挖掘纳米粒子数据集,在MODENA-COST行动中编译

S. Miert, Jan Creylman, G. Verheyen
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引用次数: 2

摘要

与微米尺寸的纳米材料相比,工程纳米材料(ENM)具有新的或增强的物理化学特性,但也可能具有增加的毒性潜力。动物和体外试验通常用于研究(纳米)材料的毒性作用。ENM的数量及其物理化学参数使得它不可能仅用于体内和体外测试,并且建模技术也被用于发现ENM参数与毒性之间的关系。在MODENA成本-行动联盟中编译了包含192个纳米颗粒端点信息的异构数据集。在这里,现有的数据被挖掘,以确定纳米颗粒性质和细胞死亡之间的关系,通过四种细胞毒性测定。方差分析、共线性分析、分类和回归树给出了np特性和毒性之间潜在关系的指示,但不能提供一个稳健的模型。需要更多的信息和数据点来构建经过良好验证的模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mining a Nanoparticle Dataset, Compiled Within the MODENA-COST Action
Engineered nanomaterials (ENM) have new or enhanced physico-chemical properties compared to their micron-sized counterparts, but may also have an increased toxic potential. Animal and in vitro testing are typically employed to investigate the toxic effects of (nano)materials. The sheer number of ENMs and their physico-chemical parameters make it impossible to only use in vivo and in vitro testing, and modelling technologies are also deployed to find relationships between ENM parameters and toxicity. A heterogenous dataset containing information on 192 nanoparticle endpoints was compiled within the MODENA COST-Action consortium. Here, the available data was mined to identify relationships between nanoparticle properties and cell-death as measured with four cytotoxicity assays. ANOVA, collinearity analyses and classification and regression trees gave indications on potential relations between the NP-properties and toxicity, but could not deliver a robust model. More information and datapoints are necessary to build well-validated models.
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