Search Results (1,455)

A novel composite material comprising titanium dioxide and layered double hydroxides (TiO₂/LDHs) was innovatively proposed and prepared using the co-precipitation method to overcome the shortcomings of titanium dioxide, such as low efficiency in separating electron–hole pairs induced by light and a low utilization rate of visible light. This material was used to study the visible-light-driven photocatalytic degradation of methylene blue. The experimental results show that by constructing efficient heterojunction structures through the alignment of interface band energies and regulating the interface charge transfer pathways, the recombination rate of photogenerated electron–hole pairs is significantly reduced, and the photocatalytic activity is greatly enhanced. Among the tested samples, the TiO₂/LDHs composite material with an aluminum-to-titanium molar ratio of 1:1 (AT11) demonstrated the best photocatalytic performance. Within 70 min of simulated sunlight exposure, the degradation rate of methylene blue reached 98.2%, and the optimal concentration of the catalyst was 1 g/L. The photocatalytic process follows a first-order kinetic model. After four cycles of use, the degradation efficiency of methylene blue by the AT11 composite material was 78.93%, demonstrating good stability. The free radical capture experiments indicated that the main active substances for the photocatalytic degradation of methylene blue were h⁺ and ·OH. The constructed TiO₂/LDHs heterostructure system significantly enhanced the photocatalytic performance of TiO₂ materials, which was conducive to the efficient utilization of solar energy. Full article

The extremophilic strain Vreelandella titanicae Zn11_249 was isolated from Salar de Uyuni, an environment with high salinity, among other extreme factors. This study researched the optimised production, characterisation, antioxidant activity, and cytotoxicity of exopolysaccharides (EPS) produced by this strain under different ionic stresses. Zn11_249 was cultured in a minimal medium with glucose as the sole carbon source as a control, and under kosmotropic (NaCl, 1 M) and chaotropic (LiCl, 0.3 M) conditions, yielding EPS_U1, EPS_U2, and EPS_U3, respectively. Maximum EPS production (336 mg/L) occurred under chaotropic conditions after 96 h. EPSs were characterised using the following techniques: Gas chromatography (GC-MS); Attenuated Total Reflectance Fourier Transform Infrared Spectroscopy (ATR-FTIR); Thermogravimetric Analysis (TGA); and Differential Scanning Calorimetry, (DSC). The results showed differences between the molecular weights for EPS_U1 (3.9 × 10⁴ Da), EPS_U2 (3.9 × 10⁴ Da), and EPS_U3 (5.85 × 10⁴ Da). Their monosaccharide molar ratios (%) were 40/25/25/10 in EPS_U1, 10/30/30/30 in EPS_U2, and 25/25/25/25 in EPS_U3, composed of mannose, galactose, rhamnose, and glucose, respectively. Functional group analysis confirmed their heteropolysaccharide nature. Thermal profiles suggest the potential of these exopolysaccharides as biomaterials. Antioxidant tests demonstrated significant activity against DPPH, OH, and O₂ radicals, while cytotoxicity assays showed no toxicity. These results highlight the biotechnological potential of EPSs from Veelandella titanicae Zn11_249 for biomedical and cosmetic uses. Full article

A high-performance Z-scheme heterojunction photocatalytic compound, ZnBiGdO₄/SnS₂ (ZS), was prepared for the first time using a microwave-assisted solvothermal method. ZS significantly improved the separation efficiency of photoinduced carriers and effectively broadened the response range to visible light through the unique mechanism of the Z-type heterojunction. Therefore, ZS exhibited an excellent photocatalytic performance during the degradation process of tinidazole (TNZ). Specifically, the removal rate of TNZ by ZS reached 99.63%, and the removal rate of total organic carbon (TOC) reached 98.37% with ZS as catalyst under visible light irradiation (VLIN). Compared to other photocatalysts, the photocatalytic performance of ZS was significantly better than that of ZnBiGdO₄, SnS₂, or N-doped TiO₂ (N-T). The removal rate of TNZ by ZS was 1.12 times, 1.26 times, or 2.41 times higher than that by ZnBiGdO₄, SnS₂, or N-T, respectively. The mineralization efficiency of TNZ for TOC with ZS as a catalyst was 1.15 times, 1.28 times, or 2.57 times higher than that with ZnBiGdO₄, SnS₂, or N-T as a catalyst, respectively. Free radical scavenging experiments and the electron paramagnetic resonance experiments confirmed that ZS could generate multiple reactive species such as hydroxyl radicals (•OH), superoxide anions (•O₂⁻), and photoinduced holes (h⁺) during the photocatalytic degradation process of TNZ. The photocatalytic degradation performance of ZS on TNZ under VLIN was evaluated, concurrently, the reliability, reproducibility, and stability of ZS were verified by five cycle experiments. This study explored the degradation mechanism and degradation pathway of TNZ with ZS as a catalyst under VLIN. This study not only provides new ideas for the design and preparation of Z-type heterojunction photocatalysts but also lays an important foundation for the development of efficient environmental remediation technologies for TNZ pollution. Full article

