Onoue Satomi, Kawamura Kiyoshi, Igarashi Naoko, Zhou Yu, Fujikawa Masaaki, Yamada Hiroshi, Tsuda Yoshiko, Seto Yoshiki, Yamada Shizuo
Department of Pharmacokinetics and Pharmacodynamics and Global Center of Excellence (COE) Program, School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Shizuoka 422-8526, Japan.
J Pharm Biomed Anal. 2008 Aug 5;47(4-5):967-72. doi: 10.1016/j.jpba.2008.03.026. Epub 2008 Mar 30.
We have previously demonstrated that the phototoxic potential of chemicals could be partly predicted by the determination of reactive oxygen species (ROS) from photo-irradiated compounds. In this study, ROS assay strategy was applied to 39 marketed drugs and 210 drug candidates in order to establish provisional classification criteria for risk assessment of drug-induced phototoxicity. The photosensitizing properties of 39 model compounds consisting of phototoxic and non-phototoxic chemicals, as well as ca. 210 drug candidates including 11 chemical series were evaluated using ROS assay and the 3T3 neutral red uptake phototoxicity test (NRU PT). With respect to marketed drugs, most phototoxic drugs tended to cause type I and/or II photochemical reactions, resulting in generation of singlet oxygen and superoxide. There seemed to be a clear difference between phototoxic drugs and non-phototoxic compounds in their abilities to induce photochemical reactions. A plot analysis of ROS data on the marked drugs provided classification criteria to discriminate the photosensitizers from non-phototoxic substances. Of all drug candidates tested, 35.2% compounds were identified as phototoxic or likely phototoxic on the basis of the 3T3 NRU PT, and all ROS data for these phototoxic compounds were found to be over the threshold value. Furthermore, 46.3% of non-phototoxic drug candidates were found to be in the subthreshold region. These results verify the usefulness of the ROS assay for understanding the phototoxicity risk of pharmaceutical substances, and the ROS assay can be used for screening purposes in the drug discovery stage.
我们之前已经证明,通过测定光照射化合物产生的活性氧(ROS),可以部分预测化学物质的光毒性潜力。在本研究中,将ROS检测策略应用于39种市售药物和210种候选药物,以建立药物诱导光毒性风险评估的临时分类标准。使用ROS检测和3T3中性红摄取光毒性试验(NRU PT)评估了由光毒性和非光毒性化学物质组成的39种模型化合物以及约210种包括11个化学系列的候选药物的光敏特性。对于市售药物,大多数光毒性药物倾向于引发I型和/或II型光化学反应,导致单线态氧和超氧阴离子的产生。光毒性药物和非光毒性化合物在诱导光化学反应的能力上似乎存在明显差异。对市售药物的ROS数据进行的绘图分析提供了区分光敏剂和非光毒性物质的分类标准。在所有测试的候选药物中,根据3T3 NRU PT,35.2%的化合物被鉴定为光毒性或可能具有光毒性,并且发现这些光毒性化合物的所有ROS数据均超过阈值。此外,发现46.3%的非光毒性候选药物处于亚阈值区域。这些结果证实了ROS检测对于了解药物光毒性风险的有用性,并且ROS检测可用于药物发现阶段的筛选目的。