Comparison of different test models for the assessment of cytotoxicity of composite resins

被引:55
作者
Cao, T
Saw, TY
Heng, BC
Liu, H
Yap, AUJ
Ng, ML
机构
[1] Natl Univ Singapore, Fac Dent, Dept Restorat Dent, Singapore 119074, Singapore
[2] Natl Univ Singapore, Fac Med, Dept Microbiol, Singapore 117597, Singapore
关键词
cytotoxicity test; biocompatibility; dental biomaterials; photo-polymerization;
D O I
10.1002/jat.1041
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
This study compared the use of different test models to assess the cytotoxicity of a dental composite. The cytotoxicity of a composite polymerized using two halogen-based light-curing units (LCUs) (Max LC and Astralis) and two light-emitting diode LCUs (E-light and Freelight) served as the basis of comparison. Disk-shaped specimens (7 mm diameter, 2 mm high) were fabricated using the four different light sources. The specimens were used in several cytotoxicity test models: direct and indirect contact tests as well as an extract test with an established cell line L-929. The cells were stained with neutral red after cell-material contact for 48 h. Neutral red-stained areas (in mm(2), for direct and indirect tests) and absorbance readings (for extract tests) were analysed statistically using ANOVA and the Tukey post hoc test, with P < 0.05 considered to be significantly different. Good correlation between direct and indirect contact tests (r = 0.903) was found. The extract test was the least correlated among the three tests. It was found that the E-light + Freelight-cured composite elicited cytotoxicity from the correlated studies. Uncured specimens were most detrimental to the cells in all tests. Our data demonstrated that composite cured with light-emitting diode LCUs were cytotoxic to L-929 cells. Different test models were found to give rise to different findings. Thus, a good cell-material contact method would replicate more closely the physiological situation in vivo. This in turn would give more clinically relevant results. Copyright (c) 2005 John Wiley & Sons, Ltd.
引用
收藏
页码:101 / 108
页数:8
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