(1) Background: Water, comprising about 70–80% of cellular mass, is the most abundant constituent of living cells. Upon exposure to ionizing radiation, water undergoes radiolysis, generating a variety of reactive species, including free radicals and molecular products. Among these, hydroxyl radicals (^•OH) are particularly damaging due to their very high reactivity and their capacity to induce oxidative injury to vital biomolecules such as DNA, membrane lipids, and proteins. From a radiation-chemical perspective, this study investigates the selective scavenging ability of molecular hydrogen (H₂) toward ^•OH radicals, with the aim of evaluating its potential as an antioxidant and radioprotective agent; (2) Methods: We employed our Monte Carlo track chemistry simulation code, IONLYS-IRT, to model the time-dependent yields of ROS in a neutral, aerated aqueous environment. The simulations included varying concentrations of dissolved H₂ and, for comparison, cystamine—a well-known sulfur-containing radioprotector and antioxidant. Irradiation was simulated using 300 MeV protons, chosen to mimic the radiolytic effects of low linear energy transfer (LET) radiation, such as that of ⁶⁰Co γ-rays or fast (>1 MeV) electrons; (3) Results: Our simulations quantitatively demonstrated that H₂ selectively scavenges ^•OH radicals. Nevertheless, its scavenging efficiency was consistently lower than that of cystamine, which produced a faster and more pronounced suppression of ^•OH due to its higher reactivity and superior radical-quenching capacity; (4) Conclusions: Molecular hydrogen offers several unique advantages, including low toxicity, high diffusivity, selective scavenging of ^•OH radicals, and well-documented anti-inflammatory effects. Although it is less potent than cystamine in terms of radical-scavenging efficiency, its excellent safety profile and biological compatibility position H₂ as a promising radioprotector and antioxidant for therapeutic applications targeting radiation-induced oxidative stress and inflammation. Full article

A centrosymmetric dinuclear complex, [Dy₂(H₂dapp)₂(μ-OH)₂(H₂O)₂]·4TCNQ·2CH₃OH, was synthesized using the TCNQ^·− radical anion (TCNQ = 7,7,8,8-tetracyanoquino-dimethane) and pentadentate nitrogen-containing Schiff base ligand (H₂dapp = 2,6-diacetylpyridine)-bis(2-pyridylhydrazone). In the Dy₂ dimer, the two Dy^III ions adopt eight-coordinated geometries intermediate between D_4d and D_2d symmetries, linked by two OH⁻ groups, with ferromagnetic Dy-Dy interactions. The TCNQ^·− radical anions are uncoordinated, and they pack tightly into antiparamagnetic dimers to balance the system charge. Under zero field, weak magnetic relaxation was observed, with an approximate Δ_eff = 2.82 K and τ₀ = 6.88 × 10⁻⁶ s. This might be attributed to the short intermolecular Dy···Dy distance of 7.97 Å, which could enhance intermolecular dipolar interactions and quantum tunneling of magnetization (QTM). Full article

Lithocarpus litseifolius, a traditional sweet tea rich in dihydrochalcones, relies on plant nutrients for secondary metabolite accumulation. However, nutrient distribution patterns during leaf development and its relationship with secondary metabolites remain inadequately characterized. This study examined mineral elements, carbon and nitrogen metabolites, and primary dihydrochalcones in L. litseifolius leaves at various developmental stages, and analyzed their interrelationships. Mineral nutrients such as phosphate (P), potassium (K), magnesium (Mg), zinc (Zn), boron (B), and copper (Cu), along with trilobatin, were most abundant in the youngest leaves. Conversely, calcium (Ca), iron (Fe), sulfur (S), manganese (Mn), selenium (Se), sugars, soluble protein, amino acids, chlorophyll, and carotenoids predominantly accumulated in old leaves, paralleling the distribution of phlorizin. Nitrogen (N) and molybdenum (Mo) concentrations were higher in mature leaves. In young leaves, P, K, Mg, S, Mn, Zn, and B positively correlated with phlorizin and trilobatin, while N, chlorophyll, carotenoids, and fructose correlated negatively. Trilobatin was the primary contributor to hydroxyl radical (·OH) scavenging capacity. Redundancy analysis highlighted N, P, Mg, B, Zn, Cu, Fe, Mo, and Se as key mineral nutrients influencing phlorizin and trilobatin accumulation. These findings offer insights for mineral nutrient management and effective utilization of L. litseifolius. Full article

