Search Results (5,660)

Polyetheretherketone (PEEK) is a high-performance thermoplastic polymer with low surface energy, chemical inertness, and a highly crystalline structure, which limit durable adhesion to resin-based materials and require improved bonding strategies. This in vitro study evaluated the effect of incorporating multifunctional methacrylate (TMPTMA) and acrylate monomers (A-TMPT and A-DPH) into an experimental primer on the 24 h shear bond strength (SBS) of resin cement to PEEK (n = 6 per group). Experimental primers were prepared by adding varying amounts (100–500 µL) of each multifunctional monomer to a UDMA/MMA-based primer, and SBS was measured after cementation with a dual-cure resin cement. TMPTMA-containing primers produced median SBS values of approximately 10–12 MPa, while acrylate-based primers showed slightly higher values, particularly at higher concentrations, reaching up to ~15.8 MPa; however, no statistically significant improvement over the control group was observed (p > 0.05). Failure modes were predominantly mixed across all conditions. These findings indicate that multifunctional monomers, despite their potential to enhance cross-link density and wetting, do not substantially overcome the intrinsic adhesion-resistant nature of polished PEEK. The results underscore that monomer modification alone is insufficient and that effective adhesion to PEEK likely requires integrated strategies combining chemical activation with mechanical surface conditioning. Full article

Conductive hydrogels are promising materials for fabricating flexible wearable strain sensors. However, their practical application remains limited by several challenges, including poor mechanical strength, unstable sensitivity, restricted stretchability, and poor structural durability. In this study, a zirconium-reinforced conductive hydrogel (PSPZr) with a dual chemical–physical cross-linked network was designed and developed. In the structural framework, polypyrrole-decorated silk fibroin (SF/PPy) functioned as a conductive reinforcing component, acrylamide and sulfobetaine methacrylate constituted the flexible polymer basis, and zirconium ions (Zr⁴⁺) acted as ionic cross-linkers to construct a dual cross-linked structure and improve mechanical stability. Due to the synergistic contributions of hydrogen bonding, ionic coordination interactions, and SF/PPy, the optimized PSPZr hydrogel exhibited a tensile strength of 166 kPa and a maximum strain 559%. Additionally, it achieved improved elasticity and reliable shape recovery. Furthermore, the optimized PSPZr hydrogel exhibited a broad working range, sensitivity with a gauge factor of 2.8, rapid response, recovery kinetics, and exceptional cycling stability over 1000 stretching–releasing cycles as wearable strain sensors. This performance enabled real-time and accurate monitoring of diverse human motions. Therefore, this study presents a feasible and versatile strategy for developing mechanically robust and electrically stable conductive hydrogel, providing a new pattern for advanced applications in wearable sensors. Full article

This study investigates the effect of (3-glycidyloxypropyl)trimethoxysilane (GPTMS) passivation time on the adhesive bonding performance of aluminum substrates using an epoxy adhesive. Alkaline etching was used to generate a chemically active surface prior to silane treatment. GPTMS passivation led to the formation of silane-derived species on the aluminum surface. SEM/EDS indicated the presence of silicon-containing species. ATR-FTIR analysis showed the progressive development of siloxane (Si–O–Si) bonding with increasing passivation time. The mechanical performance of the bonded joints was evaluated using single-lap shear (SLS) testing. The SLS strength increased from 4.3 ± 1.0 MPa in the as-received substrate to 5.5 ± 1.2 MPa after etching. After GPTMS passivation, the strength reached a plateau beginning at 3 min, with a value of 13.5 ± 1.8 MPa. This corresponds to increases of 28% after etching and 223% after GPTMS passivation. This plateau behavior indicates a self-limiting interfacial process. The improved adhesion is attributed to siloxane formation within the silane layer and the chemical compatibility between GPTMS and the epoxy adhesive. A first-order conceptual semi-quantitative model was developed to relate silane surface coverage to adhesion strength. The results demonstrate that adhesion depends on both surface coverage and the development of siloxane bonding within the silane layer. This study highlights the importance of controlled passivation time in improving adhesion performance under the present experimental conditions. Full article

