Active Oxygen Species Generated from Photoexcited Fullerene (C<sub>60</sub>) as Potential Medicines:  O<sub>2</sub><sup>-</sup><sup>•</sup>versus<sup>1</sup>O<sub>2</sub>

Yoko Yamakoshi(The University of Tokyo), Naoki Umezawa(The University of Tokyo), Akemi Ryu(The University of Tokyo), Kumi Arakane(National Institute of Health Sciences), Naoki Miyata(National Institute of Health Sciences), Yukihiro Goda(The University of Tokyo), Toshiki Masumizu(National Institute of Health Sciences), Tetsuo Nagano(National Institute of Health Sciences)
Journal of the American Chemical Society
September 24, 2003
Cited by 695

Abstract

To characterize fullerenes (C(60) and C(70)) as photosensitizers in biological systems, the generation of active oxygen species, through energy transfer (singlet oxygen (1)O(2)) and electron transfer (reduced active oxygen radicals such as superoxide anion radical O(2)(-)* and hydroxyl radical *OH), was studied by a combination of methods, including biochemical (DNA-cleavage assay in the presence of various scavengers of active oxygen species), physicochemical (EPR radical trapping and near-infrared spectrometry), and chemical methods (nitro blue tetrazolium (NBT) method). Whereas (1)O(2) was generated effectively by photoexcited C(60) in nonpolar solvents such as benzene and benzonitrile, we found that O(2)(-)* and *OH were produced instead of (1)O(2) in polar solvents such as water, especially in the presence of a physiological concentration of reductants including NADH. The above results, together with those of a DNA cleavage assay in the presence of various scavengers of specific active oxygen species, indicate that the active oxygen species primarily responsible for photoinduced DNA cleavage by C(60) under physiological conditions are reduced species such as O(2)(-)* and *OH.


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