The persistence of pharmaceutical pollutants such as ciprofloxacin (CIP) in aquatic environments represents a critical environmental threat due to their potential to induce antimicrobial resistance. Photocatalysis using TiO₂-based materials offers a promising solution for their mineralization; however, the limited visible-light response of TiO₂ and charge carrier recombination restricts its overall efficiency. In this study, Nb-doped TiO₂ nanoparticles were synthesized via the sol–gel method, incorporating Nb⁵⁺, ions into the TiO₂ lattice to modulate the structural and electronic properties of TiO₂ to enhance its photocatalytic performance for CIP degradation under UV and visible irradiation. Comprehensive structural, morphological, and optical analyses revealed that Nb incorporation stabilizes the anatase phase, reduces particle size (from 21.42 nm to 10.29 nm), and induces a slight band gap widening (from 2.85 to 2.87 eV) due to the Burstein–Moss effect. Despite this blue shift, Nb-TiO₂ exhibited significantly improved photocatalytic activity under visible light, achieving 86% CIP degradation with a reaction rate 16 times higher than that of undoped TiO₂. This enhancement was attributed to improved charge separation and higher hydroxyl radical (^•OH) generation, driven by excess conduction band electrons introduced by Nb doping. Density Functional Theory (DFT) calculations further elucidated the electronic structure modifications responsible for this behavior, offering molecular-level insights into Nb dopant-induced property tuning. These findings demonstrate how targeted doping strategies can engineer multifunctional nanomaterials with superior photocatalytic efficiencies, especially under visible light, highlighting the synergy between experimental design and theoretical modeling for environmental applications. Full article

Ultrasound-responsive nanomaterials represent a promising approach for achieving non-invasive and localized drug delivery within tumor microenvironments. In this study, we developed a piezocatalysis-assisted hydrogel system that integrates reactive oxygen species (ROS) generation with stimulus-responsive drug release. The platform combines piezoelectric barium titanate (BTO) nanoparticles with a ROS-sensitive hydrogel matrix, forming an ultrasound-activated dual-function therapeutic system. Upon ultrasound irradiation, the BTO nanoparticles generate ROS—predominantly hydroxyl radicals (^•OH) and singlet oxygen (¹O₂)—through the piezoelectric effect, which triggers hydrogel degradation and facilitates the controlled release of encapsulated therapeutic agents. The composition and kinetics of ROS generation were evaluated using radical scavenging assays and fluorescence probe techniques, while the drug release behavior was validated under simulated oxidative environments and acoustic fields. Structural and compositional characterizations (TEM, XRD, and XPS) confirmed the quality and stability of the nanoparticles, and cytocompatibility was assessed using 3T3 fibroblasts. This synergistic strategy, combining piezocatalytic ROS generation with hydrogel disintegration, demonstrates a feasible approach for designing responsive nanoplatforms in ultrasound-mediated drug delivery systems. Full article

The limited data on biological potential of the genus Hypericum sect. Drosocarpium species initiated the current research aimed at the chemical characterization of samples of six selected taxa (H. barbatum, H. montbretii, H. richerii subsp. grisebachii, H. rochelii, H. rumeliacum, and H. spruneri) and the evaluation of their biological potential (antioxidant and antihyperglycaemic potential, acetylcholinesterase and monoamine oxidases inhibition). The obtained results suggest greater abundance of biologically active compounds, hypericin (H. rochelii, H. barbatum, and H. richerii subsp. grisebachii), amentoflavone (H. richerii subsp. grisebachii), quercetin and rutin (H. richerii subsp. grisebachii), and chlorogenic acid (H. richerii subsp. grisebachii, H. barbatum, H. rumeliacum), when compared to H. perforatum. Also, the scavenging potential of DPPH (median RSC₅₀ = 3.34 µg/mL), NO (median RSC₅₀ = 26.47 µg/mL) and OH radicals (median RSC₅₀ = 76.87 µg/mL) of evaluated species was higher, or at least comparable to H. perforatum, while the same trend was noticed in the case of anti-MAO-A (median IC₅₀ = 19.41 µg/mL) and antihyperglycaemic potential (inhibition of α-amylase and α-glucosidase (median IC₅₀ = 29.47 µg/mL)). The study results highlight sect. Drosocarpium species as a valuable source of biologically active secondary metabolites and suggest a wide spectrum of possible applications in the food and medicine industries. Full article

