File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Design of Multi-Functional Bio-Safe Dental Resin Composites with Mineralization and Anti-Biofilm Properties

TitleDesign of Multi-Functional Bio-Safe Dental Resin Composites with Mineralization and Anti-Biofilm Properties
Authors
Keywordsanti-biofilm activity
bioactive glass
biocompatibility
resin composite
UDMA
Issue Date1-May-2024
PublisherMDPI
Citation
Journal of Functional Biomaterials, 2024, v. 15, n. 5 How to Cite?
Abstract

This study aims to develop multi-functional bio-safe dental resin composites with capabilities for mineralization, high in vitro biocompatibility, and anti-biofilm properties. To address this issue, experimental resin composites consisting of UDMA/TEGDMA-based dental resins and low quantities (1.9, 3.8, and 7.7 vol%) of 45S5 bioactive glass (BAG) particles were developed. To evaluate cellular responses of resin composites, MC3T3-E1 cells were (1) exposed to the original composites extracts, (2) cultured directly on the freshly cured resin composites, or (3) cultured on preconditioned composites that have been soaked in deionized water (DI water), a cell culture medium (MEM), or a simple HEPES-containing artificial remineralization promotion (SHARP) solution for 14 days. Cell adhesion, cell viability, and cell differentiation were, respectively, assessed. In addition, the anti-biofilm properties of BAG-loaded resin composites regarding bacterial viability, biofilm thickness, and biofilm morphology, were assessed for the first time. In vitro biological results demonstrated that cell metabolic activity and ALP expression were significantly diminished when subjected to composite extracts or direct contact with the resin composites containing BAG fillers. However, after the preconditioning treatments in MEM and SHARP solutions, the biomimetic calcium phosphate minerals on 7.7 vol% BAG-loaded composites revealed unimpaired or even better cellular processes, including cell adhesion, cell proliferation, and early cell differentiation. Furthermore, resin composites with 1.9, 3.8, and 7.7 vol% BAG could not only reduce cell viability in S. mutans biofilm on the composite surface but also reduce the biofilm thickness and bacterial aggregations. This phenomenon was more evident in BAG7.7 due to the high ionic osmotic pressure and alkaline microenvironment caused by BAG dissolution. This study concludes that multi-functional bio-safe resin composites with mineralization and anti-biofilm properties can be achieved by adding low quantities of BAG into the resin system, which offers promising abilities to mineralize as well as prevent caries without sacrificing biological activity.


Persistent Identifierhttp://hdl.handle.net/10722/350779

 

DC FieldValueLanguage
dc.contributor.authorYun, Jiaojiao-
dc.contributor.authorBurrow, Michael F.-
dc.contributor.authorMatinlinna, Jukka P.-
dc.contributor.authorDing, Hao-
dc.contributor.authorChan, Sin Man-
dc.contributor.authorTsoi, James K.H.-
dc.contributor.authorWang, Yan-
dc.date.accessioned2024-11-02T00:38:21Z-
dc.date.available2024-11-02T00:38:21Z-
dc.date.issued2024-05-01-
dc.identifier.citationJournal of Functional Biomaterials, 2024, v. 15, n. 5-
dc.identifier.urihttp://hdl.handle.net/10722/350779-
dc.description.abstract<p>This study aims to develop multi-functional bio-safe dental resin composites with capabilities for mineralization, high in vitro biocompatibility, and anti-biofilm properties. To address this issue, experimental resin composites consisting of UDMA/TEGDMA-based dental resins and low quantities (1.9, 3.8, and 7.7 vol%) of 45S5 bioactive glass (BAG) particles were developed. To evaluate cellular responses of resin composites, MC3T3-E1 cells were (1) exposed to the original composites extracts, (2) cultured directly on the freshly cured resin composites, or (3) cultured on preconditioned composites that have been soaked in deionized water (DI water), a cell culture medium (MEM), or a simple HEPES-containing artificial remineralization promotion (SHARP) solution for 14 days. Cell adhesion, cell viability, and cell differentiation were, respectively, assessed. In addition, the anti-biofilm properties of BAG-loaded resin composites regarding bacterial viability, biofilm thickness, and biofilm morphology, were assessed for the first time. In vitro biological results demonstrated that cell metabolic activity and ALP expression were significantly diminished when subjected to composite extracts or direct contact with the resin composites containing BAG fillers. However, after the preconditioning treatments in MEM and SHARP solutions, the biomimetic calcium phosphate minerals on 7.7 vol% BAG-loaded composites revealed unimpaired or even better cellular processes, including cell adhesion, cell proliferation, and early cell differentiation. Furthermore, resin composites with 1.9, 3.8, and 7.7 vol% BAG could not only reduce cell viability in S. mutans biofilm on the composite surface but also reduce the biofilm thickness and bacterial aggregations. This phenomenon was more evident in BAG7.7 due to the high ionic osmotic pressure and alkaline microenvironment caused by BAG dissolution. This study concludes that multi-functional bio-safe resin composites with mineralization and anti-biofilm properties can be achieved by adding low quantities of BAG into the resin system, which offers promising abilities to mineralize as well as prevent caries without sacrificing biological activity.</p>-
dc.languageeng-
dc.publisherMDPI-
dc.relation.ispartofJournal of Functional Biomaterials-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectanti-biofilm activity-
dc.subjectbioactive glass-
dc.subjectbiocompatibility-
dc.subjectresin composite-
dc.subjectUDMA-
dc.titleDesign of Multi-Functional Bio-Safe Dental Resin Composites with Mineralization and Anti-Biofilm Properties -
dc.typeArticle-
dc.identifier.doi10.3390/jfb15050120-
dc.identifier.scopuseid_2-s2.0-85193074799-
dc.identifier.volume15-
dc.identifier.issue5-
dc.identifier.eissn2079-4983-
dc.identifier.issnl2079-4983-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats