Search Results (1,258)

This study examined Kefiran, an exopolysaccharide derived from milk kefir grains, as a novel biopolymer for encapsulating phenolic extracts from sunflower cake and its antimicrobial properties in the development of natural and functional food ingredients. Kefiran was obtained from kefir grains using three extraction protocols: hot water (M1), hot water with 30% trichloroacetic acid (M2), and mild heat combined with ultrasound at 60 °C (M3). The ultrasound-assisted method produced the highest carbohydrate concentration. Spectrophotometric assays (phenol–sulfuric and Bradford), Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, and water-holding capacity were employed to characterize the composition, structure, and morphology of the extracts, revealing well-preserved polysaccharide fingerprints and a highly porous microstructure, consistent with their potential application in food systems. Kefiran was then evaluated as an encapsulating agent in complex coacervation at pH 3.75, using three Kefiran-based wall formulations (M1, M2, and M3) with gum arabic and whey protein isolate (WPI) as co-wall materials, and their performance was compared with gum arabic and WPI controls. Across formulations, coacervate microcapsules achieved high encapsulation efficiencies (83–93%), tunable particle sizes, and predominantly negative zeta potentials, indicative of good colloidal stability. The Kefiran extract and coacervate microcapsules demonstrated significant antioxidant and antimicrobial activity against Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and Candida albicans, with minimum inhibitory concentrations ranging from 250 to 1000 µg/mL. The findings support ultrasound-extracted Kefiran as a multifunctional biopolymer suitable for bioactive delivery and as a natural antimicrobial component in advanced functional food formulations. Full article

Studying Bingham flows in permeable media under a periodic magnetic field enhances the understanding of yield-stress fluids for applications like oil recovery and filtration. This study combines non-Newtonian behavior with porous-medium resistance and magnetic variations, facilitating the analysis of complex flow phenomena, including oscillatory yielding and improved flow control in porous structures. The viscous potential theory is employed to streamline the mathematical processes. The utilization of linear governing partial differential equations of motion, along with appropriate nonlinear boundary conditions, yields additional simplifications. The investigation yields a nonlinear Mathieu oscillator that governs the interfacial displacement. A non-perturbative method is used to convert this nonlinear ordinary differential equation into a linear equation. A non-dimensional formulation minimizes the fundamental variables required to characterize the system by establishing a collection of dimensionless physical characteristics. The study analyzes a nonlinear Mathieu oscillator with complex coefficients to explore system dynamics related to elevation. By simplifying the variable coefficients, it enhances the examination of stability and resonance behavior. Despite inherent complexities, the work effectively clarifies fundamental concepts, contributing to a more coherent understanding of the subject. The Hartman number, magnetic field, and magnetic permeability ratio exert a destabilizing effect. Conversely, the Bingham parameter, Weber number, and periodic frequency exert a stabilizing influence. Full article

This research reports on the properties of oxide-ceramic coatings produced by plasma electrolytic oxidation in novel electrolyte solutions for implantology applications. A series of bioactive calcium-phosphate coatings was synthesized on medical-grade Ti-13Zr-13Nb alloy using the plasma electrolytic oxidation (PEO) method. Novel electrolytes enriched with calcium and phosphorus were developed, enabling the formation of coatings with tailored physicochemical and structural characteristics. A correlation was established between the electrolyte composition and the phase composition, thickness, morphology, porosity, and microhardness of the resulting coatings. The optimum coatings exhibited a Ca/P ratio close to that of natural human bone tissue, homogeneity, a well-developed porous surface topography, and controlled resorption behavior. For the first time, a mechanism of calcium-phosphate coating resorption in a biologically active environment has been proposed. It involves partial dissolution, the formation of apatite-like surface structures, and the subsequent controlled release of Ca and P ions. In vitro testing in simulated body fluid indicated the potential bioactivity of the synthesized coatings. The proposed calcium-phosphate coatings may be considered promising candidates for future implant surface modification. The results obtained are significant for the development of advanced orthopedic and dental implants, including those fabricated using additive manufacturing technologies. Full article

