Search Results (111)

Tissue engineering is a multidisciplinary field that aims to address tissue and organ failure by integrating scientific, engineering, and medial expertise. Gelatin is valued in this field for its biocompatibility; however, it faces thermal and mechanical weaknesses that limit its biomedical utility. This work proposes a strategy for improving gelatin properties by fabricating semi-interpenetrating polymer networks via in situ Diels–Alder crosslinking within gelatin colloidal solutions. Ten systems with variable polymer concentrations (2–4%) and crosslinking degrees (2–5%) were prepared and characterized. Rheological analysis revealed that elastic modulus, zero-shear viscosity, and complex viscosity were substantially enhanced, being especially dependent on the crosslinking degree, while critical strain values mostly depended on gelatin concentration. The incorporation of a synthetic Diels–Alder-crosslinked network also improved the thermal stability of gelatin hydrogels, particularly at physiological temperatures. Additionally, these systems exhibit favorable buoyancy, swelling and biodegradation profiles. Collectively, the resultant hydrogels are cytocompatible, solid-like, and mechanically robust, allowing for further tunability of their properties for specific biomedical uses, such as injectable matrices, load-bearing scaffolds for tissue repair, and 3D bioinks. Full article

Phosphorus-modified poly(vinyl alcohol) (PVA) has recently gained increasing attention as a functional polymeric matrix suitable for gel-based systems, owing to its biocompatibility, film-forming ability, and capacity to develop semi-interpenetrating networks. In this work, PVA was chemically modified through the nucleophilic substitution of its hydroxyl groups with the chloride groups of phenyl dichlorophosphate, following a literature-reported method carried out in N,N-dimethylformamide (DMF) as reaction medium, resulting in phosphorus-containing PVA networks (PVA-OP3). Hybrid gel-like films were then prepared by incorporating titanium dioxide nanoparticles (TiO₂ NPs), known for their antimicrobial activity, low toxicity, and high stability. The resulting composites were structurally, morphologically, and thermally characterized using FTIR, SEM, and thermogravimetric analysis. The incorporation of TiO₂ NPs significantly improved the thermal stability, with T₅% increasing from 240 °C for neat PVA-OP3 to 288 °C for the optimal composite, increased the char residue from 4.5% for the neat polymer to 30.1% for PVA-OP3/TiO₂-4, and enhanced antimicrobial activity against both Gram-positive and Gram-negative bacteria. These findings demonstrate that PVA-OP3/TiO₂ hybrid films possess promising potential as advanced biomaterials for biomedical, protective, and environmental applications. Full article

Proton exchange membrane fuel cells are environmentally friendly, safe clean energy devices that have the potential to change the world. Proton exchange membrane fuel cells are a promising replacement for traditional power generation devices. Nanocomposite proton exchange membranes have high energy efficiency, which allows them to be considered as a new generation of proton exchange materials. This paper presents for the first time the synthesis and properties of nanocomposite proton exchange membranes based on poly-1-vinyl-1,2,4-triazole modified with polyhydroxysulfonated fullerene. Sulfofullerene intercalated into the polymer matrix improves all key membrane properties. The PEM nanocomposites exhibit a proton conductivity of up to 1.67 mS/cm and a uniform distribution of carbon nanoparticles of up to 10 nm in size. It was established that high dispersion and stabilization of nanoparticles are ensured by the acid–base interaction of sulfofullerene with the heterocycles of the polymer matrix. Stabilization of functionalized fullerenes by a matrix of semi-interpenetrating polymer networks is an innovative approach for creating nanocomposite proton-conducting systems. The obtained fullerene-containing PEMs demonstrate a high potential for wide practical application in various fuel cells. Full article

Biocompatible electroactive hydrogels with bidirectional pH-responsive bending are important for the creation of biomedical actuators. This study developed chitosan/carboxymethylcellulose (CS/CMC) semi-interpenetrating networks (SIPNs) with different volume ratios, which were crosslinked with glutaraldehyde. The swelling and bending behaviors of SPINs were systematically characterized as a function of the pH of the solution and the magnitude of the applied electric field. The hydrogels exhibited pH-dependent bidirectional actuation, with the maximum swelling of 4.67–6.00 at pH ≈ 3.9 and minimum swelling of 1.58–2.53 at pH ≈ 5.7. The SPINs with CS/CMC = 1:1 composition achieved the highest bending angle of 77° at pH ≈ 5.7, while cathodic bending up to an angle of −13.7° was observed in basic conditions. The electromechanical response was significantly enhanced by decreasing the electrode distance and increasing the applied voltage. The observed correlation between the composition, swelling behavior, and bending performance was explained in terms of the electrostatic interactions between NH₃⁺ and COO⁻ groups present in the CS/CMC mixtures. These findings provided novel insight into the ongoing efforts for the development of non-toxic electroactive hydrogels with tailored electromechanical bending behavior necessary for use as artificial muscles and biomedical actuators. Full article

Developing conductive hydrogels that balance high conductivity, stretchability, transparency, and sensitivity for next-generation wearable sensors remains challenging due to inherent trade-offs. This study introduces a straightforward approach to fabricate a semi-interpenetrating double-network hydrogel comprising polyvinyl alcohol (PVA), polyacrylamide (PAM), and lithium chloride (LiCl) to overcome these limitations. Leveraging hydrogen bonding for energy dissipation and chemical cross-linking for structural integrity, the design achieves robust mechanical properties. The incorporation of 1 mol/L LiCl significantly enhances ionic conductivity, while also providing plasticizing and moisture-retention benefits. The optimized hydrogel exhibits impressive ionic conductivity (0.47 S/m, 113% enhancement), excellent mechanical performance (e.g., 0.177 MPa tensile strength, 730% elongation, 0.68 MJ m⁻³ toughness), high transparency (>85%), and superior strain sensitivity (gauge factors ~1). It also demonstrates rapid response/recovery and robust fatigue resistance. Functioning as a wearable sensor, it reliably monitors diverse human activities and enables novel, secure data handling applications, such as finger-motion-driven Morse code interfaces and gesture-based password systems. This accessible fabrication method yields versatile hydrogels with promising applications in health tracking, interactive devices, and secure communication technologies. Full article

This paper presents an overview of a research line developed at the Istituto Centrale per il Restauro within the CHANGES (Cultural Heritage Active Innovation for Next-Gen Sustainable Society) project, funded under the Italian National Recovery and Resilience Plan. The research was developed in different phases: a first one dedicated to the study of the deep background and the state of the art in the ICR background: history, methodologies and research in the field; a second phase was dedicated to the selection of a specific urban art mural, as a key study with conservation problems connected to some of the principal preservation treatments related to the outdoor context; the mural was also identified as a beloved icon in the public space with a profound socio-cultural meaning for the community. Nido di Vespe, created in 2014 by the artist Lucamaleonte is part of a broader artistic project called M.U.Ro-Museum of Urban Art of Rome, an open-air public art museum located in the Quadraro district in Rome, designed by the artist Diavù. A third phase focused on the research in ICR laboratories, specifically addressing: cleaning, reintegration, and protection strategies adapted to dynamic outdoor environments. A multi-step cleaning system based on polyvinyl alcohol-borax semi-interpenetrated hydrogels loaded with nanostructured fluids was developed to selectively remove spray-paint vandalism while preserving the chemically similar original pictorial layers. The reintegration phase investigated acrylic and urea-aldehyde resins as binders to produce compatible, reversible, and UV-traceable retouching and infilling materials. For surface protection, multilayer coating systems incorporating nanoparticles with antimicrobial, photocatalytic, and UV-stabilizing properties were formulated to enhance durability and chromatic stability. Laboratory tests on mock-ups simulating typical street and urban art materials and morphologies showed satisfactory results, while diagnostic investigations on Nido di Vespe provided the reference data to calibrate the experiments with real mural conditions. Cleaning tests demonstrated promising removal efficiency, influenced by the chemical composition, thickness of the overpainted layers, and surface roughness. The reintegration system met the expected performance requirements, as the tested binders provided good results and allowed the development of compatible, reversible, and distinguishable solutions. Protective coatings showed good results in terms of chromatic stability and surface integrity; however, the long-term behavior of both reintegration, cleaning, and protection systems requires further evaluation. The results achieved so far support the development of sustainable and flexible conservation strategies for the conservation of contemporary street and urban murals and will guide the future application of the selected materials and methodologies in pilot conservation interventions on the mural chosen as a meaningful case study within the broader research. Full article

