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金纳米颗粒的尺寸和形状对siRNA纳米构建体的细胞摄取和细胞内分布的影响

Gold Nanoparticle Size and Shape Effects on Cellular Uptake and Intracellular Distribution of siRNA Nanoconstructs.

作者信息

Yue Jun, Feliciano Timothy Joel, Li Wenlong, Lee Andrew, Odom Teri W

机构信息

School of Materials Science and Engineering, Nanyang Technological University , 639798, Singapore.

出版信息

Bioconjug Chem. 2017 Jun 21;28(6):1791-1800. doi: 10.1021/acs.bioconjchem.7b00252. Epub 2017 Jun 12.

Abstract

Gold nanoparticles (AuNPs) show potential for transfecting target cells with small interfering RNA (siRNA), but the influence of key design parameters such as the size and shape of the particle core is incomplete. This paper describes a side-by-side comparison of the in vitro response of U87 glioblastoma cells to different formulations of siRNA-conjugated gold nanoconstructs targeting the expression of isocitrate dehydrogenase 1 (IDH1) based on 13 nm spheres, 50 nm spheres, and 40 nm stars. 50 nm spheres and 40 nm stars showed much higher uptake efficiency compared to 13 nm spheres. Confocal fluorescence microscopy showed that all three formulations were localized in the endosomes at early incubation times (2 h), but after 24 h, 50 nm spheres and 40 nm stars were neither in endosomes nor in lysosomes while 13 nm spheres remained in endosomes. Transmission electron microscopy images revealed that the 13 nm spheres were enclosed and dispersed within endocytic vesicles while 50 nm spheres and 40 nm stars were aggregated, and some of these NPs were outside of endocytic vesicles. In our comparison of nanoconstructs with different sizes and shapes, while holding siRNA surface density and nanoparticle concentration constant, we found that larger particles (50 nm spheres and 40 nm stars) showed higher potential as carriers for the delivery of siRNA.

摘要

金纳米颗粒(AuNPs)显示出用小干扰RNA(siRNA)转染靶细胞的潜力,但诸如颗粒核心的大小和形状等关键设计参数的影响尚不完全清楚。本文描述了U87胶质母细胞瘤细胞对基于13nm球体、50nm球体和40nm星状体的靶向异柠檬酸脱氢酶1(IDH1)表达的siRNA偶联金纳米构建体不同配方的体外反应的并排比较。与13nm球体相比,50nm球体和40nm星状体显示出更高的摄取效率。共聚焦荧光显微镜显示,在孵育早期(2小时),所有三种配方都定位于内体中,但在24小时后,50nm球体和40nm星状体既不在内体中也不在溶酶体中,而13nm球体仍在内体中。透射电子显微镜图像显示,13nm球体被包裹并分散在内吞小泡中,而50nm球体和40nm星状体聚集在一起,其中一些纳米颗粒在内吞小泡之外。在我们对具有不同大小和形状的纳米构建体的比较中,在保持siRNA表面密度和纳米颗粒浓度不变的情况下,我们发现较大的颗粒(50nm球体和40nm星状体)作为siRNA递送载体显示出更高的潜力。

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