Search Results (2,145)

In this work, hydrogel nanocomposites, as films, were prepared by embedding cerium oxide nanoparticles (CeO₂NPs) within xanthan gum (Xn)/poly(vinylalcohol) (PVA) matrices. Their physicochemical properties were tuned by adjusting the ratio between components and thermal treatment conditions. The cross-linking of the polymer network was confirmed by attenuated total reflectance–Fourier transform infrared (ATR-FTIR), thermal analysis, and swelling behavior. Morphological features were evaluated by atomic force microscopy (AFM), scanning electron microscopy (SEM), while optical properties were investigated by UV–Vis spectroscopy. Undoped films displayed high transparency (~80% transmittance at 400 nm), with thermal cross-linking determined only slight yellowing and negligible changes in absorption edge (300 ± 2 nm). In contrast, CeO₂NPs incorporation increased reflectance and introduced a new absorption threshold around 400 ± 2 nm, indicating nanoparticle–matrix interactions that modify optical behavior. Sorption studies with Methylene Blue (MB) and Crystal Violet (CV) dyes highlighted the influence of nanoparticle content and cross-linking on functional performance, with thermally treated samples showing the highest efficiency (~97–98% MB and 71–83% CV removal). Overall, the results demonstrate how structural tailoring and cross-linking control the characteristics of Xn/PVA/CeO₂ nanocomposites, providing insight into their design as multifunctional hydrogel materials for environmental applications. Full article

Hydrogels are hydrophilic, soft polymer networks with high water content and mechanical properties that are tunable; they are also biocompatible. Therefore, as biomaterials, they are of interest to modern medicine. In this review, the main applications of hydrogels in essential clinical applications are discussed. Chemical, physical, or hybrid crosslinking of either synthetic or natural polymers allow for the precise control of hydrogels’ physicochemical properties and their specific characteristics for certain applications, such as stimuli-responsiveness, drug retention and release, and biodegradability. Hydrogels are employed in gynecology to regenerate the endometrium, treat infections, and prevent pregnancy. They show promise in cardiology in myocardial infarction therapy through injectable scaffolds, patches in the heart, and medication delivery. In rheumatoid arthritis, hydrogels act as drug delivery systems, lubricants, scaffolds, and immunomodulators, ensuring effective local treatment. They are being developed, among other applications, as antimicrobial coatings for stents and radiotherapy barriers for urology. Ophthalmology benefits from the use of hydrogels in contact lenses, corneal bandages, and vitreous implants. They are used as materials for chemoembolization, tumor models, and drug delivery devices in cancer therapy, with wafers of Gliadel presently used in clinics. Applications in abdominal surgery include hydrogel-coated meshes for hernia repair or Janus-type hydrogels to prevent adhesions and aid tissue repair. Results from clinical and preclinical studies illustrate hydrogels’ diversity, though problems remain with mechanical stability, long-term safety, and mass production. Hydrogels are, in general, next-generation biomaterials for regenerative medicine, individualized treatment, and new treatment protocols. Full article

Gelatin is a collagen-derived biopolymer widely used in food, pharmaceutical and biomedical applications due to its biocompatibility and gelling ability. However, gelatin hydrogels suffer from unstable mechanical strength, limited thermal resistance and susceptibility to microbial contamination. The main aim of the present study is to investigate the influence of gelatin cryostructuring followed by photo-induced menadione sodium bisulfite (MSB) chemical crosslinking on the structural and functional characteristics of mammalian and fish gelatin hydrogels. The integration of scanning electron microscopy, dielectric spectroscopy and rheological experiments provides a comprehensive view of the of molecular, morphological and mechanical properties of gelatin hydrogels under photo-induced chemical crosslinking. The SEM results revealed that crosslinked hydrogels are characterized by enlarged pores compared to non-crosslinked systems. For mammalian gelatin, multiple pores with thin partitions are formed, giving a dense and stable polymer network. For fish gelatin, large oval pores with thickened partitions are formed, preserving a less stable ordered architecture. Rheological data show strong reinforcement of the elastic and thermal stability of mammalian gelatin. The crosslinked mammalian system maintains the gel state at higher temperatures. Fish gelatin exhibits reduced elasticity retention even after crosslinking because of a different amino acid composition. Dielectric results show that crosslinking increases the portion of bound water in hydrogels considerably, but for fish gelatin, bound water is more mobile, which may explain weaker mechanical properties. Full article

