Size-Dependent Nanoparticle Uptake by Endothelial Cells in a Capillary Flow System

Patrick L. Jurney, Rachit Agarwal, K. Roy, S. Sreenivasan, Li Shi
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引用次数: 3

Abstract

An in vitro cell culture system is developed for studying the uptake characteristics of nanoparticles (NPs) by endothelial cells under shear stress. Results show that the smaller polystyrene nanospheres are uptaken more than larger nanospheres for sizes ranging from 100 nm to 500 nm for 12, 24, and 48 hrs delivery times. While the result is similar to that found in static cultures, the observed trend is different from NP delivery behaviors to a simple glass surface in a flow, where no clear size dependence was observed because of repulsive electrostatic force on marginating NPs. The trend is also opposite to the behavior found in another study of the adhesion of labeled particles onto endothelial cells in whole blood flow. The comparison shows that the reduced zeta potential of NPs in a serum-containing cell medium and particle removal by cells results in reduced repulsive electrostatic force on marginating NPs. Consequently, the uptake behaviors are dominated by Brownian diffusion and cell membrane deformation process, which favor the uptake of NPs with reduced sizes.
毛细管流动系统中内皮细胞对纳米颗粒的摄取
为研究内皮细胞在剪切应力作用下对纳米颗粒的吸收特性,建立了体外细胞培养系统。结果表明,在100 ~ 500 nm范围内,较小的聚苯乙烯纳米球在12、24和48小时的递送时间内的吸收量大于较大的纳米球。虽然结果与静态培养中发现的相似,但观察到的趋势与流动中NP传递到简单玻璃表面的行为不同,在流动中,由于对边缘NP的排斥静力,没有观察到明显的尺寸依赖性。这一趋势也与另一项研究中发现的全血流中标记颗粒粘附内皮细胞的行为相反。结果表明,NPs在含血清的细胞培养基中zeta电位的降低和细胞对粒子的去除导致边缘NPs的斥力减小。因此,吸收行为主要由布朗扩散和细胞膜变形过程控制,这有利于小尺寸NPs的吸收。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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