Search Results (2,804)

An efficient bacteriophage delivery system needs to be developed to overcome the challenges associated with phage instability, rapid diffusion, and loss of infectivity at the infection site. Hydrogels have been found to be potential carriers. Hydrogels have emerged as promising carriers due to their biocompatibility, tunable physicochemical properties and capacity for controlled release. However, the molecular factors that regulate phage–hydrogel interactions remain poorly understood. In this study, we employed an in silico framework combining molecular docking, molecular dynamics (MD) simulations, MM/PBSA binding energy calculations, machine learning-based adhesion prediction, and diffusion modeling to explore phage–hydrogel interactions at the molecular level. Surface-exposed bacteriophage proteins, such as capsid and tail proteins, were evaluated against eight different hydrogel polymers. Binding site analysis revealed the presence of multiple solvent-accessible pockets that can interact with the polymer. Docking studies showed favorable and stable interactions, with hyaluronic acid showing strong binding affinity to multiple phage proteins (−5.5 to −5.7 kcal/mol) and GelMA showing high affinity to the capsid gp10 protein (−5.6 kcal/mol). The integrity of the structural complexes was further confirmed by 100 ns MD simulations, stable RMSD and RMSF trajectories, compact structural conformations, and favorable MM/PBSA binding energies. Machine learning classification successfully differentiated high- and low-adhesion systems and identified hydrogen bonding and electrostatic interactions as key determinants of sustained yet reversible phage retention. Collectively, our findings suggest that the hydrogels enriched with charged and polar functional groups can facilitate stable but non-destructive phage binding, enabling controlled and sustained release. This study provides mechanistic insights into rational hydrogel design for phage delivery systems and highlights the potential of high-throughput computational strategies to accelerate the development of optimized phage therapeutics. Full article

Zeolitic imidazolate framework-8 (ZIF-8) is one of the most extensively studied metal–organic frameworks due to its high surface area, tunable porosity, chemical stability, and intrinsic antimicrobial activity. Recent research has focused on engineering ZIF-8 through metal doping and surface functionalization to enhance its physicochemical performance and expand its applications in food safety and environmental systems. Metal-doped ZIF-8 incorporating Cu²⁺, Fe²⁺/Fe³⁺, Ag⁺, or Mn²⁺ improves reactive oxygen species generation, enables controlled metal-ion release, and promotes synergistic bactericidal mechanisms against both Gram-positive and Gram-negative pathogens. In parallel, surface modification using biopolymers such as hyaluronic acid, chitosan, alginate, and polyethylene glycol enhances colloidal stability, reduces cytotoxicity, modulates surface charge, and improves adhesion to food-contact surfaces, thereby enhancing coating stability and sustained antimicrobial activity. These combined strategies support the development of multifunctional nanoplatforms with improved dispersibility, controlled release behavior, and compatibility with food packaging, sanitization, and water treatment applications. From a sustainability perspective, ZIF-8-based systems offer the potential to reduce reliance on conventional chemical disinfectants, minimize chemical residues, and enable the integration of biodegradable polymer matrices for safer and more environmentally responsible antimicrobial solutions. This review summarizes recent advances in synthesis strategies, structure–property relationships, antimicrobial and antibiofilm mechanisms, and environmental safety considerations. Key challenges, including scalability, regulatory acceptance, stability, and long-term ecotoxicological impact, are discussed, along with perspectives on stimuli-responsive systems, essential oil encapsulation, and smart antimicrobial coatings. Full article

Recently, more sustainable and biodegradable packaging materials have begun to attract attention in food packaging due to major, rising concerns related to plastic usage. This study aims to develop and characterize biodegradable food packaging materials, namely poly(lactic acid) (PLA) and poly(ε-caprolactone) (PCL) enriched with pomegranate peel extract (PoPE). Firstly, the optimal extract selected was a 24 h maceration of PoPE with 60% ethanol, after production with different solvents and methods. PLA- and PCL-based films were produced via melt compounding with the addition of PoPE at different concentrations (1, 3, 5 and 10%, w/w). FTIR confirmed that the PoPE did not modify the chemical backbones of PLA or PCL, with only a more pronounced O–H band in PCL, suggesting mainly non-covalent/physical interactions. UV–Vis spectroscopy showed tunable warm coloration and strong UV shielding with reduced transparency; for PLA ~3–5 wt.%, PoPE enabled near-complete UV blocking, while PCL achieved very high UV protection even at low loadings. PoPE improved toughness in PLA (3–5 wt.%) and maintained ductility in PCL (1–10 wt.%). PoPE-added PLA and PCL films maintained thermal stability up to 10 wt.% according to TGA results. DSC/XRD indicated a matrix-dependent crystallization response. PLA remained largely amorphous, whereas PoPE promoted PCL crystallinity without changing polymer crystal polymorphs. SEM images revealed homogenous dispersion of PoPE in the films. Full article