The potential of elastomeric composites reinforced with natural fillers to replace traditional synthetic materials in applications involving exposure to acidic environments offers both economic and environmental advantages. On the one hand, these materials contribute to cost reduction and the valorization of organic waste through the development of value-added products. On the other hand, the presence of wood waste in the composite structure enhances biodegradation potential, making these materials less polluting and more consistent with the principles of the circular economy. The present study aims to evaluate the behavior of composites based on Ethylene Propylene Diene Monomer (EPDM) synthetic rubber, reinforced with silica and wood sawdust, in a weakly acidic yet strongly corrosive environment—specifically, acetic acid solutions with concentrations ranging from 10% to 30%. The study also investigates the extent to which varying the proportions of the two fillers affects the resistance of these materials under such environmental conditions. Physico-chemical, structural, and morphological analyses revealed that the materials underwent chemical modifications, such as acetylation of hydroxyl groups. This process reduced the hydrophilic character of the sawdust and, combined with the formation of stable interfaces between the elastomeric matrix and the fillers during vulcanization, limited acid penetration into the composite structure. The composites in which 20 phr or 30 phr of wood sawdust were used-replacing equivalent amounts of silica from the initial 50 phr formulation-demonstrated the highest resistance to the corrosive environments. After 14 days of exposure to a 20% acetic acid solution, the composite containing 30% wood sawdust exhibited a decrease in cross-link density of only 1.44%, accompanied by a reduction in Young’s modulus of just 0.95%. At the same time, tensile strength and specific elongation increased by 22.57% and 26.02%, respectively. FTIR and SEM analysis confirmed good rubber-filler interactions and the stability of the composite structure under acidic conditions. Full article

Polyvinyl alcohol (PVA), a water-soluble, biodegradable, and biocompatible polymer, has garnered significant attention in recent years for its applications such as packaging, electronics, biomedical materials, and water treatment. However, its high flammability poses a substantial limitation in fire-sensitive environments. To address this challenge, significant research efforts have been devoted to improving the flame retardancy and suppressing the smoke toxicity of PVA through various strategies. This review presents diverse modification strategies that have been developed for PVA, including physical blending with polymers and nanofillers, chemical modifications such as esterification, acetalization, and crosslinking, and advanced surface engineering techniques such as plasma treatment, layer-by-layer assembly, and surface grafting. Beyond fire safety, these modifications enable multifunctional applications, expanding PVA use in optical, energy, sensing, and biomedical fields. Finally, this review explores current challenges, environmental considerations, and future directions for the development of sustainable, high-performance flame-retardant PVA systems. Full article

Elastin is the principal protein found in the elastic fibers of vertebrate tissues, and the water within these fibers plays a crucial role in preserving the structure and function of this hydrophobic protein. Soluble elastin was successfully obtained by repeatedly treating insoluble elastin, extracted from pig aorta, with oxalic acid. Solid-state NMR analysis was performed on the soluble elastin, focusing on conformation-dependent chemical shifts of alanine residues. This analysis revealed that cross-linked alanine residues exhibited both α-helix and random coil structures in the dry state. In contrast, the hydrated state favored random coil structures, with some distorted helices possibly present, indicating that the cross-linked configuration is relatively unstable. Similar conformational changes were observed in insoluble elastin, mirroring those found in the soluble form. Additionally, when the soluble elastin was re-cross-linked using 1,12-dodecanedicarboxylic acid and 4-hydroxyphenyl dimethylsulfonium methylsulfate, it retained a mixture of α-helix and random coil structures in the dry state. Remarkably, in the hydrated state, α-helix structures were more prominently preserved alongside random coils. These structural changes corresponded with increased stiffness of molecular chains in the hydrophobic regions compared to their state prior to re-cross-linking, even under hydrated conditions. Full article

