Developing smart, environmentally friendly, and effective antibacterial surfaces is fundamental to contrast the diffusion of human infections and diseases for applications in the biomedical and food packaging sectors. To this purpose, here we combine aluminum-doped zinc oxide (AZO) and Ag to grow nanostructured composite coatings on bioplastic polylactide (PLA) substrates. The AZO layers are grown by RF magnetron sputtering, and then functionalized with Ag in atomic form by RF magnetron sputtering and in form of nanoparticles by supersonic cluster beam deposition. We compare the morphology, wettability, and antimicrobial performance of the nanostructured coatings obtained by the two methods. The different growth modes in the two techniques used for Ag functionalization are found to produce some differences in the surface morphology, which, however, do not induce significant differences in the wettability and antimicrobial response of the coatings. The antibacterial activity is investigated against Escherichia coli and Staphylococcus aureus as representatives of Gram-negative and Gram-positive bacteria, respectively. A preferential antimicrobial action of Ag on the first species and of AZO on the second one is evidenced. Through their combination, we obtain a hybrid composite coating taking advantage of the synergistic dual action of the two materials deposited, with a total bacterial suppression within few minutes for the first species and few hours for the second one, thus representing a valuable solution as a wide-spectrum bactericidal device.

Nanostructured materials may provide a route to overcome the electrode-limiting performance in water splitting, the oxygen evolution reaction (OER), within the framework of low-cost catalysts search. However, for alloyed NiFe nanostructures, the relationship among the OER efficiency and the electrode physical characteristics (morphology, porosity, size, thickness, or mass loading) is largely unknown. This work introduces a new type of alloyed NiFe (90/10% at) nanogranular electrodes obtained by supersonic cluster beam deposition and investigates the dependence of their catalytic activity toward the OER on the film morphological and stoichiometric properties. The synthesized alloyed NiFe nanoparticles with 0.3–3.8 nm size assemble from the gas phase to form ultrathin film electrodes with thickness in the 15–88 nm range, corresponding to 5–30 μg/cm2 mass loading. The fitting of the optical spectroscopic data by an effective medium approximation model suggests that, independent of the thickness, the films have a 20% porosity and are completely hydroxydated. The resulting catalytic efficiency is independent on the film thickness, while the turnover frequency decreases with increasing electrode loading. These data suggest that an excess of catalyst mass with respect to the OER active sites is deposited in the case of thicker electrodes and sets the 15 nm film as an upper loading limit to maximize the electrocatalyst efficiency. This study represents a crucial step toward thickness optimization of NiFe electrodes to fabricate low-cost OER catalysts.

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IntroductionAs we approach the post-antibiotic era, the development of innovative antimicrobial strategies that carry out their activities through non-specific mechanisms could limit the onset and spread of drug resistance. In this context, the use of nanogranular coatings of multielement nanoparticles (NPs) conjugated to the surface of implantable biomaterials might represent a strategy to reduce the systemic drawbacks by locally confining the NPs effects against either prokaryotic or eukaryotic cells.MethodsIn the present study, two new multielement nanogranular coatings combining Ag and Cu with either Ti or Mg were synthesized by a gas phase physical method and tested against pathogens isolated from periprosthetic joint infections to address their potential antimicrobial value and toxicity in an in vitro experimental setting.ResultsOverall, Staphylococcus aureus, Staphylococcus epidermidis and Escherichia coli displayed a significantly decreased adhesion when cultured on Ti-Ag-Cu and Mg-Ag-Cu coatings compared to uncoated controls, regardless of their antibiotic resistance traits. A dissimilar behavior was observed when Pseudomonas aeruginosa was cultured for 30 and 120 minutes upon the surface of Ti-Ag-Cu and Mg-Ag-Cu-coated discs. Biofilm formation was mainly reduced by the active effect of Mg-Ag-Cu compared to Ti-Ag-Cu and, again, coatings had a milder effect on P. aeruginosa, probably due to its exceptional capability of attachment and matrix production. These data were further confirmed by the evaluation of bacterial colonization on nanoparticle-coated discs through confocal microscopy. Finally, to exclude any cytotoxic effects on eukaryotic cells, the biocompatibility of NPs-coated discs was studied. Results demonstrated a viability of 95.8% and 89.4% of cells cultured in the presence of Ti-Ag-Cu and Mg-Ag-Cu discs, respectively, when compared to negative controls.ConclusionIn conclusion, the present study demonstrated the promising anti-adhesive features of both Ti-Ag-Cu and Mg-Ag-Cu coatings, as well as their action in hampering the biofilm formation, highlighting the safe use of the tested multi-element families of nanoparticles as new strategies against bacterial attachment to the surface of biomedical implants.

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