The European Journal of Orthodontics Advance Access originally published online on February 20, 2007
The European Journal of Orthodontics 2007 29(2):198-203; doi:10.1093/ejo/cjl083
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The cytotoxicity of orthodontic metal bracket immersion media
* Institute of Medicine, Chung Shan Medical University Hospital, Taiwan
** Institute of Oral Material Science, Chung Shan Medical University Hospital, Taiwan
*** Institute of Dental Department, Chung Shan Medical University Hospital, Taiwan
Address for correspondence Tsui-Hsien Huang, Dental Department, Chung Shan Medical University Hospital, 620 Shr Jeng Road, Taichung, Taiwan, E-mail: thh{at}csmu.edu.tw
| Abstract |
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The purpose of the present study was to evaluate the cytotoxic effects of four different orthodontic metal bracket immersion media on primary human oral gingival fibroblasts (HGFs) and one permanent human osteogenic sarcoma cell line (U2OS). Four different metal brackets (Unitek, Tomy, Ormco, and Dentaurum) were immersed in buffer solutions of NaHNO3 (1 mM) with a pH of 4 or 7, as well as artificial saliva. The concentrations for the experiments were 0.01, 0.1, and 1.0 µl/ml. At the end of the period of bracket immersion, morphological observations were conducted using light microscopy. The tetrazolium reduction assay was used to detect the survival rate of the target cells. Statistical analysis was conducted using one-way analysis of variance.
The results showed microscopically no morphological changes of the HGF or U2OS cells exposed to the metal bracket immersion media. At pH 4, the survival rates of the U2OS cells and the HGFs differed statistically for the Unitek (P = 0.003) and Ormco (P = 0.000) groups. At pH 7, the survival rate for the HGFs and the U2OS cells differed statistically for the Dentaurum (P = 0.021) and Unitek (P = 0.03) groups. The results demonstrate that differing cells exhibit various cellular reactions on exposure to metal bracket immersion media, although the four types of brackets appear to be biocompatible with HGF and U2OS cells.