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Antimicrobial Silk Fibroin Methacrylated Scaffolds for Regenerative Endodontics

dc.contributor.authorNarayanam, Ramyasaketha
dc.contributor.authorCardoso, Lais M. [UNESP]
dc.contributor.authordos Reis-Prado, Alexandre H.
dc.contributor.authorde Carvalho, Ana Beatriz G. [UNESP]
dc.contributor.authorAnselmi, Caroline [UNESP]
dc.contributor.authorMahmoud, Abdel H.
dc.contributor.authorFenno, J. Christopher
dc.contributor.authorDal-Fabbro, Renan
dc.contributor.authorBottino, Marco C.
dc.contributor.institutionUniversity of Michigan–School of Dentistry
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade Federal de Minas Gerais (UFMG)
dc.contributor.institutionStony Brook University–School of Dental Medicine
dc.contributor.institutionUniversity of Michigan
dc.date.accessioned2025-04-29T18:07:45Z
dc.date.issued2024-12-01
dc.description.abstractIntroduction: Recognizing the necessity of novel disinfection strategies for improved bacterial control to ultimately favor tissue regeneration, this study developed and characterized antibiotics-laden silk fibroin methacrylated (SilkMA) scaffolds for regenerative endodontics. Methods: SilkMA-based solutions (10% w/v) containing Clindamycin (CLI) or Tinidazole (TIN) (0 – control; 5, 10, or 15% w/w) or the combination of both drugs (BiMix CLI/TIN 10%) were electrospun and photocrosslinked. Morphology and composition were assessed using scanning electron microscopy and Fourier-transform infrared spectroscopy. Additionally, swelling and degradation profiles were also determined. Cytotoxicity was evaluated in stem cells from apical papilla. Antibacterial efficacy was tested using direct and indirect contact assays against Aggregatibacter actinomycetemcomitans/Aa, Actinomyces naeslundii/An, Enterococcus faecalis/Ef, and Fusobacterium nucleatum/Fn. E. faecalis biofilm inhibition on dentin discs was specifically evaluated for BiMix-laden scaffolds. Data were statistically analyzed with a significance level of 5%. Results: Scanning electron microscopy revealed that all scaffolds had similar characteristics, including fiber morphology and bead absence. Fourier-transform infrared spectroscopy showed the incorporation of CLI and TIN into the fibers and in BiMix scaffolds. Antibiotic-laden scaffolds exhibited lower swelling capacity than the control and were degraded entirely after 45 days. Scaffolds laden with CLI, TIN, or BiMix throughout all time points did not reduce stem cells from apical papilla's viability. CLI-laden scaffolds inhibited the growth of Aa, An, and Ef, while TIN-laden scaffolds inhibited Fn growth. BiMix-laden scaffolds significantly inhibited Aa, An, Ef, and Fn in direct contact, and their aliquots inhibited An and Fn through indirect contact, with additional biofilm inhibition against Ef. Conclusions: BiMix-laden SilkMA scaffolds are cytocompatible and exhibit antimicrobial effects against endodontic pathogens, indicating their therapeutic potential as a drug delivery system for regenerative endodontics.en
dc.description.affiliationDepartment of Cariology Restorative Sciences and Endodontics University of Michigan–School of Dentistry
dc.description.affiliationDepartment of Dental Materials and Prosthodontics São Paulo State University (UNESP)–Araraquara School of Dentistry, São Paulo
dc.description.affiliationDepartment of Restorative Dentistry Minas Gerais Federal University (UFMG)–School of Dentistry, Minas Gerais
dc.description.affiliationDepartment of Dental Materials and Prosthodontics São Paulo State University (UNESP)–Sao Jose dos Campos School of Dentistry, São Paulo
dc.description.affiliationDepartment of Morphology and Pediatric Dentistry São Paulo State University (UNESP)–Araraquara School of Dentistry, São Paulo
dc.description.affiliationDepartment of Oral Biology and Pathology Stony Brook University–School of Dental Medicine
dc.description.affiliationDepartment of Biologic and Materials Sciences & Prosthodontics University of Michigan–School of Dentistry
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)–Araraquara School of Dentistry, São Paulo
dc.description.affiliationUnespDepartment of Dental Materials and Prosthodontics São Paulo State University (UNESP)–Sao Jose dos Campos School of Dentistry, São Paulo
dc.description.affiliationUnespDepartment of Morphology and Pediatric Dentistry São Paulo State University (UNESP)–Araraquara School of Dentistry, São Paulo
dc.format.extent1752-1760.e2
dc.identifierhttp://dx.doi.org/10.1016/j.joen.2024.08.004
dc.identifier.citationJournal of Endodontics, v. 50, n. 12, p. 1752-1760.e2, 2024.
dc.identifier.doi10.1016/j.joen.2024.08.004
dc.identifier.issn0099-2399
dc.identifier.scopus2-s2.0-85203415349
dc.identifier.urihttps://hdl.handle.net/11449/297799
dc.language.isoeng
dc.relation.ispartofJournal of Endodontics
dc.sourceScopus
dc.subjectClindamycin
dc.subjectregenerative endodontics
dc.subjectsilk
dc.subjecttinidazole
dc.subjecttissue engineering
dc.titleAntimicrobial Silk Fibroin Methacrylated Scaffolds for Regenerative Endodonticsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationca4c0298-cd82-48ee-a9c8-c97704bac2b0
relation.isOrgUnitOfPublication.latestForDiscoveryca4c0298-cd82-48ee-a9c8-c97704bac2b0
unesp.author.orcid0000-0002-4125-8441[8]
unesp.author.orcid0000-0001-8740-2464 0000-0001-8740-2464[9]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Ciência e Tecnologia, São José dos Campospt

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