There is a growing interest in using essential oils with phytoprotectant properties instead of synthetic pesticides to mitigate the risks of insect pesticide resistance, environmental harm, and adverse effects on non-target organisms and human health. This study focused on the effects of Coridothymus capitatus essential oil on host selection, settling behaviour, and survival of Macrosiphoniella sanborni in dual-choice and no-choice tests. The essential oil and methanol extract of C. capitatus were analyzed using Gas Chromatography–Mass Spectrometry (GC-MS) and Liquid Chromatography–Mass Spectrometry (LTQ-LC-MS Orbitrap), respectively. The antioxidant activity was also tested through the radical scavenging assay. The settling inhibitory activity in the dual-choice test increased dose-dependently from 60% to 72% for essential oil concentrations of 0.1 to 0.3% (v/v) for up to 120 min exposure, but decreased thereafter. However, under no-choice conditions, the inhibitory effect after 60 min of exposure was inversely proportional to the concentration but became proportional by the end of the experiment (72 h). After 72 h, both assays produced a mortality rate of 15% to 17%. C. capitatus was classified as a Carvacrol chemotype. Fifteen phenolic compounds were identified in the MeOH extract, and both the extract and essential oil exhibited substantial antioxidant activity. In conclusion, our findings indicate that C. capitatus essential oil affects the behaviour and survival of M. sanborni. Full article

Disinfection by ultrasound and carbon nanotubes (CNTs) provides attractive alternatives to conventional methods for water and wastewater treatment. This study explored the inactivation of Escherichia coli (E. coli) by 5 mg/L pristine short and long multi-walled CNTs (MWCNTs) and 20 kHz ultrasound individually or in combinations in DI water, Suwannee River natural organic matter (SRNOM), and sodium dodecyl sulfate (SDS) solution, respectively. The results indicated that the dispersity of MWCNTs was the single most important factor determining the inactivation rate of E. coli. The dispersity of short MWCNTs in solutions increased in the order of DI water <10 mgC/L SRNOM < 2 mM SDS. Correspondingly, the greatest log inactivation of E. coli was achieved in SDS when short MWCNTs were used alone (0.67 ± 0.12) and combined with ultrasound (1.80 ± 0.02) for 10 min. Short MWCNTs alone had a slightly greater inactivation (0.29 ± 0.07) in SRNOM solution than in DI water (0.18 ± 0.05). However, long MWCNTs had a slightly higher inactivation in DI water (0.24 ± 0.03) than short ones (0.18 ± 0.05), because of better dispersity in DI. The observed synergistic inactivation when ultrasound and short MWCNTs were used together in 2 mM SDS shows that ultrasound energized the MWCNTs more effectively when they were well dispersed, although SDS and MWCNTs can occupy the reaction sites at the cavitational bubble–water interfacial regions and scavenge •OH radicals. The results suggest that sonophysical effects are more important to inactivate E. coli than sonochemical effects. Ultrasound inactivates E. coli and/or energizes MWCNTs through the mechanisms of acoustic streaming, microstreaming, microstreamers, transient cavitation collapse-generated shock waves and microjets (transitional forms), and localized hot temperatures. The results of this study indicate that the cytotoxicity of CNTs includes impinging bacterial cells and/or direct contact with the bacteria. Full article

The increasing presence of tetracycline antibiotics (TCs) in water sources poses significant environmental and public health risks, necessitating effective treatment technologies. This study investigates the degradation of three types of TCs in water—Tetracycline (TC), Oxytetracycline (OTC), and Chlortetracycline (CTC)—using nonthermal plasma (NTP) coupled with the persulfate (PS) process. The combined NTP/PS system was optimized for various operational parameters, including PS concentration, pH, and reaction time, to achieve maximum degradation and mineralization efficiency. The results showed that the NTP/PS system achieved over 90% degradation of all TCs under optimal conditions, outperforming plasma alone treatment. The degradation kinetics followed a pseudo-first-order model, indicating a rapid initial breakdown of TCs. The degradation mechanism was elucidated through the identification of intermediate byproducts using liquid chromatography-mass spectrometry (LC-MS/MS). Free radicals, such as sulfate (SO₄^•−) and hydroxyl (^•OH) radicals, were identified as the primary reactive species responsible for TCs degradation. This study demonstrates the potential of the NTP/PS system as an efficient and sustainable solution for the removal of antibiotic contaminants from water. Further research on the scalability and application in real wastewater conditions is recommended. Full article

