Search Results (855)

Poly(lactic-co-glycolic acid) (PLGA) sustained-release systems for intra-articular (IA) delivery aim to extend joint residence time and reduce the reinjection frequency of conventional IA therapies. This review synthesizes current understanding of PLGA degradation, the acidic microenvironment inside degrading microspheres, and release behavior in joints, and surveys clinical experience with extended-release corticosteroid depots alongside emerging platforms for nonsteroidal and biologic agents. To situate PLGA within the broader IA field, we briefly summarize selected non-PLGA sustained-release approaches—such as multivesicular liposomes, hyaluronic acid conjugates, and hybrid matrices—to contextualize comparative performance and safety. For proteins and peptides, central barriers include acidification inside degrading microspheres, aggregation during fabrication and storage, and incomplete or delayed release, as illustrated by glucagon-like peptide-1 analog formulations. Mitigation strategies span pH buffering, excipient-based stabilization, and gentler manufacturing that improve encapsulation efficiency and preserve bioactivity. Translation hinges on manufacturing scale-up and quality systems that maintain critical particle attributes and enable informative in vitro–in vivo interpretation. Clinically, prolonged symptom relief after single dosing has been demonstrated for corticosteroid depots (e.g., ~50% pain reduction over 12 weeks with a single PLGA–triamcinolone injection), whereas repeat-dose safety and indication expansion beyond the knee remain active needs best addressed through multicenter trials incorporating imaging and patient-reported outcomes. Consistent real-world performance will depend on controlling batch-to-batch variability and implementing pharmacovigilance approaches suited to long dosing intervals, enabling broader clinical adoption. Full article

Dielectric characterization offers valuable insights into fruit structure, ripening, and storage stability. However, systematic studies on apples are still limited. This work elucidates the electrical and physicochemical properties of a specific variety of apples, Malus domestica, using Electrochemical Impedance Spectroscopy (EIS), a non-destructive, fast and cost-effective technique, suitable for real-time quality assessments. The apple samples were analyzed over the frequency range of 20 Hz–120 MHz at 25 °C, and impedance data were modeled using equivalent circuits and dielectric relaxation models. Physicochemical analyses confirmed a high moisture content (84%, wwb), pH 4.81, TSS 14.58 °Brix, and acidity 0.64%, which is typical of fresh Red Delicious apples. Impedance spectra revealed semicircular and Warburg elements in Nyquist plots, indicating resistive, capacitive, and diffusive processes. Equivalent circuit fitting with the proposed R-C-Warburg impedance model outperformed (R² = 0.9946 and RMSE = 6.610) the classical Cole and Double-Shell models. The complex permittivity (ε) represented a frequency-dependent ionic diffusion, space-charge polarization, and dipolar relaxation decay, while electrical modulus analysis highlighted polarization and charge carrier dynamics. The translational hopping of charge carriers was confirmed through AC conductivity following Jonscher’s power law with an exponent of ƞ = 0.627. These findings establish a comprehensive dielectric profile and advanced circuit fitting for biological tissues, highlighting a promising non-invasive approach using EIS for real-time monitoring of fruit quality, with direct applications in post-harvest storage, supply chain management, and non-destructive quality assurance in the food industry. Full article

Viologens are promising candidates for next-generation electrochromic devices due to their reversible color changes, low operating voltages, and structural tunability. However, their practical performance is often constrained by limited color range, stability issues, and poor charge delocalization. In this study, we present a detailed density functional theory (DFT) and time-dependent DFT (TD-DFT) investigation of asymmetric viologens based on the Benzyl-4,4′-dipyridyl-R (BnV-R) framework. A series of electron-donating and electron-withdrawing substituents (CN, COOH, PO₃H₂, CH₃, OH, NH₂) were introduced via either benzyl or phenyl linkers. Geometry optimizations for neutral, radical cationic, and dicationic states were performed at the CAM-B3LYP/6-31+G(d,p) level with C-PCM solvent modeling. Electronic structure, frontier orbital distributions, and redox potentials were correlated with substituent type and linkage mode. Natural Bond Orbital analysis showed that electron-withdrawing groups stabilize reduced states, while electron-donating groups enhance intramolecular charge transfer and switching kinetics. TD-DFT calculations revealed significant bathochromic and hyperchromic shifts dependent on substitution patterns, with phenyl linkers promoting extended conjugation and benzyl spacers minimizing aggregation. Radical cation stability, quantified via ΔE_red and comproportionation constants, highlighted cyano- and amine-substituted systems as particularly promising. These insights provide predictive design guidelines for tuning optical contrast, coloration efficiency, and electrochemical durability in advanced electrochromic applications. Full article

