H2O2 Concentration Research Articles

Optimization of activation by peroxidation and photo-assisted peroxidation of biochar produced from sewage sludge

Biochar from biomass, a cost-effective and sustainable alternative to pulverized activated carbon (PAC), often faces limitations in pore size and surface functionality. Hydrogen peroxide (H₂O₂) activation can enhance biochar's surface properties but requires large quantities and high concentrations, increasing production costs. Advanced oxidation methods, such as H₂O₂/UV radiation, can reduce H₂O₂ usage by generating highly reactive hydroxyl radicals (*OH). This study investigates biochar production from activated sewage biosolids using H2O2 activation and H2O2/UV radiation. Optimization was conducted via a central composite rotational design, varying activation parameters activation pH (1.5, 4.0, 7.0, 9.0, and 11.5) and H2O2 concentration (0, 10, 20, 30, and 40 vol), with methylene blue (MB) adsorption capacity as the metric. Characterization was performed using FTIR, SEM, EDS, XRD, and N2 adsorption/desorption techniques. Results indicated optimal biochar activation at pH 11.5 with 20 vol% H2O2. Activation pH was more significant than H2O2 concentration. Desirability curve analysis suggested that optimized parameters did not significantly enhance adsorption capacity, with desirability values at 93.053 %. Overall, H2O2 efficiently increased surface area by degrading the adsorbent, while H2O2/UV effectively removed impurities.

Characterization of free radical-mediated Pleurotus ostreatus polysaccharide-EGCG conjugates for chilled minced pork preservation

To improve the functions of Pleurotus ostreatus polysaccharide (POP), POP-EGCG conjugates were prepared using free radical graft polymerization reactions and were characterized using UV–vis, FT-IR, SEM, XRD, DSC, TG, particle size and potential, three-phase contact angle, and rheological tests; The antioxidant and antibacterial ability in vitro were detected. Moreover, effects of POP-EGCG on the quality of refrigerated minced pork were investigated. The results showed the optimal preparation conditions of POP-EGCG were 1 % POP, 1.3 % EGCG, 0.25 % Vc, 16 % concentration of H2O2, and reaction 17 h. The POP-EGCG showed the characteristic peak of EGCG and was a mesh honeycomb with rough and porous surface; It had higher crystallinity, increased particle size, but decreased thermal stability, solubility, and viscosity, and significantly enhanced antioxidant and antibacterial ability. The POP-EGCG effectively improved the sensory quality and inhibited lipid oxidation of chilled minced pork, and extended the shelf life of minced pork up to 9 days at 4 °C. Specifically, the TVB-N and TBARS of minced pork in the POP-EGCG group were respectively 14.93 mg/100 g and 0.9 mg MDA/kg, which were lower than the spoilage thresholds in the national standard. This study provides a theoretical basis for further development of natural antioxidants and antimicrobial agents.

Differential Oxidative Stress Management in Industrial Hemp (IH: Cannabis sativa L.) for Fiber under Saline Regimes.

In the current study, two commercial industrial hemp (IH) fiber varieties (V1: CFX-2 and V2: Henola) were assessed for their ability to regulate salt-induced oxidative stress metabolism. For 30 days, plants were cultivated in greenhouse environments with five different salinity treatments (0, 50, 80, 100, 150, and 200 mM NaCl). Hydrogen peroxide (H2O2), malondialdehyde (MDA), and lipoxygenase (LOX) and antioxidant enzymes (superoxide dismutase (SOD), catalase, guaiacol peroxidase (GPOD), ascorbate peroxidase (APX), glutathione reductase (GR), and glutathione-S-transferase (GST)) were assessed in fully expanded leaves. At 200 and 100 mM NaCl concentrations, respectively, 30 days after saline treatment, plants in V1 and V2 did not survive. At 80 mM NaCl, the leaves of V2 showed higher concentrations of H2O2, MDA, and LOX than those of V1. Higher SOD, CAT, GPOD, APX, GR, and GST activity in the leaves of V1 up to 100 mM NaCl resulted in lower levels of H2O2 and MDA. At 80 mM NaCl, V2 demonstrated the total failure of the antioxidant defense mechanism. These results reveal that V1 demonstrated stronger salt tolerance than V2, in part due to better antioxidant metabolism.

Enhanced Fenton Degradation of Tetracycline over Cerium-Doped MIL88-A/g-C3N4: Catalytic Performance and Mechanism.

