The composition of temperature‐responsive copolymer brushes based on oligo(ethylene glycol) methacrylates is tuned to obtain a collapse temperature of ∼35 °C. The chains are grafted by antibacterial magainin I peptide, whose activity is tested at different temperatures against various bacteria. The brushes switch from bactericidal to cell‐repellent below and slightly above 35 °C, respectively, due to the progressive vertical collapse of the brush.

Silica and paramagnetic silica microparticles are surface-modified by an antibacterial macromolecular coating. For this, a hydrophilic copolymer brush based on oligo(ethylene glycol) methacrylates is grown on the particle surface by surface-initiated ATRP. Then, Magainin-I, a natural antimicrobial peptide, is grafted onto the hydroxyl groups of the brush through a heterolinker. The grafting of the peptide is evidenced by fluorescence microscopy and X-ray photoelectron spectroscopy. Moreover, culturability and viability assays performed in the presence of the magainin-grafted particles prove their bactericidal properties. The rapid recovery of the bactericidal particles based on paramagnetic silica and suspended in solution is shown under magnetization. Such particles offer the advantage to treat efficiently various sensitive aqueous solutions while avoiding any dissemination of bactericidal substances in the environment. As a consequence, they are of a great interest for various applications in medical, cosmetic, or biomedical fields.

A new and facile strategy for grafting IONPs by phosphonic acic terminated PC brushes has been demonstrated and characterized in vitro.

Polyethylene glycol (PEG) is a gold standard against protein fouling. However, recent studies have revealed surprising adverse effects of PEG, namely its immunogenicity and shortened bio-circulation upon repeated dosing. This highlights a crucial need to further examine 'stealth' polymers for controlling the protein 'corona', a new challenge in nanomedicine and bionanotechnology. Poly(2-ethyl-2-oxazoline) (PEtOx) is another primary form of stealth polymer that, despite its excellent hydrophilicity and biocompatibility, has found considerably less applications compared with PEG. Herein, we performed label-free proteomics to compare the associations of linear PEG- and PEtOx-grafted nano-graphene oxide (nGO) sheets with human plasma proteins, complemented by cytotoxicity and haemolysis assays to compare the cellular interactions of these polymers. Our data revealed that nGO-PEG enriched apolipoproteins, while nGO-PEtOx displayed a preferred binding with pro-angiogenic and structural proteins, despite high similarities in their respective top-10 enriched proteins. In addition, nGO-PEG and nGO-PEtOx exhibited similar levels of enrichment of complement proteins. Both PEG and PEtOx markedly reduced nGO toxicity to HEK 293 cells while mitigating nGO haemolysis. This study provides the first detailed profile of the human plasma protein corona associated with PEtOx-grafted nanomaterials and, in light of the distinctions of PEtOx in chemical adaptability, in vivo clearance and immunogenicity, validates the use of PEtOx as a viable stealth alternative to PEG for nanomedicines and bionanotechnologies.