Novel Formulations of PEG–Silica Phase-Changing Materials (PCMs) with Applications in Passive Storage of Thermal Energy

The aim of the present study is to design new PEG–silica hybrids (PEGx–Si) as phase changing [...

Composite Hydrogels Based on Poly (Methacrilyc Acid) Reinforced with Laponite Inorganic Filler

Polymeric hydrogels are soft materials that can absorb large amounts of water or biological [...

Chitosan-Stabilized Ag Nanoparticles with Superior Biocompatibility and Their Synergistic Antibacterial Effect in Mixtures with Essential Oils

Silver nanoparticles (AgNPs) are considered a promising alternative to the use of antibiotics in fighting multidrug-resistant pathogens. However, their use in medical application is hindered by the public concern regarding the toxicity of metallic nanoparticles. In this study, rationally designed AgNP were produced, in order to balance the antibacterial activity and toxicity. A facile, environmentally friendly synthesis was used for the electrochemical fabrication of AgNPs. Chitosan was employed as the capping agent, both for the stabilization and to improve the biocompatibility. Size, morphology, composition, capping layer, and stability of the synthesized nanoparticles were characterized. The in vitro biocompatibility and antimicrobial activities of AgNPs against common Gram-negative and Gram-positive bacteria were evaluated. The results revealed that chitosan-stabilized AgNPs were nontoxic to normal fibroblasts, even at high concentrations, compared to bare nanoparticles, while significant antibacterial activity was recorded. The silver colloidal dispersion was further mixed with essential oils (EO) to increase the biological activity. Synergistic effects at some AgNP–EO ratios were observed, as demonstrated by the fractionary inhibitory concentration values. Our results reveal that the synergistic action of both polymer-stabilized AgNPs and essential oils could provide a significant efficiency against a large variety of microorganisms, with minimal side effects

Novel Coatings for Superhydrophobic/Superamphiphobic Surfaces with Tunable Morphology of Nanoparticles

Functional surfaces with special wettability properties are currently receiving a lot of attention [...

Synergistic Effects in Nanoparticle-Based Protective Coatings for Paper and Textiles

Superhydrophobic materials have attracted considerable attention during the last decades,since they allow the facile transfer of special wettability properties on various surfaces [...

Mesoporous Silica Nanoreservoirs Loaded with 1-H Benzotriazole for Active Anticorrosion Protection

In recent years, scientists are paying increased attention to the development of intelligent nanocontainers in applications such as biomedical, catalysis, and anticorrosion [1]. Preparation of anticorrosion coatings containing smart nanocontainers loaded with corrosion inhibitors, which can be initiated when the barrier coatings are damaged, favor the long-term function, as uncontrolled loss by leaching is inhibited [2]. The aim of the present study is to optimize the amount of an organic inhibitor (1-H benzotriazole (BTA)) that can be in situ encapsulated in a mesoporous silica nanocontainer, prepared by an original sol-gel formulation. Materials and methods: For the synthesis of silica mesoporous, nanoparticles loaded with BTA were used with three silica co-precursors: tetraethylorthosilicate (TEOS), phenyltriethoxysilane (PTES), and octyltriethoxysilane (OTES), at a 5/1/1 gravimetric ratio. The synthesis was carried out in the presence of a solvent (ethanol) and of a surfactant (Igepal CA-630). The pH of the sol–gel system was adjusted to ~9 by dripping an aqueous solution of NH4OH (25%). Prior to the addition to the sol–gel reaction system, BTA was completely dissolved in ethanol. Various amounts of BTA were loaded to the sol–gel systems: 0.25; 0.5; 0.75; 1; 1.25; 1.5; and 2 g (corresponding to 0.09; 0.18; 0.27; 0.35; 0.44; 0.53; and 0.70% grav. of the total amount of sol–gel mixture, respectively). Furthermore, a similar set of samples was prepared in the presence of a constant amount of rhodamine B, dissolved in ethanol. This second set was obtained in order to perform a visual evaluation of the encapsulation efficiency. Particles dimensions, size distributions, and particles charging in the final dispersions were evaluated by the dynamic light scattering (DLS) technique and Zeta potential measurements. Surface morphology was observed by SEM. The structural characteristics of the silica mesoporous particles were investigated by N2 adsorption–desorption analysis on the calcined samples. Results: During the in situ synthesis of silica nanoparticles, the aromatic molecules of the corrosion inhibitor BTA were linked via a hydrophobic interaction with the phenyl groups from the silica pores formed by the hydrophobic functions of silica co-precursors, i.e., PTES and OTES. In addition, the corrosion inhibitor was trapped inside the surfactant micelles of Igepal and encapsulated together inside the silica pores formed by the surfactant. Moreover, it was observed that only a small amount of BTA can be encapsulated in the absence of the surfactant. Conclusions: An optimized method was developed to obtain mesoporous silica nanoparticles loaded with 1-H Benzotriazole (BTA) as a corrosion inhibitor. The optimal range of the BTA concentration was found to be between 0.18 and 0.35%

