Cytotoxicities of Antibacterial Silane Coupling Agents

  • MIYAKE Kaori
    Division of Restorative Dentistry, Department of Oral Medicine, Kanagawa Dental College
  • OHASHI Katsura
    Division of Restorative Dentistry, Department of Oral Medicine, Kanagawa Dental College
  • NIHEI Tomotaro
    Division of Restorative Dentistry, Department of Oral Medicine, Kanagawa Dental College
  • SHIMIZU Tota
    Division of Prosthetics, Department of Oral and Maxillofacial Rehabilitation, Kanagawa Dental College
  • YAMAGUCHI Shinichiro
    Department of Comprehensive Dentistry, Kanagawa Dental College
  • KONDO Yukishige
    Department of Industrial Chemistry, Tokyo University of Science
  • YOSHINO Norio
    Department of Industrial Chemistry, Tokyo University of Science
  • TERANAKA Toshio
    Division of Restorative Dentistry, Department of Oral Medicine, Kanagawa Dental College

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Other Title
  • 抗菌性シランカップリング剤の細胞毒性

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Abstract

We have considered that decreasing the surface free energy of the tooth surface may help prevent caries and periodontal disease. Recently, we successfully synthesized two antibacterial silane coupling agents, N-allyl-N-decyl-N-methyl-N-trimethoxysilylpropylammonium iodide (10-I) and N-allyl-N-methyl-N-trimethoxysilylpropyl-N-octadecylammonium iodide (18-I). The aim of this study was to investigate the cytotoxicities of these modifier agents. Glass plates were dipped in 20 mmol/l of 10-I and 18-I solutions for 1 hour at 20℃, and then were sterilized with ethylene oxide gas for 24 hours at 35℃. The modified glass plates were immersed in cell culture medium (MO5) for 24 hours at 37℃ to examine the toxicity of the extraction procedure. The extracted medium (100%) was diluted with the MO5 into ten different concentrations (0.5-50%). 0.5 ml of the V79 cell suspension (100 cells/ml) was seeded on a 24-well cell culture plate and pre-incubated for 6 hours at 37℃ in a 5% CO2 atmosphere. After removal of MO5, 0.5 ml of the extracts containing MO5 was poured onto the cell culture of V79 cells. After 6-day cultivation, cells were stained with 0.1% methylene blue solution, and calculated. The cytotoxicities of various modified agents were evaluated according to the 50% inhibitory concentration (IC50). The IC50 value of 18-I was 18.8%, while that of 10-I was more than 100%. These results suggest that 10-I has no cytotoxicity, whereas 18-I has moderate cytotoxicity.

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