Peroxide Oxidation Research Articles

Establishment of Physalis alkekengi cell suspension culture: time-dependent behavior of genes related to the steroidal compounds, key enzymes, and physalins under static magnetic field.

Cell suspension culture has the potential to be a valuable source for the bioactive compound productions. In this study, an optimized procedure was established for callus and cell suspension culture of Physalis alkekengi for the first time, and the impact of static magnetic field (SMF, 6 mT) was studied on the high-value metabolic compounds through investigation of signaling molecules and gene expressions at the late log-to-stationary phase. Results showed that the growth regulators of 6-benzyl amino purine (BAP, 1.5mg-1 L) and 1-naphthaleneacetic acid (NAA, 0.4mg-1 L) induced the highest fresh weight, callus rate, callus index, and total withanolides. Cell suspension culture was established in the liquid MS medium supplied with BAP (1.5mg-1 L) and NAA (0.1mg-1 L). SMF application decreased slightly the cell growth and viability and enhanced the number of round-shaped cells. The hydrogen peroxide (H2O2) and nitric oxide (NO) levels increased at an all-time series after SMF exposure, and their maximum contents were observed after 12h. A significant alteration of malondialdehydecontent was also identified after 12h of SMF exposure. The expression of 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGR), 1-deoxyD-xylulose 5-phosphate synthase (DXS), squalene synthase (SQS), sterol Δ7-reductase (DWF5), and C-7,8 sterol isomerase (HYD1) genes was upregulated significantly after 24 and 48h. An increase in the total withanolides was related to more activity of HMGR and DXS enzymes in SMF-exposed cells and the maximum physalin A (12.8mgg-1 DW) and physalin B (1.92mgg-1 DW) obtained after 24h compared to controls. Findings suggest that SMF can play a supportive factor in inducing steroidal compounds in P. alkekengi through modulating H2O2 and NO levels and the related-gene expressions.

Microplastic pollution and ecological risk assessment of a pond ecosystem.

Microplastic (MP) pollution has been observed in various ecosystems as a result of the rapid increase in plastic production over the past half-century. Nevertheless, the extent of MP pollution in different ecosystems, particularly in freshwater ecosystems, has not been well-studied, and there are limited investigations on this particular topic, specifically in Türkiye. Here, we quantify the occurrence and distribution of MPs in surface water samples collected from Topçu Pond (Türkiye) for the first time. Water samples were collected at five stations and filtered (30 L for each station) through stacked stainless steel sieves (5mm, 328µm, and 61µm mesh size) with a diameter of 30cm. The abundance, size, color, shape, and type of collected debris samples were analyzed after the wet peroxide oxidation process. MP particles were observed in all samples at an average abundance of 2.4 MPs/L. The most abundant MP size class and type were 0-999µm and fiber respectively. On the other hand, prevalent colors were black and colorless in general. According to the Raman analysis results, the identified MP derivatives were polypropylene (40%), polyamide (30%), ethylene acrylic acid (20%), and polyvinylchloride (10%). Moreover, the pollution load index (PLI) index was used to determine the pollution status. PLI values were determined as 1.91 at station S1, 1.73 at station S2, 1.31 at station S3, 1 at station S4 and 1.24 at station S5. The PLI value determined for the overall pond was 1.4. The results of this research show that MP pollution is present in Topçu Pond and contributes to the expanding literature on MP pollution in pond ecosystems.

Depositions of airborne microplastics during the wet and dry seasons in Pathum Thani, Thailand

In this study, microplastics were monitored separately in the wet and dry deposition in the peri-urban area of Thailand. Over eighteen weeks from September 2021 to January 2022, rainwater (wet deposition) and settled microplastics (dry deposition) were systematically collected. Subsequent analyses involved the extraction, quantification, and identification of microplastics through wet peroxide oxidation, density separation, stereomicroscopic visual inspection and Fourier-transform infrared (FTIR) analysis. The results show that the wet deposition flux of microplastics was averaged at 285 numbers/m2/day while the dry deposition flux of microplastics was averaged at 199 numbers/m2/day, contributing to a total deposition flux (dry + wet) of 325 numbers/m2/day. Comparative assessments with prior studies from different locations demonstrated similarities in microplastic numbers, color and polymer types. Notably, this study found a higher microplastic deposition flux during the period when wet deposition existed than the flux during the period with only dry deposition, underscoring the important role of rainfall in adding more removal of microplastics from the atmosphere. These findings provide crucial insights into the dynamics of microplastic deposition in outdoor settings, significantly contributing to understanding the microplastic pollution cycle in the environment.

