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    Please use this identifier to cite or link to this item: https://ir.csmu.edu.tw:8080/ir/handle/310902500/15807


    Title: Assessment of the cytotoxicity of chlorhexidine by employing an in vitro mammalian test system
    Authors: Li, Yi-Ching
    Kuan, Yu-Hsiang
    Lee, Tzu-Hsin
    Huang, Fu-Mei
    Chang, Yu-Chao
    Contributors: 中山醫大口腔科學研究所
    Keywords: cell death;chlorhexidine;cytotoxicity;superoxide anion
    Date: 2014
    Issue Date: 2016-08-15T06:13:54Z (UTC)
    ISSN: 1991-7902
    Abstract: Background/purpose

    Chlorhexidine (CHX), a chlorophenyl biguanide with broad antibacterial action, has been widely used in dentistry. The initial uses of CHX in dentistry were to wash operation site and to disinfect root canals. Recently, the addition of CHX into many dental materials has improved the overall therapeutic efficacy. The aim of this study was to evaluate the potential toxicological implications of CHX employing an in vitro mammalian test system.

    Materials and methods

    Cytotoxicity, mode of cell death, and generation of superoxide anion were performed to elucidate the toxic effects of CHX on Chinese hamster ovary cells. Cytotoxicity was judged using tetrazolium bromide reduction assay. The mode of cell death was determined by flow cytometry. Superoxide anion generation was determined by the superoxide dismutase-inhibitable reduction of ferricytochrome c.

    Results

    CHX demonstrated a cytotoxic effect on Chinese hamster ovary cells in a dose-dependent and time-dependent manner (P < 0.05). The mode of cell death changed from apoptosis to necrosis as the concentrations of CHX elevated. CHX demonstrated a significant superoxide anion generation in a dose-dependent manner (P < 0.05). The addition of superoxide dismutase decreased the cytotoxicity induced by CHX (P < 0.05).

    Conclusion

    CHX was demonstrated to exhibit cytotoxicity that could disrupt the stable cellular redox balance, resulting in increasing levels of free radical generation and subsequent cell death. CHX has significant potential for cytotoxicity.
    URI: http://dx.doi.org/10.1016/j.jds.2013.02.011
    https://ir.csmu.edu.tw:8080/ir/handle/310902500/15807
    Relation: Journal of Dental SciencesVolume 9, Issue 2, June 2014, Pages 130–135
    Appears in Collections:[口腔醫學研究所] 期刊論文

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