Different Concentrations Of Hydrogen Peroxide Research Articles

Production of nutritionally active compounds from Spirulina platensis under various stress conditions

The free-floating, filamentous cyanobacteria Spirulina platensis is highly valued and in great demand worldwide for its high-value colors and phytonutrients. These compounds find use in health foods, feed, medicines, and diagnostics. The primary objective of this work was to enhance the growth of Spirulina under both oxidative and physiological stress conditions in order to maximize the synthesis of phycocyanin and carotenoid pigments. Cultures were subjected to different concentrations of hydrogen peroxide (H2O2) and sodium chloride for varying temperatures and pH levels. Under lower concentrations of H2O2 (4mM), the maximum carotenoid content was increased, but the phycocyanin content was found to be stimulated at 10mM. Moreover, the synthesis of both pigments was shown to be highest under physiological stress circumstances (40mM and 60mM NaCl concentration) and at an optimal pH of 8-9, helped by a temperature range of 25-30℃. The experimental results demonstrate that both carotenoid and phycocyanin exhibit antioxidant properties even in the presence of oxidative stress. This suggests that the aforementioned circumstances can be applied in future investigations to extract different antioxidants from S. platensis.

Clinical comparison of whitening efficacy and tooth sensitivity of different concentrations of hydrogen peroxide photoactivated with violet or blue LEDs.

This study evaluated the photoactivation of hydrogen peroxide gels at different concentrations using blue or violet LED in terms of whitening efficacy and tooth sensitivity. Forty patients were randomly divided into 4 groups: HP6V(violet LED and 6% hydrogen peroxide), HP6B(blue LED and 6% hydrogen peroxide), HP35V(violet LED and 35% hydrogen peroxide), and HP35B (blue LED and 35% hydrogen peroxide). The L*, a* and b* values were measured before, 1 week and 3 months after treatment, and the ΔE and ΔWID values were calculated. Tooth sensitivity was measured using a visual analogue scale (VAS) before, immediately after, and 24h after bleaching. The ΔE, ΔWID and bleaching sensitivity values were subjected to the ANOVA test and Bonferroni post-test. HP35V and HP35B showed higher whitening efficacy than HP6VL, while HP6V did not show statistical differences compared to the other groups. Regarding bleaching-related sensitivity, the HP6V and HP6B groups presented the lowest values when compared to HP35V and HP35B. HP6V showed whitening efficacy comparable to HP35V and HP35B but with reduced tooth sensitivity. TRIAL REGISTRATION NUMBER: NCT06165458; registration date: 12/09/2023.

In silico and in vitro analyses to investigate the effects of vitamin C on VEGF protein

ObjectivesThis study was conducted to evaluate the effects of vitamin C on apoptotic and proliferative genes in injured HepG2 cells. MethodsIn silico analysis was performed using molecular docking of chemical compounds with vascular endothelial growth factor (VEGF). The different computational tools used were AutoDock Vina, BIOVIA DISCOVERY studio, and PyMOL. Drug likeness and toxicity were analyzed by SWISS ADMET. Cells that were 60–70% confluent were treated with different concentrations of hydrogen peroxide (H2O2) (100–2000 μM) and ascorbic acid (30, 60, 90 μg/mL). The MTT cell proliferation assay was performed to compare the proliferative potential of HepG2 cells treated with H2O2 or ascorbic acid with untreated HepG2 cells using 96-well plates. ResultsThe lowest binding energy of VEGF with vitamin C –5.2 kcal/mol and L-ascorbic acid-2 glycoside −4.7 kcal/mol was observed by in silico analysis. Vitamin C was selected because it exhibited a high interaction with VEGF and fulfilled Lipinski's rule, and had better oral viability and pharmacokinetics compared to L-ascorbic acid-2 glycoside. Cell viability assays showed that vitamin C had significant apoptotic effects (P < 0.0001). After treating HepG2 cells with ascorbic acid, reduced VEGF (angiogenesis) was observed as determined by apoptotic and proliferative gene expression. Ascorbic acid treatment of HepG2 cells led to downregulation of the proliferation markers, proliferating cell nuclear antigen, Ki67, and DNA topoisomerase II alpha. Increased apoptosis after treatment with vitamin C was observed due to upregulation of p53 and annexin V. ConclusionThe results of this study showed that vitamin C inhibited the growth of cancer cells, thus protecting HepG2 cells from oxidative stress. Vitamin C exhibited antiproliferative activity as observed in silico and in vitro, as well as by the inhibited expression of genes involved in protein synthesis.

