Title
Design, syntheses, characterization, and cytotoxicity studies of novel heterobinuclear oxindolimine copper(II)-platinum(II) complexes
Author
Esther Escribano Aranda, Tiago Araújo Matias, Koiti Araki, Adriana Pires Vieira, Elaine Andrade de Mattos, Pio Colepicolo, Carolina Portela Luz, Fábio Luiz Navarro Marques, Ana Maria da Costa Ferreira
Year
2016
Journal
Journal of Inorganic Biochemistry
Abstract
Herein, the design and syntheses of two new mononuclear oxindolimine-copper(II) (1and 2) and corresponding heterobinuclear oxindolimine Cu(II)single bondPt(II) complexes (3 and4), are described. All the isolated complexes were characterized by spectroscopic techniques (UV/Vis, IR, EPR), in addition to elemental analysis and mass spectrometry. Cyclic voltammetry (CV) measurements showed that in all cases, one-electron quasi-reversible waves were observed, and ascribed to the formation of corresponding copper(I) complexes. Additionally, waves related to oxindolimine ligand reduction was verified, and confirmed using analogous oxindolimine-Zn(II) complexes. The Pt(IV/II) reduction, and corresponding oxidation, for complexes 3 and 4 occurred at very close values to those observed for cisplatin. By complementary fluorescence studies, it was shown that glutathione (GSH) cannot reduce any of these complexes, under the experimental conditions (room temperature, phosphate buffer 50 mM, pH 7.4), using an excess of 20-fold [GSH]. All these complexes showed characteristic EPR spectral profile, with parameters values gǁ > g⊥ suggesting an axially distorted environment around the copper(II) center. Interactions with calf thymus-DNA, monitored by circular dichroism (CD), indicated different effects modulated by the ligands. Finally, the cytotoxicity of each complex was tested toward different tumor cells, in comparison to cisplatin, and low values of IC50 in the range 0.6 to 4.0 μM were obtained, after 24 or 48 h incubation at 37 °C. The obtained results indicate that such complexes can be promising alternative antitumor agents.
Instrument
J-720
Keywords
Circular dichroism, DNA structure, Ligand binding, Inorganic chemistry, Biochemistry