Derya Sürmelioğlu Ceylan Hepokur, Sevim Atılan Yavuz
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引用次数: 0
摘要
本研究的目的是通过琼脂扩散试验评价两种不同含量、pH值和聚合技术的通用胶粘剂体系对小鼠成纤维细胞系(L929)的细胞毒性。G-Premio Bond (GC Europe, Belgium)和Tokuyama Universal Bond (Tokuyama, USA)是通用的通用粘合剂系统。G-Premio Bond是光聚合的,Tokuyama Universal Bond是化学聚合的,根据制造商的说明进行聚合。所有材料在Dulbecco改良Eagle培养基(DMEM)溶液中孵育72小时。每个孔中放置L929细胞1.5x10 5个细胞/ ml,使用待检测细胞毒性的粘附系统。等待添加的琼脂冻结,安装粘附系统并在倒置显微镜下检查细胞活力。等待添加的琼脂冻结,放置黏附系统,在倒置显微镜下检查细胞活力。统计学分析采用单因素方差分析(ANOVA)和Tukey事后检验。在细胞活力值方面,两种不同的通用粘接剂系统之间存在统计学上的显著差异。Tokuyama Universal Bond组细胞活力显著低于G-Premio Bond组(p <0.05)。在使用通用粘合剂系统的治疗中,可以观察到对活细胞的细胞毒性作用。结果的一致性需要不同的细胞毒性检测方法的支持。
Biocompatibility of Two Different Universal Adhesives
The aim of this study is to evaluate the cytotoxicity with agar diffusion test of two different universal adhesive systems with different content, pH, and polymerization techniques on mouse fibroblast cell lines (L929). G-Premio Bond (GC Europe, Belgium) and Tokuyama Universal Bond (Tokuyama, USA) were supplied from common universal adhesive systems. G-Premio Bond, which is light-polymerized, and Tokuyama Universal Bond adhesive systems, which are chemical-polymerized, are polymerized according to the manufacturer's instructions. All materials were incubated for 72 hours in Dulbecco's modified Eagle medium (DMEM) solution. L929 cells were placed in each wells to be 1.5x10 5 cells / ml and adhesive systems to be examined for cytotoxicity were applied. Waiting for the added agar to freeze, adhesive systems were installed and cell viability examined in an inverted microscope. Waiting for the added agar to freeze, adhesive systems were placed and cell viability examined in an inverted microscope. Statistical analysis was performed using one-way analysis of variance (ANOVA) and Tukey’s post-hoc test. A statistically significant difference was found between the two different Universal adhesive systems in terms of cell viability values. Cell viability was significantly lower in the Tokuyama Universal Bond group compared to the G-Premio Bond group (p <0.05). In treatments using universal adhesive systems, cytotoxic effects can be observed against live cells. The compatibility of the results should be supported by different cytotoxicity detection methods.