Microplastic pollution has emerged as a major environmental concern due to its persistence, widespread distribution and potential risks to ecosystems and human health. Among the various types of microplastics, fibrous microplastics (FMPs) account for 60% to 90% of all detected microplastic particles in surface waters, primarily originating from synthetic textile production, laundering, and wastewater discharge. Their elongated morphology, high aspect ratio, and complex surface chemistry differentiate them significantly from microplastic fragments or beads, creating unique challenges for effective removal in water treatment systems. In recent years, engineered biochar has attracted increasing attention as a promising and sustainable material for microplastic removal due to tunable pore structure, surface chemistry, and adsorption capacity. However, existing reviews largely discuss microplastic removal in general terms, with limited attention to the distinctive properties of textile FMPs and their implications for biochar design and performance. This review provides a comprehensive and focused analysis of the functional characteristics of biochar that enable the effective removal of textile FMPs in water systems. First, the environmental significance and physicochemical characteristics of textile-derived FMPs are summarized. Next, the major mechanisms governing biochar–microplastic interactions, including physical interception, adsorption, and aggregation processes, are discussed. The review then examines key functional characteristics of engineered biochar, such as pore structure, surface functional groups, hydrophobicity, and composite modifications, that enhance the sequestration of FMPs. Finally, current technological challenges, research gaps, and future directions for developing scalable biochar-based solutions for textile microplastic mitigation are discussed. By linking the unique properties of textile FMPs with the functional design of biochar, this review provides a framework to guide the development of more effective and sustainable treatment strategies for reducing microplastic contamination in aquatic environments. Full article

High quality factor (Q factor) resonant metasurfaces enable efficient mid-infrared (MIR) upconversion, yet their narrow operating bandwidths severely limit practical broadband detection and imaging applications. Although high Q magnetic toroidal dipole (MTD) modes exhibit outstanding momentum space ($k$-space) stability in linear optics, their application in nonlinear processes has primarily been confined to degenerate second-harmonic generation (SHG), leaving complex non-degenerate processes such as sum-frequency generation (SFG) largely unexplored. Here, we propose a tunable MIR upconversion platform based on an all-dielectric gallium phosphide (GaP) dimer metasurface. Breaking the in-plane symmetry to trigger Brillouin zone folding excites robust MTD quasi-guided modes (MTD-QGM), tightly confining the locally enhanced optical fields within the highly nonlinear GaP nanostructure. Synchronizing this high Q resonance with a spatially overlapping pump mode yields an exceptional SFG conversion efficiency of $7.9\times {10}^{-4}$, successfully translating a 3101.8 nm MIR signal to the 903 nm near-infrared band. Crucially, the intrinsic $k$-space stability of the MTD-QGM enables continuous, broadband upconversion through simple angle tuning. This mechanism effectively overcomes the narrow-band limitations characteristic of typical symmetry-protected resonators, establishing a robust paradigm for room-temperature MIR detection. Full article

Background/Objectives: Implant-associated infections remain among the most severe and clinically challenging complications in contemporary orthopedics, largely due to the formation of persistent bacterial biofilms and the limited penetration of systemically administered antibiotics into the tissue–implant interface. In this context, local antibacterial functionalization of implantable materials represents a promising strategy for the prevention of early infectious complications. The objective of this study was to develop and comparatively evaluate the antimicrobial performance of PLA-based composites loaded with antibiotics from different pharmacological classes, with a view toward their potential application in individualized 3D-printed implants. Methods: Polylactic acid (PLA)-based composites incorporating gentamicin, ciprofloxacin, doxycycline, and vancomycin were fabricated using thermal processing under conditions compatible with extrusion and fused filament fabrication. Physicochemical characterization (FTIR, TGA, SEM) was performed to assess the structure and morphology of the composites, and in vitro antibiotic release studies were conducted. Antimicrobial activity was evaluated using an agar diffusion assay against ATCC reference strains and clinical isolates of methicillin-susceptible and methicillin-resistant Staphylococcus aureus (MSSA and MRSA), Klebsiella pneumoniae, and Pseudomonas aeruginosa (n = 10 per species). The antibacterial performance of the composites was evaluated in comparison with standard commercial antibiotic disks used as qualitative reference controls. Results: Antibiotic-loaded PLA composites exhibited consistent and reproducible antibacterial activity, markedly exceeding that of neat PLA. The broadest activity spectrum was observed for PLA–ciprofloxacin (≈29–36 mm) and PLA–gentamicin (≈25–27 mm), which effectively inhibited both Gram-positive and Gram-negative clinical isolates, including MRSA and P. aeruginosa. PLA–vancomycin retained selective activity against staphylococci (≈14–15 mm), whereas PLA–doxycycline demonstrated limited efficacy against Gram-negative pathogens. Physicochemical analysis confirmed successful incorporation of antibiotics without detectable degradation of the polymer structure, while release studies demonstrated sustained antibiotic release from the composite materials. Importantly, the expected pharmacological activity profiles of the antibiotics were preserved after incorporation into the polymer matrix and subsequent high-temperature processing. Conclusions: The results demonstrate the feasibility of integrating clinically relevant antibiotics into a thermoplastic PLA matrix while preserving their selective antimicrobial activity following processing compatible with extrusion and additive manufacturing. The proposed PLA-based composites can be regarded as elements of a pharmacologically tunable antibacterial platform, offering a rationale for the development of context-dependent, biodegradable, 3D-printed implants for the local prevention of implant-associated infections in the setting of increasing antimicrobial resistance. Full article