Gao-shan-hong-jing-tian (GSHJT) Oral Liquid is a phytochemical-rich preparation derived from Rhodiola, yet its anti-hypoxic active constituents and molecular mechanisms remain poorly understood. This study aimed to identify the key anti-hypoxic phytochemicals in GSHJT Oral Liquid and clarify their mechanisms of action to support its potential use in managing acute mountain sickness (AMS). We first established and validated an HPLC method for quality control, then comprehensively profiled the chemical composition using LC-MS. Network pharmacology and molecular docking were applied to predict the core anti-hypoxic components, candidate targets and signaling pathways. The primary bioactivity was further verified through an in vitro carbonic anhydrase (CA) inhibition assay. A total of 71 constituents were identified, with kaempferol and ellagic acid emerging as the primary anti-hypoxic phytochemicals. These compounds target seven core proteins (SRC, PIK3R1, ESR1, EGFR, PTK2, IGF1R, and LYN) to regulate vascular tone, inflammation, oxidative stress, blood–brain barrier integrity, and cell survival under hypoxic conditions. By modulating pathways such as HIF-1α, PI3K/AKT, FAK/PTK2, SRC, and IGF1R, these phytochemicals ultimately influence the onset and alleviation of AMS. Enzyme inhibition assays demonstrated that kaempferol and ellagic acid inhibited CA with IC₅₀ values of 34.05 μM and 119.1 μM, respectively. Molecular docking further revealed that both compounds suppressed CA activity through a combination of hydrogen bonding and hydrophobic interactions, consistent with a zinc-bound water-anchoring mechanism. This study elucidates the phytochemical basis and molecular mechanism responsible for the anti-hypoxic effects of GSHJT Oral Liquid, providing scientific support for its potential application as a natural, plant-derived intervention for preventing and alleviating acute mountain sickness, providing scientific support for its potential application and offering a reproducible paradigm for the rational development of other Rhodiola-based phytomedicines, though further in vivo validation is required to confirm the anti-hypoxic efficacy. Full article

Zinc oxide (ZnO) nanoparticles have attracted increasing attention in wood science due to their multifunctional properties, including antimicrobial activity, UV absorption, and photocatalytic behavior. Water-based deposition protocols offer clear advantages yet typically struggle with nanoparticle aggregation and limited adhesion to lignocellulosic substrates. This work introduces a rapid and scalable waterborne protocol combining catalyst-free aqueous seeding with microwave-assisted (MWA) growth under mild conditions. Pinus pinaster veneer samples were treated via dip-coating and spraying, with single and double seeding cycles, followed by MWA growth. Protocol efficiency was assessed through ZnO retention, SEM, and EDS analysis, while the impact of the substrate was assessed via mechanical testing, ATR-FTIR spectroscopy, and colorimetry. Dip-coating achieves significantly higher precursor uptake than spraying, while repeated seeding cycles further increase ZnO loading. Results suggest that incorporation may proceed through zinc–carboxylate bonds within the wood matrix, followed by localized ZnO nanostructures development. The effective integration did not weaken the mechanical properties, while color changes were significant for dip-coated samples and noticeable for sprayed ones. Overall, this methodology provides a fast, water-based, and minimally invasive route for ZnO incorporation into wood and a scalable pathway with retained mechanical and chemical properties and limited visual impact. Full article

