1. Academic Validation
  2. Enhanced antimicrobial properties of POSS-modified composite resin with chlorhexidine-loaded bioactive glass

Enhanced antimicrobial properties of POSS-modified composite resin with chlorhexidine-loaded bioactive glass

  • J Dent. 2026 Jun:169:106633. doi: 10.1016/j.jdent.2026.106633.
Meng Wei 1 QiQi Hu 1 Qi Xie 2 TianQi Wang 3 WeiLi Xie 4
Affiliations

Affiliations

  • 1 The First Affiliated Hospital Of Harbin Medical University, School of Stomatology, Harbin Medical University, Harbin 150001, China.
  • 2 Department of Stomatology, Harbin Medical University, Harbin 150001, China.
  • 3 The First Affiliated Hospital Of Harbin Medical University, School of Stomatology, Harbin Medical University, Harbin 150001, China. Electronic address: [email protected].
  • 4 The First Affiliated Hospital Of Harbin Medical University, School of Stomatology, Harbin Medical University, Harbin 150001, China. Electronic address: [email protected].
Abstract

Introduction: The aim of this study was to develop a novel Antibacterial dental composite resin by loading chlorhexidine (CHX) onto bioactive glass (BG 45S5) and incorporating it into a resin matrix containing cage-type polyhedral oligomeric silsesquioxane (POSS) nanomonomers.

Methods: CHX was loaded onto the surface of BG 45S5 using a blending method to obtain experimental groups with different CHX concentrations. Experimental composite resins were prepared by incorporating 20 wt% CHX-loaded BG 45S5 and 40 wt% SiO₂ as inorganic Fillers into a matrix containing 4 wt% POSS nanomonomer. Materials characterization were performed using Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM), with analysis of double-bond conversion. Mechanical properties were evaluated using a universal testing machine, and fracture mechanisms were analyzed by SEM. In vitro drug release was assessed to determine chlorhexidine release behavior. Biocompatibility was evaluated using CCK-8 assays, acute oral systemic toxicity tests, and oral mucosal irritation tests. Antimicrobial activity was assessed using Bacterial growth assays, agar plate counting, and the plate diffusion method.

Results: Increasing chlorhexidine concentration resulted in particle agglomeration, reduced double-bond conversion rate, and decreased mechanical strength. Compressive strength of C2 differed significantly from that of C0 (p < 0.05), whereas flexural strength showed no significant difference (p > 0.05). At a chlorhexidine loading concentration of 2 %, the composite resin demonstrated acceptable mechanical properties. In vitro drug release demonstrated an initial rapid release phase followed by a sustained and slower release. Furthermore, CCK-8 assays showed that C2 maintained comparable cell viability to C0 at 24, 48, and 72 h (p > 0.05). In vivo evaluations revealed no significant systemic toxicity or oral mucosal irritation. C2 exhibited significant Antibacterial activity compared with C0 (p < 0.05).

Conclusions: Incorporation of 2 % CHX-loaded bioactive glass 45S5 into a POSS-modified composite resin maintained acceptable mechanical performance and provided sustained drug release, biocompatibility, and significant Antibacterial activity.

Clinical significance: The modified composite resin with a low CHX loading concentration demonstrated Antibacterial activity while maintaining acceptable mechanical performance and biocompatibility, suggesting its potential application as a bioactive restorative material.

Keywords

Antibacterial; Biocompatibility; Chlorhexidine; Dental resin composites; Polyhedral oligomeric silsesquioxane.

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