Zhi-Yi Huang, Glemarie C Hermosa, Jyun-Sain Wu, Tung-Lin Wu, Chih-Ching Chien, Chien-Shiun Liao, Yu-Tzu Huang, Hui-Min David Wang, An-Cheng Aidan Sun
{"title":"Chitosan-Based Antibacterial Bioceramic Materials for Dental Pulp Capping.","authors":"Zhi-Yi Huang, Glemarie C Hermosa, Jyun-Sain Wu, Tung-Lin Wu, Chih-Ching Chien, Chien-Shiun Liao, Yu-Tzu Huang, Hui-Min David Wang, An-Cheng Aidan Sun","doi":"10.1021/acsbiomaterials.5c00466","DOIUrl":null,"url":null,"abstract":"<p><p>Conventional clinical approaches for regenerative endodontic procedures, root canal therapy, and vital pulp therapy often lack sufficient antimicrobial efficacy, thereby increasing the risk of post-treatment apical periodontitis. To overcome this limitation, a series of antimicrobial powders (referred to as the AC<sub><i>S</i></sub> series) was synthesized through a chemical reaction between tricalcium silicate (C<sub>3</sub>S) powder and chitosan solution pretreated with acetic acid. Following this, the AC<sub><i>S</i></sub> powders were subsequently physically blended with additional C<sub>3</sub>S to enhance the mechanical properties, thereby developing a chitosan-based bioceramic composite, named the AC<sub><i>S</i></sub>-C series. The antibacterial properties of the AC<sub><i>S</i></sub>-C materials were systematically evaluated using minimum inhibitory concentration (MIC) assays, inhibition zone tests, and antibacterial assessments against <i>Escherichia coli</i> and <i>Streptococcus mutans</i> as well as biofilm testing with <i>Porphyromonas gingivalis</i>. In addition, biocompatibility was assessed through cytotoxicity tests using L929 fibroblast cells. The results revealed that the AC<sub>20</sub>-C formulation exhibited good antibacterial efficacy (exceeding 90%), maintained over 80% cell viability, exhibited a clear inhibition zone, and effectively inhibited biofilm formation. Regarding physical properties, the AC<sub><i>S</i></sub>-C materials were able to set within 30 min and possessed sufficient compressive strength. Further structural analysis using energy-dispersive X-ray spectroscopy, X-ray diffraction, and Fourier transform infrared spectroscopy verified the successful synthesis and structural integrity of the material. The AC<sub><i>S</i></sub>-C samples exhibited key functional groups, including amino, amide, Si-O, CaO, and PO<sub>4</sub><sup>3-</sup>. In this study, the AC<sub><i>S</i></sub>-C series represent promising antimicrobial bioceramic pulp-capping materials that combine effective antibacterial activity with favorable biocompatibility.</p>","PeriodicalId":8,"journal":{"name":"ACS Biomaterials Science & Engineering","volume":" ","pages":""},"PeriodicalIF":5.5000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Biomaterials Science & Engineering","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1021/acsbiomaterials.5c00466","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
Abstract
Conventional clinical approaches for regenerative endodontic procedures, root canal therapy, and vital pulp therapy often lack sufficient antimicrobial efficacy, thereby increasing the risk of post-treatment apical periodontitis. To overcome this limitation, a series of antimicrobial powders (referred to as the ACS series) was synthesized through a chemical reaction between tricalcium silicate (C3S) powder and chitosan solution pretreated with acetic acid. Following this, the ACS powders were subsequently physically blended with additional C3S to enhance the mechanical properties, thereby developing a chitosan-based bioceramic composite, named the ACS-C series. The antibacterial properties of the ACS-C materials were systematically evaluated using minimum inhibitory concentration (MIC) assays, inhibition zone tests, and antibacterial assessments against Escherichia coli and Streptococcus mutans as well as biofilm testing with Porphyromonas gingivalis. In addition, biocompatibility was assessed through cytotoxicity tests using L929 fibroblast cells. The results revealed that the AC20-C formulation exhibited good antibacterial efficacy (exceeding 90%), maintained over 80% cell viability, exhibited a clear inhibition zone, and effectively inhibited biofilm formation. Regarding physical properties, the ACS-C materials were able to set within 30 min and possessed sufficient compressive strength. Further structural analysis using energy-dispersive X-ray spectroscopy, X-ray diffraction, and Fourier transform infrared spectroscopy verified the successful synthesis and structural integrity of the material. The ACS-C samples exhibited key functional groups, including amino, amide, Si-O, CaO, and PO43-. In this study, the ACS-C series represent promising antimicrobial bioceramic pulp-capping materials that combine effective antibacterial activity with favorable biocompatibility.
期刊介绍:
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