Synthesis of strontium hexaferrite (SrFe12O19) by self-propagating high-temperature synthesis (SHS) method and investigation of the effect of milling on morphology and magnetic properties

In this research, strontium hexaferrite (SrFe12O19) was synthesized using the self-propagating high-temperature synthesis (SHS) method, and its structural and magnetic properties were investigated. Raw materials such as strontium peroxide (SrO2), iron (Fe), and iron (III) oxide (Fe2O3) were used to prepare green compact. The current research investigated the effect of milling time and speed on the morphology and magnetic properties of strontium hexaferrite, and the optimum temperature for calcination was obtained. X-ray diffraction (XRD), vibrating magnetometer (VSM), field emission scanning electron microscope (FE-SEM), transmission electron microscopy (TEM), and high-resolution transmission electron microscopy (HRTEM) were used to study the mentioned parameters and choose the optimal conditions for the synthesis of strontium hexaferrite. Milling at speeds of 100, 200, and 300 rpm for 30 and 90 min was investigated. Also, calcination was performed at temperatures of 1000, 1100, 1200, and 1300 °C for 90 min to obtain the optimal temperature. According to the results of VSM analysis, the sample milled at 300 rpm for 90 min and calcined at 1200 °C for 90 min had the highest magnetic properties. Magnetic saturation (MS), magnetic remanence (Mr), and coercivity (HC), with values of 56.43 emu/g, 30.85 emu/g, and 5705.96 Oe, were obtained for this sample. Also, FE-SEM images showing the formation of hexagonal plates with an average particle size of 380 nm after calcination were obtained for the sample with optimal parameters. TEM and HRTEM images also showed the formed particles of strontium hexaferrite with hexagonal morphology.

Influence of the Chemical Modification of Carbon Nanotube Fibers on Electrical properties and Electromechanical Response

The electromechanical response (EMR) of carbon nanotube (CNT) fibers is related to the densification process of the CNT network driven by electromagnetic force. The study of the interaction between the electrical properties and the electromechanical response of carbon nanotubes is of great theoretical significance for exploring the microstructure of carbon nanotube fibers and developing the related flexible electronic devices. This study investigated the relationship between the conductive pathway network and EMR, by analyzing the internal structural characteristics of the CNT fibers after undergoing hydrogen peroxide oxidation and iodine modification. The results show that impurities such as amorphous carbon impeded electron transport and deformation of CNT networks. After hydrogen peroxide oxidation treatment, he carbon nanotube surface impurities inside the fibres were reduced, the van der Waals forces between carbon nanotubes were increased, the deformation of the carbon nanotube network was enhanced, and the negative effect of the decrease in the elastic modulus of the fibres caused by the increase in temperature was weakened. In the case of iodine-decorated CNT fibers, carbon-iodine bonds effectively strengthened the interaction between CNTs, but hinders the contraction of the carbon nanotube network, resulting in a weaker electromechanical response. Hydrogen peroxide oxidation treatment is more beneficial than iodine modification to improve the shrinkage and deformation ability of carbon nanotube fibres in the electromechanical response.

Efficacy of chemical digestion methods to reveal undamaged microplastics from planktonic samples