Since enormous amounts of antibiotics are consumed daily by millions of patients all over the world, tons of pharmaceutical residuals reach aquatic bodies. Accordingly, our study adopted the Fenton catalytic degradation approach to conquer such detrimental pollutants. (Ce0.33Fe) MIL-88A was fabricated by the hydrothermal method; then, it was supported on the surface of g-C3N4 sheets using the post-synthetic approach to yield a heterogeneous Fenton-like (Ce0.33Fe) MIL-88A/10%g-C3N4 catalyst for degrading the tetracycline hydrochloride drug. The physicochemical characteristics of the catalyst were analyzed using FT-IR, SEM-EDX, XRD, BET, SEM, and XPS. The pH level, the H2O2 concentration, the reaction temperature, the catalyst dose, and the initial TC concentration were all examined as influencing factors of TC degradation efficiency. Approximately 92.44% of the TC was degraded within 100 min under optimal conditions: pH = 7, catalyst dosage = 0.01 g, H2O2 concentration = 100 mg/L, temperature = 25 °C, and TC concentration = 50 mg/L. It is noteworthy that the practical outcomes revealed how the Fenton-like process and adsorption work together. The degradation data were well-inspected by first-order and second-order models to define the reaction rate. The synergistic interaction between the (Ce0.33Fe) MIL-88A/10%g-C3N4 components produces a continuous redox cycle of two active metal species and the electron-rich source of g-C3N4. The quenching test demonstrates that •OH is the primary active species for degrading TC in the H2O2-(Ce0.33Fe) MIL-88A/10%g-C3N4 system. The GC-MS spectrum elucidates the yielded intermediates from degrading the TC molecules.

Synthesis of iron loaded jackfruit peel biochar through microwave heating as a stable and active heterogenous Fenton catalyst for dye degradation

Iron-loaded biochar derived from jackfruit peels (Fe-JP) was synthesised by pyrolysis in a microwave furnace and iron was loaded onto the peels prior to pyrolysis, facilitated by sonication. The primary objective of the investigation was to examine the degradation process of methylene blue (MB) dye and Acid Red 1 (AR1) dye by the using Fe-JP biochar as a heterogeneous Fenton catalyst. The investigation encompassed an examination of the impact of different operating parameters, such as pH, catalyst dosage, and H2O2 concentration. The synthesised Fenton catalyst underwent characterization using Field Emission scanning electron microscopy (FESEM), Energy Dispersive X-ray (EDX), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) techniques, Fourier transform infrared (FTIR) spectra analysis, Raman spectroscopy, Brunauer-Emmet-Teller (BET) analysis. At a pH of 3, using an initial MB dye concentration of 20 mg/L and initial AR1 dye concentration of 50 mg/L, an 8 mM H2O2 concentration, and a catalyst dose of 2 g/L, the maximum dye removal efficiency reached 96.5 % and 98 % respectively, while the total organic carbon (TOC) removal efficiency reached 68.5 % and 75 % respectively. The observed reaction time under the given experimental conditions was 120 min. The thermal stability of the biochar catalyst was found to be excellent based on the Thermogravimetric analysis (TGA) and Differential Scanning Calorimeter (DSC) studies. The catalysts that were developed demonstrated remarkable durability and negligible leaching of iron, hence enabling their repeated usage in subsequent cycles. The findings of the investigation suggest that the primary mechanism responsible for the degradation of the dye was the surface-based heterogeneous Fenton activity. Additionally, the effect of adsorption on the elimination of colour under varying pH conditions was examined, which had a very low influence in dye degradation (<30 %). The conducted scavenging investigations in the research have indicated the major involvement of hydroxyl radicals (OH) in the degradation process, followed by surface-bound hydroxyl radicals (OHsurface), superoxide radicals (O2−) and ultimately by singlet oxygen radicals (1O2). The study's economic analysis demonstrated that using microwave mode of heating for catalyst synthesis is both green and cost-effective. This observation suggests the possibility of practical implications in the domain of dye degradation.