An optimized method of triclosan MIPs using a Design of Experiments (DOE) strategy was developed. The concentrations of methacrylic acid (MAA, monomer), 2-hydroxyethyl methacrylate (HEMA, co-monomer), and acetonitrile (ACN, solvent) were chosen as the critical parameters for the preparation process since they affect imprinting efficacy, morphological structure, and release profile of the material. A Box–Behnken design was utilized for the evaluation of how these factors influence the imprinting factor (IF). The optimized formulation revealed proper IF value indicating efficient molecular recognition. FTIR analysis validated the presence of acrylate-based bonds in the network structure. In addition, SEM images indicated a porous and aggregated structure of MIPs, which facilitated the accessibility of imprinted cavities. Release kinetics revealed two-phase profiles characterized by a moderate initial stage followed by sustained release up to 48 h. The Korsmeyer–Peppas model represented a better correlation (R² = 0.9754) compared to other kinetic models, implying complex diffusion-controlled release processes. Finally, MD simulations confirmed the experimental findings since MAA exhibited higher binding frequencies with triclosan than HEMA, proving its dominant role in molecular recognition. Full article

Adobe construction, as part of earthen architecture, is a traditional building technique that is widely used but particularly vulnerable to the effects of water and other climatic factors. This article analyses the physical and mechanical behaviour of three different grain sizes of adobe specimens, classified according to the predominant presence of coarse aggregates (CA), fine aggregates (FA), and fine aggregates with plant fibres (AF). In order to assess their response to climatic scenarios, these specimens are subjected to wetting–drying cycles (3, 5, and 7 cycles) and accelerated weathering tests (E) under controlled laboratory conditions. The main objective is to determine the influence of particle size distribution and the incorporation of plant fibres on the strength, stiffness, durability, and hydraulic behaviour of the material. For this purpose, an experimental programme was developed based on compression, modulus of elasticity, ultrasonic, abrasion, hydraulic erosion, and capillary absorption tests, and carried out at different stages of deterioration. Thus, six specimens were analysed for each of the five time points studied (0, 3, 5, 7, E) and for each proposed particle size distributions, giving a total of 450 samples analysed. The results show that the coarse mix exhibits greater overall mechanical stability, whereas the fine mix is more sensitive to the action of water. Although the addition of fibres improves ductility and resistance to surface erosion, it alters the porous structure of the material. Overall, the results confirm that particle size distribution and fibre reinforcement decisively influence the durability of adobe. Full article

The present study addresses the fabrication of porous gyroid architectures by additive manufacturing from preceramic polymer feedstocks. Photocurable emulsions were engineered by combining a silicone powder with acrylate monomers and dispersing an emulsified secondary phase of calcium nitrate. The formulations showed light-curing behaviour compatible with digital light processing vat photopolymerization (DLP-VPP), enabling high-fidelity replication of triply periodic minimal surface (TPMS) gyroids (designed porosity: 85 vol.%). After pyrolysis in nitrogen at 700 °C, the lattices converted into CaO–SiO₂-derived amorphous matrices embedding an in situ turbostratic/pyrolytic carbon fraction, as suggested by the photothermal response and preliminary impedance behaviour, although the latter was measured in liquid electrolyte and therefore does not isolate electronic transport. To improve robustness during polymer-to-ceramic conversion, pharmaceutical borosilicate waste glass (BASG) was added as a passive filler (30–70 wt.%). The waste-glass phase acts as a passive filler that improves processing robustness and can mitigate shrinkage-induced damage during pyrolysis, while remaining electrically insulating (dielectric) and therefore not directly contributing to electronic conduction. The resulting structures combine high surface-to-volume ratio, controlled open porosity, and structural integrity with electrochemical responsiveness under the adopted test conditions, making them promising architected platforms for electrochemical components where interconnected porosity is advantageous. Full article