Multilayer packaging—engineered by integrating complementary materials such as plastics, paper, and aluminum—has become a cornerstone technology for enhancing shelf life, minimizing spoilage, and reinforcing the mechanical integrity of packaging formats including films, pouches, and bottles. In this study, a laminate was developed by thermally bonding polylactic acid (PLA) with a poly(butylene adipate-co-terephthalate) (PBAT)/thermoplastic starch (TPS) matrix embedded with silver nanoparticles (Ag-NPs) at 0–3 wt.%. The resulting structures were systematically evaluated for their barrier performance, physicochemical characteristics, and antimicrobial functionality. Fourier-transform infrared (FTIR) spectroscopy confirmed the absence of chemical interactions between Ag-NPs and the polymer matrix, indicating physical dispersion rather than chemical bonding. However, at higher loading (3 wt.%), scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX) revealed notable nanoparticle aggregation. Functionally, the multilayer films demonstrated markedly improved water vapor barrier properties compared to single-layer PBAT/TPS films. Migration studies showed that silver release increased with nanoparticle concentration and was significantly enhanced under acidic conditions relative to distilled water. Importantly, Ag-NP-incorporated laminates exhibited pronounced antibacterial activity against Staphylococcus aureus. Collectively, these findings highlight the potential of Ag-NP-enriched, starch-based multilayer laminates as next-generation active packaging systems that combine with effective microbial control. Full article

Mucoadhesive drug delivery systems have emerged as a promising strategy to enhance the therapeutic efficacy of pharmaceuticals by improving drug residence time, bioavailability, and site-specific targeting. Among various materials investigated, biopolysaccharides have gained significant attention due to their biocompatibility, biodegradability, non-toxicity, and inherent mucoadhesive properties. Natural polymers such as chitosan, alginate, pectin, hyaluronic acid, and cellulose derivatives exhibit strong interactions with mucosal surfaces through hydrogen bonding, electrostatic interactions, and polymer chain entanglement. These properties enable prolonged drug retention at mucosal sites, controlled drug release, and enhanced permeation across biological barriers. Mucoadhesive biopolysaccharides have been explored for diverse routes of administration, including oral, buccal, nasal, ocular, vaginal, and pulmonary delivery. Furthermore, chemical modification and nanostructuring of these polymers have expanded their functionality, enabling targeted delivery of small molecules, proteins, peptides, and nucleic acids. This review highlights the mechanisms of mucoadhesion, key biopolysaccharides used in drug delivery, formulation approaches, and recent advances in their application as versatile platforms for novel therapeutic delivery systems. The continued development of mucoadhesive biopolysaccharide-based carriers holds substantial potential for improving treatment outcomes and patient compliance. Full article

