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.

Our work presents, for the first time, a comprehensive study of the synthesis of fully metallic platinum nanoparticles (Pt-NPs) involving the ablation process in double distilled water using a KrF excimer laser. To obtain detailed information on Pt-NP morphology and optical properties, prepared colloids were characterized using High Resolution Scanning Transmission Electron Microscopy (HR-STEM) with advanced capabilities for Energy Dispersive X-ray Analysis (EDX), UV/Vis optical spectroscopy, and Direct Analysis in Real Time—Mass Spectrometry (DART-MS). The influence of the applied laser fluence and laser repetition rate (RR) values on the characteristics of the obtained Pt-NPs and the ablation process, respectively, were also analyzed. Spherical and spherical-like nanoparticles exhibiting aggregation were produced. The Pt-NP mean size values were between 2.2 ± 1.2 nm and 4.0 ± 1.0 nm, while their interplanar distance measurements showed a face-centered cubic (FFC) Pt lattice (111), as revealed by HR–STEM measurements, for all investigated samples. The smallest mean size of 2.2 nm of the Pt-NPs was obtained using a 2.3 J cm⁻² laser fluence at a 10 Hz RR, and the narrowest size distribution of the NPs was obtained with a 2.3 J cm⁻² laser fluence at a 40 Hz RR. A linear dependence of the Pt-NP diameters versus the laser repetition rate was found at a constant fluence of 2.3 J cm⁻². The proposed eco-friendly synthesis route of Pt-NPs, because of its relative simplicity, has the potential for use in industrial production.

In this paper, we report on results of a systematic study of porous morphologies obtained using anodization of HVPE-grown crystalline GaN wafers in HNO₃, HCl, and NaCl solutions. The anodization-induced nanostructuring is found to proceed in different ways on N- and Ga-faces of polar GaN substrates. Complex pyramidal structures are disclosed and shown to be composed of regions with the degree of porosity modulated along the pyramid surface. Depending on the electrolyte and applied anodization voltage, formation of arrays of pores or nanowires has been evidenced near the N-face of the wafer. By adjusting the anodization voltage, we demonstrate that both current-line oriented pores and crystallographic pores are generated. In contrast to this, porosification of the Ga-face proceeds from some imperfections on the surface and develops in depth up to 50 μm, producing porous matrices with pores oriented perpendicularly to the wafer surface, the thickness of the pore walls being controlled by the applied voltage. The observed peculiarities are explained by different values of the electrical conductivity of the material near the two wafer surfaces.