Toxicological assessment of cadmium exposure through Hyphantria cunea larvae on the predation fitness of Arma chinensis

Heavy metals are defined as an abiotic factor that affects the efficiency of biological pest control. This study constructed a cadmium (Cd)-polluted artificial diets–Hyphantria cunea–Arma chinensis food chain to analyze the effects of Cd exposure on the ability of A. chinensis to control H. cunea. The results revealed that Cd was transferred through the artificial diet to H. cunea larvae and A. chinensis nymphs via a biological amplification effect. After feeding on Cd-accumulated H. cunea larvae, the body weight of A. chinensis nymphs reduced, mortality increased, developmental duration prolonged, and the expression of growth regulatory genes (EX, cycE, and MER) decreased. Cd activated the antioxidant defense system of the nymphs, accompanied by a significant enhancement in the contents of H2O2 and MDA, marked damage to the midgut sub-microstructure, and a remarkable induction in the expression of genes crucial for the mitochondrial pathway/ER stress–apoptosis pathway. Cd significantly diminished the contents of total amino acids, glucose, free fatty acids, and expression of the genes (HK2, PFK, IDH1, and IDH2) essential for the TCA cycle and glycolysis in the nymphs. The preference of the A. chinensis nymphs to Cd-treated H. cunea larvae was evidently reduced. Cd diminished the search-ability, food intake, instantaneous attack rate, and maximum theoretical daily food intake but prolonged the feeding time of the nymphs. Taken together, Cd exposure reduces the ability of A. chinensis nymphs to control H. cunea and provides a new challenge for the efficiency of insect pest control using natural enemies. These findings have important reference value for optimizing pest control strategies in heavy metal polluted areas.

Application of Trichoderma asperellum spore powder helps maintain ionic balance and photosystem II activity in wolfberry in saline soil

The mechanisms how Trichoderma enhances plant salt tolerance remain to be further dissected. Trichoderma asperellum spore powder (TS) was supplemented to saline soil around the stem base of potted wolfberry (Lycium chinense), and the role of Trichoderma asperellum in ameliorating salt tolerance of wolfberry was investigated with emphasis on ionic balance and photosystems II (PSII) activity. Plant dry weight was significantly increased by TS supplement, suggesting that Trichoderma asperellum promoted wolfberry growth in saline soil. As TS supplement elevated leaf and root K+/Na+ by increasing K+ content and decreasing Na+ content, Trichoderma asperellum improved ionic balance in wolfberry under saline soil stress, and the mechanism depended on that Trichoderma asperellum raised root Na+ exclusion and blocked root K+ loss. Consequentially, oxidative stress was ameliorated by Trichoderma asperellum according to lower leaf lipid peroxidation and H2O2 content in plants with TS supplement. Moreover, PSII was protected against oxidative injury and could maintain higher photochemical efficacy with TS supplement. K and J steps in prompt chlorophyll fluorescence transients were lowered by TS supplement, suggesting that Trichoderma asperellum alleviated salt-induced inhibition on electron transport at both PSII donor and acceptor sides, and consistently, more PSII centers became reactive. In addition, higher delayed chlorophyll fluorescence transients under TS supplement corroborated that Trichoderma asperellum enhanced whole PSII performance. Overall, Trichoderma asperellum helped maintain ionic balance by preventing K+ loss and elevating Na+ exclusion in roots and protect PSII by alleviating oxidative stress in wolfberry cultivated in saline soil.

Design and synthesis of a novel chiral photoacoustic probe and accurate imaging detection of hydrogen peroxide in vivo.

Nanocatalytic medicine, which aims to accurately target and effectively treat tumors through intratumoral in situ catalytic reactions triggered by tumor-specific environments or markers, is an emerging technology. However, the relative lack of catalytic activity of nanoenzymes in the tumor microenvironment (TME) has hampered their use in biomedical applications. Therefore, it is crucial to develop a highly sensitive probe that specifically responds to the TME or disease markers in the TME for precision diagnosis and treatment of diseases. In this work, a chiral photoacoustic (PA) nanoprobe (D/L-Ce@MoO3) based on the H2O2-catalyzed TME activation reaction was constructed in a one-step method using D-cysteine (D-Cys) or L-cysteine (L-Cys), polymolybdate, and cerium nitrate as raw materials. The designed and synthesized D/L-Ce@MoO3 chiral nanoprobe can perform in situ, non-invasive, and precise imaging of pharmacological acute liver injury. In vivo and in vitro experiments have shown that the D/L-Ce@MoO3 probe had chiral properties, the CD signal decreased upon reaction with H2O2, and the absorption and PA signals increased with increasing H2O2 concentration. This is because of the catalytic reaction between Ce ions doped in the nanoenzyme and the high expression of H2O2 caused by drug-induced liver injury to produce ·OH, which has a strong oxidizing property to kill tumor cells and destroy the Mo-S bond in the probe, thus converting the chiral probe into an achiral polyoxometalate (POM) with PA signal.