Deep eutectic solvent (DES) extraction is a green and efficient technology. As a substitute for organic reagents, DESs are widely used to extract active ingredients from traditional Chinese medicine. This study established an environmentally friendly and efficient method for extracting astaxanthin (AST) from Phaffia rhodozyma (PR) using ultrasound-assisted deep eutectic solvents (DESs-UAE). The astaxanthin content was determined by high-performance liquid chromatography (HPLC). Six types of deep eutectic solvents composed of DL-menthol and selected hydrogen bond donors were prepared and evaluated, among which the DL-menthol–acetic acid system showed superior extraction performance. Response surface methodology (RSM) was employed to optimize extraction parameters (ultrasonic power, time, and temperature), and the optimal conditions were determined as follows: ultrasonic power 420 W, ultrasonic time 20 min, and ultrasonic temperature 60 °C, achieving an AST extraction rate of 62% (2.49 mg/g). Compared with conventional organic solvent extraction, DESs exhibited a significantly higher AST extraction rate from PR, except for dimethyl sulfoxide (DMSO). Scanning electron microscopy (SEM) analysis demonstrated that DES-UAE treatment disrupted the cellular structure of PR, resulting in numerous surface pores; this facilitated the release of intracellular bioactive components and significantly improved AST extraction efficiency. The PR extract showed no significant cytotoxicity and could effectively promote L929 cell proliferation. It concentration-dependently increased superoxide dismutase (SOD) activity and decreased malondialdehyde (MDA) content in H₂O₂-induced oxidative stress L929 cells, thereby alleviating oxidative damage. Additionally, it concentration-dependently upregulated type I collagen expression in these cells, ameliorated the decline in collagen synthesis function, and exerted a protective effect against cellular oxidative damage. This study provides a green alternative to toxic solvents and offers important theoretical and chemical support for the extraction of natural products and the high-value utilization of Phaffia rhodozyma (PR). Deep eutectic solvents have emerged as promising green alternatives to hazardous organic solvents, yet hydrophobic DESs tailored for lipophilic astaxanthin extraction from Phaffia rhodozyma and the linkage between extraction performance and anti-aging bioactivity remain insufficiently explored. Here, an ultrasound-assisted hydrophobic deep eutectic solvent extraction strategy was constructed to acquire astaxanthin, aiming to overcome low efficiency and environmental risks of conventional organic extraction techniques. Six DL-menthol-based DESs were prepared and screened, and DL-menthol–acetic acid possessed the optimal extraction capacity. Key extraction parameters were optimized via response surface methodology, and the maximum astaxanthin extraction recovery reached 62% (2.49 mg/g) under 420 W ultrasonic power, 20 min treatment and 60 °C. This yield was markedly higher than that of most common organic solvents; though comparable extraction effect was obtained with DMSO, the adopted DES possessed outstanding low-toxic and biodegradable superiorities that DMSO cannot match. SEM characterization verified that the combined treatment destroyed yeast cell structure and formed porous morphology, which accelerated intracellular astaxanthin release and accounted for improved extraction efficiency. Biological assays proved the extract possessed good biosafety and proliferation-promoting effect on L929 cells. It effectively relieved cellular oxidative injury by elevating the SOD level and reducing MDA accumulation in oxidative damaged cells, and upregulated type I collagen expression to mitigate aging-related collagen loss. This work develops an eco-friendly and high-efficiency extraction route for lipophilic active substance, confirms the practical value of hydrophobic DES, and provides experimental basis for high-value utilization of Phaffia rhodozyma resources. Full article

Polyester (PET) fibers are widely used to reinforce asphalt materials; however, their smooth and hydrophobic surfaces limit interfacial bonding and restrict their reinforcing efficiency. This study develops an eco-friendly surface modification method based on the chemical modification of gallic acid (GA) and aminosilane (KH792) to enhance the compatibility between PET fibers and asphalt. Modified fibers with various molar ratios of GA/KH792 were prepared and incorporated into asphalt mastic. Their performance was evaluated using softening point, cone penetration, dynamic shear rheometer (DSR), multiple stress creep recovery (MSCR), linear amplitude sweep (LAS), and bending beam rheometer (BBR) tests, combined with interfacial interaction analysis and scanning electron microscopy (SEM). The results show that surface modification significantly improves the reinforcing effect of PET fibers. In particular, the co-modified fiber with a GA/KH792 ratio of 1:1 exhibits the best performance, with increases of 27% in softening point and 105% in shear strength, as well as notable improvements in rutting resistance, fatigue performance, and temperature stability. Interfacial indices and SEM observations confirm enhanced adhesion, dispersion, and load transfer capacity. However, the improvement in low-temperature performance is limited. Overall, GA/KH792 chemical modification effectively enhances fiber asphalt interfacial interaction and provides a simple and sustainable approach for developing high-performance asphalt materials. Full article