Metastructures, waveguides composed of multiple unit cells (meta-atoms), have gained significant attention for controlling wave propagation in engineering applications, especially in the context of elastic and acoustic waves. However, existing metastructures often lack sufficient tunable functionality to dynamically control both elastic vibration and acoustic wave transmission using a single external parameter. This study introduces a phase-change material (PCM)-embedded meta-atom, where a core mass is connected to an outer shell by Archimedean spiral bridges. The solid–liquid phase transition of PCM induces a notable change in the effective shear modulus, enabling dynamic wave control. The mechanism for bandgap formation transitions from Bragg scattering in the solid PCM state to local resonance in the liquid state. Core rotation, driven by the phase transition, is key to generating flat bands and low-frequency locally resonant bandgaps at high temperatures. Temperature-dependent, mode-selective transmission behavior is observed, with transverse vibrations and acoustic waves exhibiting opposite blocking and transmission characteristics at the same frequency. This design provides a promising approach for decoupling sound and vibration management, using temperature control driven by the PCM phase transition. The work contributes to multifunctional metastructures with applications in adaptive noise control, structural health monitoring, and tunable vibration isolation systems. Full article

The management of complex acute and chronic wounds remains a formidable challenge in modern medicine, underscoring the urgent need for advanced therapeutic strategies that accelerate healing, prevent infection, and promote functional tissue regeneration. Electrospun nanofibers have attracted considerable attention in the biomedical field due to their extracellular matrix-like architecture, high surface area, interconnected porosity, and tunable physicochemical composition, which drive advances in wound regeneration, tissue engineering, and biopolymer-based therapeutics. In wound healing, nanofibrous dressings composed of natural polymers such as chitosan, gelatin, collagen, and cellulose promote cell attachment and proliferation, support angiogenesis, and enable infection control while delivering bioactive agents, thereby addressing significant challenges related to inflammation, biocompatibility, and antimicrobial resistance. In tissue engineering, aligned and hierarchically organized scaffolds fabricated from biopolymers such as collagen, gelatin, chitosan, and cellulose enhance the guided orientation of cells, differentiation, and functional regeneration of neural, musculoskeletal, vascular, and skin tissues. In addition to their conventional regenerative applications, recent studies have demonstrated that electrospun biopolymer nanofibers can be used in multifunctional biomedical platforms, including smart and stimuli-responsive systems for drug delivery, biosensing, regenerative interfaces, and wearable medical technologies. The integrated constructs that incorporate diagnostic or therapeutic functionalities, hybrid fabrication approaches that combine 3D printing with electrospinning, and intelligent biopolymer frameworks that enable telemedicine, real-time physiological monitoring, and personalized regenerative therapies offer new opportunities for developing improved biomedical systems. Overall, these advances position electrospun nanofiber systems as promising biomaterials for next-generation biomedical innovation. This review summarizes recent progress in tissue-engineered scaffolds, wound dressings, fabrication strategies for integrative therapeutics, and wearable devices with transformative potential for biomedical applications. Finally, the review addresses significant challenges related to scalability and clinical translation. It offers perspectives on future directions, including the integration of artificial intelligence and the regeneration of complex skin appendages, which will shape the next generation of nanofiber-based wound-healing therapies. Full article