Experimental study on single crystal diamond CMP based on Fenton reaction and analysis of oxidation mechanism

Single crystal diamond (SCD) is an ultra-hard semiconductor material with exceptional chemical inertness, posing challenges for conventional oxidants to induce oxidation. The highly electronegative and potent ·OH produced by the Fenton reaction possesses significant importance in enabling efficient and high-quality polishing of SCD. This study delved into optimizing the Fenton reaction polishing slurry through orthogonal experiments and explored its influence on SCD CMP concerning various mechanical factors. Findings indicated that pH value, Fe3O4 concentration, and H2O2 concentration had a significant impact on the material removal rate (MRR) and surface roughness of SCD CMP, with Fe3O4 particle size playing a comparatively minor role. The optimized Fenton reaction polishing slurry achieved a peak MRR of 742.7 nm/h and a minimum surface roughness Ra of 0.240 nm. The acidic Fenton reaction polishing slurry generated H+ and ·OH, which interacted with the surface of SCD, forming an oxidation layer consisting of C–O/C–H and CO groups, thereby facilitating SCD material removal. This study provides a theoretical basis for the broader application of the Fenton reaction in SCD CMP at scale.

Biochar with KMnO4-hematite modification promoted foxtail millet growth by alleviating soil Cd and Zn biotoxicity

The excessive accumulation of Cd and Zn in soil poisons crops and threatens food safety. In this study, KMnO4-hematite modified biochar (MnFeB) was developed and applied to remediate weakly alkaline Cd-Zn contaminated soil, and the heavy metal immobilization effect, plant growth, and metal ion uptake of foxtail millet were studied. MnFeB application reduced the phytotoxicity of soil heavy metals; bioavailable acid-soluble Cd and Zn were reduced by 57.79% and 35.64%, respectively, whereas stable, non-bioavailable, residual Cd and Zn increased by 96.44% and 32.08%, respectively. The chlorophyll and total protein contents and the superoxide dismutase (SOD)activity were enhanced, whereas proline, malondialdehyde, the H2O2 content, glutathione reductase (GR), ascorbate peroxidase (APX) and catalase (CAT) activities were reduced. Accordingly, the expressions of GR, APX, and CAT were downregulated, whereas the expression of MnSOD was upregulated. In addition, MnFeB promoted the net photosynthetic rate and growth of foxtail millet plants. Furthermore, MnFeB reduced the levels of Cd and Zn in the stems, leaves, and grains, decreased the bioconcentration factor of Cd and Zn in shoots, and weakened the translocation of Cd and Zn from roots to shoots. Precipitation, complexation, oxidation-reduction, ion exchange, and π-π stacking interaction were the main Cd and Zn immobilization mechanisms, and MnFeB reduced the soil bacterial community diversity and the relative abundance of Proteobacteria and Planctomycetota. This study provides a feasible and effective remediation material for Cd- and Zn-contaminated soils.

Combined Effect of Subsurface Water Retention Technology and Arbuscular Mycorrhizal Fungi on Growth, Physiology and Biochemistry of Argan Seedlings under Field Conditions.

The argan (Argania spinosa L. Skeels) ecosystem is severely degrading in arid and semi-arid lands due to climate change, particularly in terms of density loss and reforestation failure. Thus, it is important to adopt innovative effective sustainable practices to optimize the densification and reforestation success of the argan tree. The purpose of the present research was to investigate the combined effect of subsurface water retention technology (SWRT) and the use of native arbuscular mycorrhizal fungi (AMF) on edaphic, growth, physiological and biochemical parameters of field-grown argan seedlings in the Essaouira region, Morocco. In this experiment, one-year-old argan seedlings were transplanted in the absence and presence of biodegradable plastic and AMF. Our findings revealed that the application of SWRT enhanced soil profile moisture up to 640% at 40 cm depth compared to the control. The combination of this technology with AMF also improved soil fertility. Furthermore, the application of SWRT, with or without AMF, significantly enhanced argan seedling height (208 and 168%, respectively), stomatal conductance (54 and 33%, respectively), and chlorophyll fluorescence (21 and 20%, respectively). Similarly, the combined application of SWRT and AMF significantly improved protein and sugar content (36 and 57%, respectively), as well as antioxidant enzyme activities (peroxidase and polyphenol oxidase) and chlorophyll pigments content compared to the control. However, this treatment reduced malondialdehyde and H2O2 content in the argan leaves. As a summary, SWRT technology combined with AMF may be used as a valuable strategy to promote the success of argan reforestation and to limit soil erosion and desertification in arid and semi-arid climates.