The impact of counterion structure, especially variations in constitutional and stereochemical isomers, on the properties and performance of AABSs remains under-explored. This study investigates how structural variations, particularly the stereochemistry of diammonium cyclohexane (DACH) counterions, influence the self-assembly behavior of AABSs. Four AABSs: undecanoyl-glycine, -L-alanine, -L-valine, and -L-leucine, were paired with six DACH counterions representing cis/trans isomers of 1,2-, 1,3-, and 1,4-DACH. Critical micelle concentrations (CMCs) were determined via conductimetry, and micellar sizes were measured using dynamic light scattering. The degree of counterion binding (β) was calculated to probe micelle stability, while geometry-optimized structures of the DACH isomers were obtained using density functional theory. Lastly, pH measurements were taken to probe the protonation of DACH counterions at their natural pH, where both the DACH counterion and AABS headgroups intrinsically behave as buffers. Results indicate that while surfactant hydrophobicity primarily dictates CMC in other AABS/DACH combinations, trans-1,3-DACH leads to consistently higher CMCs. This deviation likely arises from its structural conformation, which positions the amine groups an intermediate distance of ~4.4–4.5 Å apart, allowing a small fraction of divalently charged counterions to form strong electrostatic bridging pockets at the micelle interface. These interactions dominate over headgroup effects, leading to elevated and surfactant-independent CMC values. Regarding size and other unusual trends in the systems, cis- isomers formed slightly larger micelles, and trans-1,4-DACH induces abnormal aggregation in undecanoyl-glycine leading to temperature dependent gel formation. These findings highlight the significant influence of counterion structure on AABS behavior and support counterion design as a strategy for enhancing surfactant performance in sustainable applications. Full article

Selenium nanoparticles (SeNPs) show great potential for sustainable agriculture, but their green synthesis and practical application still need further optimization. This study established a green synthesis method for SeNPs using lyophilized rose (Rosa rugosa Thunb.) powder as both a reducing and stabilizing agent to reduce sodium selenite (Na₂SeO₃), key parameters, including template concentration, Na₂SeO₃/VC ratio, and reaction temperature were systematically optimized. This process yielded stable, spherical SeNPs with optimal properties, exhibiting a diameter of 90 nm and a zeta potential of −35 mV. Structural characterization confirmed that selenium forms chelation complexes through carboxyl and hydroxyl oxygen-binding sites. The SeNPs exhibited exceptional stability (retained 426 days at 25 °C) and pH tolerance (pH 4–10), though divalent cations (Ca²⁺) triggered aggregation. In agricultural application tests, 5 mg/L SeNPs increased tomato plant biomass by 84% and antioxidant capacity by 152% compared to controls, and the biosynthesis pathways of salicylic acid and jasmonic acid were upregulated. Moreover, the SeNPs exhibited strong concentration-dependent antifungal activity against several major pathogens. Among these pathogens, tomato gray mold (Botrytis cinerea) was the most sensitive, as evidenced by its low EC₅₀ (4.86 mg/L) and sustained high inhibition rates, which remained substantial even at 1 mg/L and reached 94% at 10 mg/L. These findings highlight SeNPs as a friendly alternative for minimizing agrochemical use in sustainable agriculture. Full article

Salmonella is a major zoonotic pathogen and phage cocktails offer a novel strategy against its infections. This study aimed to characterize Salmonella phages and assess the efficacy of various phage combinations, both in vitro and in vivo. Three phages (PJN012, PJN042, PJN065) were isolated, showing stability across a broad range of temperatures and pH values, and lacking genes associated with lysogenicity, virulence, and antibiotic resistance. Combined with two known phages (PJN025, vB_SalS_JNS02), they formed cocktails tested for lytic activity against S. Enteritidis and S. Typhimurium. Phage cocktails (comprising 2–5 phages) that demonstrated efficacy in vitro were validated using Galleria mellonella models. For S. Enteritidis strain 015, prophylactic cocktail C18 increased larval survival to 90% at 48 h (vs. 3% control). For S. Typhimurium strain 024, phage cocktail 26 showed the best therapeutic effect when co-injected with the bacterium, with a survival rate of up to 85% at 96 h, compared to 30% in the positive control group. Biofilm assays showed cocktails inhibited formation more effectively (e.g., at 24 h, C14 and C17 reduced biofilm formation by 93.74% and 94.21%, respectively) than removed established ones. The cocktails depended on bacterial type, phage genera, combinations, and incubation time. Robust in vitro screening remains crucial for optimizing phage formulations despite potential in vivo discrepancies. Full article

