| Literature DB >> 24700480 |
Qin Dai1, Carl Walkey, Warren C W Chan.
Abstract
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.Entities:
Keywords: PEGylation; cell targeting; nanoparticles; polymers; surface chemistry
Mesh:
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Year: 2014 PMID: 24700480 DOI: 10.1002/anie.201309464
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336