The application of polymer “brushes”, with their unique physicochemical properties, has led to a radical change in the way we functionalize biomaterials or formulate hybrids; however, their attractive traits can be largely surpassed by applying different polymer topologies, beyond the simple linear chain. Cyclic and loop brushes provide enhanced steric stabilization, improved biopassivity, and lubrication compared to their linear analogues. Focusing on poly­(2-ethyl-2-oxazoline) (PEOXA), an emerging polymer in nanobiotechnology, we systematically investigate how topology effects determine the structure of PEOXA brushes and to what extent technologically relevant properties such as protein resistance, nanomechanics, and nanotribology can be tuned by varying brush topology. The highly compact structure of cyclic PEOXA brushes confers an augmented entropic barrier to the surface, efficiently hindering unspecific interactions with biomolecules. Moreover, the intrinsic absence of chain ends at the cyclic-brush interface prevents interdigitation when two identical polymer layers are sheared against each other, dramatically reducing friction. Loop PEOXA brushes present structural and interfacial characteristics that are intermediate between those of linear and cyclic brushes, which can be precisely tuned by varying the relative concentration of loops and tails within the assembly. Such topological control allows biopassivity to be progressively increased and friction to be tuned.

Surface-initiated Cu(0)-mediated controlled radical polymerization (Si-CuCRP) can be successfully applied to fabricate poly[(oligoethylene glycol)methyl ether methacrylate] (POEGMA) brushes in one pot, presenting a grafting-density gradient across the surface. This is achieved by continuously varying the distance (d) between a copper plate, used as a source of Cu species, and the initiator-functionalized substrate. X-ray photoelectron spectroscopy (XPS) analysis of monolayers of Cu Iselective ligands demonstrates that a higher concentration of activator species diffuses to the initiating substrate in areas closer to the copper plate, a progressive decrease in activator concentration being observed upon increasing the distance between the two surfaces. As confirmed by the SI-CuCRP kinetics measured at different positions along the gradient, radical-termination reactions between propagating chains limit the grafting density of POEGMA grafts where the diffusion of activators is favored (i.e., at d → 0). This effect decreases with increasing d, ultimately yielding a gradual variation of POEGMA grafting density across the substrate. We have investigated the influence of grafting-density variation across the gradient on the swelling of POEGMA brushes as well as on their nanomechanical and nanotribological properties, measured by a combination of variable angle spectroscopic ellipsometry (VASE), colloidal-probe atomic force microscopy (CP-AFM), and lateral force microscopy (LFM). The results of these tests highlight how loosely grafted POEGMA chains incorporating a substantial amount of water can be significantly deformed by a shearing AFM probe, exhibit relatively high friction, and generate friction-vs-load (F f −L) profiles that follow a sublinear trend described by a Johnson− Kendall−Roberts (JKR) modeltypical of deformable films of high surface energy. In contrast, more densely packed POEGMA brushes incorporate less solvent and display very low friction, with F f −L data following a linear progression according to Amontons' law.

The introduction of different types and concentrations of crosslinks within poly(hydroxyethyl methacrylate) (PHEMA) brushes influences their interfacial, physicochemical properties, ultimately governing their adsorption of proteins. PHEMA brushes and brush-hydrogels were synthesized by surface-initiated, atom-transfer radical polymerization (SI-ATRP) from HEMA, with and without the addition of di(ethylene glycol) dimethacrylate (DEGDMA) or tetra(ethylene glycol) dimethacrylate (TEGDMA) as crosslinkers. Linear (pure PHEMA) brushes show high hydration and low modulus and additionally provide an efficient barrier against nonspecific protein adsorption. In contrast, brush-hydrogels are stiffer and less hydrated, and the presence of crosslinks affects the entropy-driven, conformational barrier that hinders the surface interaction of biomolecules with brushes. This leads to the physisorption of proteins at low concentrations of short crosslinks. At higher contents of DEGDMA or in the presence of longer TEGDMA-based crosslinks, brush-hydrogels recover their antifouling properties due to the increase in interfacial water association by the higher concentration of ethylene glycol (EG) units.