In this study, polyvinyl alcohol (PVA) and chitosan (CS) were used as the base materials, and ethyl lauroyl arginate (LAE) as the antibacterial agent to prepare biodegradable bilayer composite films (P/C-L), whose properties compared with those of the monolayer films (P-C-L) of identical composition. Scanning electron microscopy (SEM) results revealed that the P/C-L films formed a compact microstructure with tight interlayer adhesion. Fourier transform infrared spectroscopy (FTIR) confirmed the presence of intermolecular hydrogen bonds within the P/C-L films without the formation of new chemical bonds, and X-ray diffraction (XRD) indicates that the crystallinity of the P/C-L films was dominated by that of PVA. P/C-L films exhibited a dual-surface structure with a hydrophobic CS layer and a hydrophilic PVA layer, broadening their potential application range. The P/C-L films demonstrated superior water resistance and light transmittance to the P-C-L films. When the LAE content increased from 0% to 10%, the P/C-L films displayed a more stable range of variation concerning visible light transmittance, water contact angle (CS layers), and moisture absorption than that of the P-C-L films, with the corresponding changing values being 86.86% to 62.09%, 96.79°to 72.46°, and 8.35% to 19.78%, respectively. Regarding antibacterial properties, the P/C-L films exhibited significantly enhanced activity across all LAE concentrations. Notably, P/C-L films at 2% LAE already outperformed P-C-L films at 4% LAE. At an LAE content of 10%, the inhibition zone diameters of the P/C-L films against E. coli and S. aureus reached 39.42 mm and 42.15 mm, which were 12.71 mm and 13.10 mm larger than those of the P-C-L films, corresponding to increases of 47.58% and 45.09%, respectively. In addition, both the P/C-L bilayer films and the P-C-L films could achieve complete biodegradation within 30 days under laboratory soil burial conditions. These findings suggest that P/C-L films show advantageous overall characteristics, highlighting their strong potential in the field of sustainable active food packaging. Full article

Low-dimensional (0D/1D/2D) nanomaterials exhibit unique physical and chemical properties different from general bulk materials due to enhanced surface and interface contributions and quantum confinement effects, which strongly modulate electronic structures. Boron, with atomic number 5, can form multicenter bonds and enables the construction of structurally diverse nanomaterials across different dimensionalities. In this review, boron-based low-dimensional materials are systematically organized from 0D clusters to 1D nanostructures and 2D sheets, and their optical and electrical properties are discussed in relation to structural factors such as dimensionality. This review provides an integrated perspective on how dimensional expansion and structural design govern the optical and electrical properties of boron-based nanomaterials. Full article

This study evaluated the effectiveness of maleic anhydride polypropylene (MAPP) in improving the mechanical performance and interfacial adhesion of lignocellulosic fiber-reinforced polypropylene (PP) composites. Based on Scanning Electron Microscopy (SEM) investigations, the relationship between fiber fraction, MAPP content, mechanical characteristics, and fracture morphology was the main focus. The test results showed that the stiffness and tensile strength of the composites increased with the addition of MAPP. The esterification reaction between the anhydride groups of MAPP and the hydroxyl groups of the fibers strengthened the interphase covalent bond, with the 46:50:4 composition producing the highest elastic modulus of 79.67 MPa and maximum tensile stress of 11.01 MPa. The dense interphase zone, few gaps, and no dominant fiber tension were all confirmed by SEM morphology, and also indicated effective stress transfer from the PP matrix to the fibers. However, the toughness of the material decreased significantly with increasing stiffness. Due to strong plastic deformation in the PP matrix that is not tightly attached to the fibers, the composition without MAPP (30:70:0) shows high impact energy and breaking strain, reaching 25.39 kJ/m² and 121.26%, respectively. The increase in chemical bonding at 4% MAPP content limits the mobility of the polymer chains, making it more brittle. In addition, even though MAPP is still present in the system, increasing the fiber fraction above 60% causes agglomeration, decreased homogeneity, and increased voids due to limited matrix wetting, ultimately deteriorating the mechanical properties. Tensile stress and elastic modulus have a very strong positive correlation (R² = 0.93), while impact energy and strain have a good correlation (R² = 0.89). The results overall showed that the ideal MAPP dosage is in the range of 4% before interface saturation occurs and confirmed that MAPP efficiency is determined by the balance between fiber composition, MAPP quantity, and dispersion homogeneity. Full article

