Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/107149
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dc.contributor.authorPaulo, Siri-
dc.contributor.authorLaranjo, Mafalda-
dc.contributor.authorAbrantes, Ana M.-
dc.contributor.authorCasalta-Lopes, João-
dc.contributor.authorSantos, Kathleen-
dc.contributor.authorGonçalves, Ana C.-
dc.contributor.authorPaula, Anabela Baptista-
dc.contributor.authorMarto, Carlos Miguel-
dc.contributor.authorRibeiro, Ana Bela Sarmento-
dc.contributor.authorCarrilho, Eunice-
dc.contributor.authorSerra, Arménio C.-
dc.contributor.authorBotelho, Maria F.-
dc.contributor.authorFerreira, Manuel M.-
dc.date.accessioned2023-06-12T08:57:28Z-
dc.date.available2023-06-12T08:57:28Z-
dc.date.issued2019-06-06-
dc.identifier.issn1996-1944-
dc.identifier.urihttps://hdl.handle.net/10316/107149-
dc.description.abstract(1) Background: Bisphosphonate-related osteonecrosis of the jaw (BRONJ) is one of the most often seen side effects in patients treated with nitrogen-containing bisphosphonates (BPs), a post-surgical non-healing wound condition. Since calcium phosphate (CP) compounds are able to adsorb zoledronate (ZOL) when used as a drug delivery vehicle, we aimed to verify if these ceramics might have a potential protective effect for soft tissues surrounding surgical osseous wounds. (2) Methods: The chemical reaction between ZOL and CP compounds was evaluated through ultraviolet-visible spectroscopy and elemental analysis. A primary culture of human gingival fibroblasts (HGF) was established as a model to evaluate the cytotoxicity of the association of ZOL (5-500 μM) and of ZOL/biphasic calcium phosphates (BCP). Metabolic activity, cell viability, types of cell death, the cell cycle through, and the migration ability of human gingival fibroblasts were evaluated. (3) Results: ZOL was adsorbed by biphasic calcium phosphate compounds in an aqueous solution. The HGF were sensitive to ZOL toxicity; nevertheless, ZOL/BCP showed a significant protective effect regarding metabolic activity, cell viability, and cell migration. (4) Conclusions: BCP interaction with ZOL reduces or abolishes its toxicity in HGF. This finding represents a potential solution for BRONJ in the case of patients undergoing therapy with ZOL.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationFCT, COMPETE-FEDER (Strategic Project PEst-C/SAU/UI3282/2013 and UID/NEU/04539/2013)pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectbiomaterialspt
dc.subjectbiomineralizationpt
dc.subjectbisphosphonate-related osteonecrosis of the jawpt
dc.subjectcellular biologypt
dc.subjectgingival fibroblastspt
dc.subjectosteonecrosispt
dc.subjectzoledronatept
dc.titleSynthetic Calcium Phosphate Ceramics as a Potential Treatment for Bisphosphonate-Related Osteonecrosis of the Jawpt
dc.typearticlept
degois.publication.firstPage1840pt
degois.publication.issue11pt
degois.publication.titleMaterialspt
dc.peerreviewedyespt
dc.identifier.doi10.3390/ma12111840-
degois.publication.volume12pt
dc.date.embargo2019-06-06*
dc.identifier.pmid31174333-
uc.date.periodoEmbargo0pt
item.fulltextCom Texto completo-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
item.grantfulltextopen-
item.cerifentitytypePublications-
crisitem.author.researchunitCIBIT - Coimbra Institute for Biomedical Imaging and Translational Research-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCEMMPRE - Centre for Mechanical Engineering, Materials and Processes-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0003-0689-6007-
crisitem.author.orcid0000-0003-4185-7871-
crisitem.author.orcid0000-0001-7795-795X-
crisitem.author.orcid0000-0001-9269-5417-
crisitem.author.orcid0000-0002-4142-4841-
crisitem.author.orcid0000-0002-5759-5557-
crisitem.author.orcid0000-0001-8664-2757-
crisitem.author.orcid0000-0001-7202-1650-
crisitem.author.orcid0000-0002-5968-6161-
Appears in Collections:I&D IBILI - Artigos em Revistas Internacionais
FMUC Medicina - Artigos em Revistas Internacionais
I&D ICBR - Artigos em Revistas Internacionais
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