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Physiologically-based Pharmacokinetic (PBPK) Model of TiO_2 Nanoparticles' Bio-distribution in Rat Tissues

机译:TiO_2纳米粒子在大鼠组织中的生物分布的基于生理的药代动力学(PBPK)模型

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The emerging of nanotechnology has increasingly gained expansions and applications in various materials science research and development. However, the exposure to nanoparticles and engineered nanomaterials can lead to adverse biological effects because the small sizes of nanoparticles can enter the human body and deposit in the organs or translocate from the intake area to the secondary organs and can cause inflammation. One of the most used nanoparticles is TiO_2, which is commonly found in skin care and household products. It is still unclear how TiO_2 nanoparticles are remained in human bodies after exposing. In the present study, we develop a physiologically-based pharmacokinetic (PBPK) model to predict the bio-distribution of TiO_2 concentrations in rat tissues. The model is validated with an existing in-vivo study in rats. We also extend our PBPK model to predict cell death caused by TiO_2 nanoparticles in the rat liver using a dose-response model. The dose-response model accounts for the interplay between the cellular accumulation of TiO_2 due to cell's particle uptake and the dilution of TiO_2 due to cell division. Our developing framework, which can be scaled-up to understand the effects in human system, has a potential to provide the health risk data and to help regulate the human exposure to TiO_2 nanoparticles.
机译:纳米技术的兴起已在各种材料科学研究和开发中得到越来越多的扩展和应用。但是,暴露于纳米颗粒和工程纳米材料会导致不利的生物学影响,因为小尺寸的纳米颗粒会进入人体并沉积在器官中,或从摄入区域转移到次级器官,并可能引起炎症。最常用的纳米颗粒之一是TiO_2,它通常在皮肤护理和家用产品中发现。暴露后仍不清楚TiO_2纳米粒子如何保留在人体中。在本研究中,我们开发了一种基于生理的药代动力学(PBPK)模型,以预测TiO_2浓度在大鼠组织中的生物分布。该模型已在大鼠中进行了一项现有的体内研究验证。我们还使用剂量反应模型扩展了PBPK模型,以预测由TiO_2纳米颗粒引起的大鼠肝脏细胞死亡。剂量反应模型解释了由于细胞颗粒吸收引起的TiO_2细胞积累与由于细胞分裂引起的TiO_2稀释之间的相互作用。我们正在开发的框架可以扩大规模以了解对人体系统的影响,有潜力提供健康风险数据并帮助调节人类对TiO_2纳米粒子的暴露。

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