Search Results (2,773)

This review aims to provide a comprehensive overview of how oxidative stress drives inflammation, structural remodeling, and clinical expression of childhood asthma, while critically appraising emerging redox-sensitive biomarkers and antioxidant-focused preventive and therapeutic strategies. Oxidative stress arises when reactive oxygen species (ROS) and reactive nitrogen species (RNS) outpace airway defenses. This surplus provokes airway inflammation: ROS/RNS activate nuclear factor kappa-B (NF-κB) and activator protein-1 (AP-1), recruit eosinophils and neutrophils, and amplify type-2 cytokines. Normally, an antioxidant network—glutathione (GSH), enzymes such as catalase (CAT) and superoxide dismutase (SOD), and nuclear factor erythroid 2-related factor 2 (Nrf2)—maintains redox balance. Prenatal and early exposure to fine particulate matter <2.5 micrometers (µm) (PM_2.5), aeroallergens, and tobacco smoke, together with polymorphisms in glutathione S-transferase P1 (GSTP1) and CAT, overwhelm these defenses, driving epithelial damage, airway remodeling, and corticosteroid resistance—the core of childhood asthma pathogenesis. Clinically, biomarkers such as exhaled 8-isoprostane, hydrogen peroxide (H₂O₂), and fractional exhaled nitric oxide (FeNO) surge during exacerbations and predict relapses. Therapeutic avenues include Mediterranean-style diet, regular aerobic exercise, pharmacological Nrf2 activators, GSH precursors, and mitochondria-targeted antioxidants; early trials report improved lung function and fewer attacks. Ongoing translational research remains imperative to substantiate these approaches and to enable the personalization of therapy through individual redox status and genetic susceptibility, ultimately transforming the care and prognosis of pediatric asthma. Full article

Poly (3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) stands out as a renowned commercial conducting polymer composite, boasting extensive and promising applications in the realm of film electronics. In this study, we have made a concerted effort to overcome the inherent drawbacks of PEDOT:PSS films (especially, high moisture absorption, mechanical damage vulnerability, insufficient substrate adhesion ability, etc.) by uniformly blending them with polydimethylsiloxane polyurea (PDMS-PUa) and silica (SiO₂) nanoparticles through a feasible mechanical stirring process, which effectively harnesses the intermolecular interactions, as well as the morphological and structural characteristics, among the various components. The Si−O bonds within PDMS-PUa and the −CH₃ groups attached to Si atoms significantly enhance the hydrophobicity of the composite film (as evidenced by a water contact angle of 132.89° under optimized component ratios). Meanwhile, SiO₂ microscopically modifies the surface morphology, resulting in increased surface roughness. This composite film not only maintains high conductivity (1.21 S/cm, in contrast to 0.83 S/cm for the PEDOT:PSS film) but also preserves its hydrophobicity and electrical properties under rigorous conditions, including high-temperature exposure (60–200 °C), ultraviolet (UV) aging (365.0 nm, 1.32 mW/cm²), and abradability testing (2000 CW abrasive paper, drag force of approximately 0.98 N, 40 cycles). Furthermore, the film demonstrates enhanced resistance to both acidic (1 mol/L, 24 h) and alkaline (1 mol/L, 24 h) environments, along with excellent self-cleaning and de-icing capabilities (−6 °C), and satisfactory adhesion (Level 2). Notably, the dried composite film can be re-dispersed into a solution with the aid of isopropanol through simple magnetic stirring, and the sequentially coated films also exhibit good surface hydrophobicity (136.49°), equivalent to that of the pristine film. This research aims to overcome the intrinsic performance drawbacks of PEDOT:PSS-based materials, enabling them to meet the demands of complex application scenarios in the field of organic electronics while endowing them with multifunctionality. Full article

