Department of Pharmacokinetics and Pharmacodynamics and Global Center of Excellence Program, School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan.
J Pharm Biomed Anal. 2010 Sep 5;52(5):781-6. doi: 10.1016/j.jpba.2010.02.029. Epub 2010 Feb 25.
The aim of the present study was to provide an intercalator-based photogenotoxicity (IBP) assay as a high-throughput in vitro screening system for predicting the photogenotoxic potential of pharmaceutical substances. The conditions of the high-throughput IBP assay using thiazole orange (TO), a fluorescent intercalating dye, were optimized and validated by a fluorescence titration experiment and reproducibility/robustness test. The IBP assay was applied to 27 phototoxic and 5 weak/non-phototoxic commercially available compounds, and other phototoxicity screenings were also carried out for comparison; these included the reactive oxygen species (ROS) assay for overall phototoxic potential and the DNA-photocleavage assay for photogenotoxic risk. According to the results from the comparative experiments, a decreased level of intercalated TO in the IBP assay could theoretically be related to the DNA-photocleaving behaviors of phototoxic drugs, but not to their ROS-generating abilities. The IBP assay could predict the photodynamic DNA impairment caused by irradiated drugs with a prediction accuracy of 78%. These findings suggest that the IBP assay could be a fast and reliable tool for predicting the photogenotoxic potential of a large number of drug candidates at early stages of drug discovery.
本研究旨在提供一种基于嵌入剂的光毒性(IBP)测定法作为高通量体外筛选系统,以预测药物物质的潜在光毒性。通过荧光滴定实验和重现性/稳健性测试,优化并验证了使用噻唑橙(TO),一种荧光嵌入染料的高通量 IBP 测定法的条件。该 IBP 测定法应用于 27 种光毒性和 5 种弱/非光毒性市售化合物,并进行了其他光毒性筛选进行比较;这些包括用于整体光毒性潜力的活性氧(ROS)测定法和用于光基因毒性风险的 DNA 光裂测定法。根据比较实验的结果,IBP 测定法中嵌入 TO 的水平降低理论上可能与光毒性药物的 DNA 光裂行为有关,但与它们产生 ROS 的能力无关。IBP 测定法可以预测辐照药物引起的光动力 DNA 损伤,预测准确性为 78%。这些发现表明,IBP 测定法可能是一种快速可靠的工具,可在药物发现的早期阶段预测大量候选药物的光基因毒性潜力。