Dental Resin Composites Reinforced by Rough Core-Shell SiO 2 Nanoparticles with a Controllable Mesoporous Structure

A porous structure within filler particles may improve interfacial bonding between the resin matrix and fillers for the preparation of dental resin composites (DRCs). In this study, rough core-shell SiO (rSiO ) nanoparticles with controllable mesoporous structures were synthesized via an oil-water b...

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Veröffentlicht in:ACS applied bio materials 2019-10, Vol.2 (10), p.4233-4241
Hauptverfasser: Wang, Yazi, Hua, Hongfei, Yu, Yejia, Chen, Guoyin, Zhu, Meifang, Zhu, X X
Format: Artikel
Sprache:eng
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Zusammenfassung:A porous structure within filler particles may improve interfacial bonding between the resin matrix and fillers for the preparation of dental resin composites (DRCs). In this study, rough core-shell SiO (rSiO ) nanoparticles with controllable mesoporous structures were synthesized via an oil-water biphase reaction system and characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), and N adsorption-desorption measurements. The influence of the mesoporous shell thickness of rSiO and mass ratio between rSiO and smooth SiO (sSiO ) on the physical and mechanical properties of DRCs was studied. The rSiO with a thin mesoporous shell could form a strong physical interlocking with the resin matrix, which improved the mechanical properties with the exception of flexural modulus. The mechanical properties were further optimized by mixing rSiO and sSiO . The flexural strength and compressive strength of the DRC at a mass ratio of 5:5 increased by 24.3% and 16.8%, respectively, compared with the DRC filled with sSiO alone. There is no statistically significant difference in the flexural modulus between these two DRCs ( > 0.05). The DRCs in this study showed excellent biocompatibility on the human dental pulp cells (HDPCs) as demonstrated by the cytotoxicity tests. The use of rSiO provides a promising approach to develop strong, durable, and biocompatible DRCs.
ISSN:2576-6422
2576-6422
DOI:10.1021/acsabm.9b00508