Cytotoxicity of zinc, copper and rhodium complexes with 1,10-phenanthroline or 2,9-dimethyl-1,10-phenanthroline in cultured vascular endothelial cells

  • Hara Takato
    Faculty of Pharmaceutical Sciences, Tokyo University of Science
  • Matsuzaki Hiroka
    Faculty of Pharmaceutical Sciences, Tokyo University of Science
  • Nakamura Takehiro
    Faculty of Pharmaceutical Sciences, Tokyo University of Science
  • Yoshida Eiko
    Faculty of Pharmaceutical Sciences, Tokyo University of Science
  • Ohkubo Takanori
    Department of Chemistry, Faculty of Science, Tokyo University of Science
  • Maruyama Hiroki
    Department of Chemistry, Faculty of Science, Tokyo University of Science
  • Yamamoto Chika
    Department of Environmental Health, Faculty of Pharmaceutical Sciences, Toho University
  • Saito Shinichi
    Department of Chemistry, Faculty of Science, Tokyo University of Science Division of Bio-organometallics, Research Institute for Science and Technology, Tokyo University of Science
  • Kaji Toshiyuki
    Faculty of Pharmaceutical Sciences, Tokyo University of Science Division of Bio-organometallics, Research Institute for Science and Technology, Tokyo University of Science

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Organic-inorganic hybrid molecules, which have organic structure and metal atoms, can exhibit various biological activities that are distinctly different from their components. Consequently, organic-inorganic hybrid molecules are considered an effective tool to analyze biological systems. Herein, we investigated the cytotoxicity of zinc, copper, and rhodium complexes, with either 1,10-phenanthroline or 2,9-dimethyl-1,10-phenanthroline as a common ligand, in cultured vascular endothelial cells. The copper complexes, that is, dichloro(1,10-phenanthroline) copper and dichloro(2,9-dimethyl-1,10-phenanthroline) copper, exhibited high cytotoxicity accompanied by considerable accumulation inside the cells. Potassium tetrachloro(1,10-phenanthroline) rhodate also exhibited cytotoxicity and considerable accumulation. Thus, it was found that the cytotoxicity of organic-inorganic hybrid molecules to vascular endothelial cells depends on the interaction between the intramolecular metal and ligand, which facilitates their uptake by the cells.

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