Affiliation:
1. Endodontic Section, Faculty of Dental Medicine, Rangsit University, Pathumtanee 12000, Thailand
2. Research Office, Faculty of Dentistry, Mahidol University, Bangkok 10400, Thailand
3. Department of Oral Biology, Faculty of Dentistry, Mahidol University, Bangkok 10400, Thailand
Abstract
ABSTRACT
Objective: To evaluate the cytotoxic and the proliferative effect of cuttlefish bone on MC3T3-E1 osteoblast cell line. Materials and Methods: MC3T3-E1 cells were treated with 0.5, 1, 5, 25, 50, 100, or 200 μg/ml cuttlefish bone powder (CBP). Cytotoxicity was evaluated using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. This assay was also used to determine cell proliferation over 16 days of treatment with 0.5, 25, or 100 μg/ml CBP. Results: CBP was not cytotoxic to MC3T3-E1 cells at any concentration. The percentage of cell viability in the 0.5–200 μg/ml CBP groups dose dependently decreased from 107.52 ± 11.03 to 92.48 ± 5.60%; however, the differences between the groups or the negative control group were not significant. At 16 days, 0.5, 25, and 100 μg/ml CBP groups showed 123.19 ± 10.07%, 126.02 ± 15.69%, and 133.33 ± 11.74% proliferation, respectively, that were significantly higher than that of the control group. Conclusion: These results indicate that CBP promotes osteoblast proliferation and may be a potential material to increase the number of osteoblasts in a bone defect in the oral cavity.
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