The use of nanoparticles (NPs) as reinforcements in polymeric coatings allows for direct interaction with the polymeric chains of the matrix, resulting in a synergistic process through physical (electrostatic forces) and chemical interactions (bond formation) for the improvement of the mechanical properties with relatively low weight concentrations of the NPs. In this investigation, different nanocomposite polymers were synthesized from the crosslinking reaction of the hydroxy-terminated polydimethylsiloxane elastomer. Different concentrations (0, 2, 4, 8, and 10 wt%) of TiO₂ and SiO₂ nanoparticles synthesized by the sol-gel method were added as reinforcing structures. The crystalline and morphological properties of the nanoparticles were determined through X-ray diffraction (XRD), Raman spectroscopy, and transmission electron microscopy (TEM). The molecular structure of coatings was through infrared spectroscopy (IR). The crosslinking, efficiency, hydrophobicity, and adhesion degree of the study groups were evaluated with gravimetric crosslinking tests, contact angle, and adhesion tests. It was observed that the crosslinking efficiency and surface adhesion properties of the different nanocomposites obtained were maintained. A slight increase in the contact angle was observed for the nanocomposites with 8 wt% compared to the polymer without reinforcements. The mechanical tests of indentation hardness and tensile strength following the ASTM E-384 and ISO 527 standards, respectively, were performed. As the nanoparticle concentration increased, a maximum increase of 157% in Vickers hardness, 71.4% in elastic modulus, and 80% in tensile strength was observed. However, the maximum elongation remained between 60 and 75%, ensuring that the composites did not become brittle.

Self-healing polymer-based coatings have emerged as a new generation of adaptive protective materials capable of restoring their structure and function after damage. This review provides a comprehensive analysis of current strategies enabling autonomous or externally triggered repair in polymeric films, including encapsulation, reversible chemistry, and microvascular network formation. Emphasis is placed on polymer–inorganic hybrid composites and vitrimeric systems, which integrate barrier protection with stimuli-responsive healing and recyclability. Comparative performance across different matrices—epoxy, polyurethane, silicone, and polyimine—is discussed in relation to corrosion protection and biomedical interfaces. The review also highlights how dynamic covalent and supramolecular interactions in hydrogels enable self-repair under physiological conditions. Recent advances demonstrate that tailoring interfacial compatibility, healing kinetics, and trigger specificity can achieve repeatable, multi-cycle recovery of both mechanical integrity and functional performance. A representative selection of published patents is also shown to illustrate recent technological advancements in the field. Finally, key challenges are identified in standardizing evaluation protocols, ensuring long-term stability, and scaling sustainable manufacturing. Collectively, these developments illustrate the growing maturity of self-healing polymer coatings as multifunctional materials bridging engineering, environmental, and biomedical applications.

The addition of nanostructures to polymeric materials allows for a direct interaction between polymeric chains and nanometric structures, resulting in a synergistic process through the physical (electrostatic forces) and chemical properties (bond formation) of constituents for the modification of their properties and potential cutting-edge materials. This study explores a novel in situ synthesis method for PDMS-%SiO₂ nanoparticle composites with varying crosslinking degrees (PDMS:TEOS of 15:1, 10:1, and 5:1); particle concentrations (5%, 10%, and 15%); and sol-gel catalysts (acidic and alkaline). This investigation delves into the distinct physical and chemical properties of silicon nanoparticles synthesized under acidic (SiO₂-a) and alkaline (SiO₂-b) conditions. A characterization through Raman, FT-IR, and XPS analyses confirms particle size and agglomeration differences between both the SiO₂-a and SiO₂-b particles. Similar chemical environments, with TEOS and ethanol by-products, were detected for both systems. The results on polymer composites elucidate the successful incorporation of SiO₂ nanoparticles into the PDMS matrix without altering the PDMS’s chemical structure. However, the presence of nanoparticles did affect the relative intensities of specific vibrational modes over composites from −35% to 24% (Raman) and from −14% to 59% (FT-IR). The XPS results validate the presence of Si, O, and C in all composites, with significant variations in atomic proportions (C/Si and O/Si) and Si and C component analyses through deconvolution techniques. This study demonstrates the successful in situ synthesis of PDMS-SiO₂ composites with tunable properties by controlling the sol-gel and crosslinking synthesis parameters. The findings provide valuable insights into the in situ synthesis methods of polymeric composite materials and their potential integration with polymer nanocomposite processing techniques.

Polydimethylsiloxane (PDMS) has been extensively employed in electrical insulation applications owing to its excellent thermal stability, hydrophobicity, and dielectric properties. However, its inherent mechanical limitations require structural reinforcement to enhance its performance under more demanding operational conditions. In this study, the mechanical, thermal, and surface properties of PDMS-SiO₂ nanocomposites synthesized via in situ sol–gel process was systematically investigated. The influence of different SiO₂ nanoparticle concentrations (5, 10, and 15 wt%), sol–gel catalyst type (acidic and alkaline), and tetraethyl orthosilicate (TEOS) crosslinking agent ratios (15:1, 10:1, 5:1) was evaluated. Tensile mechanical testing, dynamic mechanical analysis (DMA), and thermogravimetric analysis (TGA) revealed that the incorporation of SiO₂ notably improved both the mechanical strength and thermal stability of the composites. The 5-15b and 10-15a composites exhibited the highest tensile stress and viscoelastic modulus among all samples. Furthermore, the composites retained key functional properties, including hydrophobicity, high volumetric electrical resistivity (~10¹¹ Ω·cm), and strong adhesion. These findings confirm the potential of in situ PDMS-SiO₂ nanocomposites for use as high-performance insulating coatings in advanced electrical applications.

Plant cell, tissue, and organ cultures are increasingly used as controlled platforms for producing pharmaceutically important specialized metabolites. Their productivity can be improved through elicitors, plant biostimulant-like substances, microbial inputs, and nano-enabled delivery systems. However, the regulatory interpretation of these inputs is not determined only by their biological mechanism. It also depends on product composition, formulation, intended use, exposure scenario, and label claim. This review analyzes how elicitors, plant biostimulants, biofertilizer- and bioinput-related concepts, and nano-enabled inputs are positioned within selected regulatory frameworks in the European Union, United States, Canada, Brazil, India, China, and Mexico. The analysis shows that current frameworks increasingly emphasize product identity, efficacy substantiation, safety evidence, and labeling, but they remain fragmented for multifunctional materials that may simultaneously affect nutrient-related processes, abiotic stress tolerance, defense signaling, growth regulation, and specialized metabolism. Nano-enabled and encapsulated formulations create additional challenges because they can modify uptake, persistence, bioavailability, release behavior, residue profiles, and non-target exposure compared with conventional formulations. A clearer distinction is therefore needed between contained biotechnological use in plant biofactories and open-environment agricultural applications. Future regulatory development should move toward formulation-level assessment, claim-specific evidence, nanospecific characterization, traceability, and harmonized terminology to support innovation while ensuring safety, reproducibility, and regulatory clarity.