As the increasing demand for clean-label, plant-based, and functional food systems, bigels, an innovative biphasic structured system composed of both hydrogels and oleogels, have emerged as promising research focus for delivering functional ingredients in the food, pharmaceutical, and cosmetic fields. Plant-based bigels, formulated from edible biopolymers and vegetable oils, represent a sustainable and regulatory-compliant delivery platform. This review critically reviews the recent advances in the structural design and stabilization of plant-based bigels, with an emphasis on the regulation of phase behavior and interfacial interactions. Advanced strategies, including stimuli-responsive gelation, Pickering interfaces, and semi-interpenetrating networks, are explored to improve stability and enable targeted gastrointestinal release. Applications in the delivery of polyphenols, omega-3 fatty acids, lipophilic vitamins, and probiotics are highlighted, underscoring the relationship between structural construction and delivery performance. Furthermore, current challenges and potential solutions concerning stability enhancement, bioavailability improvement, and industrial scalability are outlined. Future research directions are proposed to address existing gaps and to further exploit the potential of plant-based bigels for functional compound delivery. Full article

The anthrone-based dummy molecularly imprinted membrane (DIM) was successfully synthesized using a semi-interpenetrating polymer network (semi-IPN) approach for the selective recognition and adsorption of fluorene and phenanthrene in aqueous systems. Fourier-transform infrared spectroscopy (FTIR) confirmed the successful incorporation of functional groups, while scanning electron microscopy (SEM) revealed a uniform porous morphology favorable for analyte diffusion. Thermogravimetric analysis (TGA) demonstrated good thermal stability, and Brunauer–Emmett–Teller (BET) and Barrett–Joyner–Halenda (BJH) analyses indicated an enhanced surface area and mesoporous structure that supported improved adsorption performance. Adsorption isotherm studies revealed favorable adsorption behavior, with the maximum adsorption capacities of the DIM calculated to be 130.857 mg/g for fluorene and 453.030 mg/g for phenanthrene. The imprinting factors (IFs) were approximately 2.01 for fluorene and 2.17 for phenanthrene, confirming the successful imprinting effect. The recovery values achieved were 86.61% for fluorene and 92.40% for phenanthrene, demonstrating the efficiency and selectivity of the fabricated membrane. These results highlight the potential application of the anthrone-based DIM in the environmental monitoring of polycyclic aromatic hydrocarbons (PAHs). Full article

Self-healing coatings can replace conventional coatings and are capable of self-healing and continuing to protect the substrate after coating damage. In this study, two types of self-healing resins were synthesized as coatings: Type-A via Diels–Alder crosslinking of furfuryl-modified diglycidyl ether bisphenol A with bismaleimide, and Type-B through epoxy blending/curing to form a semi-interpenetrating network. FTIR and Raman spectroscopy confirmed the formation of Diels–Alder (DA) bonds, while GPC tests indicated incomplete monomer conversion. Both resins were applied to glass and wood substrates, with performance evaluated through TGA, colorimetry (ΔE), gloss analysis, and scratch-healing tests (120 °C/30 min). The results showed that Type-A resins had a higher healing efficiency (about 80% on glass substrates and 60% on wood substrates), while Type-B resins had a lower healing rate (about 65% on glass substrates and 55% on wood substrates). However, Type-B is more heat-resistant, has a slower decomposition rate between 300 and 400 °C, higher gloss retention, and less color difference (ΔE) between wood and glass substrates. The visible light transmission of Type-B (74.14%) is also significantly higher. Full article

Deep coalbed methane (CBM) reservoirs are characterized by high hydrocarbon content and are considered an important strategic resource. Due to their inherently low permeability and porosity, horizontal well drilling is commonly employed to enhance production, with the length of the horizontal section playing a critical role in determining CBM output. However, during extended horizontal drilling, wellbore instability frequently occurs as a result of drilling fluid invasion into the coal formation, posing significant safety challenges. This instability is primarily caused by the physical intrusion of drilling fluids and their interactions with the coal seam, which alter the mechanical integrity of the formation. To address these challenges, interpenetrating and semi-interpenetrating network (IPN/s-IPN) hydrogels have gained attention due to their superior physicochemical properties. This material offers enhanced sealing and support performance across fracture widths ranging from micrometers to millimeters, making it especially suited for plugging applications in deep CBM reservoirs. A self-degradable interpenetrating double-network hydrogel particle plugging agent (SSG) was developed in this study, using polyacrylamide (PAM) as the primary network and an ionic polymer as the secondary network. The SSG demonstrated excellent thermal stability, remaining intact for at least 40 h in simulated formation water at 120 °C with a degradation rate as high as 90.8%, thereby minimizing potential damage to the reservoir. After thermal aging at 120 °C, the SSG maintained strong plugging performance and favorable viscoelastic properties. A drilling fluid containing 2% SSG achieved an invasion depth of only 2.85 cm in an 80–100 mesh sand bed. The linear viscoelastic region (LVR) ranged from 0.1% to 0.98%, and the elastic modulus reached 2100 Pa, indicating robust mechanical support and deformation resistance. Full article

