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CeO2/TiO2 nanostructures enhance adsorption and photocatalytic degradation of organic compounds in aqueous suspension
摘要： Mixed oxide interfaces are critical in the delivery of active components in photocatalytic processes. Cerium doped TiO2 photocatalysts were prepared using a hydrothermal route to manipulate the morphology of the photocatalyst and improve the interaction between CeO2 and TiO2 nanoparticles. These changes were compared with the photocatalytic activity and adsorption capacity of the solids. The photocatalysts were used to degrade polyvinylpyrrolidone (PVP) and methylene blue (MB) as test compounds. A low photodegradation rate of PVP (0.0001 min?1 and 0.0005 min?1 under visible and UV light, respectively) was observed using Ce-doped photocatalysts, with no adsorption. The high adsorption capacity of MB (34.46 mg g?1) proved that the local morphology of the nanostructured CeO2/TiO2 photocatalysts is more important than the amount of CeO2 in the sample, and the main role of the CeO2 on mixed photocatalysts is to improve thermal stability during the synthesis. XRD, XPS, BET surface area, UV–vis and TEM techniques confirmed this conclusion. The rate of degradation of MB by the Ce-doped photocatalyst decreased dramatically when using the singlet oxygen scavenger L-Histidine (0.0214 min?1 to 0.0001 min?1), indicating a photocatalysis sensitized by the dye, under visible and UV light.
关键词： Cerium,Photosensitization,Reactive oxygen species,Adsorption,Morphology
更新于2025-09-23 15:23:52
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Enzymatic sensor for phenols based on titanium dioxide generating surface confined ROS after treatment with H2O2
摘要： Titanium dioxide (TiO2) is a popular material as host matrix for enzymes. We now evidence that TiO2 can accumulate and retain reactive oxygen species after treatment by hydrogen peroxide (H2O2) and support redox cycling of a phenolic analyte between horseradish peroxidase (HRP) and an electrode. The proposed detection scheme is identical to that of second generation biosensors, but the measuring solution requires no dissolved H2O2. This significantly simplifies the analysis and overcomes issues related to H2O2 being present (or generated) in the solution. The modified electrodes showed rapid stabilization of the baseline, a low noise level, fast realization of a steady-state current response, and, in addition, improved sensitivity and limit of detection compared to the conventional approach, i.e. in the presence of H2O2 in the measuring solution. Hydroquinone, 4-aminophenol, and other phenolic compounds were successfully detected at sub-μM concentrations. Particularly, a linear response in the concentration range between 0.025 and 2 μM and LOD of 24 nM was demonstrated for 4-aminophenol. The proposed sensor design goes beyond the traditional concept with three sensors' generations offering a new possibility for the development of enzymatic sensors based on peroxidases and the formation of ROS on titania after treatment with H2O2.
关键词： Hydroperoxyl species,Titanium dioxide,Horseradish peroxidase,Bioelectrochemistry,Hydrogen peroxide
更新于2025-09-23 15:23:52
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Carteolol hydrochloride reduces visible light-induced retinal damage in?vivo and BSO/glutamate-induced oxidative stress in?vitro
摘要： The purpose of this study was to determine whether carteolol eye drops, a b-adrenoceptor antagonist used as an intraocular hypotensive agent, has protective effects against the light-induced oxidative stress in retina. Dark-adapted pigmented rats were pre-treated with topical carteolol ophthalmic solution or saline and then exposed to visible light. The effects on electroretinogram (ERG), morphology, oxidative stress, and expression of mRNAs in the retinas were determined. The L-buthionine-(S,R)-sulfoximine (BSO)/glutamate-induced oxidative stress in 661 W cells, a murine photoreceptor cell line, was evaluated by cell death assays, production of reactive oxygen species (ROS), and activation of caspase. In vivo studies showed that exposure to light caused a decrease in the amplitudes of ERGs and the outer nuclear layer (ONL) thickness and an increase of the 8-hydroxy-20-deoxyguanosine (8-OHdG)-positive cells in the ONL. These changes were significantly reduced by pre-treatment with carteolol. Carteolol also significantly up-regulated the mRNA levels of thioredoxin 1 and glutathione peroxidase 1 compared to saline-treated group. Moreover, carteolol and timolol, another b-adrenoceptor antagonist, significantly inhibited BSO/glutamate-induced cell death and reduced caspase-3/7 activity and ROS production in vitro. Therefore, carteolol could protect retina from light-induced damage with multiple effects such as enhancing the antioxidative potential and decreasing the intracellular ROS production.
