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Current status and future perspective of computational toxicology in drug safety assessment under ontological intellection

机译:本体主义在本体主义中的药物安全评估计算毒理学现状与未来视角

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摘要

For the safety assessment of pharmaceuticals, initial data management requires accurate toxicological data acquisition, which is based on regulatory safety studies according to guidelines, and computational systems have been developed under the application of Good Laboratory Practice (GLP). In addition to these regulatory toxicology studies, investigative toxicological study data for the selection of lead compound and candidate compound for clinical trials are directed to estimation by computational systems such as Quantitative Structure-Activity Relationship (QSAR) and related expert systems. Furthermore, in the "Go" or "No-Go" decision of drug development, supportive utilization of a scientifically interpretable computational toxicology system is required for human safety evaluation. A pharmaceutical safety evaluator as a related toxicologist who is facing practical decision needs not only a data-driven Artificial Intelligence (AI) system that calls for the final consequence but also an explainable AI that can provide comprehensive information necessary for evaluation and can help with decision making. Through the explication and suggestion of information on the mechanism of toxic effects to safety assessment scientists, a subsidiary partnership system for risk assessment is ultimately to be a powerful tool that can indicate project-vector with data weight for the corresponding counterparts. To bridge the gaps between big data and knowledge, multi-dimensional thinking based on philosophical ontology theory is necessary for handling heterogeneous data for integration. In this review, we will explain the current state and future perspective of computational toxicology related to drug safety assessment from the viewpoint of ontology thinking.
机译:对于药物的安全评估,初始数据管理需要准确的毒理数据采集,这是根据指导方针的监管安全性研究,并在良好实验室实践(GLP)的应用下制定了计算系统。除了这些调节毒理学研究外,用于选择铅化合物和临床试验的候选化合物的调查毒理学研究涉及通过计算系统(例如定量结构 - 活动关系(QSAR)和相关专家系统的计算系统。此外,在药物开发的“GO”或“NO-GO”决定中,人类安全评估需要支持科学解释的计算毒理学系统的支持。作为一个有关毒理位学家的药物安全评估员不仅需要一种数据驱动的人工智能(AI)系统,可以要求最终后果,也可以提供可解释的AI,可以提供评估所需的全面信息,并可以帮助决策制作。通过对安全评估科学家有毒效应机制的信息,风险评估的子公司伙伴关系系统最终是一个强大的工具,可以指示具有对应对应物数据权重的项目 - 向量。为了弥合大数据和知识之间的差距,基于哲学本体论理论的多维思维是处理异构数据进行集成所必需的。在本综述中,从本体论思维的观点来说,我们将解释当前与药物安全评估相关的计算毒理学的视角。

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