Background/Objectives: The global increase in multidrug-resistant (MDR) bacterial infections underscores the urgent need for effective and sustainable antimicrobial alternatives. This study investigates the antimicrobial activity of exometabolite-based formulations (ExAFs), derived from the cell-free supernatants (CFS) of native lactic acid bacteria (LAB) applied individually or in combination thereof, against MDR-Escherichia coli strain L1PEag1. Methods: Fourteen ExAFs were screened for inhibitory activity using time–kill assays, and structural damage to bacterial cells was assessed via scanning and transmission electron microscopy (SEM/TEM). The most potent formulation was further characterized by liquid chromatography–tandem mass spectrometry (LC–MS/MS) employing a Sequential Windowed Acquisition of All Theoretical Fragment Ion Mass Spectra (SWATH) approach for untargeted metabolite profiling. Results: Among the tested formulations, E10, comprising CFS from Weissella cibaria UTNGt21O, exhibited the strongest inhibitory activity (zone of inhibition: 17.12 ± 0.22 mm), followed by E1 (CFS from Lactiplantibacillus plantarum Gt28L and Lactiplantibacillus plantarum Gt2, 3:1 v/v) and E2 (Gt28L CFS + EPS from Gt2, 3:1 v/v). Time–kill assays demonstrated rapid, dose-dependent bactericidal activity: E1 and E10 achieved >98% reduction in viable counts within 2–3 h, at 1× MIC, while E2 sustained 98.24% inhibition over 18 h, at 0.25× MIC. SEM and TEM revealed pronounced ultrastructural damage, including membrane disruption, cytoplasmic condensation, and intracellular disintegration, consistent with a membrane-targeting mode of action. Metabolomic profiling of E10 identified 22 bioactive metabolites, including lincomycin, the proline-rich peptide Val–Leu–Pro–Val–Pro–Gln, multiple flavonoids, and loperamide. Several compounds shared structural similarity with ribosomally synthesized and post-translationally modified peptides (RiPPs), including lanthipeptides and lassopeptides, suggesting a multifaceted antimicrobial mechanism. Conclusions: These findings position ExAFs, particularly E10, as promising, peptide-rich, bio-based antimicrobial candidates for food safety or therapeutic applications. The co-occurrence of RiPP analogs and secondary metabolites in the formulation suggests the potential for complementary or multi-modal bactericidal effects, positioning these compounds as promising eco-friendly alternatives for combating MDR pathogens. Full article

Escherichia coli O157:H7 has been an important foodborne pathogen causing severe disease in humans worldwide. It is challenging to control E. coli O157:H7 due to its intrinsic acid resistance, ability to survive in various environments, and the emergence of antimicrobial resistance. Recent research showed that phages are promising antibacterial agents. A phage (Φ241) infecting 48 E. coli O157:H7 strains from various sources was previously isolated from an industrial cucumber fermentation at pH 3.7 and 5% NaCl. The efficacy of phage Φ241 infection was evaluated in this study in four representative model food systems (beef broth, cucumber juice, cucumber juice supplemented with NaCl, and apple juice). Pronounced differences in phage effectiveness were found in the tested food systems, and impacted by pH, salinity, and multiplicity of infection. The potential of this phage is evident in beef broth and cucumber juice, where 4- to 6-log reduction in host concentration was achieved within 3 to 5 h. However, apple juice (pH 3.55) completely inhibited host growth and phage infection. Overall, the study shows the high potential of Φ241 as an antibacterial agent to improve food safety. Future research will incorporate a cocktail of phages targeting E. coli O157:H7 to mitigate phage resistance development. Full article

Metal–air batteries have excellent theoretical energy density and economic advantages through abundant anode materials and open cathode structures. However, the actual energy efficiency of metal–air batteries is much lower than the theoretical value due to the effect of polarization voltage during battery operation, limiting the power output and thus hindering their practical application. This review systematically dissects the origins of polarization: slow oxygen reduction/evolution reaction (ORR/OER) kinetics, interfacial resistance, and mass transfer bottlenecks. We highlight cutting-edge strategies to mitigate polarization, including atomic-level engineering of air cathodes (e.g., single-atom catalysts, low Pt catalysts), biomass-derived 3D porous electrodes, and electrolyte innovations (additives to inhibit corrosion, solid-state electrolytes to improve stability). In addition, breakthroughs in metal–H₂O₂ battery design using concentrated liquid oxygen sources are discussed. Together, these advances alleviate the battery polarization bottleneck and pave the way for practical applications of metal–air batteries in electric vehicles, drones, and deep-sea devices. Full article