Carbon dioxide (CO₂) hydrate slurries have emerged as promising candidates for cold thermal energy storage (CTES) and refrigeration systems due to their high latent heat, controllable flow behavior, and environmentally friendly nature. These slurries are formed by dispersing solid CO₂ hydrate particles in a liquid phase, forming a multiphase system with tunable thermophysical and rheological properties. The performance of these slurries is dependent on nucleation kinetics, particle sizes and their distribution, solid content, and thermal transport characteristics under flow conditions. This review paper gives an assessment of CO₂ hydrate slurries from a thermofluid’ perspective by focusing on key aspects such as hydrate nucleation mechanisms, viscosity behavior, shear response, thermal conductivity, convective heat transfer, and slurry stability. Particular attention is given to the role of surfactants and nanoparticle additives that enhance hydrate formation and improve slurry performance. The addition of nanofluids is discussed both in terms of their effect on thermal properties as well as in flow stability. Full article

This review explores the catalytic conversion of carbon dioxide (CO₂) into glycerol carbonate (GC), positioning this pathway as a sustainable strategy that couples environmental mitigation with the valorization of surplus glycerol from biodiesel production. Glycerol carbonate maintains extensive industrial utility as a green solvent, chemical intermediate, and functional component in polymers, cosmetics, and packaging. Distinct from prior literature, this study specifically evaluates the use of amorphous silica from rice husk ash (RHA) as a sustainable, low-cost support, analyzing the synergistic effect between Nb₂O₅, NiO, and ionic liquids in hybrid catalyst architectures. The review evaluates diverse catalytic frameworks, with a primary focus on heterogeneous systems. Silica-based materials are highlighted, particularly those synthesized from rice husk ash, which is an abundant amorphous silica source. The sol–gel method is identified as a robust route for engineering porous matrices with high surface areas and tunable structural properties. Furthermore, the doping of silica with metal oxides, such as niobium oxide (Nb₂O₅) and nickel oxide (NiO), is discussed as a strategic approach to introduce synergistic acid–base sites and redox properties that facilitate CO₂ activation. The integration of ionic liquids into hybrid systems is also examined as a promising frontier to enhance reaction kinetics and selectivity. Finally, this review delineates the nexus between agro-industrial waste management and the reduction in greenhouse gas emissions, proposing a circular economy framework for the biodiesel value chain. Full article

Two-dimensional (2D) heterostructures offer tunable electronic structures and synergistic interactions that enhance electrocatalytic activity beyond the limits of single-component materials. However, the same atomically thin interfaces that enable high performance also introduce inherent mechanical, chemical, and electronic vulnerabilities, giving rise to complex and coupled degradation pathways. In this review, we provide a systematic overview of degradation in 2D heterojunction electrocatalysts during electrochemical operation, covering failure mechanisms, operando characterization, and stabilization strategies. Degradation is governed by interfacial strain accumulation, bubble-induced stress and delamination, galvanic corrosion, and selective leaching, while stability can be improved through interfacial coupling, structural confinement, and controlled reconstruction. These insights provide practical design guidelines for developing robust 2D heterostructures for electrochemical energy conversion. Full article

One of the main sources of microplastic pollution in aquatic ecosystems is municipal wastewater, and preserving the ecological security of water depends on its effective removal. In this study, a potential multi-functionalized nanocomposite (NH₂-MIL-101(Fe)/CS/GO), which consists of an iron-based metal–organic framework (NH₂-MIL-101(Fe)) integrated with chitosan (CS) as a biopolymer matrix and graphene oxide (GO) as a conductive support, was exploited to enhance microplastic removal via different adsorptive hydrophilic/hydrophobic interactions. According to adsorption tests, the removal efficiencies of NH₂-MIL-101(Fe)/CS/GO for polyethylene terephthalate (PET) and polystyrene (PS) microplastics (25–30 μm) were 93.8% and 89.7%, respectively, at pH 6.2 and for 40 min of contact time. Adsorption isotherms were well fitted to both the Langmuir and the Freundlich models, and the maximum adsorption capacities of PET and PS were 321.4 and 255.1 mg·g⁻¹, respectively. The removal efficiency reached 92.5% after six cycles. The proposed MOF-based CS/GO nanocomposite provides an efficient and durable method of controlling microplastic contamination in urban wastewater. The developed multi-functionalized nanocomposite offers excellent electrostatic and hydrophobic synergy through a large surface area and π–π interactions for GO, positively charged CS, and a very high surface area with tunable porosity for the amino–MIL-101 (Fe) moiety. The proposed MOF-based nanocomposite provides an effective and persistent method of reducing microplastic contamination in constructed wetlands and water/wastewater treatment plants. Full article

