Polyethylene Glycol Backfilling Mitigates the Negative Impact of the Protein Corona on Nanoparticle Cell Targeting

被引:312
作者
Dai, Qin [1 ,2 ]
Walkey, Carl [1 ,2 ]
Chan, Warren C. W. [1 ,2 ]
机构
[1] Univ Toronto, Inst Biomat & Biomed Engn, Terrence Donnelly Ctr Cellular & Biomol Res, Dept Chem Mat Sci & Engn, Toronto, ON M5S 3G9, Canada
[2] Univ Toronto, Dept Chem Engn, Toronto, ON M5S 3G9, Canada
关键词
cell targeting; nanoparticles; PEGylation; polymers; surface chemistry; GOLD NANOPARTICLES; QUANTUM-DOT; SIZE; DELIVERY; CHEMISTRY; MECHANISM; THERAPY;
D O I
10.1002/anie.201309464
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In protein-rich environments such as the blood, the formation of a protein corona on receptor-targeting nanoparticles prevents target recognition. As a result, the ability of targeted nanoparticles to selectively bind to diseased cells is drastically inhibited. Backfilling the surface of a targeted nanoparticle with polyethylene glycol (PEG) molecules is demonstrated to reduce the formation of the protein corona and re-establishes specific binding. The length of the backfilled PEG molecules must be less than the length of the ligand linker; otherwise, PEG interferes with the binding of the targeting ligand to its corresponding cellular receptor.
引用
收藏
页码:5093 / 5096
页数:4
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