| Literature DB >> 28294482 |
Giulia Morgese1,2, Behzad Shirmardi Shaghasemi3, Valerio Causin4, Marcy Zenobi-Wong2, Shivaprakash N Ramakrishna1, Erik Reimhult3, Edmondo M Benetti1.
Abstract
Cyclic poly-2-ethyl-2-oxazoline (PEOXA) ligands for superparamagnetic Fe3 O4 nanoparticles (NPs) generate ultra-dense and highly compact shells, providing enhanced colloidal stability and bio-inertness in physiological media. When linear brush shells fail in providing colloidal stabilization to NPs, the cyclic ones assure long lasting dispersions. While the thermally induced dehydration of linear PEOXA shells cause irreversible aggregation of the NPs, the collapse and subsequent rehydration of similarly grafted cyclic brushes allow the full recovery of individually dispersed NPs. Although linear ligands are densely grafted onto Fe3 O4 cores, a small plasma protein such as bovine serum albumin (BSA) still physisorbs within their shells. In contrast, the impenetrable entropic shield provided by cyclic brushes efficiently prevents nonspecific interaction with proteins.Entities:
Keywords: core-shell nanoparticles; polymer brushes; polymer topology; polyoxazolines; surface functionalization
Year: 2017 PMID: 28294482 DOI: 10.1002/anie.201700196
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336