Histocompatibility of Light-Curing Composites Used in Pediatric Dentistry in Human Oral Fibroblast Cells.

Milad Arab-Nozari, Ehsan Zamani, Mehdi Evazalipour, Banafsheh Soleimani, Ali Jorbonian, Azam Nahvi
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Abstract

Statement of the problem: Tooth-colored composites are used to repair caries lesions and other dental defects, particularly in anterior regions in children. Although a wide range of composites is using, little attention has been paid to the important indicators such as biological profiles or products released from these materials.

Purpose: The current study aimed to compare the histocompatibility and cytotoxicity of light-curing resin used to repair children's teeth with different brands (3M, DenFil, and Opallis) in curing times of 20 and 40 seconds in human oral fibroblast cells (HGF1).

Materials and method: In this in vitro study, Three types of flow composites (3M, Opallis, and DenFil), all at A2 shade, were used. The composites were at 4×2mm with separate exposure times of 20 and 40 seconds. MTT test was used to determine the cytotoxicity of composites on oral fibroblast cells. This test is based on the conversion of tetrazolium bromide to a purple compound known as formazan that its color intensity can be evaluated using the ELISA. The higher intensity of the color reveals the higher survival rate of the mitochondria, which indicates less toxicity. One-way variance analysis and unpaired t-test were used to compare the cytotoxicity of each brand in two conditions of 20 and 40 seconds of curing. Statistical significance was considered when p< 0.05.

Results: 3M and Opallis composites were significantly reduced vitality of cells compared to control group in both 20s and 40s curing status. While DenFil brand did not show marked cytotoxicity. In each brand, there are no significant deference between 20s and 40s curing times.

Conclusion: Histocompatibility depends on the type of composite resin. In the current study, DenFil brand showed the highest histocompatibility, followed by 3M and Opallis.

Abstract Image

Abstract Image

儿童牙科用光固化复合材料在人口腔成纤维细胞中的组织相容性研究。
问题说明:牙齿颜色的复合材料用于修复龋齿损伤和其他牙齿缺陷,特别是在儿童的前牙区域。虽然复合材料的使用范围很广,但很少注意这些材料的重要指标,如生物特征或释放的产品。目的:本研究旨在比较不同品牌(3M、DenFil和Opallis)光固化树脂在人口腔成纤维细胞(HGF1)固化20秒和40秒时用于修复儿童牙齿的组织相容性和细胞毒性。材料和方法:在体外研究中,使用3种流动复合材料(3M、Opallis和DenFil),均为A2遮光。复合材料分别在4×2mm上曝光20秒和40秒。采用MTT法测定复合材料对口腔成纤维细胞的细胞毒性。该测试是基于溴化四氮唑转化为一种紫色化合物,称为福马甲酸,其颜色强度可以使用ELISA进行评估。颜色越深,表明线粒体存活率越高,毒性越小。采用单因素方差分析和非配对t检验比较各品牌在腌制20秒和40秒两种情况下的细胞毒性。p< 0.05为差异有统计学意义。结果:与对照组相比,3M和Opallis复合材料在20s和40s的固化状态下,细胞活力均明显降低。而DenFil品牌未表现出明显的细胞毒性。在每个品牌中,20岁和40岁之间的固化时间没有显著差异。结论:组织相容性取决于复合树脂的类型。在本研究中,DenFil品牌的组织相容性最高,3M和Opallis次之。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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