Generating luminescent Graphene quantum Dots from Tryptophan: Fluorosensors for hydrogen peroxide in cancer cells

Herein, we report a single step synthesis of highly fluorescent Graphene Quantum Dots (GQDs) using tryptophan and glycerol as precursors via pyrolysis. The morphological and functional characterization of the prepared GQDs was performed using PXRD, FTIR, TEM, XPS and zeta potential measurements. The prepared GQDs found their practical application in ultrasensitive detection of an emerging potential cancer biomarker, H2O2, by exploiting the fluorescence quenching behaviour of H2O2. To evaluate the detection sensitivity, a series of various concentrations of H2O2 was spiked to biomatrices like, serum and MCF-7 (human breast cancer cell line) cell lysate medium. A remarkably low limit of detection (LOD) was found in serum medium (139.5 pM) which further improved in MCF-7 cell lysate medium (LOD 61.43 pM). Moreover, the sensing capacity of the GQDs was further validated in presence of various physiological variables such as glucose, cholesterol, insulin and nitrite. Sensing assay was also carried out in HaCaT (human keratinocyte cell line) cell lysate medium to compare the performance of our prepared sensor but the non-linearity of the F0/F versus H2O2 concentration plot pointed towards the conduciveness of the MCF-7 cell lysate medium for sensitive detection of H2O2.The mechanism behind the sensing was also explored using spectroscopic methods.

The Increase in the Peroxidase Activity of the Cytochrome C with Substitutions in the Universal Binding Site Is Associated with Changes in the Ability to Interact with External Ligands.

Cytochrome c (CytC), a one-electron carrier, transfers electrons from complex bc1 to cytochrome c oxidase (CcO) in the electron-transport chain. Electrostatic interaction with the partners, complex bc1 and CcO, is ensured by a lysine cluster near the heme forming the Universal Binding Site (UBS). We constructed three mutant variants of mitochondrial CytC with one (2Mut), four (5Mut), and five (8Mut) Lys->Glu substitutions in the UBS and some compensating Glu->Lys substitutions at the periphery of the UBS for charge compensation. All mutants showed a 4-6 times increased peroxidase activity and accelerated binding of cyanide to the ferric heme of CytC. In contrast, decomposition of the cyanide complex with ferrous CytC, as monitored by magnetic circular dichroism spectroscopy, was slower in mutants compared to WT. Molecular dynamic simulations revealed the increase in the fluctuations of Cα atoms of individual residues of mutant CytC compared to WT, especially in the Ω-loop (70-85), which can cause destabilization of the Fe…S(Met80) coordination link, facilitation of the binding of exogenous ligands cyanide and peroxide, and an increase in peroxidase activity. It was found that only one substitution K72E is enough to induce all these changes, indicating the significance of K72 and the Ω-loop (70-85) for the structure and physiology of mitochondrial CytC. In this work, we also propose using a ferro-ferricyanide buffer as a substrate to monitor the peroxidase activity of CytC. This new approach allows us to determine the rate of peroxidase activity at moderate (200 µM) concentrations of H2O2 and avoid complications of radical formation during the reaction.

Abatement and biotoxicity assessment of chlorpyrifos residue from green coffee beans: Effect of non-thermal plasma generated ozone and nitric oxide species