Temperature-induced instability in early-age rheology poses a major challenge to the pumpability and application of robotic plastering mortars. This study systematically investigates the temperature-dependent effects of a high-viscosity (75,000 mPa·s) hydroxyethyl methyl cellulose (HEMC) on the rheological properties and early microstructural evolution of mortars at 5 °C, 20 °C, and 40 °C. Mortars with HEMC dosages from 0 to 0.25 wt% were tested using rheological measurements, ultrasonic pulse velocity (UPV), and complementary microstructural analyses (XRD, FTIR, and SEM–EDS). Results show that HEMC reduced the initial static yield stress while monotonically increasing plastic viscosity, with the thickening effect more pronounced at higher temperatures. Notably, at 40 °C, the initial plastic viscosity of a 0.25% HEMC mix reached 14.4 Pa·s, a 133% increase compared to the control group. HEMC also effectively retarded the time-dependent increase in yield stress and stabilized plastic viscosity, thereby mitigating the adverse influence of elevated temperature. UPV confirmed that HEMC delayed microstructural formation, in agreement with the observed retardation of hydration reactions. At 40 °C, a 0.10% HEMC dosage postponed the percolation threshold from 67 min to 150 min, highlighting its strong retardation effect. Microstructural tests further revealed that HEMC delayed CH formation, refined C–S–H gels, and reduced the crystallinity of AFt, supporting the rheological and ultrasonic findings. A statistically significant, moderate-to-strong correlation (r = 0.88, R² = 0.77, p < 0.001) was established between static yield stress and UPV, indicating that macroscopic rheological resistance responds to microstructural evolution. Based on these results, the recommended HEMC dosages to achieve stable rheological performance are 0.05–0.10% at 5 °C, 0.10–0.15% at 20 °C, and 0.15–0.20% at 40 °C. Full article

Periodontitis is a chronic oral inflammatory disease whose treatment is often hindered by poor drug retention, prolonged therapeutic regimens, and the rise of antibiotic resistance. In this study, we developed a Hydrogel@ZIF-8@metronidazole (Hydrogel@ZIF-8@MNZ) nanocomposite dressing for targeted, sustained, and in situ antimicrobial therapy. This system integrates ZIF-8, a pH-responsive metal–organic framework, with the antimicrobial agent metronidazole (MNZ), encapsulated within a crosslinked hydrogel matrix to enhance stability and retention in the oral environment. Drug release studies demonstrated that MNZ release was significantly accelerated under acidic conditions (pH 5.0), mimicking the periodontal microenvironment. The Hydrogel@ZIF-8 composite achieved a maximum MNZ adsorption capacity of 132.45 mg·g⁻¹, with a spontaneous and exothermic uptake process best described by a pseudo-second-order kinetic model, suggesting chemisorption as the dominant mechanism. The nanoplatform exhibited strong pH-responsive behavior, with enhanced drug release under acidic conditions and potent dose-dependent bactericidal activity against Fusobacterium nucleatum (Fn). At the highest tested concentration, bacterial survival was reduced to approximately 30%, with extensive membrane disruption observed through live/dead fluorescence microscopy. In summary, the stimuli-responsive Hydrogel@ZIF-8@MNZ nanocomposite offers an intelligent and effective therapeutic strategy for periodontitis. By tailoring its action to the disease microenvironment, this platform enables sustained and localized antibacterial therapy, addressing major challenges in the treatment of chronic oral infections. Full article

In this study, nanostructured ferberites (FeWO₄) were synthesized via hydrothermal routes in an acidic medium. It was then investigated as an efficient photocatalyst for degrading organic dye molecules, with methylene blue (MB) as a model pollutant. The formation mechanism of ferberite revealed that the physical form of the precursor, FeSO₄·7H₂O, acts as a decisive factor in morphological evolution. Depending on whether it is in a solid or dilute solution form, two distinct nanostructures are produced: nanoplatelets and self-organized microspheres. Both structures are composed of stoichiometric FeWO₄ (Fe: 49%, W: 51%) in a single monoclinic phase (space group P2/c:1) with high purity and crystallinity. The p-type semiconductor behavior was confirmed using Mott–Schottky model and the optical analysis, resulting in small band gap energies (≈1.7 eV) favoring visible absorption light. Photocatalytic tests under simulated solar irradiation revealed rapid and efficient degradation in less than 10 min under near-industrial conditions (pH 5). This was achieved using only a ferberite catalyst and a low concentration of H₂O₂ (4 mM) without additives, dopants, or artificial light sources. Advanced studies based on photocurrent measurements, trapping and stability tests were carried out to identify the main reactive species involved in the photocatalytic process and better understanding of photodegradation mechanisms. These results demonstrate the potential of nanostructured FeWO₄ as a sustainable and effective photocatalyst for water purification applications. Full article