High-permeability reservoirs at the extra-high water-cut stage commonly exhibit preferential flow, limited sweep expansion, and complex remaining-oil occurrence. To clarify the pore-scale mechanisms controlling waterflood sweep and remaining-oil retention, this study integrates CT-assisted core flooding and microfluidic chip visualization using a high-permeability sandstone core from the Guantao Formation in the Bohai Bay Basin. The CT-assisted core flooding experiment was used to quantify the stage-wise evolution of pores swept by the water phase, while the microfluidic experiment was used to visualize displacement pathways, local bypassing, and remaining-oil morphology under controlled pore-network conditions. The results show that waterflood sweep exhibits clear stage-wise evolution. During the low water-cut stage, injected water preferentially advances through large pore channels, resulting in limited sweep efficiency. With increasing water cut, pores newly swept by the water phase gradually shift from large pores to medium and small pores, accompanied by increasing displacement pressure. Under the present experimental conditions, the lower radius limit of pores newly swept by the water phase is approximately 7.54 μm, corresponding to a capillary force of about 0.9 MPa. When the injected volume exceeds approximately 2.5 PV, the sweep efficiency approaches a plateau and increases only from 0.72 to 0.75 at 5.0 PV, indicating that approximately 25% of the pore space remains difficult to be effectively swept. Image-based classification indicates that remaining oil can be divided into six occurrence types: clustered, porous, columnar, dead-end, film-like, and granular. Clustered and porous are the dominant occurrence types, accounting for a combined 59.7% of the total remaining oil. Pore-structure heterogeneity controls the microscopic sweep boundary through the combined effects of intra-unit structural dispersion and cross-unit structural contrast, which together regulate capillary resistance, seepage resistance, preferential flow, local bypassing, and remaining-oil retention. Microfluidic observations further show that permeability contrast and displacement velocity affect pore-scale displacement pathways and remaining-oil morphology. These findings provide experimental evidence for understanding the lower sweep-radius limit and remaining-oil occurrence mechanisms in high-permeability heterogeneous reservoirs at the extra-high water-cut stage, while the chip-scale velocity effects should be interpreted as pore-scale mechanistic evidence and require further validation before field-scale application. Full article

Transforming existing structural surfaces into sensing interfaces offers a promising route for scalable hydrogen monitoring in hydrogen-handling facilities, where leakage poses significant safety risks, addressing the limitations of conventional point-based sensors. In this study, a surface-integrated ZnFe₂O₄–CNT (ZFC) composite coating is developed as a potentially retrofit-compatible sensing solution to enable hydrogen sensing directly on cementitious materials, combining material-level functionality with data-driven concentration prediction. The ZFC composite was synthesized via a hydrothermal method followed by CNT functionalization and composite formation, and was then applied onto cement-based substrates using a thickness-controlled coating approach. Structural and morphological characterization (XRD, FESEM, TEM, BET) confirmed the formation of a hierarchical, porous architecture, while hydrogen sensing performance was evaluated under controlled thermo-hygrometric conditions (24–72 °C, 32–87% RH) at 10,000 ppm H₂. The sensor exhibited stable and reversible responses, with optimal performance at 39–52 °C and a minimum response time of 18 s. An XGBoost model enabled accurate prediction of hydrogen concentration, achieving R² ≈ 0.92 and RMSE ≈ 820 ppm under dynamic exposure. These results demonstrate that coupling redox-active oxide surfaces with conductive CNT networks enables effective surface-based chemiresistive sensing under realistic conditions. The proposed system transforms conventional cementitious materials into smart, surface-integrated hydrogen sensing systems, offering a scalable and retrofit-compatible approach for real-time monitoring in hydrogen-related infrastructure. Full article

Achieving precise control over anticancer drug release remains one of the key challenges in modern pharmaceutical development, as it directly determines therapeutic efficacy, systemic toxicity, and patient outcomes. This review critically evaluates recent advances in three major formulation strategies: polymeric solid dispersions, cyclodextrin-based inclusion complexes, and metal–organic frameworks (MOFs), with a particular focus on their capacity to tailor anticancer drug release. Over the past decade, polymeric solid dispersions and cyclodextrin-based carriers have played a central role in improving the dissolution and bioavailability of poorly water-soluble anticancer agents, while also enabling modified release profiles through rational formulation design. Increasing structural complexity, including ternary systems and supramolecular assemblies, reflects a shift toward more controllable delivery platforms. In recent years, MOFs have emerged as highly adaptable porous materials capable of supporting controlled and stimuli-responsive release. The integration of imaging agents, magnetic components, and photothermal functionalities has further enabled the design of multifunctional and theranostic platforms. Taken together, these technologies reflect a shift from conventional solubility enhancement toward structurally engineered systems designed to achieve predictable and controlled drug release. Continued advances in material design and formulation strategies are expected to further refine release kinetics and support the development of next-generation anticancer therapies aligned with the growing demand for precision medicine. Full article