Candida albicans, listed by WHO as a priority fungal (yeast) pathogen, can cause invasive infections resistant to drugs, thus demanding novel strategies of disinfection. This study examines the inactivation, reactivation in darkness, and susceptibility to fluconazole of an antifungal-resistant C. albicans strain through UVC photolysis, chemical oxidation, and photooxidation using hydrogen peroxide (H₂O₂), peroxydisulfate (PDS), or peroxymonosulfate (PMS). Tests were performed in deionized water over very short treatment times (0–80 s). Also, standardized CLSI methods for antifungal sensitivity studies and morphological microscopic views were carried out. The fungus disinfection order was UVC/H₂O₂ > UVC/PDS > UVC/PMS > UVC. The photooxidation processes followed pseudo-first-order kinetics, with the highest rate constant for the UVC/H₂O₂ process. Direct oxidation, photoinactivation, and attacks of radical species were responsible for the inactivation of the antifungal-resistant microorganism. The fluconazole susceptibility of yeasts was significantly decreased (from 64 to 8 µg mL⁻¹) by the action of UVC/H₂O₂. A low reactivation in the dark and strong changes in the yeast morphology were found, indicating that the use of UVC light and radical-based processes is an effective alternative for fluconazole-resistant yeasts and could be promising to deal with hospital wastewater loaded with resistant fungi. Full article

The search for broad-spectrum antimicrobial products that do not generate resistance upon multiple applications has led to increased scientific and clinical interest in ozonated oils. The aim of this preliminary study was to evaluate the physico-chemical structure and antimicrobial properties of 1–12 h ozonated extra virgin olive oil produced in a veterinary clinic with a medical-grade generator. Prolonging the ozonation time causes a decrease in the iodine index, followed by significant increases in viscosity, acidity index, and peroxide values (p < 0.001). Other similar studies using industrial generators obtained satisfactory clinical results at peroxide values between 335 and 3590 mEq O₂/Kg. Contrary to these established minimum thresholds, we found that ozonated olive oil with a peroxide index of 184 and 224 mEq O₂/Kg exhibits fungicidal and bactericidal effects, demonstrating significant differences (p < 0.05) between tested and control samples for strains such as Staphylococcus aureus, E. faecalis, and E. coli. The 12 h ozonated oil showed itself to be efficient in the treatment of a 3-year-old cat presenting a chronic infected wound. The results encourage more detailed investigations of the antimicrobial effect of ozonated oils obtained with medical-grade generators and their evaluation on bacterial strains isolated from different individuals, followed by clinical evaluations and standardization. Full article

In this study, cerium with different ratios (x = 0 (zero), 0.1, 0.15, 0.5) was added to the PrMn structure as an A-site material to evaluate characteristic behavior as a potential cathode material for solid oxide fuel cells. The Pr_xCe_1−xMnO_3−δ electrocatalysts were synthesized using the sol–gel combustion method and were assessed for their electrochemical, phase, and structural properties, as well as desorption and reducibility capabilities. Phase changes, from orthorhombic to cubic structures observed upon cerium additions, were evaluated via the X-Ray diffraction method. X-Ray photoelectron spectroscopy (XPS) showed the valence states of the surface between the Ce⁴⁺/Ce³⁺ and Pr⁴⁺/Pr³⁺ redox pairs, while oxygen temperature programmed desorption (O₂-TPD) analysis was used to evaluate the oxygen adsorption and desorption behavior of the electrocatalysts. Redox characterization, evaluated via hydrogen atmosphere temperature-programmed reduction (H₂-TPR), revealed that a higher cerium ratio in the structure lowered the reduction temperature, suggesting a better dynamic oxygen exchange capability at a lower temperature for the Pr_0.5Ce_0.5MnO_3−δ catalyst compared to the electrochemical behavior analysis by the electrochemical impedance spectroscopy method. Moreover, the symmetrical cell tests with Pr_0.5Ce_0.5MnO_3−δ electrodes showed that, when combined with scandia-stabilized zirconia (ScSZ) electrolyte, the overall polarization resistance was reduced by approximately 28% at 800 °C compared to cells with yttria-stabilized zirconia (YSZ) electrolyte. Full article

Pt/TiO₂ and Pt-Eu₂O₃/TiO₂ catalysts were prepared via the impregnation method for catalytic oxidation of CO. The Pt-2Eu₂O₃/TiO₂ catalyst exhibited better CO oxidation activity as well as greater SO₂ resistance than the Pt/TiO₂ catalyst. For the inlet gas consisting of 0.8% CO, 5% O₂, and balanced N₂, the lowest complete conversion temperatures (T₁₀₀) of CO were 120 °C and 140 °C for the Pt-2Eu₂O₃/TiO₂ and Pt/TiO₂ catalysts, respectively. During the 72 h SO₂-resistance test at 200 °C under an inlet gas composition of 0.8% CO, 5% O₂, 15% H₂O, 50 ppm SO₂, and balanced N₂, the CO conversion on the Pt-2Eu₂O₃/TiO₂ catalyst remained >99%, while that on the Pt/TiO₂ catalyst gradually decreased to 77.8%. Pre-loading 2 wt% Eu₂O₃ on TiO₂ enhanced the dispersion of Pt, increased the proportion of Pt⁰, and facilitated the adsorption and dissociation of H₂O, all of which promoted CO oxidation. SO₂ preferentially occupied the Eu₂O₃ sites by forming stable sulfates on the Pt-2Eu₂O₃/TiO₂ catalyst, which protected the Pt active sites from poisoning. The OH* species produced from the dissociation of H₂O played a significant role in promoting CO oxidation through the formation of COOH* as the key reaction intermediate. The developed Pt-2Eu₂O₃/TiO₂ catalyst has great application potential in terms of the removal of CO from industrial flue gases. Full article

