Cytotoxicity of four denture adhesives on human gingival fibroblast cells

Authors

  • Yoon Lee Department of Conservative Dentistry, Wonju Severance Christian Hospital, Yonsei University, Wonju, Republic of Korea
  • Jin-Soo Ahn Department of Dental Biomaterials Science, School of Dentistry, Seoul National University, Seoul, Republic of Korea
  • Young-Ah Yi Department of Dentistry, Inje University Seoul Paik Hospital, Seoul, Republic of Korea
  • Shin-Hye Chung Department of Dental Biomaterials Science, School of Dentistry, Seoul National University, Seoul, Republic of Korea
  • Yeon-Jee Yoo Department of Conservative Dentistry and Dental Research Institute, School of Dentistry, Seoul National University, Seoul, Republic of Korea
  • Sung-Won Ju Department of Dental Biomaterials Science, School of Dentistry, Seoul National University, Seoul, Republic of Korea
  • Ji-Yun Hwang Nutrition Education Major, Graduate School of Education, Sangmyung University, Seoul, Republic of Korea
  • Deog-Gyu Seo Department of Conservative Dentistry and Dental Research Institute, School of Dentistry, Seoul National University, Seoul, Republic of Korea

DOI:

https://doi.org/10.3109/00016357.2014.954266

Keywords:

cytotoxicity, denture adhesive, flow cytometric apoptosis assay, human gingival fibroblast, MTT assay, scanning electron microscope

Abstract

Objective. The purpose of this study was to compare the cytotoxicity of four denture adhesives on human gingival fibroblast cells. Materials and methods. Immortalized human gingival fibroblasts were cultured with one of four different denture adhesives, Polident, Protefix, Staydent or Denfix-A, which was placed in insert dishes (10% w/v concentration) for 48 h. The MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] assay and flow cytometric apoptosis assay were used to evaluate cell viability and apoptosis rates. The fibroblasts were also examined under a scanning electron microscope. Results. The MTT assay showed that all denture adhesives resulted in a significantly lower cell viability compared to the control cells propagated in normal culture medium (p < 0.05), with Staydent demonstrating the lowest cell viability. According to the flow cytometric apoptosis assay, Staydent and Protefix showed significantly higher apoptosis rates than the control group (p < 0.05), whereas Polident and Denfix-A did not demonstrate any significant differences (p > 0.05). Staydent showed the highest apoptosis rate. Scanning electron microscopy showed that the cells of the Staydent group underwent cytoplasmic membrane shrinkage, with cell free areas containing residual fragments of the membrane of dead cells. Conclusions. The four denture adhesives evaluated in this study imparted cytotoxic effects on human gingival fibroblast cells. Staydent showed the highest toxicity.

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Published

2015-02-17