Bioadhesive materials capable of operating under aqueous conditions are of considerable interest for biomedical and materials science applications. Peptide-based systems represent an attractive platform for such materials due to their structural tunability, inherent biocompatibility, and ability to form supramolecular networks through noncovalent interactions. In this work, a focused library of tyrosine-containing dehydropeptides was designed and synthesized to investigate how molecular architectures influence self-assembly, hydrogel formation and adhesive properties. The peptides were synthesized using a solution-phase Boc strategy and systematically varied with respect to N-terminal protection and C-terminal functionality. The N-protected dehydropeptides formed supramolecular hydrogels through multiple gelation triggers, including pH reduction and heating–cooling cycles. Rheological characterization confirmed the formation of viscoelastic networks with tunable mechanical properties, with storage moduli reaching tens of kilopascals depending on peptide structure. Scanning electron microscopy revealed dense fibrous nanostructures consistent with supramolecular hydrogel formation. The N,C-deprotected dehydropeptides displayed reduced gelation propensity but formed cohesive films with measurable adhesive performance toward hydrophilic substrates. Lap-shear tests demonstrated high shear strengths for the hydrophilic films, highlighting their structural robustness under stress. Overall, this study provides insights into the structure–property relationships governing tyrosine-containing dehydropeptide assemblies and demonstrates their potential as minimalistic building blocks for supramolecular adhesive materials. Full article

Improving the interfacial compatibility between cellulose and poly(butylene adipate-co-terephthalate) (PBAT) is critical for enhancing the performance of PBAT-based composites. Here, microcrystalline cellulose (MCC) was homogeneously silanized at the molecular chain level using t-hexyldimethylchlorosilane (TDMS-Cl) as the modifier, yielding t-hexyldimethylsilylated cellulose (TDMS-Cell). TDMS-Cell/PBAT composite films were then prepared by solution blending and casting in tetrahydrofuran (THF). Structural characterizations confirmed the successful grafting of TDMS-Cl onto cellulose chains, resulting in TDMS-Cell with a degree of substitution of approximately 2. Microstructural observations combined with thermal analysis revealed that TDMS-Cell exerted a dual effect on the crystallization behavior of PBAT: it acted as a heterogeneous nucleating agent that increased the crystallization temperature, while the pronounced steric hindrance simultaneously suppressed crystal growth. Mechanical testing showed that simultaneous strengthening and toughening were achieved at an optimal TDMS-Cell loading of 3–5 wt%. Specifically, the tensile strength increased from ~16 MPa for neat PBAT to 21 MPa (31.25% improvement), and the elongation at break increased from ~700% to 964% (37.7% improvement). In addition, the incorporation of an appropriate amount of TDMS-Cell effectively enhanced the surface hydrophobicity of the composite films. At higher filler loading, however, solvent evaporation-induced phase separation led to self-aggregation of TDMS-Cell, which in turn deteriorated both the mechanical properties and surface hydrophobicity of the composites. Overall, this work systematically elucidates the structure–property relationships of silanized cellulose/PBAT composites in a homogeneous solution system, providing a rational basis for interfacial design and property optimization of PBAT/biomass-based composite materials. The prepared TDMS-Cell/PBAT composite films with balanced mechanical strength, tunable crystallization behavior, and improved surface hydrophobicity exhibit great potential for practical applications in high-performance flexible packaging materials, functional film substrates, lightweight composite structural components, and tunable hydrophobicity coating substrates. Full article

The oxygen evolution reaction (OER), serving as the anodic bottleneck in electrochemical water splitting for hydrogen production, severely limits the overall energy conversion efficiency due to its sluggish kinetics. Developing efficient and stable electrocatalysts based on earth-abundant elements is a critical challenge for advancing clean energy technologies. In recent years, silicate materials have demonstrated significant potential in alkaline OER catalysis owing to their unique stable silicon-oxygen tetrahedral framework and flexibly tunable metal-oxygen-silicon electronic coordination environments. This review systematically summarizes recent progress in silicate-based materials, including natural clay mineral supports such as halloysite, for OER electrocatalysis. It focuses on controllable synthesis strategies for silicate materials and provides an in-depth analysis of the regulation mechanisms for their electronic structure and surface properties through defect engineering, anion vacancy construction, and bimetallic/non-metallic heteroatom doping. Particular emphasis is placed on research pathways that utilize natural silicate clay minerals as both supports and silicon sources to construct high-performance composite catalytic materials via innovative structural design and interface engineering. Systematic studies indicate that precisely modulated silicate-based catalysts exhibit excellent electrochemical activity and long-term stability in the alkaline OER process. This review offers perspectives on the future development of efficient and stable silicate-based catalytic systems for renewable energy conversion. Full article