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Novel antibacterial and apatite forming restorative composite resin incorporated with hydrated calcium silicate

BACKGROUND: White Portland cement is a calcium silicate material. It exhibits antibacterial properties and is biocompatible. In addition, calcium silicate-based materials are known to release calcium ions and form apatite. The purpose of this study was to develop a novel bioactive restorative resin...

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Autores principales: Yang, Song-Yi, Han, A Ruem, Choi, Ji-Won, Kim, Kwang-Mahn, Kwon, Jae-Sung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10053114/
https://www.ncbi.nlm.nih.gov/pubmed/36978203
http://dx.doi.org/10.1186/s40824-023-00364-z
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author Yang, Song-Yi
Han, A Ruem
Choi, Ji-Won
Kim, Kwang-Mahn
Kwon, Jae-Sung
author_facet Yang, Song-Yi
Han, A Ruem
Choi, Ji-Won
Kim, Kwang-Mahn
Kwon, Jae-Sung
author_sort Yang, Song-Yi
collection PubMed
description BACKGROUND: White Portland cement is a calcium silicate material. It exhibits antibacterial properties and is biocompatible. In addition, calcium silicate-based materials are known to release calcium ions and form apatite. The purpose of this study was to develop a novel bioactive restorative resin composite with antibacterial and apatite forming properties to prevent tooth caries at the interface of teeth and restorative materials, by incorporation of hydrated calcium silicate (hCS) derived from white Portland cement. METHODS: To prepare the experimental composite resins, a 30 wt% light-curable resin matrix and 70 wt% filler, which was mixed with hCS and silanized glass powder were prepared in following concentrations: 0, 17.5, 35.0, and 52.5 wt% hCS filler. The depth of cure, flexural strength, water sorption, solubility, and antibacterial effect were tested. After immersion in artificial saliva solution for 15, 30, 60, and 90 days, ion concentration by ICP-MS and apatite formation using SEM-EDS, Raman spectroscopy and XRD from experimental specimens were analyzed. RESULTS: All experimental groups showed clinically acceptable depths of cure and flexural strength for the use as the restorative composite resin. Water sorption, solubility, released Ca and Si ions increased with the addition of hCS to the experimental composite resin. Experimental groups containing hCS showed greater antibacterial effects compared with the 0 wt% hCS filler group (p < 0.05). The 52.5 wt% hCS filler group produced precipitates mainly composed of Ca and P detected as hydroxyapatite after immersion in artificial saliva solution for 30, 60, and 90 days. CONCLUSIONS: This results show that composite resins containing hCS filler is effective in antibacterial effects. hCS has also apatite formation ability for reducing gap size of microleakage by accumulating hydroxyapatite precipitates at the restoration-tooth interface. Therefore, novel composite resin containing hCS is promising bioactive resin because of its clinically acceptable physiochemical properties, antibacterial properties, and self-sealing potential for prevention of microleakage for longer usage of restorations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40824-023-00364-z.
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spelling pubmed-100531142023-03-30 Novel antibacterial and apatite forming restorative composite resin incorporated with hydrated calcium silicate Yang, Song-Yi Han, A Ruem Choi, Ji-Won Kim, Kwang-Mahn Kwon, Jae-Sung Biomater Res Research Article BACKGROUND: White Portland cement is a calcium silicate material. It exhibits antibacterial properties and is biocompatible. In addition, calcium silicate-based materials are known to release calcium ions and form apatite. The purpose of this study was to develop a novel bioactive restorative resin composite with antibacterial and apatite forming properties to prevent tooth caries at the interface of teeth and restorative materials, by incorporation of hydrated calcium silicate (hCS) derived from white Portland cement. METHODS: To prepare the experimental composite resins, a 30 wt% light-curable resin matrix and 70 wt% filler, which was mixed with hCS and silanized glass powder were prepared in following concentrations: 0, 17.5, 35.0, and 52.5 wt% hCS filler. The depth of cure, flexural strength, water sorption, solubility, and antibacterial effect were tested. After immersion in artificial saliva solution for 15, 30, 60, and 90 days, ion concentration by ICP-MS and apatite formation using SEM-EDS, Raman spectroscopy and XRD from experimental specimens were analyzed. RESULTS: All experimental groups showed clinically acceptable depths of cure and flexural strength for the use as the restorative composite resin. Water sorption, solubility, released Ca and Si ions increased with the addition of hCS to the experimental composite resin. Experimental groups containing hCS showed greater antibacterial effects compared with the 0 wt% hCS filler group (p < 0.05). The 52.5 wt% hCS filler group produced precipitates mainly composed of Ca and P detected as hydroxyapatite after immersion in artificial saliva solution for 30, 60, and 90 days. CONCLUSIONS: This results show that composite resins containing hCS filler is effective in antibacterial effects. hCS has also apatite formation ability for reducing gap size of microleakage by accumulating hydroxyapatite precipitates at the restoration-tooth interface. Therefore, novel composite resin containing hCS is promising bioactive resin because of its clinically acceptable physiochemical properties, antibacterial properties, and self-sealing potential for prevention of microleakage for longer usage of restorations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40824-023-00364-z. BioMed Central 2023-03-29 /pmc/articles/PMC10053114/ /pubmed/36978203 http://dx.doi.org/10.1186/s40824-023-00364-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Yang, Song-Yi
Han, A Ruem
Choi, Ji-Won
Kim, Kwang-Mahn
Kwon, Jae-Sung
Novel antibacterial and apatite forming restorative composite resin incorporated with hydrated calcium silicate
title Novel antibacterial and apatite forming restorative composite resin incorporated with hydrated calcium silicate
title_full Novel antibacterial and apatite forming restorative composite resin incorporated with hydrated calcium silicate
title_fullStr Novel antibacterial and apatite forming restorative composite resin incorporated with hydrated calcium silicate
title_full_unstemmed Novel antibacterial and apatite forming restorative composite resin incorporated with hydrated calcium silicate
title_short Novel antibacterial and apatite forming restorative composite resin incorporated with hydrated calcium silicate
title_sort novel antibacterial and apatite forming restorative composite resin incorporated with hydrated calcium silicate
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10053114/
https://www.ncbi.nlm.nih.gov/pubmed/36978203
http://dx.doi.org/10.1186/s40824-023-00364-z
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