Onoue Satomi, Yamauchi Yukinori, Kojima Takashi, Igarashi Naoko, Tsuda Yoshiko
Analytical Research and Development, Pfizer Global Research and Development, Nagoya Laboratories, Pfizer Japan Inc., 5-2 Taketoyo, Aichi, 470-2393, Japan.
Pharm Res. 2008 Apr;25(4):861-8. doi: 10.1007/s11095-007-9383-4. Epub 2007 Aug 1.
Monitoring of reactive oxygen species (ROS) generation from photoirradiated compounds would be effective for the prediction of the phototoxic potential. The aim of this investigation was to clarify the possible role of biomimetic vehicle systems on the photochemical properties of phototoxic compounds, focusing on the singlet oxygen generation.
Nine phototoxic and one non-phototoxic compounds (200 microM), dissolved in Tween 20, sodium laurate, or sodium dodecyl sulfate (SDS) micellar solution, were exposed to UVA/B light (250 W/m2), and singlet oxygen generation was monitored by RNO bleaching methodology. Photochemical properties of photosensitizers were also evaluated by UV measurement, and the interaction of photosensitizers with surfactant micelles was assessed by Z-potential and NMR spectroscopic analyses.
All phototoxic compounds tended to generate singlet oxygen under light exposure in the all micellar solutions tested. There appeared to be some differences in photoreactivity of both cationic and anionic photosensitizers among the micelles tested, whereas ROS data on anthracene, dissolved in three micellar solutions, were found to be quite similar. Photosensitizers exhibited no significant changes in UV spectral patterns among the dissolving micellar solutions. Addition of cationic photosensitizer at the final concentration of 100 microM into 100 mM SDS solution resulted in the 20 mV increase of zeta potential and transition of NMR spectral pattern, which would reflect the electrostatic interaction with anionic micelles.
Based on the data obtained, the photoreactivity of photosensitizing molecules, especially cationic and anionic photosensitizers, strongly depends on the physicochemical properties of the microenvironment.
监测光照射化合物产生的活性氧(ROS)对于预测光毒性潜力将是有效的。本研究的目的是阐明仿生载体系统对光毒性化合物光化学性质的可能作用,重点是单线态氧的产生。
将九种光毒性化合物和一种非光毒性化合物(200 microM)溶解在吐温20、月桂酸钠或十二烷基硫酸钠(SDS)胶束溶液中,暴露于UVA/B光(250 W/m2)下,通过RNO漂白法监测单线态氧的产生。还通过紫外测量评估了光敏剂的光化学性质,并通过Z电位和核磁共振光谱分析评估了光敏剂与表面活性剂胶束的相互作用。
在所有测试的胶束溶液中,所有光毒性化合物在光照下都倾向于产生单线态氧。在所测试的胶束中,阳离子和阴离子光敏剂的光反应性似乎存在一些差异,而溶解在三种胶束溶液中的蒽的ROS数据非常相似。光敏剂在溶解的胶束溶液中的紫外光谱模式没有显著变化。在100 mM SDS溶液中加入终浓度为100 microM的阳离子光敏剂会导致zeta电位增加20 mV,并使核磁共振光谱模式发生转变,这反映了与阴离子胶束的静电相互作用。
根据获得的数据,光敏分子,尤其是阳离子和阴离子光敏剂的光反应性强烈依赖于微环境的物理化学性质。