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基于虚拟细胞的分析的实际应用:肝细胞系中重复暴露实验的模拟。

Practical use of the Virtual Cell Based Assay: Simulation of repeated exposure experiments in liver cell lines.

机构信息

Chemical Safety and Alternative Methods Unit, EURL ECVAM, Directorate F - Health, Consumers and Reference Materials, Joint Research Centre, European Commission, Ispra, Italy.

Chemical Safety and Alternative Methods Unit, EURL ECVAM, Directorate F - Health, Consumers and Reference Materials, Joint Research Centre, European Commission, Ispra, Italy.

出版信息

Toxicol In Vitro. 2017 Dec;45(Pt 2):233-240. doi: 10.1016/j.tiv.2016.10.007. Epub 2016 Oct 14.

Abstract

The Virtual Cell Based Assay (VCBA) was applied to simulate the long-term (repeat dose) toxic effects of chemicals, including substances in cosmetics and personal care products. The presented model is an extension of the original VCBA for simulation of single exposure and is implemented in a KNIME workflow. This work illustrates the steps taken to simulate the repeated dose effects of two reference compounds, caffeine and amiodarone. Using caffeine, in vitro experimental viability data in single exposure from two human liver cell lines, HepG2 and HepaRG, were measured and used to optimize the VCBA, subsequently repeated exposure simulations were run. Amiodarone was then tested and simulations were performed under repeated exposure conditions in HepaRG. The results show that the VCBA can adequately predict repeated exposure experiments in liver cell lines. The refined VCBA model can be used not only to support the design of long term in vitro experiments but also practical applications in risk assessment. Our model is a step towards the development of in silico predictive approaches to replace, refine, and reduce the in vivo repeated dose systemic toxicity studies in the assessment of human safety.

摘要

基于虚拟细胞的检测方法(VCBA)被应用于模拟化学品的长期(重复剂量)毒性效应,包括化妆品和个人护理产品中的物质。所提出的模型是原始 VCBA 的扩展,用于模拟单次暴露,并在 KNIME 工作流程中实现。本工作说明了模拟两种参考化合物,咖啡因和胺碘酮的重复剂量效应所采取的步骤。使用咖啡因,测量了来自两种人源肝细胞系 HepG2 和 HepaRG 的单次暴露的体外实验存活率数据,并用于优化 VCBA,随后进行了重复暴露模拟。然后测试了胺碘酮,并在 HepaRG 中进行了重复暴露条件下的模拟。结果表明,VCBA 可以充分预测肝细胞系中的重复暴露实验。经过改进的 VCBA 模型不仅可用于支持长期体外实验的设计,还可用于风险评估中的实际应用。我们的模型是朝着开发计算机预测方法迈出的一步,以替代、改进和减少在评估人类安全性时重复剂量全身毒性的体内研究。

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