Kato Masashi, Ohtake Hiroto, Sato Hideyuki, Seto Yoshiki, Onoue Satomi
Department of Pharmacokinetics and Pharmacodynamics, School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan.
Department of Pharmacokinetics and Pharmacodynamics, School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan.
Toxicol Lett. 2017 Aug 15;278:59-65. doi: 10.1016/j.toxlet.2017.07.852. Epub 2017 Jul 8.
The present study aimed to verify the feasibility of an enzymatic reactive oxygen species (eROS) assay to evaluate the phototoxic risk of compounds after their metabolization. The eROS assay was designed based on the combined use of an in vitro drug metabolism system and a ROS assay. The incubation time of compounds with human hepatic S9 fractions was optimized with the use of fenofibrate (FF), a typical phototoxicant with metabolite-related phototoxicity, and the reproducibility and robustness of the eROS assay were examined using FF. The eROS assay was applied to 12 phototoxic compounds, including 7 phototoxicants with metabolite-related phototoxicity, to clarify the assay performance. According to the eROS data on singlet oxygen generation from FF and metabolic conversion profiles of FF and fenofibric acid, the incubation time of chemicals with human hepatic S9-mix was determined to be 4min. The singlet oxygen-based evaluation system in the eROS assay was found to be acceptable as a high-throughput assay because of its favorable intra-/inter-day reproducibility (coefficient of variation: ca. 8%) and robustness (Z'-factor: 0.23). Singlet oxygen data on phototoxicants with phototoxic metabolites tended to exceed 120% of control, suggesting the feasibility of the eROS assay to evaluate metabolite-related phototoxic potentials. However, further data accumulation is still needed to improve the assay performance because the eROS assay provided false predictions for some compounds. The present eROS assay may be applicable in part for evaluating the phototoxic risk of drug candidates after their metabolization in the early stage of drug discovery.
本研究旨在验证酶促活性氧(eROS)测定法评估化合物代谢后光毒性风险的可行性。eROS测定法是基于体外药物代谢系统和活性氧测定法的联合使用而设计的。使用非诺贝特(FF)对化合物与人肝S9组分的孵育时间进行了优化,非诺贝特是一种典型的具有代谢物相关光毒性的光毒性物质,并使用FF检测了eROS测定法的重现性和稳健性。将eROS测定法应用于12种光毒性化合物,包括7种具有代谢物相关光毒性的光毒性物质,以阐明该测定法的性能。根据FF产生单线态氧的eROS数据以及FF和非诺贝特酸的代谢转化谱,确定化学品与人肝S9混合物的孵育时间为4分钟。由于其良好的日内/日间重现性(变异系数:约8%)和稳健性(Z'因子:0.23),eROS测定法中基于单线态氧的评估系统被认为是一种可接受的高通量测定法。具有光毒性代谢物的光毒性物质的单线态氧数据往往超过对照的120%,表明eROS测定法评估代谢物相关光毒性潜力的可行性。然而,由于eROS测定法对某些化合物提供了错误的预测,仍需要进一步积累数据以提高测定法的性能。目前的eROS测定法可能部分适用于在药物发现的早期阶段评估候选药物代谢后的光毒性风险。