Although it has been proposed that the ability of such complexes to induce apoptosis in tumour cells in vitro derives from their facility to generate free radicals, the relationship between apoptotic Selleck IWR-1 activity and the reactive species produced is not clear [35], [36], [37],
[38] and [39]. The aim of the present study was to determine the effects of imine ligands and low molecular weight Gly-derived ligands on the capacity of the respective Cu(II) complexes to catalyse the generation of reactive oxygen species (ROS) by hydrogen peroxide in the presence of the bicarbonate/carbon dioxide pair. Additionally, the two classes of complexes were compared with respect to their effects on the copper uptake and growth of human neuroblastoma cells. Reagents of analytical grade or better were purchased from Sigma, Aldrich, RG7204 mouse Merck or Fisher Scientific. Solutions were prepared with distilled water that had been purified using a Millipore Milli-Q system, and buffers were pre-treated with Chellex-100 to remove contaminating metal ions. The concentration of hydrogen peroxide was determined spectrophotometrically
(ε240 nm = 43.6 M−1 cm−1) [40]. Condensation of the amine ligands 1,3-diaminepropane (pn), ethylenediamine (en), 2-aminoethyl pyridine (epy) or 8-aminoquinoline (amiquin) with isatin (isa), followed by metallation with Cu(II) perchlorate, yielded the Cu(II)–isatin–diimine complexes [Cu(isa-pn)](ClO4)2, [Cu(isa-en)(H2O)]ClO4·2H2O, [Cu(isa-epy)2](ClO4)2·2H2O and [Cu(isa-amiquin)(H2O)]ClO4 as previously reported [41], [42] and [43]. The structures of the complexes ( Fig. 1) were confirmed by elemental analysis and comparison
of their UV–visible (UV–VIS) and EPR spectra with literature data. Cu(II) complexes with the ligands tetraglycine ([CuII(H-2G4)]−), triglycine ([CuII(H-2G3)]−) and glycylglycylhistidine ([CuII(H-2GGH)]−) were prepared by mixing an aqueous solution of Cu(II) chloride with 1.25 Transmembrane Transporters modulator equivalents of the peptide solution. The structures of the complexes were confirmed by comparison of their UV–VIS and EPR spectra with published data for these compounds [44], [45], [46] and [47]. Both classes of complexes showed to be structurally stable in aqueous solutions at all conditions used in experiments. Reaction mixtures (final volume = 1.00 mL) containing bicarbonate (25 mM), ascorbate (maintained in stock buffer solution pH = 4.0, 100 μM), hydrogen peroxide (3 mM) and DHR (50 μM) in 10 mM phosphate buffer (pH 7.4) were incubated in the presence or absence of Cu(II) sulphate or Cu(II)–imine complexes (50 μM) in order to assay the generation of oxygen-derived radicals with the capacity to bring about the one-electron oxidation of DHR generating DHR•+ (measured spectrophotometrically at 500 nm; ε = 7.88 × 104 M− 1 cm−1) [11]. Reaction mixtures (final volume = 1.