The present study aimed to assess the eighteen month follow-up patient-centered outcomes of a simple and predictable protocol for 3D-printed functional complete dentures manufactured using an improved poly(methyl methacrylate) (PMMA)–nanoTiO₂. A detailed morphological and structural characterization of the PMMA–TiO₂ nanocomposite, using SEM, EDX, XRD, and AFM, after 3D-printing procedure and post-wearing micro-CT, was also performed. Methods: A total of 35 fully edentulous patients were enrolled in this prospective study. A 0.4% TiO₂-nanoparticle-reinforced PMMA composite with improved mechanical strength, morphologically and structurally characterized, was used according to an additive computer-aided design and computer-aided manufacturing (CAD/CAM) protocol for complete denture fabrication. The protocol proposed involved a three-step appointment process. Before denture insertion, 1 week, 12 month, and 18-month follow up patients were evaluated via the Visual Analogue Scale (VAS, 0–10) and Oral Health Impact Profile for Edentulous Patients (OHIP-EDENT), with a higher score meaning poor quality of life. Results: A total of 45 complete denture sets were inserted. OHIP-EDENT scored significantly better after 18 months of denture wearing, 20.43 (±4.42) compared to 52.57 (±8.16) before treatment; mean VAS was improved for all parameters assessed. Conclusions: Within the limitations of this study, we can state that the proposed workflow with the improved material used is a viable treatment option for patients diagnosed with complete edentulism.

Identical carbonization and KOH activation procedures result in very similar activated carbons with ultra-high BET surface area (up to ∼3500 m² g⁻¹) when applied to several types of precursors: pine, spruce, and larch cones, and bark/wood chips.

The aim of this study is to design, develop and evaluate new biohybrid sponges based on polymers (collagen and polyvinyl alcohol) with and without indomethacin as anti-inflammatory drug model to be used for tissue regeneration in wound healing. Type I fibrillar collagen in the form of a gel and different concentrations of polyvinyl alcohol were mixed together to prepare composite gels. Both control samples, without indomethacin and with indomethacin, were obtained. All samples were crosslinked with glutaraldehyde. By freeze-drying of hydrogels, the spongious forms (matrices) were obtained. The matrices were characterized by FT-IR spectroscopy, scanning electron microscopy (SEM), water absorption, enzymatic degradation and in vitro indomethacin release. The pharmacological effect of the spongious biohybrid matrices was determined on an experimental model of burns induced to Wistar rats. The SEM images showed a porous structure with interconnected pores. Collagen sponges present a structure with pore sizes between 20 and 200 µm, which became more and more compact with polyvinyl alcohol addition. The FT-IR showed interactions between collagen and polyvinyl alcohol. The enzymatic degradation indicated that the most stable matrix is the one with the ratio 75:25 of collagen:polyvinyl alcohol (ACI75), the other ones being degradable in time. The kinetic data of indomethacin release from matrices were fitted with different kinetic models and highlighted a biphasic release of the drug. Such kinetic profiles are targeted in skin wound healing for which important aspects are impaired inflammation and local pain. The treatment with sponges associated with anti-inflammatory drug had beneficial effects on the healing process in experimentally induced burns compared to the corresponding matrices without indomethacin and the classical treated control group.

The commonly used electrode Pt supported on a carbon (Pt/C) catalyst has demonstrated underperforming electrochemical durability in proton exchange membrane fuel cell (PEMFC) harsh operation conditions, especially in terms of Pt electrochemical instability and carbon corrosion. Gold nanoparticles (AuNPs) are considered one of the best alternative catalysts of PtNPs due to their remarkable selectivity for oxygen reduction reaction (ORR) and electrochemical stability in strong acid conditions, attributes which are ideal for practical PEMFC applications. In this work, we propose a new, facile and low-cost approach to prepare AuNPs supported on reduced graphene oxide nanocompounds (AuNPs/rGO). The morphological and structural properties of the as-prepared AuNPs/rGO were studied using various microscopic and spectroscopic techniques, namely, Raman Spectroscopy, Scanning Electron Microscopy (SEM), Scanning Transmission Electron Microscopy (STEM), X-Ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), specific surface area (Brunauer–Emmett–Teller, BET). A mesoporous structure with narrow pore size distribution centered at 2 nm approximately, where the pores are regular and interconnected was successfully fabricated. The prepared catalyst was exposed to an accelerated stress test (potential cycles between −0.8 and +0.2 in KOH 1 M solution). The voltammetric stability test indicated a slight degradation after 1500 cycles. The electrochemical stability was assigned to the combined effect of AuNPs formed during chemical synthesis and to graphene oxide support.