Viscosupplementation with intra-articular hyaluronic acid (HA) is a key therapeutic option for osteoarthritis (OA), yet the field is hampered by clinical controversies and an outdated classification of available products. This comprehensive review critically analyzes the current landscape, moving from a mechanical to a biological paradigm of HA’s mechanism of action. We argue that the traditional HA product classification based solely on molecular weight is insufficient, as it conflates chemically distinct products. Therefore, we propose a new, two-tiered classification framework: the primary distinction is based on chemical structure, separating linear (non-modified) HA from cross-linked (chemically modified) HA. Linear HA is then sub-classified by molecular weight (Low, Intermediate, and High), while cross-linked HA is defined as a separate category of hydrogels with a ultra-high effective molecular weight. Within this clearer framework, we analyze the central controversy between formulations, highlighting the pivotal emergence of high-concentration, high-molecular-weight (>2 million Dalton) linear HA. These formulations not only challenge the durability rationale for cross-linking by providing year-long efficacy but also possess a superior biological profile for chondroprotection, preserving chondrocyte viability and function. Furthermore, we explore the expanding frontier of combination therapies, where linear HA serves as the ideal physiological scaffold for agents like corticosteroids, PRP and other injectable orthobiologics such as bone marrow aspirate and stromal vascular fraction. Full article

Sugar beet pulp (SBP) is a by-product from the sugar industry with low value. As a feed, SBP needs to be dried. However, the drying process takes too much energy, leading to potential environmental issues caused by coal use. This paper raised and tried a crosslinking method to shorten the drying process, save energy consumption, and increase the value of SBP. This paper aimed to reduce the water-holding ability of SBP while obtaining animal feed with higher nutritional value. First, the crosslinking method was used to evaluate its dryness–strengthening effect. Second, three factors were evaluated: operating temperature, solution pH, and cationic concentration. Third, a kinetic study was performed on the drying process of SBP through its crosslinking with macro-elements (Ca²⁺, Cu²⁺) using drying models; the characterization of Ca²⁺-SBP and Cu²⁺-SBP using FTIR, SEM, and XRD; and possible drying mechanisms, which were discussed using an egg box model and a simple quantum chemical calculation. Results showed that the dryness–strengthening and value-adding idea is more practical through a Ca²⁺-crosslinking method, rather than through crosslinking with Cu²⁺. Under experimental conditions, wet SBP with 2 g of dry base reacts to Ca²⁺ under optimized conditions of 1000 mg/L Ca²⁺ solution at pH 6.0 and 40 °C for 135 min, with a moisture content of 5.23 g/g as a water-holding index. Compared with SBP, the moisture content of the crosslinking SBP on a dry basis was reduced by ~30–40%. The Midilli–Kucuk model was the most suitable model to describe the hot-air drying process of SBP, while Ca²⁺ or Cu²⁺ can crosslink to the galacturonic acid in pectin and form an “egg-box” model. SBP binds with Ca²⁺ or Cu²⁺ through its carboxyl groups, as testified by a combination analysis of FTIR, SEM, and XRD. As a result, the SBP dried through the Ca²⁺-crosslinking or Cu²⁺-crosslinking method can be directly used as a feed additive with good economic benefit and without the post-treatment problem as a bio-sorbent. Full article

