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采用荧光嵌入染料的药物物质光遗传毒性高通量筛选策略。

High-throughput screening strategy for photogenotoxic potential of pharmaceutical substances using fluorescent intercalating dye.

机构信息

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.

出版信息

J Pharm Biomed Anal. 2010 Sep 5;52(5):781-6. doi: 10.1016/j.jpba.2010.02.029. Epub 2010 Feb 25.

Abstract

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.

摘要

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。

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