Chlorpyrifos (CP) is an organophosphate pesticide (OPP) that is widely used in coffee plantations to mitigate the impacts of insects and maximize productivity. However, the environmental persistence of CP has become an issue. Non-thermal plasma (NTP) generated ozone and nitric oxide (NO) species have demonstrated the ability to remediate organic contaminants and promote plant growth. In this study, the washing of CP-contaminated green coffee beans (GCBs) by using plasma activated water (PAW) via ozone and NO dominated species was investigated, respectively. The results revealed degradation efficiencies of 89 and 87 % for ozone and NO dominated treatment, respectively. The concentration of hydroxyl radicals in ozone plasma-activated water (PAW), crucial for initiating and sustaining CP degradation, decreased from 25 μM after 30 min of treatment to 5 μM after 150 min. The concentration of H2O2 remained steady at 1.6 μM while NO2- concentration increased gradually from 0.37 to 3.06 mM during the treatment. Nevertheless, NO dominated NTP treatment resulted in the darkening of the GCBs, whereas ozone NTP treatment brought no physical changes. Therefore, ozone NTP treatment is recommended for large-scale treatments. Moreover, three degradation mechanisms were proposed based on the identified intermediate products (IPs) from liquid chromatography-mass spectrometry (LC-MS) analysis. The cytotoxic effects of these residual IPs after ozone dominated NTP washing were examined using human colon cancer-derived HT29 cells. The results showed cell viability increased to 90 and 95 % when exposed to ozone NTP-treated GCBs for 90 and 120 min, respectively.

Enhancing volatile fatty acid production from food waste by H2O2-moderate temperature thermal pretreatment: Treating waste with waste in coal mining areas

Supplementing carbon sources in sewage treatment plants with organic matter from food waste is crucial for resource recycling in coal mining areas. In this study, a moderate-temperature H2O2 method was used to pretreat food waste from a coal mining area. The changes in the properties of the pretreated food waste and their influence on volatile fatty acids (VFAs) production during anaerobic fermentation were investigated. Additionally, the nitrogen and phosphorus removal rates obtained when glucose and fermentation slurry of food waste (FSFW) were used as carbon sources in the sewage treatment system were compared. Compared with untreated food waste, the soluble chemical oxygen demand (SCOD) increased by 58 % after pretreatment with 0.25 % H2O2 at 60 ℃, and the viscosity and oil content decreased significantly, which caused VFAs production to increase from 15,267 mg COD/L to 50,774 mg COD/L. When the H2O2 concentration increased to 2.0 %, the SCOD increased to 153 %, and the viscosity and oil content further decreased, but the VFAs production decreased to 7477 mg COD/L. This occurred because large quantities of ammonia nitrogen was formed at higher H2O2 doses, which inhibited VFAs formation. Moreover, the nitrogen removal rate was higher when FSFW was used as a carbon source than when glucose was used as a carbon source.

Cell stiffening is a label-free indicator of reactive oxygen species-induced intracellular acidification

Reactive oxygen species (ROS) are important secondary messengers involved in a variety of cellular processes, including activation, proliferation, and differentiation. Hydrogen peroxide (H2O2) is a major ROS typically kept in low nanomolar range that causes cell and tissue damage at supraphysiological concentrations. While ROS have been studied in detail at molecular scale, little is known about their impact on cell mechanical properties as label-free biomarker for stress response. Here, we exposed human myeloid precursor cells, T-lymphoid cells and neutrophils to varying concentrations of H2O2 and show that elevated levels of mitochondrial superoxide are accompanied by an increased Young’s modulus. Mechanical alterations do not originate from global modifications in filamentous actin and microtubules but from cytosolic acidification due to lysosomal degradation. Finally, we demonstrate our findings to be independent of the presence of H2O2 and that stiffening seems to be a general response of cells to stress factors lowering cytosolic pH.

Copper Single-Atom-Based Metal-Organic Framework for Ultrasound-Enhanced Nanocatalytic Therapy.

Chemodynamic therapy (CDT) is an emerging therapeutic modality triggered by endogenous substances in the tumor microenvironment (TME) to generate reactive oxygen species. However, the mild acid pH, low H2O2 concentration, and overexpressed glutathione can suppress the CDT efficiency. Herein, ultrasound (US)-triggered Cu2+-based single-atom nanoenzymes (FA-NH2-UiO-66-Cu, FNUC) are constructed with the performance of target and glutathione depletion. In the TME, the single-atom Cu sites of FNUC consume glutathione and the FNUC:Cu+ generates •OH via peroxidase-like activity. The US-activated FNUC exhibits a fast •OH generation rate, a low Michaelis constant, and a large •OH concentration, indicating the cavitation effect of US promotes the •OH generation. Meanwhile, the tumor target of FNUC is confirmed by NIR-II fluorescence imaging, in which it is modified with IR-1061. Combined with the antitumor performance of FNUC in vitro and in vivo, the novel Cu-based SAzymes can achieve efficient and precise cancer treatment.