Background/Objectives: Photothermal therapy (PTT) is an emerging minimally invasive strategy in biomedicine that converts near-infrared (NIR) light into localized heat for the targeted inactivation of pathogens and tumor cells. Methods and Results: In this study, we report the synthesis and characterization of thermoresponsive nanogels composed of poly (N-isopropylacrylamide-co-N-isopropylmethylacrylamide) (PNIPAM-co-PNIPMAM) semi-interpenetrated with polypyrrole (PPy), yielding monodisperse particles of 377 nm diameter. Spectroscopic analyses—including ¹H-NMR, FTIR, and UV-Vis—confirmed successful copolymer formation and PPy incorporation, while TEM images revealed uniform spherical morphology. Differential scanning calorimetry established a volumetric phase transition temperature of 38.4 °C, and photothermal assays demonstrated a ΔT ≈ 10 °C upon 10 min of 850 nm NIR irradiation. In vitro antimicrobial activity tests against Pseudomonas aeruginosa (ATCC 15692) showed a dose-time-dependent reduction in bacterial viability, with up to 4 log CFU/mL. Additionally, gentamicin-loaded nanogels achieved 38.7% encapsulation efficiency and exhibited stimulus-responsive drug release exceeding 75% under NIR irradiation. Conclusions: Combined photothermal and antibiotic therapy yielded augmented bacterial killing, underscoring the potential of PPy-interpenetrated nanogels as smart, dual-mode antimicrobials. Full article

Polygalacturonic acid (PGA), derived from the natural plant polysaccharide, pectin, has been suggested as a biomaterial for implantable medical devices and tissue engineering; particularly in the field of bone implant materials. As a negatively charged polysaccharide, PGA can be considered similar to hyaluronic acid, a component of the extracellular matrix (ECM). PGA-based biomaterials may therefore exhibit favorable biocompatibility with surface chemistry mimicking the natural ECM. In this study, we synthesized semi-interpenetrating polymer networks (SIPNs) incorporating PGA, and conducted physical characterization and in vitro biocompatibility studies. Biocompatibility testing revealed the SIPNs to be cytocompatible, with the PGA component conferring some resistance to the adherence of the macrophage cell line RAW264.7. In addition, SIPNs did not support the fusion of primary murine macrophages into foreign body giant cells (FBGCs). Macrophage adherence and FBGC formation on implanted biomaterial surfaces are important events in the progression of a foreign body response. Our in vitro studies suggest that PGA-based materials may offer desirable biocompatibility profiles, holding promise for future clinical applications. Full article

Cellulose, a widely abundant natural polymer, is well recognized for its remarkable properties, such as biocompatibility, degradability, and mechanical strength. Conductive hydrogels, with their unique ability to conduct electricity, have attracted significant attention in various fields. The combination of cellulose and conductive hydrogels has led to the emergence of cellulose-based conductive hydrogels, which show great potential in flexible electronics, biomedicine, and energy storage. This review article comprehensively presents the latest progress in cellulose-based conductive hydrogels. Firstly, it provides an in-depth overview of cellulose, covering aspects like its structure, diverse sources, and classification. This emphasizes cellulose’s role as a renewable and versatile material. The development and applications of different forms of cellulose, including delignified wood, bacterial cellulose, nanocellulose, and modified cellulose, are elaborated. Subsequently, cellulose-based hydrogels are introduced, with a focus on their network structures, such as single-network, interpenetrating network, and semi-interpenetrating network. The construction of cellulose-based conductive hydrogels is then discussed in detail. This includes their conductive forms, which are classified into electronic and ionic conductive hydrogels, and key performance requirements, such as cost-effectiveness, mechanical property regulation, sensitive response to environmental stimuli, self-healing ability, stable conductivity, and multifunctionality. The applications of cellulose-based conductive hydrogels in multiple areas are also presented. In wearable sensors, they can effectively monitor human physiological signals in real time. In intelligent biomedicine, they contribute to wound healing, tissue engineering, and nerve regeneration. In flexible supercapacitors, they offer potential for green and sustainable energy storage. In gel electrolytes for conventional batteries, they help address critical issues like lithium dendrite growth. Despite the significant progress, there are still challenges to overcome. These include enhancing the multifunctionality and intelligence of cellulose-based conductive hydrogels, strengthening their connection with artificial intelligence, and achieving simple, green, and intelligent large-scale industrial production. Future research directions should center around exploring new synthesis methods, optimizing material properties, and expanding applications in emerging fields, aiming to promote the widespread commercialization of these materials. Full article

