PHYSICOCHEMICAL AND BIOLOGICAL PROPERTIES OF REMINERALIZING, POLYMERIC ACP COMPOSITES.
PHYSICOCHEMICAL AND BIOLOGICAL PROPERTIES OF REMINERALIZING, POLYMERIC ACP COMPOSITES.
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发表时间:
2011
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通讯作者:
JM Antonucci;D. Škrtić
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作者:
JM Antonucci;D. Škrtić
Because of their potential to regenerate mineral lost to tooth decay and their biocompatibility, amorphous calcium phosphate (ACP) polymeric composites have recently attracted attention as a new generation of bioactive dental materials in preventive dentistry, orthodontics and endodontics. Embedded in polymerized methacrylate matrices and exposed to saliva-like, aqueous milieu, ACP fillers convert spontaneously into thermodynamically stable apatite, and during this conversion, release in a sustained manner, sufficient levels of remineralizing Ca and PO4 ions to stimulate mineral recovery [1–3]. For over a decade, research in our group has been focused on structure/composition/property relationships for an appreciation of the interactions between various types of bioactive ACP fillers, their polymeric resin phases and simulated oral environments. Specifically, we strived to improve the dispersion of ACP filler throughout the polymer matrix and control critical physicochemical properties of the composites via fine-tuning of the resin phases. So far, the biological apects of ACP composites were much less explored. One of the physicochemical parameters, the degree of vinyl conversion (DVC) attained upon polymerization, was conveniently used as an indirect predictor of materials’ tendency to leach residual monomers and their potentially harmful effects on cells. In this study, both physicochemical and biological properties of potentially remineralizing ACP composites based on two visible light curable methacrylate resin formulations were evaluated for dental application as orthodontic adhesives and endodontic root canal sealers. Both types of biomimetic ACP composites were expected to attain high DVC without the excessive polymerization shrinkage (PS) and/or polymerization shrinkage stress (PSS) while maintaining desirable remineralizing potential and mechanical stability. To test this hypothesis, the experimental orthodontic and endodontic copolymers and their ACP composites were assessed for DVC, PS and PSS, water sorption, hygroscopic expansion, mechanical strength and ion release. In vitro cytotoxicity of both formulations was evaluated by examining the morphology and viability of osteoblast-like cells exposed to materials’ extracts and compared to the relevant commercial controls. Additionally, leachability of the endodontic ACP copolymers and composites was quantitatively assessed by 1H nuclear magnetic resonance (1H NMR) spectroscopy. It was assumed that, due to the high DVCs attained in the experimental endodontic formulations, the leachability, and in turn, their cytotoxicity will not exceed the cytotoxicity of the commercial control.