In ulcerative colitis (UC), the therapeutic efficacy of nanoparticle (NP)-based drug delivery systems is limited by premature drug release, uptake or degradation of NPs during their passage through the harsh gastrointestinal tract (GIT) environment, poor colon targeting, and rapid NP clearance caused by diarrhea symptoms. This study focused on designing an advanced spatiotemporally controlled nanohybrid hydrogel drug delivery system to overcome these challenges. We developed a pH- and temperature-responsive polysaccharide-based hydrogel composed of chitosan (CS), β-glycerol phosphate disodium salt pentahydrate (GP), hydroxypropyl cellulose (HPC), and collagen type I (Col I), designated as CS/HHPC/Col I-GP. The hydrogel exhibited a dense and uniform porous reticular structure, with an average pore diameter of 127.45 ± 2.22 μm. The equilibrium swelling ratio of the CS/HHPC/Col I-GP was determined to be 32.10 ± 1.11 g/g, indicating excellent swelling capacity and sustained structural stability over 6 h—making it suitable for sustained drug release in the intestinal tract. Then, the prepared curcumin nanoparticles (CurNPs) were encapsulated into the CS/HHPC/Col I-GP hydrogel to form the CS/HHPC/Col I-GP-CurNPs composite. The polysaccharide-based hydrogel shell of the formulation withstood harsh gastrointestinal conditions, enabled targeted adhesion to the colon, and was specifically degraded by colonic enzymes. The CurNPs released in the colon benefit from their negatively charged characteristics, enabling accumulation at the positively charged inflamed sites and achieving sustained Cur release. The results of the gastrointestinal digestion simulation experiment showed that the cumulative release of CS/HHPC/Col I-GP-CurNPs was only 12.33 ± 2.17% in simulated gastric fluid (SGF) and reached 96.91 ± 1.98% in simulated colonic fluid (SCF) after 60 h. Cell and animal experimental data confirmed that the formulation significantly alleviated colitis symptoms by modulating the repolarization of pro-inflammatory M1 macrophages to anti-inflammatory M2 phenotypes and deactivating the TLR4/MyD88/NF-κB pathway. Furthermore, the integrity of the intestinal mucosal barrier and the gut microbiota were enhanced. This study provides a promising strategy for the oral drug treatment of UC. Full article

Two-dimensional molybdenum disulfide (MoS₂) has emerged as a promising candidate for next-generation electronics and optoelectronics; however, its scalable synthesis with precise control over domain size and film continuity remains challenging. Herein, we report a physical vapor deposition (PVD)-assisted chemical vapor deposition (CVD) strategy for the controllable growth of high-quality monolayer MoS₂. By thermally evaporating an ultrathin (3 nm) MoO₃ precursor film, spontaneous post-deposition dewetting yields a porous honeycomb morphology that significantly enhances vapor–solid reaction kinetics during subsequent sulfurization. Crucially, by modulating the argon carrier gas flow rate to regulate the local sulfur chemical potential, we achieve distinct growth regimes: a high flow rate (70 sccm) suppresses nucleation density, enabling isolated triangular and hexagonal single crystals with lateral dimensions up to 500 μm, whereas a reduced flow rate (50 sccm) promotes high-density nucleation and coalescence into continuous centimeter-scale polycrystalline films. Comprehensive structural and optical characterizations, including atomic force microscopy, Raman spectroscopy, photoluminescence, and X-ray photoelectron spectroscopy, confirm that the synthesized MoS₂ exhibits prototypical monolayer thickness (~0.7 nm), well-defined local crystallinity and a direct bandgap emission at 1.84 eV. This work establishes a robust, scalable, and highly tunable route for synthesizing large-area 2D TMDs tailored for advanced device integration. Full article

Stress shielding (SS) after cementless total hip arthroplasty arises from the stiffness mismatch between conventional Ti-6Al-4V femoral stems (110 GPa) and cortical bone (10–30 GPa). The β-type Ti-33.6Nb-4Sn (TNS) alloy femoral stem addresses this limitation through a continuous Young’s modulus gradient (~70 GPa proximally to ~40 GPa distally) achieved by localized heat treatment of a single homogeneous alloy. This review synthesizes a translational research program encompassing material characterization, finite element modeling (FEM), preclinical animal studies, and prospective clinical follow-up of up to seven years. FEM demonstrated favorable proximal micromotion well below the osseointegration threshold, with physiological proximal stress concentration concordant with clinical outcomes. At seven years, SS grade distribution was significantly lower in the TNS group than in Ti-6Al-4V controls, with SS frequency reduced in Gruen Zones 2, 3, and 6, and no stem-related failures; however, third-degree SS was still observed in 11 of 34 evaluable cases (32%), indicating that modulus-gradient optimization alone is insufficient to fully prevent SS. TNS alloy is currently the only β-type titanium alloy clinically applied in joint prostheses. Remaining challenges include stem geometry optimization, additive manufacturing-based porous structures, and dual-energy X-ray absorptiometry-based bone density quantification. Future directions encompass long-term follow-up, cyclic fatigue FEM simulations, and expansion to fracture fixation devices and dental implants. Full article

