Pristine, carboxylated, and hybrid multi-walled carbon nanotubes exert potent antioxidant activities in in vitro-cell free systems.

Multi-walled carbon nanotubes (MWCNTs) are tubular-shaped carbon allotropes, composed of multiple concentric graphene cylinders. The extended systems of conjugated double bonds, that MWCNTs are constituted by, provide them with high electron affinities, enabling them to act as electron donors or acceptors. Consequently, their potential biomedical applications, as synthetic antioxidant agents, are of particular interest. Based on the above, the purpose of the present study was to evaluate the intrinsic antioxidant properties of pristine and carboxylated MWCNTs, as well as of novel hybrid nanocomposites of MWCNTs and inorganic nanoparticles. To this end, after the synthesis and characterization of MWCNTs, their antiradical, reducing, and antigenotoxic properties were assessed in cell-free assays, using a methodological approach that has been recently proposed by our research group. According to our results, most of the tested MWCNTs exhibited strong antioxidant activities. More elaborately, the hybrid material of MWCNTs and ferrous oxide nanoparticles, i.e., CNTs@Fe3O4, showed robust scavenging capacities in all free-radical scavenging assays examined. As regards reducing properties, the pristine MWCNTs, i.e., CNTs-Ref, exhibited the greater electron donating capacity. Finally, in terms of antigenotoxic properties, the hybrid material of MWCNTs and silicon carbide nanoparticles, i.e., CNTs@SiC, exhibited potent ability to inhibit the formation of peroxyl radicals, thus preventing from the oxidative DNA damage. Conclusively, our findings suggest that the MWCNTs of the study could be considered as promising broad-spectrum antioxidants, however, further investigations are required to evaluate their toxicological profile in cell-based and in vivo systems.

Toxicity assessment of core-shell and superabsorbent polymers in cell-based systems.

The identification of health risks arising from occupational exposure to submicron/nanoscale materials is of particular interest and toxicological investigations designed to assess their hazardous properties can provide valuable insights. The core-shell polymers poly (methyl methacrylate)@poly (methacrylic acid-co-ethylene glycol dimethacrylate) [PMMA@P (MAA-co-EGDMA)] and poly (n-butyl methacrylate-co-ethylene glycol dimethacrylate)@poly (methyl methacrylate) [P (nBMA-co-EGDMA)@PMMA] could be utilized for the debonding of coatings and for the encapsulation and targeted delivery of various compounds. The hybrid superabsorbent core-shell polymers poly (methacrylic acid-co-ethylene glycol dimethacrylate)@silicon dioxide [P (MAA-co-EGDMA)@SiO2] could be utilized as internal curing agents in cementitious materials. Therefore, the characterization of their toxicological profile is essential to ensure their safety throughout manufacturing and the life cycle of the final products. Based on the above, the purpose of the present study was to assess the acute toxic effects of the above mentioned polymers on cell viability and on cellular redox state in EA. hy926 human endothelial cells and in RAW264.7 mouse macrophages. According to our results, the examined polymers did not cause any acute toxic effects on cell viability after any administration. However, the thorough evaluation of a panel of redox biomarkers revealed that they affected cellular redox state in a cell-specific manner. As regards EA. hy926 cells, the polymers disrupted redox homeostasis and promoted protein carbonylation. Concerning RAW264.7 cells, P (nBMA-co-EGDMA)@PMMA caused disturbances in redox equilibrium and special emphasis was placed on the triphasic dose-response effect detected in lipid peroxidation. Finally, P (MAA-co-EGDMA)@SiO2 activated cellular adaptive mechanisms in order to prevent from oxidative damage.

Smart Composite Materials with Self-Healing Properties: A Review on Design and Applications.

Research on self-healing materials spans multiple academic disciplines and employs a variety of methodologies. Nature has been a major source of inspiration for developing self-healing materials and will likely continue to inspire innovative ideas in this field. This review article covers the principles of self-healing mechanisms, focusing on both autonomous and non-autonomous procedures. It explores both intrinsic and extrinsic self-healing abilities by considering their components, structures, and design. Additionally, a detailed analysis of the application of these materials across various sectors is provided, including aerospace, automotive, marine, energy, medical and healthcare, military, and construction. Finally, the review paper highlights the advancements in encapsulation technologies for microcapsules, their thermal stability, their mechanical properties, and the compatibility of healing agents with the matrix, which play a crucial role in the effectiveness of self-healing processes.

Triggerable Super Absorbent Polymers for Coating Debonding Applications.

This study aims to examine how core-shell super absorbent polymers (SAPs) can be effective in relation to recycling processes by using them as triggerable materials in coating binders. Super absorbent polymers are partially cross-linked, three-dimensional polymer networks that can absorb and retain water. Coatings based on an acrylic binder, including SAPs, were applied onto plastic substrates of acrylonitrile-butadiene-styrene/polycarbonate. The incorporation of 1 wt.% and 5 wt.% SAPs into the coatings resulted in the debonding of the coatings from the substrates under a steam treatment. The trigger mechanism for the core-shell hydrophilic SAPs relies on the different abilities of the core and shell materials to be swollen. Therefore, under the influence of steam, SAPs can enhance their shape due to water absorption and the breaking of the inorganic shell. This results in the reduction of the attachment between the primer layer and both the top coating and the substrate, thus enabling the detachment of the top coating from the corresponding substrate. The obtained results from this study can be considered as potential formulations for plastic recycling applications in industries.

Encapsulation and release of corrosion inhibitors into titania nanocontainers.

Titania nanocontainers were synthesized through a two-step process and then loaded with 8-hydroxyquinoline (8-HQ) and p-toluenesulfonic acid (p-TSA). The size of the containers was 242 +/- 10 nm as determined by Scanning Electron Microscopy (SEM). X-Ray Diffraction Analysis (XRD) showed that the titania nanocontainers consist of anatase and rutile crystalline phases. The presence of 8-HQ and p-TSA in the nanocontainers was confirmed with Fourier Transform Infrared Spectroscopy (FT-IR). The loading of the inhibitors in the nanocontainers was estimated with Thermo Gravimetric Analysis (TGA). The loading amount of 8-HQ is 3.56% w/w and that of p-TSA is 6.13%. Based on the size of the nanocontainers and the assumption that they are not broken, the amount of approximately with 2.83 x 10(6) molecules of 8-HQ and 3.86 x 10(6) molecules of p-TSA per nanocontainer was estimated. Furthermore, release studies of 8-HQ and p-TSA in a corrosive environment were studied by potentiodynamic measurements showing that the inhibitors are released from the nanocontainers, suppressing the corrosion activities. SEM and Dynamic Light Scattering (DLS) measurements confirmed that the nanocontainers are not agglomerated and keep their shape after suspension in 0.5 M NaCI solution for more than 72 hours.