Naringinase consists of two enzymes: α-L-rhamnosidase and β-D-glucosidase. The enzyme was immobilized on a carrier prepared from carob gum activated with polyethyleneimine. Cross-linking with dextran aldehyde was used to improve the stability of the immobilization. Knowledge of the characteristics of naringinase subunits is important for developing efficient and selective enzymatic reactions involving flavonoids. This study aimed to characterize two subunits of naringinase—α-L-rhamnosidase and β-D-glucosidase—free, immobilized on a magnetic polysaccharide carrier and cross-linked with dextran aldehyde. The characterization of free, immobilized, and stabilized naringinase, as well as α-L-rhamnosidase and β-D-glucosidase, included the effect of pH and temperature on enzyme activity, as well as the determination of their stability depending on the pH and temperature of the environment, and the determination of kinetic constants. Immobilization and subsequent stabilization of naringinase did not affect the optimal pH for the activity of α-L-rhamnosidase and β-D-glucosidase. Immobilization caused a change in the optimal temperature for the activity of α-L-rhamnosidase and β-D-glucosidase from 60 to 65°. Cross-linking of immobilized naringinase with dextran aldehyde increased the temperature stability of its subunits. Cross-linking also altered the pH stability profile of β-D-glucosidase. Immobilization and stabilization of naringinase slightly reduced the maximum reaction rate for α-L-rhamnosidase and β-D-glucosidase compared to the free enzyme. As a result of immobilization, the enzymes’ affinity for substrates for both subunits decreased. Full article

The investigation into the complementary roles of essential oils (EOs) and organic acids in enhancing rumen physiology is increasingly gaining recognition within the field of animal nutrition. Essential oils are known for their antimicrobial effects, which can specifically target certain microbial populations in the rumen, thereby impacting fermentation processes, methane output, and nutrient digestion. In addition, the integration of organic acids plays a crucial role in stabilizing rumen pH and steering the metabolic activities of bacterial populations toward propionate production, a process essential for energy metabolism in ruminants. The concurrent use of essential oils and organic acids may yield synergistic benefits that could further optimize ruminal fermentation efficiency, enhance feed conversion rates, and lower methane emissions. This systematic review used the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines. The literature search was meticulously designed to encompass parameters related to ruminant species, feed additives, essential oils, organic acids, synergistic effects, and rumen physiology. The efficacy of both organic acids and essential oils is highly dependent on their concentration and the specific combinations utilized. When certain essential oils are used in conjunction with selected organic acids, they may mitigate any potential negative effects on fermentation, thereby fostering a more favorable environment for the proliferation of beneficial microbial communities. Understanding the relationship between essential oils and organic acids is essential for the formulation of diets that enhance rumen health while concurrently reducing environmental pressures through diminished methane emissions. Future research should prioritize long-term in vivo investigations to gain more comprehensive insights into the interactions among these dietary components and identify the optimal combinations for ruminant feeding strategies. Full article

This study evaluated the potential of silibinin linoleate (SL), a natural derivative of silibinin, as an antioxidant to improve the thermal stability of sunflower oil (SF). SL was synthesized through green technology by enzymatic esterification, using mild reaction conditions. SL was added to high-oleic SF samples at three concentrations (200, 400, and 600 ppm), and the oils were subjected to heating at 180 °C for 4 and 8 h. Oxidative stability, fatty acid composition, and nutritional indices were analyzed. The results showed that 600 ppm SL provided the strongest antioxidant effect, significantly reducing oxidation parameters after 8 h of heating, in addition to the following values: peroxide value (PV) 14.22 ± 0.31 meq O₂/kg, p-anisidine value (p-AV) 22.85 ± 0.34, inhibition of oxidation (IO) 56.41 ± 0.31%, and total oxidation value (TOTOX) 51.30 ± 0.39. FTIR spectroscopy confirmed that SL effectively protected the triglyceride structure and limited the formation of oxidation by-products. SL demonstrated a protective effect against thermal oxidation in sunflower oil, with its efficacy being clearly dose-dependent. At 600 ppm, SL showed comparable or superior activity to BHT. However, this effect was specific to the highest tested concentration and does not indicate superiority across all concentrations. These findings suggest that SL has potential as a natural antioxidant for improving oil stability, but further studies are needed to validate SL as a practical and scalable alternative to synthetic antioxidants in the food industry. Full article

