Kim Eun Ji, Youn Nam Hee, Yi Jung-Sun, Kim Joo Hwan, Cho Ye-Jin, Nam Ki Taek, Park Ki Sook, Lee Jong Kwon
Toxicological Evaluation and Research Department, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Cheongju, 28159 Republic of Korea.
Severance Biomedical Science Institute, Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, Seoul, 03722 Republic of Korea.
Toxicol Res. 2021 Feb 8;37(4):435-442. doi: 10.1007/s43188-020-00078-7. eCollection 2021 Oct.
In vivo phototoxicity testing is important for predicting drug-induced phototoxicity in humans. Currently, there is no internationally validated in vivo test method for the photosafety evaluation of pharmaceuticals. In this study, we evaluated the phototoxicity of systemically administered drugs using SD rats. We first determined the appropriate ultraviolet A (UVA) dose using 8-methoxypsoralen, a well-known phototoxic drug. Compared to lower and higher UVA doses, we found that a UVA dose of 10 J/cm allowed for the detection of phototoxic responses in both a dose- and time-dependent manner. We next performed a phototoxicity study using seven pharmaceutical drugs which included known phototoxic and non-phototoxic drugs using a UVA dose of 10 J/cm. In order to improve the accuracy of our assessment, we evaluated both gross skin findings as well as histopathological findings. Using gross skin findings alone resulted in an accuracy of 85.7% which could be increased to 100% accuracy when the gross skin findings were combined with histopathological findings. This study suggests that the inclusion of histopathological findings increases the accuracy of the phototoxicity evaluation of systemically administered drugs in SD rats. In conclusion, we found that for studying drug-induced phytotoxicity, a 10 J/cm UVA dose serves as the optimal radiation dose, and that the inclusion of histopathological findings increases the accuracy of the phototoxicity evaluation of the drugs.
体内光毒性测试对于预测药物在人体中引起的光毒性很重要。目前,尚无用于药物光安全性评估的国际认可的体内测试方法。在本研究中,我们使用SD大鼠评估了全身给药药物的光毒性。我们首先使用一种知名的光毒性药物8-甲氧基补骨脂素确定了合适的紫外线A(UVA)剂量。与较低和较高的UVA剂量相比,我们发现10 J/cm的UVA剂量能够以剂量和时间依赖性方式检测到光毒性反应。接下来,我们使用七种药物进行了光毒性研究,其中包括已知的光毒性和非光毒性药物,UVA剂量为10 J/cm。为了提高评估的准确性,我们评估了皮肤大体表现以及组织病理学表现。仅使用皮肤大体表现时准确性为85.7%,当将皮肤大体表现与组织病理学表现相结合时,准确性可提高到100%。本研究表明,纳入组织病理学表现可提高SD大鼠中全身给药药物光毒性评估的准确性。总之,我们发现对于研究药物引起的植物毒性,10 J/cm的UVA剂量是最佳辐射剂量,并且纳入组织病理学表现可提高药物光毒性评估的准确性。