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Multifunctional aloe vera-based biomaterial for vital pulp therapy: an in vivo evaluation

dc.contributor.authorNamazi, Sharon S.
dc.contributor.authorOliveira, Pedro Henrique Chaves de [UNESP]
dc.contributor.authorMcDonald, Neville J.
dc.contributor.authorCavalcanti, Bruno
dc.contributor.authorSasaki, Hajime
dc.contributor.authorBottino, Marco C.
dc.contributor.authorDal-Fabbro, Renan
dc.date.accessioned2026-04-07T14:22:12Z
dc.date.issued2025-11-17
dc.description.abstractThis study aimed to evaluate the effects of Gelatin methacryloyl/Aloe vera (GelMA/AV) scaffolds, both alone and in combination with mineral trioxide aggregate (MTA), on pulp inflammatory response and mineralized tissue formation in a rat model of pulp exposure. GelMA/AV nanofibers (70:30) were fabricated via electrospinning and photocrosslinked. Twenty-four rats were randomly assigned to three groups (n = 8/ group): GelMA/AV, GelMA/AV + MTA, and MTA (control). Following pulp exposure of the first upper molars (n = 2/animal), the materials were placed over the exposed pulp as the pulp capping agent, and MTA was applied or not, depending on the group. The cavities were then sealed with glass ionomer. Animals were euthanized at 7 or 28 days post-procedure for histological, immunohistochemical, and micro-computed tomography (micro-CT) analyses. Data were analyzed using one-way or two-way ANOVA at a 5% significance level. Micro-CT analysis at 28 days revealed new hard tissue formation in the pulp chamber across all groups. GelMA/AV + MTA demonstrated comparable mineralized volume and tissue mineral density to MTA. Histologically, the GelMA/AV + MTA group exhibited a significantly lower cell count than the MTA and GelMA/AV groups at 28 days. However, for macrophage polarization, the GelMA/AV + MTA exhibited a similar expression of CD163-positive (M2) and iNOS-positive (M1) cells compared to the MTA. Lastly, GelMA/AV + MTA also showed expression of nestin and DMP1 at 28 days, indicating active mineralization. In conclusion, a thin GelMA/AV sublayer beneath MTA preserves MTA-driven mineralization but does not reduce pulp inflammation or enhance mineralization beyond MTA in this model. Optimization of AV dosing/formulation and longer follow-up are necessary before clinical translation.
dc.description.affiliationDepartment of Cariology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, 1011 N. University Ave, 48109, Ann Arbor, MI, USA
dc.description.affiliationDepartment of Preventive and Restorative Dentistry, School of Dentistry, São Paulo State University, Araçatuba, São Paulo, Brazil
dc.description.affiliationDepartment of Biomedical Engineering, College of Engineering, University of Michigan, Ann Arbor, MI, USA
dc.description.affiliationUnespDepartment of Preventive and Restorative Dentistry, School of Dentistry, São Paulo State University, Araçatuba, São Paulo, Brazil
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1195080637
dc.identifier.dimensionspub.1195080637
dc.identifier.doi10.1007/s10266-025-01258-3
dc.identifier.issn1618-1247
dc.identifier.issn1618-1255
dc.identifier.orcid0000-0002-1593-7926
dc.identifier.orcid0000-0003-3336-2537
dc.identifier.orcid0000-0001-8740-2464
dc.identifier.orcid0000-0002-4125-8441
dc.identifier.orcid0000-0002-0455-4823
dc.identifier.pmcidPMC13011884
dc.identifier.pmid41247659
dc.identifier.urihttps://hdl.handle.net/11449/320804
dc.publisherSpringer Nature
dc.relation.ispartofOdontology; p. 1-10
dc.rights.accessRightsAcesso abertopt
dc.rights.sourceRightsoa_all
dc.rights.sourceRightshybrid
dc.sourceDimensions
dc.titleMultifunctional aloe vera-based biomaterial for vital pulp therapy: an in vivo evaluation
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication8b3335a4-1163-438a-a0e2-921a46e0380d
relation.isOrgUnitOfPublication.latestForDiscovery8b3335a4-1163-438a-a0e2-921a46e0380d
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatubapt

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