Standardisation and validation of methods for microplastics research is essential. A major methodological challenge is the removal of planktonic organisms from marine water samples allowing for the identification of microplastics associated to planktonic communities. To improve the reproducibility and accuracy of digestion methods for the removal of planktonic biomass, we compared and modified existing chemical digestion methods. These digestion methods included an acidic digestion using nitric acid, alkaline digestions with potassium hydroxide (alkaline 1 digestion) and sodium hydroxide from drain cleaner (alkaline 2 digestion), an oxidative digestion using sodium dodecyl sulfate with hydrogen peroxide, and an enzymatic digestion using enzyme drain clean pellets. Chemical digestion of three densities of zooplankton communities (high, medium, and low) in the presence of five commonly found environmental microplastic pollutants (polyamide, polyethylene, polyethylene terephthalate, polypropylene, and polystyrene) were performed for each treatment. The chemical treatments were assessed for (i) their digestion efficiency of zooplankton communities by different biomass densities, and (ii) their impact on microplastic particles through the comparison of both chemical (Raman spectroscopy) and physical (length, width, and visual) changes, between the pre-treatment and post-treatment microplastic particles. The alkaline 1, alkaline 2 and oxidative methods demonstrated significantly better digestion efficiency (p < 0.05) than the modified enzymatic and acidic treatments. The acidic, alkaline 1, and alkaline 2, treatments caused the most damages to the microplastic particles. We suggest future studies to implement the oxidative digestion method with sodium dodecyl sulfate and hydrogen peroxide because of its high digestion efficiency, and low damage to microplastic particles. This method is similar to the wet peroxide oxidation digestion method used throughout the literature but can be implemented at a lower cost.

Effect of SiO2 passivation layer on nanoporous Si photocathode under the density of SiO2 passivation layer

This study presents the fabrication and comparative evaluation of SiO2/Si photoelectrodes employing two distinct SiO2 oxidation methods. Each SiO2/Si photoelectrodes was successfully generated based on uniform SiO2 layers a top nanoporous Si that have thicknesses of 2.7 nm via hydrogen peroxide oxidation (H2O2 oxidation) and 1.8 nm via nitric acid oxidation of Si (NAOS). Notably, the thin NAOS-formed SiO2 layer resulted in a measured suboxide density approximately 4.8 times lower (0.5192 × 1014 atoms/cm2) than that of the H2O2 oxidation (2.4969 × 1014 atoms/cm2). The presence of this SiO2 layer not only passivates defects but also improves electrical properties. As a result, the photocurrent density of the NAOS-formed SiO2/Si photoelectrode notably outperformed that of the H2O2-formed counterpart (about 1.7 times). This enhancement is attributed to the consistent passivation effects and improved electrical properties achieved due to NAOS-formed SiO2. This study contributes to a deeper understanding of how the SiO2 passivation layer can be utilized to improved photocurrent density.

Protective effects of polysaccharide extracted from green alga Chaetomorpha linum against zinc and copper-induced testicular toxicity in male mice

This study aimed to investigate the effects of copper (CuSO4) and zinc (ZnSO4) overload on male reproductive toxicity and the potential of a polysaccharide extracted from green alga Chaetomorpha linum (PS) in mitigating their toxicities. Adult male mice strain of 25 ± 2 g of weight was subdivided into eight groups. Group 1 served as control; group 2 received PS (200 mg/kg), and groups 3 and 4 received intraperitoneally zinc (60 mg/kg b.w) and copper (33 mg/kg b.w), respectively. Group 5 received both zinc (60 mg/kg b.w) and copper (33 mg/kg b.w), group 6 received zinc (60 mg/kg b.w) associated with PS (200 mg/kg), group 7 received copper (33 mg/kg b.w) associated with PS (200 mg/kg), and group 8 received zinc (60 mg/kg b.w) and copper (33 mg/kg b.w) associated with PS (200 mg/kg). Results suggested that ZnSO4 and CuSO4 significantly decreased the functional sperm parameters. Furthermore, extended exposure to these elements increased oxidative stress biomarkers, including malondialdehyde (MDA) as a measure of lipid peroxidation and advanced oxidation protein products (AOPP) indicating protein oxidative damage. This process also reduces the activity of antioxidant enzymes such as glutathione (GSH) and glutathione peroxidase (GPx), which neutralize and catalyze free radicals. Histopathological changes in mice testis were also studied. However, the co-treatments with PS significantly reduced these effects and promoted the reproductive parameters in male mice. In conclusion, PS exhibited protective effects against zinc and copper-induced reproductive toxicity, making it a potential adjuvant treatment for testicular toxicity.