Preliminary Studies on Silica Nanoparticles Preparation as Transport Vectors for Curcumin

Mesoporous silica nanoparticles (MSN) are currently central to studies in different scientific areas [...

Adjusting Some Properties of Poly(methacrylic acid) (Nano)Composite Hydrogels by Means of Silicon-Containing Inorganic Fillers

The present work aims to show how the main properties of poly(methacrylic acid) (PMAA) hydrogels can be engineered by means of several silicon-based fillers (Laponite XLS/XLG, montmorillonite (Mt), pyrogenic silica (PS)) employed at 10 wt% concentration based on MAA. Various techniques (FT-IR, XRD, TGA, SEM, TEM, DLS, rheological measurements, UV-VIS) were used to comparatively study the effect of these fillers, in correlation with their characteristics, upon the structure and swelling, viscoelastic, and water decontamination properties of (nano)composite hydrogels. The experiments demonstrated that the nanocomposite hydrogel morphology was dictated by the way the filler particles dispersed in water. The equilibrium swelling degree (SDe) depended on both the pH of the environment and the filler nature. At pH 1.2, a slight crosslinking effect of the fillers was evidenced, increasing in the order Mt pKaMAA (pH 5.4; 7.4; 9.5), the Laponite/Mt-containing hydrogels displayed a higher SDe as compared to the neat one, while at pH 7.4/9.5 the PS-filled hydrogels surprisingly displayed the highest SDe. Rheological measurements on as-prepared hydrogels showed that the filler addition improved the mechanical properties. After equilibrium swelling at pH 5.4, G’ and G” depended on the filler, the Laponite-reinforced hydrogels proving to be the strongest. The (nano)composite hydrogels synthesized displayed filler-dependent absorption properties of two cationic dyes used as model water pollutants, Laponite XLS-reinforced hydrogel demonstrating both the highest absorption rate and absorption capacity. Besides wastewater purification, the (nano)composite hydrogels described here may also find applications in the pharmaceutical field as devices for the controlled release of drugs

Synergistic Antioxidant Activity and Enhanced Stability of Curcumin Encapsulated in Vegetal Oil-Based Microemulsion and Gel Microemulsions

Curcumin, due to its antioxidant, antibacterial, anti-inflammatory, and antitumoral activity, has attracted huge attention in applications in many fields such as pharmacy, medicine, nutrition, cosmetics, and biotechnology. The stability of curcumin-based products and preservation of antioxidant properties are still challenges in practical applications. Stability and antioxidant properties were studied for curcumin encapsulated in O/W microemulsion systems and three related gel microemulsions. Only biodegradable and biocompatible ingredients were used for carriers: grape seed oil as oily phase, Tween 80, and Plurol® Diisostearique CG as a surfactant mix, and ethanol as a co-solvent. For the gel microemulsions, water-soluble polymers, namely Carbopol® 980 NF, chitosan, and sodium hyaluronate were used. The influence of UVC irradiation and heat treatment on the degradation kinetics of curcumin in the formulations was studied. Because of the antioxidant character of the microemulsion oily phase, the possibility of a synergistic effect between grape seed oil and curcumin was explored. In this study, the high efficiency of the studied drug delivery systems to ensure protection from external degradative factors was confirmed. Also, the influence of the encapsulation in microemulsion and derived gel microemulsion systems on the antioxidant capacity curcumin was studied, and a synergistic effect with vegetal oil was demonstrated