The application of lipases in biphasic oil–water emulsions offers an efficient and sustainable alternative to conventional chemical synthesis. However, the natural immiscibility of these phases is a substantial limitation. To address this issue, we proposed a dual-stabilized emulsion system combining a nonionic emulsifier (Kolliphor^® CS 20) and cross-linked polyacrylic acid (Carbopol^® Ultrez 10), exceeding conventional single-stabilized systems. The activity of Candida antarctica lipase B (CALB), both in its free form and immobilized onto an IB-D152 support, was investigated in the prepared emulsion system. The olive oil emulsion stabilized with 10.0% Kolliphor^® CS 20 and 0.1% Carbopol^® Ultrez 10 significantly enhanced the lipolytic activity of immobilized CALB (156.27 ± 3.91 U/g of support), compared to the activity obtained in the emulsion stabilized only with 10.0% Kolliphor^® CS 20 (71.11 ± 3.86 U/g of support). On the other hand, the activity of immobilized CALB in the emulsion containing 5.0% Kolliphor^® CS 20 and 0.1% Carbopol^® Ultrez 10 (62.22 ± 3.85 U/g of support) was lower than in the corresponding system without Carbopol^® Ultrez 10 (72.03 ± 4.63 U/g of support), stabilized with only 5.0% Kolliphor^® CS 20. Furthermore, immobilization onto IB-D152 led to lipase hyperactivation, with activity approximately eight-fold higher than that of free CALB. This dual emulsion stabilization strategy not only improves emulsion stability but also enhances lipase activity, offering new opportunities for scalable, high-performance biocatalysis using emulsions in industrial applications. Full article

Epoxidized soybean oil (ESO) is the oxidation product of soybean oil with hydrogen peroxide and either acetic or formic acid obtained by converting the double bonds into epoxy groups, which is non-toxic and of higher chemical reactivity. Oxidized soybean oil (ESO) has gained significant attention as a renewable and environmentally friendly alternative to petroleum-based epoxy resins. Derived from soybean oil through epoxidation of its unsaturated fatty acids, ESO offers a bio-based platform with inherent flexibility, low toxicity, and excellent chemical resistance. When used as a reactive diluent or primary component in epoxy formulations, ESO enhances the sustainability profile of coatings, adhesives, and composite materials. This study explores the mechanical properties of ESO-based epoxy systems, with particular attention to formulation strategies, crosslinking agents, and performance trade-offs compared to conventional epoxies. The incorporation of ESO not only reduces the reliance on fossil resources but also imparts tunable thermal and mechanical properties, making it suitable for a range of industrial and eco-friendly applications. The results underscore the potential of ESO as a viable component in next-generation green materials, contributing to circular economy and low-impact manufacturing. For the application of these materials in pultrusion and FW technologies, the Taguchi method is used to determine the most influential process parameters. Full article

Bio-based nanofibers are gaining increasing attention in nanotechnology owing to their high surface area, interconnected porosity, and capacity to incorporate bioactive compounds. Among natural polymers, gelatin is particularly attractive because of its abundance, low cost, biodegradability, and versatile physicochemical properties. When processed by electrospinning, gelatin combines its amphiphilic nature with the structural advantages of nanofibers, enabling efficient interactions with a wide range of molecules. Nevertheless, pure gelatin nanofibers have drawbacks, such as poor mechanical strength and high-water solubility. To address these limitations, strategies including polymer blending, chemical and physical crosslinking, and multilayer biomaterials have been developed, resulting in improved stability, functionality, and application-specific performance. Therefore, this review summarizes recent advances in the fabrication and functionalization of gelatin nanofibers, highlighting how processing parameters and gelatin source influence electrospinning outcomes and fiber properties. Key applications are also discussed, with emphasis on biomedical, food, environmental, and biosensing. Therefore, gelatin nanofibers represent a sustainable and versatile biomaterial with high potential for advanced technological applications. Full article

Hydrogels have garnered significant attention as multifunctional materials in next-generation rechargeable batteries due to their high ionic conductivity, mechanical flexibility, and structural tunability. This review presents a comprehensive overview of hydrogel types—including natural, synthetic, composite, carbon-based, conductive polymer, and MOF hydrogels—and their synthesis methods, such as chemical crosslinking, self-assembly, and irradiation-based techniques. Characterization tools like SEM, XRD, and FTIR are discussed to evaluate their microstructure and performance. In rechargeable batteries systems, hydrogels enhance ionic transport and mechanical stability, particularly in lithium-ion, sodium-ion, zinc-ion, magnesium-ion, and aluminum-ion batteries. Despite their advantages, hydrogels face challenges such as limited mechanical strength, reduced stability under extreme conditions, and scalability issues. Current research focuses on advanced formulations, self-healing mechanisms, and sustainable materials to overcome these limitations. This review highlights the pivotal role of hydrogels in shaping the future of flexible, high-performance, and environmentally friendly secondary batteries. Full article