Trichothecenes are the most common Fusarium mycotoxin contaminants of grains and their related products. Searching for effective adsorbents remains a major challenge in mycotoxicology, due to the low polarity and bulky chemical structure of type A trichothecenes. This study aimed to investigate in silico chitosan binding to type A trichothecenes such as diacetoxyscirpenol (DAS), neosolaniol (NEO), T-2 toxin (T2), and HT-2 toxin (HT2) and to study in vitro the devil fish chitosan biosorption capacity under two pH conditions (pHs 3 and 8). Molecular dynamic experiments showed that the chitosan monomers D-glucosamine and N-acetyl-D-glucosamine mostly bound to trichothecenes through the O in hydroxyls and glycosidic bonds and through their functional groups containing nitrogen. DAS exhibited a 9.44-, 6.39-, and 4.54-fold increase in the number of intermolecular contacts with chitosan compared to NEO, HT2 and T2, respectively. Moreover, in vitro experiments showed that at pH 3, chitosan exhibited a significant DAS sorption efficiency of 31.60% (p < 0.005), corresponding to a mass-normalized sorption capacity of 126.4 ng/mg. In contrast, no significant differences in sorption were observed at pH 8 (p > 0.05). Regarding NEO, T2, and HT2, no significant adsorption was detected under either pH condition (p > 0.05). This study is the first attempt to elucidate chitosan’s capacity to bind DAS and propose a mechanism for that interaction. Full article

The development of advanced and efficient oil–water separation technologies is crucial, and membrane fouling remains one of the primary obstacles hindering the sustainable development of membrane technology. Separation membranes, which differ in pore size and material composition, can be selected based on specific environmental conditions and application requirements. In the study, a composite enhanced PVDF membrane with a complex coordination aggregation structure and abundant hydroxyl groups was prepared by introducing a citric acid–Fe(III) complex coating onto the PVDF surface using tannic acid as an interfacial adhesive layer. Citric acid (CA) molecules participate in competitive cross-linking. The carboxylic acid groups (-COOH) of CA form ionic bonds with Fe³⁺. This promotes the formation of a complex cross-linked network inside the coating. It also successfully introduces additional hydrophilic groups. Consequently, a TA-Fe/CA composite coating system is constructed. The optimized modified membrane exhibited superior performance, with a water contact angle (WCA) of 14° and complete wetting within 0.5 s. The pure water flux reached 20,473.16 L/m²·h. Compared to the pristine membrane, the modified membrane demonstrated significantly enhanced hydrophilicity, underwater oleophobicity, and antifouling properties. During the separation of surfactant-stabilized toluene emulsions, the PVDF-TA-Fe/CA membrane showed higher separation efficiency and permeate flux than both the PVDF and PVDF-TA membranes. Furthermore, the modified membrane demonstrated excellent chemical stability, long-term durability, and thermal stability. Full article

Binding affinity prediction is about estimating the degree to which a drug binds to a protein. Predicting the binding affinity between a drug and a protein in a computational process helps researchers filter huge libraries of compounds before performing expensive biochemical lab experiments. Currently, there is interest in predicting binding affinity through computational pattern recognition or machine learning methods instead of the classical physics-inspired methods, which are computationally intractable except for tiny chemical compounds. In the last five years, several machine learning-based methods have been presented, whose experimental validations have achieved increasing Pearson coefficients while trained and tested in the PDBBind 2016 and CASF 2016 databases, respectively. These methods have an important diversity of architectures that provide different properties. The aim of this paper is to discern which binary properties (existence or absence) of these methods make them return higher Pearson coefficients. Basically, the properties introduced are related to the level of structural knowledge, the presence of 3D information, and the introduction of the relationship between the drug and the protein in the input of the model. The t-test confirms that the important binary properties for having a high Pearson coefficient are the protein (or part of the protein) being represented and introduced into the computational model as a graph, the pocket and the drug–protein interaction being part of the input, and incorporating the distance between atoms and the type of chemical bonds into the model. Full article