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流量会影响纳米颗粒被内皮细胞摄取。

Flow Rate Affects Nanoparticle Uptake into Endothelial Cells.

机构信息

Institute of Biomaterials and Biomedical Engineering, University of Toronto, Toronto, Ontario, M5S 3G9, Canada.

Terrence Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario, M5S 3E1, Canada.

出版信息

Adv Mater. 2020 Jun;32(24):e1906274. doi: 10.1002/adma.201906274. Epub 2020 May 8.

Abstract

Nanoparticles are commonly administered through systemic injection, which exposes them to the dynamic environment of the bloodstream. Injected nanoparticles travel within the blood and experience a wide range of flow velocities that induce varying shear rates to the blood vessels. Endothelial cells line these vessels, and have been shown to uptake nanoparticles during circulation, but it is difficult to characterize the flow-dependence of this interaction in vivo. Here, a microfluidic system is developed to control the flow rates of nanoparticles as they interact with endothelial cells. Gold nanoparticle uptake into endothelial cells is quantified at varying flow rates, and it is found that increased flow rates lead to decreased nanoparticle uptake. Endothelial cells respond to increased flow shear with decreased ability to uptake the nanoparticles. If cells are sheared the same way, nanoparticle uptake decreases as their flow velocity increases. Modifying nanoparticle surfaces with endothelial-cell-binding ligands partially restores uptake to nonflow levels, suggesting that functionalizing nanoparticles to bind to endothelial cells enables nanoparticles to resist flow effects. In the future, this microfluidic system can be used to test other nanoparticle-endothelial cell interactions under flow. The results of these studies can guide the engineering of nanoparticles for in vivo medical applications.

摘要

纳米粒子通常通过全身注射给药,这使它们暴露于血流的动态环境中。注射的纳米粒子在血液中移动,并经历广泛的流速,这会对血管产生不同的剪切率。这些血管由内皮细胞排列,已经证明在循环过程中内皮细胞会摄取纳米粒子,但很难在体内描述这种相互作用对流动的依赖性。在这里,开发了一种微流控系统来控制纳米粒子与内皮细胞相互作用时的流速。在不同的流速下定量测定了金纳米粒子进入内皮细胞的情况,结果发现流速增加会导致纳米粒子摄取减少。内皮细胞对增加的流剪切表现出摄取纳米粒子的能力降低。如果以相同的方式剪切细胞,则随着纳米粒子流速的增加,其摄取量会减少。用内皮细胞结合配体修饰纳米粒子表面可部分恢复至非流动水平的摄取,这表明使纳米粒子功能化以与内皮细胞结合可使纳米粒子抵抗流动效应。将来,这种微流控系统可用于在流动条件下测试其他纳米粒子-内皮细胞相互作用。这些研究的结果可以指导用于体内医学应用的纳米粒子的工程设计。

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