A chemical platform for post-polymerization methods was developed, starting from the ecodesign and enzymatic synthesis of safe and sustainable bio-based polyesters containing discrete units of itaconic acid. This unsaturated bio-based monomer enables the covalent linkage of molecules that can impart desired properties such as hydrophilicity, flexibility, permeability, or affinity for biological targets. Molecular descriptor-based computational methods, which are generally used for modeling the pharmacokinetic properties of drugs (ADME), were employed to predict in silico the hydrophobicity (LogP), permeability, and flexibility of virtual terpolymers composed of different polyols (1,4-butanediol, glycerol, 1,3-propanediol, and 1,2-ethanediol) with adipic acid and itaconic acid. Itaconic acid, with its reactive vinyl group, acts as a chemical platform for various post-polymerization functionalizations. Poly(glycerol adipate itaconate) was selected because of its higher hydrophilicity and synthetized via solvent-free enzymatic polycondensation at 50 °C to prevent the isomerization or crosslinking of itaconic acid. The ecotoxicity and marine biodegradability of the resulting oligoester were assessed experimentally in order to verify its compliance with safety and sustainability criteria. Finally, the viability of the covalent linkage of biomolecules via Michael addition to the vinyl pendant of the oligoesters was verified using four molecules bearing thiol and amine nucleophilic groups: N-acetylcysteine, N-Ac-Phe-ε-Lys-OtBu, Lys-Lys-Lys, and glucosamine. Full article

Crosslinked hyaluronic acid dermal fillers are widely used for non-permanent aesthetic enhancement, offering safe and effective solutions for facial volume restoration. Specific formulations are designed for targeted facial regions, with highly crosslinked hydrogels often recommended for volumizing areas such as the jawline, chin, and cheeks due to their structural properties. While elasticity and viscosity are commonly evaluated, broader comparative analyses remain limited. In this study, we assess five commercially available HA-based fillers with similar HA concentrations, all optimised for volume enhancement. Alongside widely used reference products, we evaluate BtHCROSS 2%^®, a novel formulation not previously compared to established fillers. We examined the degree of chemical modification, mechanical viscoelastic behaviour, susceptibility to enzymatic degradation by hyaluronidase, and injection force. While all tested fillers are suitable for volume restoration, BtHCROSS 2%^® demonstrates a distinctive combination of mechanical adaptability, structural support, enzymatic resistance, and low injection force, making it a versatile option for practitioners. Full article

Anion exchange ionomer (AEI) binders are critical to the performance of alkaline electrochemical devices (i.e., fuel cells, electrolyzers, and batteries), as they facilitate ion transport, provide structural integrity, and improve the overall performance and lifespan of these devices. These binders not only ensure ion transport but also provide mechanical stability to the electrode materials. Recently, there has been significant progress in designing AEIs that are more compatible with existing electrode materials and electrolytes. This review summarizes the different types of AEI binders, focusing on their chemical structure, functionalization, conductivity, and how they affect the performance of alkaline fuel cells, specifically, anion exchange membrane fuel cells (AEMFCs). It also discusses how factors like functional groups, polymer backbone and side-chain flexibility, and ion exchange capacity balance conductivity, mechanical strength, and water uptake (WU). Recent advances in material design, such as polymer blends, composites, and crosslinked ionomers, as well as electrode setup, such as asymmetric ionomer electrodes, are explored as methods for improving stability and ion transport. The main challenges facing AEIs, including water management, alkaline degradation, phase separation, mechanical robustness, and long-term durability, are discussed along with strategies for overcoming them. Finally, we outline future research directions for developing scalable, economical solutions and integrating these binders with new electrode materials to help improve the performance and stability of next-generation AEMFCs. Full article