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Comparison of the internalization of targeted dendrimers and dendrimer-entrapped gold nanoparticles into cancer cells

机译:比较目标树枝状聚合物和树枝状聚合物包埋的金纳米粒子进入癌细胞

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摘要

Dendrimer-based nanotechnology significantly advances the area of targeted cancer imaging and therapy. Herein, we compared the difference of surface acetylated fluorescein isocyanate (FI) and folic acid (FA) modified generation 5 (G5) poly(amidoamine) dendrimers (G5.NHAc-FI-FA), and dendrimer-entrapped gold nanoparticles with similar modifications ([(Au 0 ) 51.2 -G5.NHAc-FI-FA]) in terms of their specific internalization to FA receptor (FAR)-overexpressing cancer cells. Confocal microscopic studies show that both G5.NHAc-FI-FA and [(Au 0 ) 51.2 -G5.NHAc-FI-FA] exhibit similar internalization kinetics regardless of the existence of Au nanoparticles (NPs). Molecular dynamics simulation of the two different nanostructures reveals that the surface area and the FA moiety distribution from the center of the geometry are slightly different. This slight difference may not be recognized by the FARs on the cell membrane, consequently leading to similar internalization kinetics. This study underlines the fact that metal or inorganic NPs entrapped within dendrimers interact with cells in a similar way to that of dendrimers lacking host NPs. © 2009 Wiley Periodicals, Inc. Biopolymers 91: 936–942, 2009. This article was originally published online as an accepted preprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at biopolymers@wiley.com
机译:基于树状聚合物的纳米技术极大地推动了靶向癌症成像和治疗领域的发展。在这里,我们比较了表面乙酰化的荧光素异氰酸酯(FI)和叶酸(FA)修饰的第5代(G5)聚(酰胺基胺)树状聚合物(G5.NHAc-FI-FA)和包裹有树状聚合物的金纳米颗粒的区别([(Au 0)51.2 -G5.NHAc-FI-FA])在它们对过表达FA受体(FAR)的癌细胞的特异性内在化方面。共聚焦显微镜研究表明,无论存在Au纳米颗粒(NPs),G5.NHAc-FI-FA和[(Au 0)51.2 -G5.NHAc-FI-FA]都显示出相似的内在动力学。两种不同的纳米结构的分子动力学模拟表明,从几何中心开始的表面积和FA部分的分布略有不同。细胞膜上的FAR可能无法识别出这种细微的差异,因此导致相似的内在动力学。这项研究强调了这样一个事实,即树枝状聚合物中截留的金属或无机NP与细胞相互作用的方式与缺乏宿主NP的树枝状聚合物类似。 ©2009 Wiley Periodicals,Inc.生物聚合物91:936-942,2009。本文最初在线发布为可接受的预印本。 “在线发布”日期对应于预印本版本。您可以通过发送电子邮件至生物聚合物编辑部biopolymers@wiley.com索取预印本的副本。

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