Porous bilayer Ni–Co and sandwiched Ni–Co–Ni electrodes were fabricated by combining aqueous electrodeposition with high-temperature molten-salt Al deposition and subsequent electrochemical dissolution in NaCl–KCl–AlF₃ melt at 750 °C. The study aimed to determine how the initial layer architecture controls phase evolution, porous structure formation, and hydrogen evolution performance in alkaline media. SEM/EDS and XRD analyses showed that the two electrode designs followed different reaction pathways during molten-salt treatment. In the Ni–Co system, Al reacted predominantly with Co, leading mainly to Co–Al intermetallic formation and, after dissolution, to a highly open coral-like porous network. In contrast, the Ni–Co–Ni architecture promoted mainly Ni–Al phase formation and produced a more compact porous surface with a Ni-rich outer layer. Despite these morphological differences, both layered porous electrodes outperformed untreated Ni and porous Ni in 1 M NaOH. At −0.6 V vs. RHE, porous Ni–Co and NiCo–Ni reached current densities of −162 and −141 mA·cm⁻², respectively, compared with −87 mA·cm for porous Ni and −45 mA·cm for flat Ni. The Ni–Co–Ni sandwiched electrode showed the most favourable HER kinetics and benchmark performance, with the lowest Tafel slope (111 mV·dec) and the lowest potentials at −10 and −100 mA·cm (−0.132 and −0.556 V, respectively). These results demonstrate that the electrocatalytic response of molten-salt-derived porous Ni-based electrodes is governed not only by porosity development but also by the spatial arrangement of metallic layers prior to Al infiltration and dealloying. Full article

Transition-metal oxide/layered double hydroxide (LDH) electrodes often suffer from insufficient utilization of active sites, sluggish electron/ion transport, and limited cycling stability at high rates. Here, La-doped ZnCo₂O₄/MnCo-LDH nanoflowers serve as the positive electrode and Ti-supported Sb-doped SnO₂ (Ti/Sb-SnO₂) serves as the negative electrode for constructing an asymmetric supercapacitor. A stepwise hydrothermal route, La-doping regulation, and ethylenediamine-assisted morphology control transform stacked nanosheets into open porous nanoflowers with a specific surface area of 382.5 m² g⁻¹, thereby exposing more electroactive sites and shortening OH⁻ diffusion pathways. La³⁺-induced lattice distortion and defect-related oxygen species further tune the electronic structure and improve interfacial charge-transfer kinetics. The optimized La-ZnCo₂O₄/MnCo-LDH electrode delivers 2130 F g⁻¹ at 1 A g⁻¹ and retains 1993 F g⁻¹ after 10,000 cycles at 3 A g⁻¹. The Ti/Sb-SnO₂ negative electrode provides 673 F g⁻¹ at 1 A g⁻¹ and 302 F g⁻¹ at 15 A g⁻¹. The assembled device operates stably from 0 to 1.8 V in 2 M KOH and achieves 69 Wh kg⁻¹ and 13,500 W kg⁻¹. Full article

This study presents a sodium alginate/chitosan/activated carbon (SA/CS/AC) gel microspheres loaded with Citrus reticulata peel allelochemicals for continuous inhibition of Microcystis aeruginosa by controlled release. Preparation parameters were optimized via response surface methodology (RSM) for improved algal inhibition, yielding an optimal formulation: 1.97% SA, 0.76% CS, 0.31% AC. The optimized gel microspheres showed a 7-day inhibition rate of 85.17 ± 2.49%, consistent with the predicted 85.29%. Characterization revealed that AC optimized the gel’s porous structure and surface functionality, providing more adsorption sites for allelochemicals. This helps improve the loading capacity of the gel microspheres and enables stable sustained release, with a cumulative release of 70% over 25 days. Algal inhibition declined slightly from day 7 to 30 due to allelochemical depletion but remained 76.27%, versus 30.58% for the blank SA/CS/AC carrier and 52.81% for the allelochemical-loaded SA/CS gel microspheres. AC thus synergistically strengthens algal inhibition by elevating allelochemical loading and prolonging activity, providing a feasible strategy for sustainable cyanobacterial bloom control. Full article