关键词： Antioxidative potential,Oxidative stress,Carteolol hydrochloride,Light-induced retinal damage,Reactive oxygen species
更新于2025-09-23 15:23:52
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Photodynamic therapy versus systemic antibiotic for the treatment of periodontitis in a rat model
摘要： Backgroup: To compare the therapeutic effect of photodynamic therapy (PDT) with Toluidine blue O hydrogel versus systemic antibiotic (SA) in treating periodontitis on rats. Methods: Thirty-two Wistar rats were divided into 4 groups and treated differently: Negative Control (NC) group, normal rats; Positive Control (PC) group, rats with periodontitis; SA group, rats with periodontitis treated with systemic antibiotic; PDT group, rats with periodontitis treated with PDT. After treatment, Gingival sulcus bacterial load was measured by counting the colony forming units per milliliter (CFU ml-1). The tooth and periodontal tissues were histologically processed to analyze histological and immunohistochemical profile. Gingival samples were obtained to quantify interleukyn-1 beta (IL-1β) and tumor necrosis factor-alpha (TNF-α) levels. Results: Gingival sulcus bacteria load is significantly lower in PDT group compared to the SA group. The histological analysis showed that some extremely effective repair signs of periodontal tissue were presented in PDT group, such as no periodontal pocket, no bone resorption, few inflammatory cells, massive fibroblasts and collagen fibers. Several effective repair signs of periodontal tissue were also observed in SA group, such as shallow periodontal pocket, small amount of inflammatory cells, substantial fibroblasts and collagen fibers. There were lower COX-2, MMP-8 and RANK immunolabeling, higher OPG immunolabeling in PDT group compared with SA group. The IL-1β and TNF-α levels in PDT group were lower than those in NC group, but higher than those in SA group. Conclusions: PDT was effective to treat experimental periodontitis and was superior to systemic metronidazole as a treatment for periodontitis.
关键词： Cytokine(s),Reactive oxygen species (ROS),Antimicrobial(s),Periodontitis
更新于2025-09-23 15:23:52
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A turn-on two-photon fluorescent probe for detecting lysosomal hydroxyl radicals in living cells
摘要： The detection of reactive oxygen species (ROS) in biological systems and its imaging is of great importance. Among them, the hydroxyl radical (?OH) stands out as one of the most reactive, playing an important role in many physiological and pathological processes. Here we report a two-photon (TP) turn-on fluorescent probe with good selectivity and sensitivity towards ?OH. The molecular design of this naphthalene-indoline compound enables it to accurately target lysosomes in its non-fluorescent (“off”) state, where interaction with ?OH gives rise to the fluorescent (“on”) state and allows for the imaging of ?OH generation in living mouse embryonic fibroblast (MEF) cells. The present study provides an approach for improving our understanding of the role of ?OH in biological processes.
关键词： Lysosomes,Two-photon absorption,Biosensors,Fluorescent Probes,Reactive Oxygen Species
更新于2025-09-23 15:23:52
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Quantitative control and identification of copper species in Cu–SAPO-34: a combined UV–vis spectroscopic and H2-TPR analysis
摘要： A series of Cu–SAPO-34 catalysts with different copper contents were prepared using a modified ion-exchange method, i.e., impregnation–activation. Controlled amounts of well-dispersed active copper species and integrated physical properties were obtained by this method. The Cu–SAPO-34 catalysts retained the CHA structure, high specific surface area, and pore volume of the H–SAPO-34. Based on a combined analysis of UV–vis spectra and H2-TPR, these common laboratory techniques enabled the identification of the different copper species present in the catalysts. Only isolated copper ions balanced by two framework charges were present in the catalysts at copper contents ≤ 0.8 wt%. With increasing the Cu content, isolated Cu2+ ions charge-balanced by one negative charge became dominant. Further higher Cu contents could result in formation of copper oxides after consumption of all ion-exchange sites.
关键词： Cu–SAPO-34,Copper species,NH3-SCR,H2-TPR,Impregnation–activation
更新于2025-09-23 15:23:52
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Graphitic Carbon Nitride with Carbon Vacancies for Photocatalytic Degradation of Bisphenol A
摘要： Photocatalysis is intensely employed to remove refractory organic pollutants in water, but suffers from low efficiency due to rapid recombination of photogenerated electrons and holes. Here, carbon vacancies modified g-C3N4 (VC-C3N4) is prepared via a handy two-step calcination method and firstly applied in the photocatalytic removal of bisphenol A (BPA). Compared to pristine g-C3N4, the photocatalytic degradation activity of VC-C3N4 for BPA is largely enhanced, whose kinetic constant (k) of BPA degradation is 1.65 times as that of pristine g-C3N4. The enhanced photocatalytic performance of VC-C3N4 is ascribed to critical role of carbon vacancies: On the one hand, carbon vacancies serve as the reservoir of photogenerated electrons to inhibit the recombination of photogenerated holes and electrons. On the other hand, carbon vacancies as conversion centers transfer trapped photogenerated electrons to absorbed O2 for generation of abundant superoxide radical (?O2-), which takes a dominant effect in the photocatalytic degradation process.