Toxicological assessment of the Achyrocline satureioides aqueous extract in the Caenorhabditis elegans alternative model

ABSTRACT Achyrocline satureioides, popularly called “marcela” in Brazil, is used in traditional medicine in South America. A. satureioides, inflorescences are used for many conditions, including to minimize the Sars-Cov-2 symptoms. Therefore, the aim of this study was to determine the toxicity profile of A. satureioides aqueous extract (ASAE), using the Caenorhabditis elegans (C. elegans) alternative model. Survival, reproduction, development, and transgenerational assays were performed. The effects of ASAE were investigated under conditions of thermal stress and presence of oxidant hydrogen peroxide (H2O2). In addition, C. elegans strains containing high antioxidant enzyme levels and elevated lineages of daf-16, skn-1 and daf-2 regulatory pathways were examined. The ASAE LC50 value was found to be 77.3 ± 4 mg/ml. The concentration of ASAE 10 mg/ml (frequently used in humans) did not exhibit a significant reduction in worm survival at either the L1 or L4 stage, after 24 or 72 hr treatment. ASAE did not markedly alter the body area. In N2 strain, ASAE (10 or 25 mg/ml) reversed the damage initiated by H2O2. In addition, ASAE protected the damage produced by H2O2 in strains containing significant levels of sod-3, gst-4 and ctl − 1,2,3, suggesting modulation in these antioxidant systems by this plant extract. ASAE exposure activated daf-16 and skn-1 stress response transcriptional pathways independently of daf-2, even under extreme stress. Data suggest that ASAE, at the concentrations tested in C. elegans, exhibits a reliable toxicity profile, which may contribute to consideration for safe use in humans.

Myricetin ameliorates cognitive impairment in 3×Tg Alzheimer’s disease mice by regulating oxidative stress and tau hyperphosphorylation

BackgroundAlzheimer's disease is characterized by abnormal β-amyloid (Aβ) plaque accumulation, tau hyperphosphorylation, reactive oxidative stress, mitochondrial dysfunction and synaptic loss. Myricetin, a dietary flavonoid, has been shown to exert neuroprotective effects in vitro and in vivo. Here, we aimed to elucidate the mechanism and pathways involved in the protective effect of myricetin. MethodsThe effect of myricetin was assessed on Aβ42 oligomer-treated neuronal SH-SY5Y cells and in 3×Tg mice. Behavioral tests were performed to assess the cognitive effects of myricetin (14 days, ip) in 3×Tg mice. The levels of beta-amyloid precursor protein (APP), synaptic and mitochondrial proteins, glycogen synthase kinase3β (GSK3β) and extracellular regulated kinase (ERK) 2 were assessed via Western blotting. Flow cytometry assays, immunofluorescence staining, and transmission electron microscopy were used to assess mitochondrial dysfunction and reactive oxidative stress. ResultsWe found that, compared with control treatment, myricetin treatment improved spatial cognition and learning and memory in 3×Tg mice. Myricetin ameliorated tau phosphorylation and the reduction in pre- and postsynaptic proteins in Aβ42 oligomer-treated neuronal SH-SY5Y cells and in 3×Tg mice. In addition, myricetin reduced reactive oxygen species generation, lipid peroxidation, and DNA oxidation, and rescued mitochondrial dysfunction via the associated GSK3β and ERK 2 signalling pathways. ConclusionsThis study provides new insight into the neuroprotective mechanism of myricetin in vitro in cell culture and in vivo in a mouse model of Alzheimer’s disease.

Mechanistic aspect of copper selenide as an electrocatalyst for the detection of hydrogen peroxide in gaseous phase

The electrocatalytic properties of copper selenide for hydrogen peroxide detection in a gas phase were investigated using cyclic and square-wave voltammetry. Copper selenide demonstrated significant electrocatalytic activity towards hydrogen peroxide oxidation in a basic medium containing polyacrylic acid as a gas-absorbing polyelectrolyte. Experimental data were corroborated by a brief theoretical analysis and simulations based on a two-electron irreversible electrode mechanism of a dissolved redox couple. The voltammetric response of a conventional glassy carbon electrode modified with copper selenide showed a linear correlation with hydrogen peroxide concentration over a range of 3.0 × 10−5 to 1.0 × 10−3 mol L−1 in solution.Practical application of this method for gaseous hydrogen peroxide detection was explored using screen-printed electrodes (SPE) coated with a thin film of polyacrylic acid containing medium, with copper selenide serving as a modifier of the working electrode. The detectable concentration range of gaseous hydrogen peroxide using the modified SPE spanned picomolar concentrations. The statistical parameters of the calibration line in terms of LOQ, LOD and R2 are 4.1 × 10−6, 1.2 × 10−6 mol L−1, and 0.996, which correspond very closely to the gas concentrations of 6.1 × 10−12 to 6.1 × 10−11 mol L−1.