Growing consumer demand for healthier meat products with clean-label ingredients has increased interest in plant-based fortification strategies. The present study evaluated the effects of a multicomponent cereal supplement comprising rice (35%), buckwheat (20%), oats (20%), and corn (25%) on the physicochemical, functional, oxidative, hydrolytic, and sensory properties of meat patties. Four formulations were prepared with 0% (control), 5%, 10%, and 15% supplement inclusion. At higher inclusion levels of the cereal supplement, the patties showed reduced moisture, protein, and fat contents, while ash and carbohydrate levels increased. Conversely, ash content increased from 1.38% to 2.82%, and carbohydrates rose to 8.99%. pH remained stable (5.92–6.04), whereas aw decreased significantly at 10% (0.921) and 15% (0.889) inclusion (p < 0.05). Functional tests showed dose-dependent improvements in water-binding capacity, which increased from 65.98% in the control to 71.58% at 10% supplement, and in fat retention, which rose from 38.3% to 54.14% under the same conditions, with optimal performance observed at 10% inclusion. TBARS values in 10% and 15% formulations were 13–20% lower than control throughout storage (p < 0.05). The increase in acid number was significantly slower in supplemented patties, indicating that the cereal blend effectively inhibited lipid hydrolysis during storage. Sensory evaluation revealed maximal acceptability at 10% inclusion, with declines at 15% due to grainy texture and flavor dilution. These findings establish 10% multicomponent cereal supplementation as a promising strategy to enhance yield, shelf-life stability, and consumer appeal of meat patties without compromising processing parameters. Full article

Berry pomace is a valuable source of dietary fiber (DF) with promising applications in functional food development. This study aimed to evaluate and compare the technological and rheological properties of soluble (SDF) and insoluble (IDF) fiber fractions isolated from cranberry, black currant, lingonberry, and sea buckthorn pomace. SDF fractions demonstrated higher water solubility and lower swelling capacity, compared with IDF fractions. Meanwhile, water and oil retention capacities depended on fiber type and the sources of pomace. Fractionation notably affected color parameters, with SDFs generally being lighter. Rheological analysis revealed pseudoplastic, shear-thinning behavior in all SDF samples, with viscosity dependent on both pH and shear rate. In particular, the black currant SDF demonstrated higher yield stress compared to other SDFs, suggesting enhanced resistance to deformation and superior structural stability under low shear conditions. The consistency coefficient varied across samples, indicating differences in gel-forming potential. These findings highlight the importance of berry source and fiber fraction in determining functionality. The distinct hydration, binding, and rheological properties suggest that both SDF and IDF from berry pomace can be strategically applied as thickeners, stabilizers, or texture enhancers in food systems. This study supports the valorization of berry by-products as sustainable and functional ingredients in the formulation of fiber-enriched foods. Full article

Arsenic pollution in potable water is a significant worldwide health concern. This study systematically evaluates current progress in adsorption technology, the most promising restorative approach, to provide a definitive framework for future research and use. The methodology entailed a rigorous evaluation of 91 peer-reviewed studies (2012–2025), classifying adsorbents into three generations: (1) Natural adsorbents (e.g., agricultural/industrial wastes), characterized by cost-effectiveness but limited capacities (0.1–5 mg/g); (2) Engineered materials (e.g., metal oxides, activated alumina), which provide dependable performance (84–97% removal); and (3) Advanced hybrids (e.g., MOFs, polymer composites), demonstrating remarkable capacities (60–300 mg/g). The primary mechanisms of removal are confirmed to be surface complexation, electrostatic interactions, and redox precipitation. Nevertheless, the critical analysis indicates that despite significant laboratory efficacy, substantial obstacles to field implementation persist, including scalability limitations (approximately 15% of materials are evaluated beyond laboratory scale), stability concerns (e.g., structural collapse of MOFs at extreme pH levels), and elevated costs (e.g., MOFs priced at approximately $230/kg compared to $5/kg for alumina). The research indicates that the discipline must transition from only materials innovation to application science. Primary objectives include the development of economical hybrids (about $50/kg), the establishment of uniform WHO testing standards, and the implementation of AI-optimized systems. The primary objective is to attain sustainable solutions costing less than $0.10 per cubic meter that satisfy worldwide deployment standards via multidisciplinary cooperation. Full article