纳米医学
表面改性
纳米颗粒
聚乙二醇化
材料科学
纳米技术
量子点
硅烷
赫拉
内吞作用
胶体
配体(生物化学)
生物分子
组合化学
化学工程
化学
有机化学
细胞
聚乙二醇
受体
生物化学
工程类
复合材料
作者
Emile Drijvers,Jing Liu,Aranit Harizaj,Ulrich Wiesner,Kevin Braeckmans,Zeger Hens,Tangi Aubert
标识
DOI:10.1021/acsami.9b12398
摘要
PEGylation, which has traditionally been the method of choice to enhance the colloidal stability of nanostructures designed for biological applications and to prevent nonspecific protein adsorption, is now being challenged by short zwitterionic ligands. Inspired by the zwitterionic nature of cell membranes, these ligands have the potential to push forward the field of nanoparticles for nanomedicine. In this work, we report a thorough analysis of the surface chemistry of silica-coated luminescent CdSe/CdS quantum dots functionalized with either PEG-silane or zwitterionic sulfobetaine-silane by quantitative nuclear magnetic resonance spectroscopy. We demonstrate the differences in the cellular uptake propensity between particles with these two ligands. Although both ligands offer good colloidal stability in a crowded cell culture medium, the zwitterionic-functionalized nanoparticles with an optimized ligand density showed to be more easily endocytosed by HeLa cells. This approach can readily be transferred to other nanoparticle systems offering a wealth of unique properties, with great potential for intracellular bioapplications.
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