Platinum-Particle-Assisted Etching of Low-, Moderately-, and Highly-Doped p-Type Silicon: Change of Composite Porous Structure

Metal-assisted etching (metal-assisted chemical etching) is an efficient method to fabricate porous silicon (Si). When using platinum (Pt) particles as metal catalysts in metal-assisted etching, a composite porous structure of straight macropores formed beneath the Pt particles and a mesoporous layer formed on the entire surface of Si can be fabricated. The formation mechanism of the composite structure is still open to discussion. We previously demonstrated that the ratio of mesoporous layer thickness to macropore depth showed a large value (approximately 1.1) in the case of highly-doped p-Si. In this study, we investigated the composite structure formation by using p-Si substrates with different doping densities and etching solutions with different concentrations of hydrogen peroxide (H2O2). There was not significant difference in the structures formed on low- and moderately-doped Si, despite the large difference in doping density. The ratio of mesoporous layer thickness to macropore depth increased within the range approximately from 0.1 to 0.4 with increasing the H2O2 concentration in the case of low- and moderately-doped Si, but it did not change in the case of highly-doped Si. We discussed the observation results based on the spatial distribution of hole consumption and the band structures at Pt/Si and Si/electrolyte interfaces.

Effect of whitening toothpastes with different hydrogen peroxide concentrations: Penetration into the pulp chamber and color change

ObjectivesThis study evaluated the efficacy of simulated brushing with toothpastes containing different concentrations of hydrogen peroxide (HP) in pulp chamber penetration and color change. Also, physical-chemical properties (concentration, pH and viscosity) were evaluated. MethodsForty-nine premolars were divided into seven groups (n = 7): untreated (control); whitening gel (White Class 6 %, 6 %BG) with one 90 min application (6 %BG 90 min) and 14 applications of 90 min (6 %BG 14×90 min); toothpastes (Colgate Luminous White Glow 3 %, 3 %TP; Crest 3D White Brilliance 4 %, 4 %TP; Colgate Optic White Pro-Series 5 %, 5 %TP) and 6 %BG toothbrushing for 14 applications of 90 s. HP penetration into the pulp chamber was measured through UV–Vis spectrophotometry and color change with a spectrophotometer (ΔEab, ΔE00, and ΔWID). Initial concentration, pH, and viscosity were measured through Titration, Digital pH-meter, and Rheometer, respectively. Statistical analysis used one-way ANOVA and Tukey's test (α = 0.05). Results6 %BG (14×90 min) and 4 %TP groups showed acidic pH and higher concentrations of HP in the pulp chamber compared to the other groups (p < 0.05). On the other side, 3 %TP and 5 %TP groups showed alkaline pH, higher viscosity between the toothpastes and lower HP penetration (p < 0.05). The 6 %BG AH (14×90 min) group exhibited the most significant color change (ΔEab, ΔE00, and ΔWID) (p < 0.05). ConclusionsBrushing with whitening toothpaste with an acidic pH leads to greater HP penetration into pulp chamber; but, even when a high concentrated HP whitening toothpaste was used, a lower whitening effect was observed when compared to a two-week at-home bleaching. Clinical SignificanceWhitening toothpastes containing up to 5 % HP produced lower whitening effect than two-week at-home bleaching. Additionally, HP was detected within the pulp chamber which can potentially impact in tooth sensitivity.

Influence of blue and violet LED and infrared laser on the temperature of bleaching protocols in different concentrations of hydrogen peroxide

BackgroundThe photo-acceleration of bleaching gels by lights has been extensively researched. However, the induced temperature increase during this process needs to be further evaluated to prevent damage to the dental pulp. Therefore, the objective of this study was to evaluate the surface and intrapulpal temperature kinetics of different concentrations of hydrogen peroxide (HP) gels photo-accelerated by blue or violet light and infrared laser. MethodsThe whitening gels at concentrations of HP35, HP15, and HP6 % were irradiated with blue and violet LED/laser on the surface of a human canine tooth. The surface temperature variation (∆Ts) was evaluated using a pH meter, while the intrapulpal temperature variation (∆Ti) was assessed using a digital thermometer at intervals of 1, 15, and 30 min. Statistical analysis was conducted using a Two-way repeated measures ANOVA test, and Bonferroni post-test was applied at a significance level of 5 %. ResultsAll violet LED photo-accelerated groups showed a higher increase in ∆Ts compared to the blue LED/laser groups. However, there were no significant differences between the groups for ∆Ti. ConclusionAlthough the photo-acceleration of HP35 and HP15 % gels with violet LED/laser has a greater increase in surface temperature compared to HP6 % gel, the different light systems do not significantly increase the intrapulpal temperature.