Single-factor and orthogonal experiments were conducted to investigate the biological characteristics of Dichomitus squalens strains isolated from wild fruiting bodies collected in Tekes County, Xinjiang Uygur Autonomous Region. Building upon the optimal mycelial culture conditions identified, domestication cultivation studies were performed, including experiments to induce fruiting body formation. Liquid strains were inoculated into substrates to monitor developmental stages from primordia formation to mature fruiting bodies, with macroscopic characteristics recorded throughout the cultivation process. Crude polysaccharides were extracted from the cultivated fruiting bodies using the water extraction and ethanol precipitation method. The scavenging rates of these polysaccharides against hydroxyl radicals (OH⁻) and superoxide anion radicals (O₂⁻) were measured to evaluate their in vitro antioxidant activity. Results demonstrated that the optimal growth conditions for D. squalens were as follows: sucrose as the preferred carbon source, yeast extract powder as the optimal nitrogen source, a pH of 5.0, and a temperature of 30 °C. Among these factors, pH exerted the most significant influence on the mycelial growth rate, followed by nitrogen source, carbon source, and temperature. Mature fruiting bodies developed approximately 57 days after inoculation with liquid strains. The crude polysaccharide extraction yield from the cultivated fruiting bodies reached 7.07%, with a total polysaccharide content of 24.69% in the extract. The crude polysaccharides exhibited potent radical scavenging activity: at a concentration of 5.0 mg/mL, the hydroxyl radical scavenging rate was 56.74%, while the superoxide anion radical scavenging rate reached 78.3%. These findings indicate that D. squalens possesses significant antioxidant potential. Full article

Volvariella volvacea, a fungal species of Volvariella within the Pluteaceae family, is predominantly cultivated in southern China. Polysaccharides, the primary bioactive constituents of V. volvacea, exhibit diverse pharmacological activities. However, current cultivation practices face challenges due to the genetic heterogeneity of strains, leading to inconsistent content and compositional variability of polysaccharides and other functional components. ARTP, denoting atmospheric and room-temperature plasma, is a technology capable of generating plasma jets at ambient pressure with temperatures ranging from 25 to 40 °C. These jets feature high concentrations of highly reactive species, including but not limited to excited-state helium atoms, oxygen atoms, nitrogen atoms, and OH radicals. This study aims to develop high-yielding exopolysaccharide (EPS) strains through integrated ARTP mutagenesis and genome shuffling, thereby overcoming current cultivation bottlenecks. ARTP mutagenesis and genome shuffling significantly boosted EPS production in V. volvacea. ARTP generated nine stable mutants with >20% higher EPS yields. Subsequent genome shuffling (three rounds of protoplast fusion) produced the hybrid strain SL212, which achieved 46.85 g/L of EPS, an 111.67% increase over that of the parent strain under identical conditions. Metabolomics and transcriptomics analyses revealed that differential metabolites and genes were mainly enriched in galactose metabolism, ABC transporter pathways, and the tricarboxylic acid cycle. These pathways enhance monosaccharide biosynthesis and generate ATP, providing both precursors and energy for polysaccharide polymerization, thereby driving EPS overproduction. Preliminary mechanistic analysis identified the key contributing factors driving the elevated polysaccharide biosynthesis. Full article

Orpiment (As₂S₃), a yellow mineral pigment widely used in historical artworks, undergoes degradation that seriously threatens the integrity of Dunhuang murals. Reactive oxygen species (ROS) exist widely in air, which may be one reason for the color change of pigments. This study aims to investigate the degradation effects and mechanisms of four ROS—hydroxyl radical (·OH), singlet oxygen (¹O₂), peroxynitrite anion (ONOO⁻), and hydrogen peroxide (H₂O₂)—on orpiment. By simulating chemical reaction systems, the interaction processes between different ROS and orpiment were qualitatively and quantitatively analyzed, and the degradation capacities of each ROS on orpiment were evaluated. The experiments show that all ROS can induce orpiment degradation, among which ·OH exhibits the strongest degradation capacity due to its high oxidation potential, while ¹O₂, ONOO⁻, and H₂O₂ have relatively minor impacts on orpiment aging. It is the first time that a study has confirmed that ROS (especially ·OH) may drive orpiment degradation in environments, contributing to the increasing number of conservation strategies for artworks. Full article