Adachi Tamiko, Satou Yuko, Satou Hiroko, Shibata Hiroshi, Miwa Satoko, Iwase Yumiko, Yamamoto Toshinobu, Nishida Atsuyuki, Masutomi Naoya
Research Division, Safety Research Laboratories, Mitsubishi Tanabe Pharma Corporation, Kisarazu, Chiba, Japan.
Research Division, Safety Research Laboratories, Mitsubishi Tanabe Pharma Corporation, Kisarazu, Chiba, Japan
Int J Toxicol. 2015 Jan-Feb;34(1):16-23. doi: 10.1177/1091581814559397. Epub 2014 Nov 28.
Phototoxicity has a strong impact on drug development. Although several animal models have been developed to quantitatively assess human risks, none have been validated for standardized use. In this study, we validated an in vivo phototoxicity model using Long-Evans (LE) rats treated with 4 well-known phototoxic drugs, namely 8-methoxypsoralen, lomefloxacin, sparfloxacin, and pirfenidone. Daily macroscopic observations of skin and eyes, ophthalmological examinations 4 days after dosing, and blood sampling for toxicokinetics (TKs) were performed after exposure of treated animals to ultraviolet, and dose-dependent eye and/or skin reactions were noted for all compounds. Margins of safety were calculated when possible and correlated well with known relative phototoxicity of the 4 compounds. We conclude that the present in vivo phototoxicity assay using LE rats with TK analysis can be used to quantitatively predict the risk of pharmaceutical phototoxicity in humans.
光毒性对药物研发有重大影响。尽管已经开发了几种动物模型来定量评估人类风险,但尚无模型经过验证可用于标准化应用。在本研究中,我们使用Long-Evans(LE)大鼠验证了一种体内光毒性模型,这些大鼠用4种著名的光毒性药物进行处理,即8-甲氧基补骨脂素、洛美沙星、司帕沙星和吡非尼酮。在经处理的动物暴露于紫外线后,每天对皮肤和眼睛进行宏观观察,给药4天后进行眼科检查,并采集血液进行毒代动力学(TKs)分析,所有化合物均观察到剂量依赖性的眼睛和/或皮肤反应。在可能的情况下计算了安全边际,并且与这4种化合物已知的相对光毒性相关性良好。我们得出结论,目前使用LE大鼠并进行TK分析的体内光毒性试验可用于定量预测药物对人类的光毒性风险。