Alleviation of arsenic stress in pakchoi by foliar spraying of engineered nanomaterials.

Addressing heavy metal contamination in leafy vegetables is critically important due to its adverse effects on human health. In this study, we investigated the inhibitory effects of foliar spraying with four nanoparticles (CeO2, ZnO, SiO2, and S NPs) on arsenic (As) stress in pakchoi (Brassica rapa var. Chinensis). The findings reveal that foliar application of ZnO NPs at 1 ~ 2.5 mg plant-1 and CeO2 NPs at 5 mg plant-1 significantly reduces As in shoots by 40.9 ~ 47.3% and 39.4%, respectively. Moreover, 5 mg plant-1 CeO2 NPs increased plant height by 6.06% and chlorophyll a (Chla) content by 30.2% under As stress. Foliar spraying of CeO2 NPs at 0.2-5 mg plant-1 also significantly enhanced superoxide dismutase (SOD) activity in shoots by 9.4 ~ 13.9%, lowered H2O2 content by 42.4 ~ 53.25%, and increased root protein contents by 79 ~ 109.2%. CeO2 NPs regulate the As(III)/As(V) ratio, aiding in As efflux from roots and thereby reducing As toxicity to plants. In vitro digestion experiments reveal that the consumption of CeO2 NPs carries the lowest health risk of As. In addition, foliar spraying of ZnO NPs at 1 ~ 2.5 mg plant-1 can suppress plant As uptake by modulating enzyme activity, reducing leaf damage, and enhancing chlorophyll content. The study demonstrates that high CeO2 NP concentrations and suitable ZnO NP concentrations can alleviate As toxicity in pakchoi, consequently reducing human health risks.

Ultrasensitive detection of H2O2 via electrochemical sensor by graphene synergized with MOF-on-MOF nanozymes.

An electrochemical sensor was developed for the detection of hydrogen peroxide (H2O2),utilizing the synergistic effects of graphene (Gr) and MOF-on-MOF nanozymes (FeCu-NZs). Initially, Fe-MOF with peroxide-like activity is synthesized using a solvothermal method. Subsequently, the organic ligand on its surface binds Cu2+, enhancing the enzyme-like activity further. The resulting FeCu-NZs exhibit a distinctive electrochemical signal in response to H2O2. Moreover, integrating FeCu-NZs with Gr significantly amplifies the electrochemical signal and effectively reduces the sensor's detection limit. The developed sensor exhibited linear ranges of 0.1-3800 μM, with a limit of detection (LOD) of 0.06 μM. Additionally, FeCu-NZs catalyze H2O2 to generate abundant •OH radicals, and colorimetric detection of H2O2 is facilitated using the color rendering principle of 3,3',5,5'-tetramethylbenzidine (TMB). Notably, this detection method was applied to determine H2O2 concentrations in real samples, achieving a recovery exceeding 95.7%. In summary, this research provides a practical platform for the construction of traditional nanozymes and the integration of electrochemical systems, which have broad applications in food analysis, environmental monitoring, and medical diagnosis.

Specificity of DNA damage formation induced by femtosecond near-infrared laser filamentation in water

We investigated the deoxyribonucleic acid (DNA) damage induced by laser filamentation, which was generated by focusing femtosecond near-infrared Ti:Sapphire laser light in water at several repetition rates ranging from 1000 Hz to 10 Hz. Using plasmid DNA (pUC19), the single-strand break, double-strand break, nucleobase lesions, and the fragmented DNA were analyzed and quantified by agarose gel electrophoresis. Additionally, the H2O2 concentration after irradiation was determined. We observed that (1) the DNA damage per laser shot and (2) the enzyme-sensitive base lesions per total DNA damage decreased as the laser repetition rate increased. Furthermore, (3) extraordinarily short DNA fragments were likely to be produced, compared with those produced using X-rays, and (4) most OH radicals could be eliminated by recombination to generate H2O2, preventing them from damaging the DNA. The Monte-Carlo simulation of the strand break formation implies that the observed dependency of strand break efficiency on the laser repetition rate is mainly due to diffusion of DNA molecules. These findings quantitatively and qualitatively revealed that an intense laser pulse induces a specific DNA damage profile that is not induced by X-rays, a sparsely ionizing radiation source.