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Bifunctional naringenin-laden gelatin methacryloyl scaffolds with osteogenic and anti-inflammatory properties

dc.contributor.authorCardoso, Lais M.
dc.contributor.authorde Carvalho, Ana Beatriz G. [UNESP]
dc.contributor.authorAnselmi, Caroline [UNESP]
dc.contributor.authorMahmoud, Abdel H.
dc.contributor.authorDal-Fabbro, Renan
dc.contributor.authorBasso, Fernanda G. [UNESP]
dc.contributor.authorBottino, Marco C.
dc.contributor.institutionUniversity of Michigan–School of Dentistry
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionStony Brook University–School of Dental Medicine
dc.contributor.institutionUniversity of Michigan
dc.date.accessioned2025-04-29T18:42:33Z
dc.date.issued2024-09-01
dc.description.abstractObjective: To fabricate and characterize an innovative gelatin methacryloyl/GelMA electrospun scaffold containing the citrus flavonoid naringenin/NA with osteogenic and anti-inflammatory properties. Methods: GelMA scaffolds (15 % w/v) containing 0/Control, 5, 10, or 20 % of NA w/w were obtained via electrospinning. The chemical composition, fiber morphology/diameter, swelling/degradation profile, and NA release were investigated. Cytotoxicity, cell proliferation, adhesion and spreading, total protein/TP production, alkaline phosphatase/ALP activity, osteogenic genes expression (OCN, OPN, RUNX2), and mineralized nodules deposition/MND with human alveolar bone-derived mesenchymal stem cells (aBMSCs) seeded on the scaffolds were assessed. Moreover, aBMSCs seeded on the scaffolds and stimulated with tumor necrosis factor-alpha/TNF-α were submitted to collagen, nitric oxide/NO, interleukin/IL-1α, and IL-6 production assessment. Data were analyzed using ANOVA and t-student/post-hoc tests (α = 5 %). Results: NA-laden scaffolds presented increased fiber diameter, lower swelling capacity, and faster degradation profile over 28 days (p < 0.05). NA release was detected over time. Cell adhesion and spreading, and TP production were similar between GelMA and GelMA+NA5 % scaffolds, while cell proliferation, ALP activity, OCN/OPN/RUNX2 gene expression, and MND were higher for GelMA+NA5 % scaffolds (p < 0.05). Cells seeded on control scaffolds and TNF-α-stimulated presented higher levels of NO, IL-1α/IL-6, and lower levels of collagen (p < 0.05). In contrast, cells seeded on GelMA+NA5 % scaffolds showed downregulation of inflammatory markers and higher collagen synthesis (p < 0.05). Significance: GelMA+NA5 % scaffold was cytocompatible, stimulated aBMSCs proliferation and differentiation, and downregulated inflammatory mediators’ synthesis, suggesting its therapeutic effect as a multi-target bifunctional scaffold with osteogenic and anti-inflammatory properties for bone tissue engineering.en
dc.description.affiliationDepartment of Cariology Restorative Sciences and Endodontics University of Michigan–School of Dentistry, 1011 N. University Avenue
dc.description.affiliationDepartment of Dental Materials and Prosthodontics São Paulo State University (UNESP)–São Jose dos Campos School of Dentistry, Eng. Francisco Jose Longo 777, SP
dc.description.affiliationDepartment of Morphology and Pediatric Dentistry São Paulo State University (UNESP)–Araraquara School of Dentistry, Humaitá 1680, SP
dc.description.affiliationDepartment of Oral Biology and Pathology Stony Brook University–School of Dental Medicine, 100 Nicolls Road
dc.description.affiliationDepartment of Phisiology and Pathology São Paulo State University (UNESP) Araraquara School of Dentistry, SP
dc.description.affiliationDepartment of Biomedical Engineering College of Engineering University of Michigan
dc.description.affiliationUnespDepartment of Dental Materials and Prosthodontics São Paulo State University (UNESP)–São Jose dos Campos School of Dentistry, Eng. Francisco Jose Longo 777, SP
dc.description.affiliationUnespDepartment of Morphology and Pediatric Dentistry São Paulo State University (UNESP)–Araraquara School of Dentistry, Humaitá 1680, SP
dc.description.affiliationUnespDepartment of Phisiology and Pathology São Paulo State University (UNESP) Araraquara School of Dentistry, SP
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipNational Institutes of Health
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdFAPESP: #2019/16886-4
dc.description.sponsorshipIdFAPESP: #2022/03788-7
dc.description.sponsorshipIdCNPq: 303574/2022-4
dc.format.extent1353-1363
dc.identifierhttp://dx.doi.org/10.1016/j.dental.2024.06.019
dc.identifier.citationDental Materials, v. 40, n. 9, p. 1353-1363, 2024.
dc.identifier.doi10.1016/j.dental.2024.06.019
dc.identifier.issn0109-5641
dc.identifier.scopus2-s2.0-85196028382
dc.identifier.urihttps://hdl.handle.net/11449/299493
dc.language.isoeng
dc.relation.ispartofDental Materials
dc.sourceScopus
dc.subjectBone
dc.subjectElectrospinning
dc.subjectFlavonoids
dc.subjectGelatin methacryloyl
dc.subjectInflammation
dc.subjectRegeneration
dc.titleBifunctional naringenin-laden gelatin methacryloyl scaffolds with osteogenic and anti-inflammatory propertiesen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationca4c0298-cd82-48ee-a9c8-c97704bac2b0
relation.isOrgUnitOfPublication.latestForDiscoveryca4c0298-cd82-48ee-a9c8-c97704bac2b0
unesp.author.orcid0000-0002-3189-1542 0000-0002-3189-1542[3]
unesp.author.orcid0000-0002-4125-8441[5]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Ciência e Tecnologia, São José dos Campospt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt

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