/MCTES in the framework of the project “Institute for Research and Innovation in Health Sciences”(POCI-01-0145-FEDER-007274). Fundação para a Ciência e Tecnologia (FCT) is also acknowledged for Catarina Coelho’s PhD grant (SFRH/BDE/108971/2015). This work was also supported by the Applied Molecular Biosciences Unit-UCIBIO, which is financed by national funds from FCT/MCTES (UID/Multi/04378/2019). The authors would also want to acknowledge Rui Rocha from CEMUP for the contribution with SEM analysis and Dra. Rosário Soares from the University of Aveiro for the help with XRD data.
dc.language.isoeng
dc.publisherNature Publishing Group
dc.relationinfo:eu-repo/grantAgreement/FCT/POR_NORTE/SFRH%2FBDE%2F108971%2F2015/PT
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UID%2FMulti%2F04378%2F2019/PT
dc.relation.ispartofScientific Reports, vol.10(1):19098
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.meshAnimals
dc.subject.meshAnti-Bacterial Agents / pharmacology
dc.subject.meshBone Substitutes / pharmacology
dc.subject.meshBone Transplantation / methods
dc.subject.meshCell Line
dc.subject.meshDurapatite / pharmacology
dc.subject.meshMagnesium Oxide / pharmacology
dc.subject.meshMice
dc.subject.meshOsteoblasts / drug effects
dc.titleThe antibacterial and angiogenic effect of magnesium oxide in a hydroxyapatite bone substitute
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.1038/s41598-020-76063-9
dc.relation.publisherversionhttps://www.nature.com/articles/s41598-020-76063-9
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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