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首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >Effects of monomers eluted from dental resin restoratives on osteoblast-like cells.
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Effects of monomers eluted from dental resin restoratives on osteoblast-like cells.

机译:从牙科树脂修复剂洗脱的单体对成骨细胞样细胞的影响。

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摘要

Resin-modified glass-ionomer (RMGIC) has been demonstrated to exhibit inhibition on the growth and differentiation of osteoblasts on its surface. In this study, the hypothesis that the different levels of inhibitory effects on osteoblasts of resin restoratives depend on elution of unpolymerized monomers was examined. Release of monomers from cured specimens of Bis-GMA/TEGDMA-composites, MMA-resin cements, or HEMA-containing RMGIC was determined and osteoblast-like MC3T3-E1 cells were cultured in the presence of 100-10 microg/mL of TEGDMA, 10-1 microg/mL of MMA, or 400-50 microg/mL of HEMA according to the release concentrations. Cell proliferation, alkaline phosphatase (ALP) activity, the expression of osteoblastic markers, and mineralized tissue formation were evaluated. TEGDMA and MMA at the concentrations tested did not affect the growth of MC3T3-E1 and exhibited little harmful effects on their differentiation and mineralization. On the contrary, HEMA inhibited proliferation, ALP activities, the expression of osteocalcin, and mineralized tissue formation at 200 microg/mL or more. These results indicate that HEMA at the concentrations similar to that observed in elution tests affected osteoblastic proliferation, differentiation, and mineralization, suggesting that elution of unreacted HEMA could be the main component of the adverse effects of RMGIC on osteoblast-like cells and influences of resin restoratives on the osteoblasts are possibly dependant on release characteristics of unpolymerized monomers.
机译:已证明树脂改性的玻璃离聚物(RMGIC)在其表面上表现出对成骨细胞生长和分化的抑制作用。在这项研究中,检验了对树脂修复剂对成骨细胞不同程度的抑制作用取决于未聚合单体洗脱的假设。确定了Bis-GMA / TEGDMA复合材料,MMA树脂水泥或含HEMA的RMGIC固化样品中的单体释放,并在100-10 microg / mL TEGDMA存在的情况下培养了成骨细胞样MC3T3-E1细胞,根据释放浓度,可使用10-1微克/毫升的MMA或400-50微克/毫升的HEMA。评价细胞增殖,碱性磷酸酶(ALP)活性,成骨细胞标志物的表达以及矿化组织的形成。所测试浓度的TEGDMA和MMA不会影响MC3T3-E1的生长,并且对其分化和矿化几乎没有有害作用。相反,在200 microg / mL或更高的浓度下,HEMA抑制增殖,ALP活性,骨钙素的表达以及矿化组织的形成。这些结果表明,与洗脱试验中观察到的浓度相似的HEMA影响成骨细胞的增殖,分化和矿化,这表明未反应的HEMA洗脱可能是RMGIC对成骨样细胞和树脂影响的主要成分。成骨细胞上的修复剂可能取决于未聚合单体的释放特性。

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