Covalent crosslinking of weak polyelectrolyte brushes widens the tuning potential for their swelling, nanomechanical, and nanotribological properties, which can be simultaneously adjusted by varying the crosslinker content and the pH of the surroundings. We demonstrate that this is especially valid for poly­(hydroxyethyl methacrylate) (PHEMA) brushes and brush hydrogels, and their ionizable, succinate-modified derivatives (PHEMA-SA), covalently crosslinked with different amounts of di­(ethylene glycol) dimethacrylate (DEGDMA) during surface-initiated atom transfer radical polymerization (SI-ATRP). Atomic force microscopy (AFM) methods highlight how pristine PHEMA films are stiff and display high coefficients of friction in water. Their succinate derivatives swell profusely in aqueous media. Under acidic conditions they are neutral, compliant, and lubricious, with apparent Young’s moduli (E*) lying between 10 and 30 kPa. Their contact mechanical behavior can be described by either the Johnson–Kendall–Roberts (JKR) or the Derjaguin–Müller–Toporov (DMT) model, depending on crosslinker content. In contrast, under basic conditions, brushes and brush hydrogels become charged, expand, and present a rigid, electrostatic barrier toward the AFM probe. Friction is extremely low at relatively low applied loads, whereas it increases at higher loads, to an extent that is regulated by the number of crosslinks within the films.

Despite the wide range and versatility of polymer-grafting methods to produce biopassive interfaces, commonly applied polymer brushes suffer from an intrinsic lack of long-term stability when incubated in aqueous media under physiological conditions. The robustness of brush films in such environments can be greatly improved by applying a hydrophobic, "protecting" layer

The affinity of surfaces toward proteins is found to be a key parameter to govern the synthesis of polymer brushes by surface-initiated biocatalytic atom transfer radical polymerization (SI-bioATRP). While the "ATRPase" hemoglobin (Hb) stimulates only a relatively slow growth of protein repellent brushes, the synthesis of thermoresponsive grafts can be regulated by switching the polymer's attraction toward proteins across its lower critical solution temperature (LCST). Poly(N-isopropylacrylamide) (PNIPAM) brushes are synthesized in discrete steps of thickness at temperatures above LCST, while the biocatalyst layer is refreshed at T< LCST. Multistep surface-initiated biocatalytic ATRP demonstrates a high degree of control, results in high chain end group fidelity and enables the synthesis of multiblock copolymer brushes under fully aqueous conditions. The activity of Hb can be further modulated by tuning the accessibility of the heme pocket within the protein. Hence, the multistep polymerization is accelerated at acid pH, where the enzyme undergoes a transition from its native to a molten globule conformation. The controlled synthesis of polymer brushes by multistep SI-bioATRP highlights how a biocatalytic synthesis of grafted polymer films can be precisely controlled through the modulation of the polymer's interfacial physicochemical properties, in particular of the affinity of the surface toward proteins. This is not only of importance to gain a predictive understanding of surface-confined enzymatic polymerizations, but also represents a new way to translate bioadhesion into a controlled functionalization of materials.

The interaction between weak polyacid brushes and metal ions can lead to the formation of a wide variety of complex structures across the polymer grafts. In the case of poly­(hydroxyethyl methacrylate) brushes derivatized with succinate side groups (PHEMA-SA), the coordination with Zn2+ or Ca2+ species can be tuned by varying the solution pH, below and above the pK a of the polyacid brush. Attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) indicates that Zn2+ ions generate relatively weak, localized monodentate bridges along PHEMA-SA grafts at basic pH. These Zn2+–brush conjugates swell profusely in water, are compliant and very lubricious, as observed by combining variable angle spectroscopic ellipsometry (VASE), quartz crystal microbalance with dissipation (QCM-D), and atomic force microscopy (AFM) methods. In contrast, incubation of PHEMA-SA brushes with Ca2+ or Zn2+ at acidic pH leads to the formation of more extended, bidentate linkages forming a physical network between the metal centers and the surrounding grafts. This type of coordination causes brush dehydration and the stiffening of the films, as well as high friction, due to the energy dissipation required to perturb the dense, brush physical network by the shearing AFM probe. Regulating the interaction between metal ions and ionizable polymer brushes emerges as a versatile and easily accessible tool to control the interfacial properties of grafted polymer films. The achieved modulation of nanomechanical and nanotribological characteristics is technologically relevant, in that it allows both function and performance to be tuned for widely applicable polymer coatings.

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