Emerging Roles of Xanthine Oxidoreductase in Chronic Kidney Disease.

Xanthine Oxidoreductase (XOR) is a ubiquitous, essential enzyme responsible for the terminal steps of purine catabolism, ultimately producing uric acid that is eliminated by the kidneys. XOR is also a physiological source of superoxide ion, hydrogen peroxide, and nitric oxide, which can function as second messengers in the activation of various physiological pathways, as well as contribute to the development and the progression of chronic conditions including kidney diseases, which are increasing in prevalence worldwide. XOR activity can promote oxidative distress, endothelial dysfunction, and inflammation through the biological effects of reactive oxygen species; nitric oxide and uric acid are the major products of XOR activity. However, the complex relationship of these reactions in disease settings has long been debated, and the environmental influences and genetics remain largely unknown. In this review, we give an overview of the biochemistry, biology, environmental, and current clinical impact of XOR in the kidney. Finally, we highlight recent genetic studies linking XOR and risk for kidney disease, igniting enthusiasm for future biomarker development and novel therapeutic approaches targeting XOR.

Novel Properties of Old Propranolol-Assessment of Antiglycation Activity through In Vitro and In Silico Approaches.

Hypertension has earned the "silent killer" nickname since it may lead to a number of comorbidities, including diabetes and cardiovascular diseases. Oxidative stress and protein glycation play vital roles in the pathogenesis of hypertension. Several studies have shown that they profoundly account for vascular dysfunction, endothelial damage, and disruption of blood pressure regulatory mechanisms. Of particular note are advanced glycation end products (AGEs). AGEs alter vascular tissues' functional and mechanical properties by binding to receptors for advanced glycation end products (RAGE), stimulating inflammation and free radical-mediated pathways. Propranolol, a nonselective beta-adrenergic receptor antagonist, is one of the most commonly used drugs to treat hypertension and cardiovascular diseases. Our study is the first to analyze propranolol's effects on protein glycoxidation through in vitro and in silico approaches. Bovine serum albumin (BSA) was utilized to evaluate glycoxidation inhibition by propranolol. Propranolol (1 mM) and BSA (0.09 mM) were incubated with different glycating (0.5 M glucose, fructose, and galactose for 6 days and 2.5 mM glyoxal and methylglyoxal for 12 h) or oxidizing agents (chloramine T for 1 h). Biomarkers of protein glycation (Amadori products (APs), β-amyloid (βA), and advanced glycation end products (AGEs)), protein glycoxidation (dityrosine (DT), kynurenine (KYN), and N-formylkynurenine (NFK)), protein oxidation (protein carbonyls (PCs), and advanced oxidation protein products (AOPPs)) were measured by means of colorimetric and fluorimetric methods. The scavenging of reactive oxygen species (hydrogen peroxide, hydroxyl radical, and nitric oxide) and the antioxidant capacity (2,2-diphenyl-1-picrylhydrazyl radical and ferrous ion chelating (FIC) assays)) of propranolol were also evaluated. Additionally, in silico docking was performed to showcase propranolol's interaction with BSA, glycosides, and AGE/RAGE pathway proteins. The products of protein glycation (↓APs, ↓βA, ↓AGEs), glycoxidation (↓DT, ↓KYN, ↓NFK), and oxidation (↓PCs, ↓AOPPs) prominently decreased in the BSA samples with both glycating/oxidizing factors and propranolol. The antiglycoxidant properties of propranolol were similar to those of aminoguanidine, a known protein oxidation inhibitor, and captopril, which is an established antioxidant. Propranolol showed a potent antioxidant activity in the FIC and H2O2 scavenging assays, comparable to aminoguanidine and captopril. In silico analysis indicated propranolol's antiglycative properties during its interaction with BSA, glycosidases, and AGE/RAGE pathway proteins. Our results confirm that propranolol may decrease protein oxidation and glycoxidation in vitro. Additional studies on human and animal models are vital for in vivo verification of propranolol's antiglycation activity, as this discovery might hold the key to the prevention of diabetic complications among cardiology-burdened patients.

