Photocatalytic remediation represents a potential sustainable solution to the abatement of xenobiotic pollutants released within the water environment. Aeroxide® P25 titanium dioxide nanoparticles (TiO2 NPs) are well-known as one of the most efficient photocatalysts in several applications, and have also been investigated in water remediation as suspended powder. Recently, their application in the form of thin films has been revealed as a potential alternative to avoid time-consuming filtration processes. Polymers represent suitable substrates to immobilize TiO2 NPs, allowing further production of thin films that can be exploited as a photoactive coating for environmental remediation. Nevertheless, the methods adopted to immobilize TiO2 NPs on polymer matrix involve time-consuming procedures and the use of several reactants. Here, titanium dioxide-based nanocomposites (NCx) were obtained through a new approach based on Methyl Methacrylate in situ bulk polymerization and were compared with a blended mixture (BL). Their morphology and chemical–physical properties were investigated through Thermogravimetric Analysis (TGA), Differential Scanning Calorimetry (DSC), UV–Vis, and Raman spectroscopies. It was revealed that the in situ approach deeply influences the chemical–physical interactions between the polymer matrix and TiO2 NPs. Photocatalytic experiments revealed the boosted photodegradation activity of NCx thin films, induced by the in situ approach. The photodegradation of paraquat and acetaminophen was also ascertained.
Nanocomposites obtained by the decoration of graphene-based materials with silver nanoparticles (AgNPs) have received increasing attention owing to their antimicrobial activity. However, the complex synthetic methods for their preparation have limited practical applications. This study aims to synthesize novel NanoHybrid Systems based on graphene, polymer, and AgNPs (namely, NanoHy-GPS) through an easy microwave irradiation approach free of reductants and surfactants. The polymer plays a crucial role, as it assures the coating layer/substrate compatibility making the platform easily adaptable for a specific substrate. AgNPs’ loading (from 5% to 87%) can be tuned by the amount of Silver salt used during the microwave-assisted reaction, obtaining spherical AgNPs with average sizes of 5–12 nm homogeneously distributed on a polymer-graphene nanosystem. Interestingly, microwave irradiation partially restored the graphene sp2 network without damage of ester bonds. The structure, morphology, and chemical composition of NanoHy-GPS and its subunits were characterized by means of UV-vis spectroscopy, thermal analysis, differential light scattering (DLS), Field Emission Scanning Electron Microscopy (FE-SEM), Energy Dispersive X-ray analysis (EDX), Atomic Force Microscopy (AFM), and High-Resolution Transmission Electron Microscopy (HRTEM) techniques. A preliminary qualitative empirical assay against the typical bacterial load on common hand-contacted surfaces has been performed to assess the antibacterial properties of NanoHy-GPS, evidencing a significative reduction of bacterial colonies spreading.
A recent approach in the treatment of diseased cells/ tissues is the use of smart, stimuli-responsive nanomaterials. Wellknown examples include photosensitizer agents that after light irradiation at a specific wavelength generate singlet oxygen species (strongly cytotoxic) or self-assembled supramolecular structures, which blow up cancer cells by releasing their payload upon an external stimulus, thus making cancer cells swell and burst (so-called "nanobombs"). In this work we synthesized and characterized a polymeric star-like pentaporphyrin system (5P) that, depending on the photoexcitation wavelength selected, can act either as a photosensitizer or as a nanobomb. The 5P compound was characterized by using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, nuclear magnetic resonance, UV−vis, and fluorescence spectroscopy techniques. The hydrodynamic size of the 5P compound in physiological buffer solution, as determined by dynamic light spectroscopy, pointed to the formation of aggregates. The toxicity and the blow-up capability of 5P were tested on human neuroblastoma (SH-SY5Y cell line). Results demonstrated that the 5P system can work as a light-triggered nanobomb for targeted cell death. In fact, while the cell's treatment with the compound in the darkness did not induce cell toxicity, the 5P irradiation with laser light at wavelengths of 458 or 405 nm resulted in the generation of singlet oxygen species or a true explosion in a cellular environment, respectively.
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