Industrial textile wastewater containing both heavy metals and dyes has been massively produced. In this study, semi-interpenetrating polymer network structures of sodium alginate (SA)/polyvinyl alcohol (PVA)/κ-carrageenan (CG) aerogel beads were synthesized for their simultaneous reduction. The SA/PVA/CG aerogel beads were synthesized through a cost-effective and environmentally friendly method using naturally abundant biopolymers without toxic cross-linkers. The SA/PVA/CG aerogel beads were spheres with a size of 3.8 $\pm$ 0.1 mm, exhibiting total pore areas of 15.2 m²/g and porous structures (pore size distribution: 0.04–242.7 μm; porosity: 93.97%) with abundant hydrogen bonding, high water absorption capacity, and chemical resistance. The adsorption capacity and mechanisms of the SA/PVA/CG aerogel beads were investigated through kinetic and isotherm experiments for heavy metals (Cu(II), Pb(II)), cationic dye (methylene blue, MB), and anionic dye (acid blue 25, AB)) in both single and binary systems. The maximum adsorption capacities of the SA/PVA/CG aerogel beads based on the Langmuir model of Cu(II), Pb(II), and MB were 85.17, 265.98, and 1324.30 mg/g, respectively. Pb(II) showed higher adsorption affinity than Cu(II) based on ionic properties, such as electronegativity and hydration radius. The adsorption of Cu(II), Pb(II), and MB on the SA/PVA/CG aerogel beads was spontaneous, with heavy metals and MB exhibiting endothermic and exothermic natures, respectively. Full article

Purpose: To fabricate 3D-printed, biodegradable conjunctival gelatin methacrylate (GelMA) inserts that can release polyvinyl alcohol (PVA) when exposed to an ocular surface enzyme. Method: In this work, biodegradable conjunctival inserts were 3D-printed using a stereolithography-based technique. The release of PVA from these insert formulations (containing 10% GelMA and 5% PVA (P-Gel-5%)) was assessed along with different mathematical models of drug release. The biodegradation rates of these inserts were studied in the presence of a tear-film enzyme (matrix metalloproteinase-9; MMP9). The morphology of the inserts before and after enzymatic degradation was monitored using scanning electron microscopy. Results: The 3D-printed P-Gel-5% inserts formed a semi-interpenetrating network, which was mechanically stronger than GelMA inserts. The PVA release graphs demonstrate that at the end of 24 h, 222.7 ± 20.3 µg, 265.5 ± 27.1 µg, and 242.7 ± 30.4 µg of PVA were released when exposed to 25, 50, and 100 µg/mL of MMP9, respectively. The release profiles of the P-Gel-5% containing hydrogels in the presence of different concentrations of MMP9 showed the highest linearity with the Korsmeyer–Peppas model. The results suggest that the degradation rate over 24 h is a function of MMP9 enzyme concentration. Over 80% of P-Gel-5% inserts were degraded at the end of 8 h, 12 h, and 24 h in the presence of 100, 50, and 25 µg/mL MMP9 enzyme solutions, respectively. Conclusions: These results demonstrate the potential for 3D printing of GelMA for use as conjunctival inserts. These inserts could be used to deliver PVA, which is a well-known therapeutic agent for dry eye disease. PVA release is influenced by multiple mechanisms, including diffusion and enzymatic degradation, which is supported by morphological studies and biodegradation results. Full article