关键词： ?O2- species,bisphenol A,carbon vacancies,g-C3N4,photocatalytic degradation
更新于2025-09-23 15:23:52
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Influence of Mg doping on the structural, morphological, optical, thermal, and visible-light responsive antibacterial properties of ZnO nanoparticles synthesized via co-precipitation
摘要： Mg-doped zinc oxide (Zn1-xMgxO, where x = 0.000, 0.001, 0.003, 0.005, and 0.010 M) nanoparticles (MgZnO NPs) were synthesized via a co-precipitation method and subjected to various analyses for application as functional additives in food packaging. The MgZnO NPs were successfully formed at approximately 360 °C and showed an increase in the optical band gap with respect to the increase in the concentration of Mg doping. The X-ray diffraction and scanning electron microscopy analyses of MgZnO NPs confirmed the formation of hexagonal wurtzite structure and rod-like morphology. X-ray photoelectron spectra revealed that the Mg (1s) peaks centered at 1303.35 and 1303.38 eV were ascribed to the presence of Mg2+ replacing Zn2+. Transmission electron microscopy images showed rod shapes with the length of 208–650 nm and width of 84–142 nm. Various concentrations of synthesized MgZnO NPs were investigated against a gram-negative (Escherichia coli - DH5α) bacterial strain under light and dark conditions. Among the studied samples, 0.010 M MgZnO NPs of concentration 3 mg/mL showed the best antibacterial activity under the light condition. MgZnO NPs revealed uneven ridges on the outer surface, which promote the diffusion ability of Zn2+ and increased production of reactive oxygen species, and consequently lead to bacterial lysis. Furthermore, this study demonstrates excellent feasibility for the application of MgZnO NPs as fillers with good antibacterial activity, especially in antimicrobial food packaging applications.
关键词： Mg doping,reactive oxygen species,antibacterial activity,nanorod,ZnO
更新于2025-09-23 15:23:52
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Miniaturized electrochemiluminescent biochip prepared on gold nanoparticles-loaded mesoporous silica film for visual detection of hydrogen peroxide released from living cells
摘要： Au nanoparticles (NPs) has been widely used for the detection of intracellular H2O2 to enhance the electron transfer process. But AuNPs are easy to aggregate in the live cells environment. Herein we report a rapid, reliable and low-cost electrochemiluminescent (ECL) biochip integrated by AuNPs-loaded mesoporous silica film (MSF) to detect H2O2 released by macrophage cells. The MSF was employed as a template to load AuNPs within the nanochannels to avoid aggregation. H2O2 could be catalyzed by AuNPs to promote the ECL reaction of luminol molecules in solution. The ECL intensity was significantly enhanced, and the peak potential was negatively shifted by 400 mV due to the excellent electrocatalytic ability of AuNPs. The integrated biochip demonstrated good reproducibility, with a wide linear range of 0.1–200 μM and an LOD of 25.3 nM. The reliability was evaluated by applying for the assessment of antioxidant activity of resveratrol using RAW 264.7 macrophage model. The AuNPs-loaded MSF integrated biochip can be easily adapted to the development of improved devices in biosensing, lab-on-a-chip, and nanofluidic systems.
关键词： Gold nanoparticles,Biochip array,Electrochemiluminescence,Reactive oxygen species,Mesoporous silica
更新于2025-09-23 15:23:52
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Protection mechanisms of periphytic biofilm to photocatalytic nanoparticles (PNPs) exposure
摘要： Researchers are devoting great effort to combine photocatalytic nanoparticles (PNPs) with biological process to create efficient environmental purification technologies (i.e. intimately coupled photobiocatalysis). However, little information is available to illuminate the responses of multispecies microbial aggregates against PNP exposure. Periphytic biofilm, as a model multispecies microbial aggregate, was exposed to three different PNPs (CdS, TiO2, and Fe2O3) under Xenon lamp irradiation. There were no obvious toxic effects of PNP exposure on periphytic biofilm as biomass, chlorophyll content and ATPase activity were not negatively impacted. Enhanced production of extracellular polymetric substances (EPS) is the most important protection mechanism for periphytic biofilm against PNPs exposure. Although PNPs exposure produced extracellular superoxide radicals and caused intracellular reactive oxygen species (ROS) accumulation in periphytic biofilm, the interaction between EPS and PNPs could mitigate production of ROS while superoxide dismutase could alleviate biotic ROS accumulation in periphytic biofilm. The periphytic biofilms changed their community composition in the presence of PNPs by increasing the relative abundance of phototrophic and high nutrient metabolic microorganisms (Families Chlamydomonadaceae, Cyanobacteriacea, Sphingobacteriales and Xanthomonadaceae). This study provides insight into the protection mechanisms of microbial aggregates against simultaneous photogenerated and nanoparticle toxicity from PNPs.
关键词： community composition,EPS,reactive oxygen species,Periphytic biofilm,photocatalyst,nanoparticles
更新于2025-09-23 15:23:52