To mitigate the consumption of active sites on co-catalysts by H₂O₂ and to enhance the efficiency and stability of co-catalytic Fenton reactions, an external circulation two-stage packed-bed reactor (ECTPBR) was developed using DPW (diatomite plate@polydopamine@WC) as a co-catalyst to degrade 4-nitrophenol (4-NP). Under suitable conditions, the ECTPBR could achieve over 91.97% 4-NP degradation, with low iron sludge production (11.97 mg/L) and minimal tungsten leaching (3.6363 mg/L). The two-stage strategy enabled spatial separation of Fe³⁺ reduction and Fenton reactions, minimizing the loss of active sites on DPW, ensuring long-term system stability, and reducing the toxicity of 4-NPdegradation products. In addition, external circulation enhanced mass transfer and improved resistance to shock loads. These advantages suggest that the ECTPBR may serve as an effective strategy for applying co-catalytic Fenton reactions in the treatment of toxic and refractory organic wastewater. Full article

Adenosine deaminase (ADA) is one of the most important enzymes in nucleoside metabolism, regulating the levels of adenosine and deoxyadenosine triphosphate (ADT/dATP) on either side of the cell membrane. This small protein (weighing approximately 40 kDa) exhibits deamination properties towards other pharmaceuticals built on adenine as the leading structure, which requires co-administration of ADA inhibitors. 3′-deoxyadenosine (Cordycepin, Cord) is an active compound isolated from the fungus Cordyceps, which has been used in traditional Chinese medicine for over 2000 years. Its anticancer activity is likely related to the inhibition of primer elongation of lagging strands during genetic information replication. Unfortunately, Cord is rapidly deaminated by ADA into inactive 3′-deoxyinosine, necessitating its co-administration with ADA inhibitors. Here, for the first time, the synthesis and discussion of the oxidised form of Cord are presented. The 7,8-dihydro-8-oxo-3′-deoxyadenosine (Cord^OXO) exhibits high resistance to ADA because of its syn conformation, as shown experimentally by UV spectroscopy and RP-HPLC monitoring. Theoretical Density Functional based Tight Binding (DFTB) studies of the Michaelis complex ADA-Cord^OXO have revealed significant distance increases between the “active” H₂O molecule and C6 of the 8-oxo-adenine moiety of Cord^OXO, i.e., 4 Å as opposed to 2.7 Å in the cases of ADA-dAdo and Cord. In conclusion, it can be postulated that the conversion of Cord to Cord^OXO enhances its therapeutic potential; however, this needs to be verified in vitro and in vivo. It should be emphasised that the therapeutic effect, if any, can be achieved theoretically without ADA inhibitors, e.g., pentostatin, thus reducing adverse effects. These promising preliminary results, presented here, warrant further investigations. Full article

A series of Ce-doped α-MnO₂ catalysts (Ce_XMn_1−XO₂, x = 0.04, 0.07, 0.10) were synthesized by a simple in situ hydrothermal method. It was confirmed by characterization methods such as XRD, Raman, N₂ adsorption–desorption and SEM confirmed that the introduction of Ce significantly regulated the microstructure of α-MnO₂, specifically manifested as the reduction in grain size, the increase in defect sites, the increase in Mn-O bond length and altered morphological structure. H₂-TPR, O₂-TPD and XPS analyses further revealed the strong interaction between Mn and Ce, accompanied by significant electron transfer (Ce³⁺ + Mn⁴⁺ → Ce⁴⁺ + Mn³⁺), thereby promoting the formation of Mn³⁺ species. In the test of toluene catalytic oxidation performance, C_e0.07Mn_0.93O₂ exhibited the most excellent catalytic activity (T₁₀₀ = 280 °C), while also having good thermal stability and water resistance. Furthermore, the degradation pathways of toluene were analyzed by TD-GC-MS technology: Toluene → Benzene → Benzaldehyde → Maleic anhydride → CO₂ and H₂O. Full article

