Development of antimicrobial peptide-loaded hydrogels as potential scaffolds for pulp-dentine complex regeneration: a comparative study

dc.commentsCEB58219por
dc.contributor.authorNoohi, Parisapor
dc.contributor.authorAbdekhodaie, Mohammad J.por
dc.contributor.authorNekoofar, Mohammad H.por
dc.contributor.authorGama, F. M.por
dc.contributor.authorSaadatmand, Maryampor
dc.contributor.authorDummer, Paul M. H.por
dc.date.accessioned2025-06-05T15:19:27Z
dc.date.embargo10000-01-01
dc.date.issued2025
dc.date.updated2025-05-26T11:21:49Z
dc.description.abstractIntroduction: As a recently developed treatment modality, regeneration of the pulp-dentin-like complex via tissue engineering approaches is the focus of considerable attention. The persistence of bacteria within the root canal spaces is well known as the major challenge of dental pulp regeneration. Antimicrobial peptides (AMPs) are short peptides with inhibitory activities against a broad spectrum of microorganisms. Methods: In the present study, antimicrobial hydrogels based on 2 photo-reactive biopolymers, that is collagen methacrylate and chitosan methacrylate, and containing 2 different AMPs, that is LLKKK18 and Tet213, were used to develop a potential scaffold with antimicrobial and regenerative features. Results: The incorporation of AMPs had no significant effect on the physical, mechanical, rheological, and morphological properties of the new systems. The optimized concentration of LLKKK18 and Tet213 had appropriate antimicrobial activity against Gram-positive Enterococcus fæcalis and did not exhibit any cytotoxicity to stem cells from the apical papilla encapsulated within the hydrogels compared to the control group without AMPs. The presence of AMPs also significantly promoted migration and differentiation of stem cells from the apical papilla. In the AMP-loaded groups, greater levels of calcified nodules deposition, alkaline phosphatase, collagen type I, dentin sialophosphoprotein, dentin matrix protein 1, and vascular endothelial growth factor A mRNA gene expression, and collagen type I and dentin sialophosphoprotein protein expression were observed. Conclusions: The results indicated the potential of engineered antimicrobial collagen methacrylate/chitosan methacrylate hydrogels for application in tissue engineering-based strategies to regenerate the pulp-dentin complex.por
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersion
dc.description.sponsorshipThe authors wish to thank Prof. Saeed Balalaie and Dr Farhad Golmohammadi for synthesizing and providing the antimicrobial peptides used in the present study, and Dr Naghmeh Meraji for her valuable comments and suggestions. This work has been supported financially by the National Institute for Medical Research Development (NIMAD) under grant number 972809. The authors deny any conflicts of interest related to this study.por
dc.distributioninternationalpor
dc.identifier.citationNoohi, P., Abdekhodaie, M. J., Nekoofar, M. H., Gama, M., Saadatmand, M., & Dummer, P. M. H. (2025, May). Development of Antimicrobial Peptide-loaded Hydrogels as Potential Scaffolds for Pulp-dentine Complex Regeneration: A Comparative Study. Journal of Endodontics. Elsevier BV. http://doi.org/10.1016/j.joen.2025.01.018por
dc.identifier.doi10.1016/j.joen.2025.01.018por
dc.identifier.issn0099-2399por
dc.identifier.pmid39914769por
dc.identifier.urihttps://hdl.handle.net/1822/96039
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherWolters Kluwer Healthpor
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0099239925000548por
dc.rightsrestrictedAccesspor
dc.subjectAntimicrobial peptidespor
dc.subjectchitosan methacrylatepor
dc.subjectcollagen methacrylatepor
dc.subjectphoto-crosslinkingpor
dc.subjectregenerative endodonticspor
dc.titleDevelopment of antimicrobial peptide-loaded hydrogels as potential scaffolds for pulp-dentine complex regeneration: a comparative studypor
dc.typearticle
dspace.entity.typePublicationen
oaire.citationConferencePlaceUnited States
oaire.citationEndPage593por
oaire.citationIssue5por
oaire.citationStartPage585por
oaire.citationVolume51por
oaire.versionVoRpor
sdum.journalJournal of Endodonticspor

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