期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 53, 期 20, 页码 5093-5096出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201309464
关键词
cell targeting; nanoparticles; PEGylation; polymers; surface chemistry
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.
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