Cytotoxic and Genotoxic Effects of Composite Resins on Cultured Human Gingival Fibroblasts

被引:19
作者
De Angelis, Francesco [1 ]
Mandatori, Domitilla [1 ,2 ]
Schiavone, Valeria [1 ,2 ]
Melito, Francesco Paolo [1 ,2 ]
Valentinuzzi, Silvia [2 ,3 ]
Vadini, Mirco [1 ]
Di Tomo, Pamela [1 ,2 ]
Vanini, Lorenzo [1 ]
Pelusi, Letizia [1 ,2 ]
Pipino, Caterina [1 ,2 ]
Del Boccio, Piero [2 ,3 ]
D'Arcangelo, Camillo [1 ]
Pandolfi, Assunta [1 ,2 ]
机构
[1] Univ G dAnnunzio, Dept Med Oral & Biotechnol Sci, I-66100 Chieti, Italy
[2] Univ G dAnnunzio, Ctr Adv Studies & Technol CAST Ex CeSI MeT, I-66100 Chieti, Italy
[3] Univ G dAnnunzio, Dept Pharm, I-66100 Chieti, Italy
关键词
dental resins; composite resins; Bis-GMA; TEGDMA; gingival fibroblast; cytotoxicity; biocompatibility; DOUBLE-STRAND BREAKS; DENTAL COMPOSITE; OXIDATIVE STRESS; MONOMERS; BIODEGRADATION; COMPONENTS; NANOPARTICLES; MACROPHAGES; ACTIVATION; INDUCTION;
D O I
10.3390/ma14185225
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The aim of the study was to evaluate the cytotoxic and genotoxic potential of five commercially available dental composite resins (CRs), investigating the effect of their quantifiable bisphenol-A-glycidyl-methacrylate (Bis-GMA) and/or triethylene glycol dimethacrylate (TEGDMA) release. Experiments were performed using the method of soaking extracts, which were derived from the immersion of the following CRs in the culture medium: Clearfil-Majesty-ES-2, GrandioSO, and Enamel-plus-HRi (Bis-GMA-based); Enamel-BioFunction and VenusDiamond (Bis-GMA-free). Human Gingival Fibroblasts (hGDFs) were employed as the cellular model to mimic in vitro the oral cavity milieu, where CRs simultaneously release various components. Cell metabolic activity, oxidative stress, and genotoxicity were used as cellular outcomes. Results showed that only VenusDiamond and Enamel-plus-HRi significantly affected the hGDF cell metabolic activity. In accordance with this, although no CR-derived extract induced a significantly detectable oxidative stress, only VenusDiamond and Enamel-plus-HRi induced significant genotoxicity. Our findings showed, for the CRs employed, a cytotoxic and genotoxic potential that did not seem to depend only on the actual Bis-GMA or TEGDMA content. Enamel-BioFunction appeared optimal in terms of cytotoxicity, and similar findings were observed for Clearfil-Majesty-ES-2 despite their different Bis-GMA/TEGDMA release patterns. This suggested that simply excluding one specific monomer from the CR formulation might not steadily turn out as a successful approach for improving their biocompatibility.
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页数:15
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