Efficient oxygen reduction to alkaline peroxide at current densities up to 500 mA cm−2 on a gas diffusion electrode with hydrophobic carbon microporous layer: Influence of fluid dynamics and reactor operation on scale-up

The two-electron electrochemical O2 reduction reaction (2e-ORR) on a gas diffusion electrode (GDE) using clean electricity is an attractive process for generating the green oxidant hydrogen peroxide (H2O2). Electrolyte flooding through the porous catalyst and diffusion layers is one of the major factors inhibiting the operational stability and longevity under industrially relevant current densities (>100 mA cm−2). This study reports for the first time that optimizing the two-phase flow and the mode of reactor operation brings about a remarkable improvement in the high current density operation (up to 500 mA cm−2) on a scalable (20 cm2 geometric area) and commercially available Sigracet 39BB GDE with the microporous carbon layer (MPL) acting as the catalyst layer. The interacting effects of current density, gas and liquid flow rates and the flooding threshold limit for the differential liquid/gas pressure were determined. While high peroxide Faradaic efficiency (FE > 95 %) was attained in a gas flow-by mode during short-term experiments, long-term stability was only established when the gas was switched to the flow-through or quasi-flow-through mode of operation. Under the latter conditions, at 500 mA cm−2 operational stability of more than 20 h was demonstrated with a peak FE of 97 % in 1.0 M KOH, at 293 K, 1 atm. It was found that optimizing the reactor operation has a profound effect during scale-up, and developing novel catalytic materials for 2e-ORR to alkaline peroxide is not warranted since a low-cost microporous carbon-based GDE is sufficient for stable and efficient operation.

Microplastic concentration, characterization, and size distribution in the Delaware Bay estuary

Microplastic (MP) pollution has been widely reported across water matrices including in estuaries, which are important for the understanding of oceanic MPs. Estuaries can greatly alter the fate, transport, size distribution, and abundance of plastic pollution. The aim of this study was to quantify and characterize MP pollution in the Delaware Bay estuary USA, including the size distribution. Samples (N = 31) were collected from the mouth of the Delaware River to the coastal ocean including multiple frontal zones across two sampling campaigns (2019 and 2022). MP were extracted from the collected particles using wet peroxide oxidation and density separation with saturated sodium chloride. Particles collected on 500 μm mesh sieves were analyzed via Fourier transform infrared (FTIR) spectroscopy. Across all samples, 324 of the 1015 particles analyzed were MP, and 11 macroplastics were observed. MP concentrations ranged from below detection to 4.12 MP/m3 (mean 0.34 ± 0.80 MP/m3). No significant differences were observed between sampling sites; nonetheless, the two highest MP concentrations were observed when sampling along frontal zones with visible debris including macroplastics. Polyethylene (53%) and polypropylene (43%) were the most abundant polymers observed. The majority of the non-plastic particles were classified as particulate natural organic matter (82% of non-plastics). Particles from samples collected during 2022 (N = 864) also had color, morphology, and two size dimensions recorded. MP particle size was significantly associated with sampling site, with the coastal ocean sampling site generally having the smallest MPs. A correlation between total post-extraction particles and total plastic particles was observed. Aspect ratios for the plastics ranged from one to 40.7, with larger ratios for fibers, with a mean (±standard deviation) of 3.39 ± 4.72 (unitless). These aspect ratios can be used to select shape factors used to estimate the total volume of MP in the studied size range. Overall, these results can help inform fate, transport, and risk assessments related to estuarine plastic pollution.