A key issue with lead-cooled fast reactors is the corrosion vulnerability of fuel cladding and core components, which will endanger the structural materials’ integrity and the operational safety of the reactor system. The FeCrAlTi-ODS (Oxide Dispersion Strengthened) alloy coatings are prepared by the Magnetron Sputtering technique under different bias voltages to shield structural elements in lead-cooled fast reactors from corrosion caused by lead-bismuth eutectic (LBE). A comprehensive study examines their mechanical attributes and resistance to LBE-induced corrosion. Compared to the bare substrate of austenitic 316L steel, the FeCrAlTi-ODS alloy coatings exhibit significantly improved binding force and hardness. The hardness (H) reaches 11.52 GPa (twice that of the bare substrate), and the elastic modulus (E) reaches 172.89 GPa. After the corrosion of bare substrate 316L steel by LBE, the oxygen element penetrated was obvious, and the Nickel element underwent selective migration. The FeCrAlTi-ODS alloy coatings show promising LBE corrosion resistance, and the FeCrAlTi-ODS alloy coating prepared under different bias can effectively protect the substrate material, which is attributed to the formation of protective FeCr₂O₄ film on the surface. The compact oxide film significantly prevents the further infiltration of the oxygen element and the migration of metal elements. Full article

Reductive stress (RS) results from the overactivity of the enzymatic and non-enzymatic antioxidant systems and from excess antioxidant agents that neutralize reactive oxygen species. Hibiscus sabdariffa Linnaeus (HSL) is a natural source of antioxidant molecules that can overload the antioxidant system. Twenty-one Wistar rats were divided into three groups: group 1 (G) G1: rats that consumed a 6% HSL infusion for one month (HSL + 6%), G2: rats that consumed a 6% HSL infusion for one month and were then given natural water for another month (HSL ± 6%), and G3: rats with natural drinking water. Renal vascular resistance (RVR) was evaluated through their responses to norepinephrine (Ne), acetylcholine (Ach), super oxide (O₂⁻), hydrogen peroxide (H₂O₂)_, and peroxynitrite (ONOO⁻). The activity of antioxidant enzymes and oxidative stress markers was evaluated. RVR was increased by Ne and H₂O₂ (p = 0.03), but it was decreased by Ach, O₂⁻, and ONOO⁻ (p = 0.01). The reduced glutathione / oxidized glutathione (GSH/GSSG) ratio and nitrates/nitrites ratio, the total antioxidant capacity, the activities of superoxide dismutase, catalase, peroxidases, glutathione peroxidase, glutathione reductase, glucose-6-phosphate, and the expression of phosphorylated NrF2 were increased (p ≤ 0.04). However, the thiol groups, adenochrome, and glutathione-S-transferase were decreased (p = 0.01) in G1 vs. G2 and G3. The excessive consumption of antioxidants provided by a 6% HSL infusion results in RS contributing to a decrease in ROS. Full article

In agriculture, the use of fructans has gained relevance due to their ability to improve plant immunity and resistance to pathogens. However, many studies use high-purity fructans, which makes their application more expensive. In this work, the efficacy of two agave fructans, one food grade from Agave tequilana Weber var. Azul (FT) and the other obtained by semi-craft extraction from A. cupreata (FC) were evaluated in comparison with reagent-grade inulin from dahlia tubers. The effectiveness of their defense response against Phytophthora capsici infection in tomato (Solanum lycopersicum L.) was analyzed by evaluating defense mechanisms, including lignin deposition, hydrogen peroxide (H₂O₂) accumulation, and β-1,3-glucanase and peroxidase activity. The results indicated that foliar application of both fructans showed protection against infection, reducing disease incidence and severity. FT fructans at lower concentration (0.5 g/L) showed the highest protection, followed by FC, while dahlia inulin showed lower effectiveness. An early and progressive accumulation of H₂O₂ was observed in fructan-treated plants, in contrast to the late increase in untreated infected plants. Also, peroxidase activity was higher in the fructan treatments, suggesting a more efficient defense response. Although lignin deposition was not directly correlated with protection against P. capsici, fructans showed potential as resistance inducers. Given their low cost, easy extraction, and zero environmental impact, agave fructans represent a viable alternative for crop protection in sustainable agricultural systems. This study opens the door to their validation in the field and their application in other economically important crops, contributing to biological control strategies with less dependence on agrochemicals. Full article