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新型喹诺酮抗菌剂的体外光毒性活性:脂质过氧化潜力。

In vitro phototoxic activities of new quinolone antibacterial agents: lipid peroxidative potentials.

作者信息

Fujita H, Matsuo I

机构信息

Department of Molecular Life Science, Tokai University School of Medicine, Kanagawa, Japan.

出版信息

Photodermatol Photoimmunol Photomed. 1994 Oct;10(5):202-5.

PMID:7880759
Abstract

To determine the fundamental photochemical properties of new quinolones that can induce photosensitivity, the in vitro phototoxicity of these drugs (enoxacin, norfloxacin, ofloxacin, ciprofloxacin, and lomefloxacin) was examined with respect to photosensitizing ability to peroxidize unsaturated lipid squalene in ethanol solution. Lomefloxacin and ciprofloxacin showed the highest efficiency in sensitization of peroxidation of the lipid. Moderate repression of peroxidation occurred by addition of sodium azide (a quencher of singlet molecular oxygen), suggesting that the nonsinglet oxygen mechanism is operative in addition to the singlet oxygen mechanism.

摘要

为了确定可引发光敏感的新型喹诺酮类药物的基本光化学性质,研究了这些药物(依诺沙星、诺氟沙星、氧氟沙星、环丙沙星和洛美沙星)在乙醇溶液中对不饱和脂质角鲨烯过氧化的光致敏能力的体外光毒性。洛美沙星和环丙沙星在脂质过氧化致敏方面表现出最高效率。添加叠氮化钠(单线态分子氧猝灭剂)后,脂质过氧化受到适度抑制,这表明除单线态氧机制外,非单线态氧机制也起作用。

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