Hydrogen peroxide serves as pivotal fountainhead for aerosol aqueous sulfate formation from a global perspective

Traditional atmospheric chemistry posits that sulfur dioxide (SO2) can be oxidized to sulfate (SO42–) through aqueous-phase reactions in clouds and gas-phase oxidation. Despite adequate knowledge of traditional mechanisms, several studies have highlighted the potential for SO2 oxidation within aerosol water. Given the widespread presence of tropospheric aerosols, SO42− production through aqueous-phase oxidation in aerosol water could have a pervasive global impact. Here, we quantify the potential contributions of aerosol aqueous pathways to global sulfate formation based on the GEOS-Chem simulations and subsequent theoretical calculations. Hydrogen peroxide (H2O2) oxidation significantly influences continental regions both horizontally and vertically. Over the past two decades, shifts in the formation pathways within typical cities reveal an intriguing trend: despite reductions in SO2 emissions, the increased atmospheric oxidation capacities, like rising H2O2 levels, prevent a steady decline in SO42− concentrations. Abating oxidants would facilitate the benefit of SO2 reduction and the positive feedback in sulfate mitigation.

The degradation of maleic acid with wet peroxide oxidation catalyzed by Al2O3-supported Cu catalyst: effect of inorganic ions

The degradation of maleic acid with wet peroxide oxidation catalyzed by Al2O3-supported Cu catalyst: effect of inorganic ions

A method for the extraction of microplastics from solid biowastes including biosolids, compost, and soil for analysis by µ-FTIR

Few methods exist detailing the extraction of microplastics from organic matrices. A validated method for the successful extraction of microplastics from solid biowastes including biosolids, compost, and soil for spectroscopic analysis by micro-Fourier transform infrared spectroscopy (µ-FTIR) was developed. Solid dry biowastes were first digested with a wet peroxide oxidation (WPO) with iron (II) solution and 30% hydrogen peroxide followed by sequential density separations with ultra-pure water and 1.8 g cm−3 NaI in an optimised sediment-microplastic isolation (SMI) unit. The average recoveries for spiked microplastics were 92, 95 and 98% for bagged compost, biosolids, and soil, respectively. This method ensures a high microplastic recovery by first chemically disintegrating biowaste aggregates without employing destructive methods like milling and allows for successful density separations where the settled fraction is isolated off from the supernatant, allowing thorough rinsing of the equipment and thus a greater transferal of particles into the vacuum filtering device. Minimal processing steps reduce the instance of introducing contamination and particle loss.•Digestion as a first step to disintegrate aggregates to release entrapped microplastics•Density separation with SMI unit with the method adapted for biowastes•Minimal steps to reduce contamination and particle loss

Sago Starch Modification by Combination of Lactic Acid Hydrolysis and Oxidation of Hydrogen Peroxide Under Ultraviolet Rotary Dryer Irradiation

Sago Starch Modification by Combination of Lactic Acid Hydrolysis and Oxidation of Hydrogen Peroxide Under Ultraviolet Rotary Dryer Irradiation

Visualizing hydrogen peroxide and nitric oxide dynamics in endothelial cells using multispectral imaging under controlled oxygen conditions

The complex interplay between hydrogen peroxide (H2O2) and nitric oxide (NO) in endothelial cells presents challenges due to technical limitations in simultaneous measurement, hindering the elucidation of their direct relationship. Previous studies have yielded conflicting findings regarding the impact of H2O2 on NO production. To address this problem, we employed genetically encoded biosensors, HyPer7 for H2O2 and geNOps for NO, allowing simultaneous imaging in single endothelial cells. Optimization strategies were implemented to enhance biosensor performance, including camera binning, temperature regulation, and environmental adjustments to mimic physiological normoxia. Our results demonstrate that under ambient oxygen conditions, H2O2 exhibited no significant influence on NO production. Subsequent exploration under physiological normoxia (5 kPa O2) revealed distinct oxidative stress levels characterized by reduced basal HyPer7 signals, enhanced H2O2 scavenging kinetics, and altered responses to pharmacological treatment. Investigation of the relationship between H2O2 and NO under varying oxygen conditions revealed a lack of NO response to H2O2 under hyperoxia (18 kPa O2) but a modest NO response under physiological normoxia (5 kPa O2). Importantly, the NO response was attenuated by l-NAME, suggesting activation of eNOS by endogenous H2O2 generation upon auranofin treatment. Our study highlights the intricate interplay between H2O2 and NO within the endothelial EA.hy926 cell line, emphasizing the necessity for additional research within physiological contexts due to differential response observed under physiological normoxia (5 kPa O2). This further investigation is essential for a comprehensive understanding of the H2O2 and NO signaling considering the physiological effects of ambient O2 levels involved.