Effect of different concentrations of hydrogen peroxide on indigenous bull sperm motility

Effect of different concentrations of hydrogen peroxide on indigenous bull sperm motility

Dissolution of contaminant Zr-DBP and corrosion of stainless steel by dissolved solution

In the nuclear spent fuel reprocessing, zirconium dibutyl phosphate (Zr-DBP) is deposited on the surface of stainless steel equipment, making spent fuel reprocessing difficult. Therefore, in this study, hydrazine carbonate ((N2H5)2CO3) was used to dissolve Zr-DBP. The effects of solid–liquid ratio, different mass fractions of (N2H5)2CO3 solutions, and (N2H5)2CO3 solutions containing different concentrations of hydrogen peroxide (H2O2) on the dissolution of Zr-DBP were investigated. The corrosion rates of different dissolution solutions on stainless steel were also investigated. When the mass fraction of (N2H5)2CO3 in solution was increased from 1 % to 20 %, the concentration of Zr(IV) at dissolution equilibrium increased from 1.05 g/L to 1.61 g/L, respectively. When the dissolution temperature was kept in the range of 25 °C to 65 °C, the increasing temperature promoted the dissolution of Zr-DBP. The presence of H2O2 induced the production of the white precipitates zirconium hydroxide (Zr(OH)4). In addition, the corrosion rate of stainless steel gradually increased from 0.00153 mm/a to 0.0138 mm/a when the concentration of H2O2 in the (N2H5)2CO3 solution was increased from 0 M to 1.5 M. The dissolution ability of Zr-DBP in different carbonate solutions was (N2H5)2CO3 ≥ ammonium carbonate ((NH4)2CO3) > sodium carbonate (Na2CO3) ≥ potassium carbonate (K2CO3).

Novel oxidation indicator films based on natural pigments and corn starch/carboxymethyl cellulose

The existing oil oxidation detection methods are unsuitable for consumers to identify oil oxidation in a domestic setting. This study aims to develop indicator films detecting the degree of lipid oxidation with the naked eye. Purple sweet potato pigment (PSP) was chosen as a color indicator due to its response to hydrogen peroxide. The novel oxidation indicator films were prepared using corn starch, carboxymethyl cellulose (CMC), and varying concentrations of PSP. Fourier transform infrared spectroscopy spectra and scanning electron microscopy analysis confirmed the successful dispersion of PSP in the films. Thermal stability, light resistance, ultraviolet light resistance, mechanical resistance, and flexibility of films containing PSP were improved, enhancing the potential application in detecting oxidized substances. All the films exhibited noticeable color changes when exposed to different concentrations of hydrogen peroxide. These differences were more pronounced with higher levels of PSP. When these films were used to determine the degree of lipid oxidation, the ∆E value of the CS-PSP-0.25 % film showed a linear relationship (R2 = 0.929) with the peroxide value, unlike other films. Therefore, it is reliable to infer the peroxide value of edible oil by observing the color of the films, which helps customers avoid consuming expired oils.

Catalytic epoxidation of palm oleic acid by heterogeneous catalysts: Optimization and kinetic model

AbstractEpoxidized vegetable oils can produce a natural‐based polymer product as chemical reaction intermediates, plasticisers, and stabilizers in polyvinyl chloride. This study aims to identify the effects of using different concentrations of hydrogen peroxide and the effect of different molar ratios of hydrogen peroxide on relative conversion to oxirane. Epoxidized palm oil was produced in situ using performic acid as epoxidation agents and titanium dioxide as a catalyst. The results indicated that a higher concentration of hydrogen peroxide at 50% concentration and the ratio of 2:1 of hydrogen peroxide to palm oil used in the in situ epoxidation of had provided a higher relative conversion to oxirane (50%) in reaction time (70 min). Fourier transformation infrared spectroscopy revealed the presence of an oxirane group at 1200 cm−1. Numerical kinetic modeling was developed with applied genetic algorithm optimization to find the process model that fit experimental data. Then, the kinetic rate, k parameters obtained k11 = 0.031 mol L−1 min−1, k12 = 3.159 mol L−1 min−1, k2 = 2.620 mol L−1 min−1 for epoxidation palm oil, and k3 = 1.19 × 10−5 mol L−1 min−1 in degradation process.

Preclinical EIS Study of the Inflammatory Response Evolution of Pure Titanium Implant in Hank's Biological Solution.

Pure titanium (Ti) is investigated in a pre-clinical study in Hank's biological solution using electrochemical methods, open circuit potential, and electrochemical impedance spectroscopy to highlight the time effect in extreme body conditions, such as inflammatory diseases, on degradability due to corrosion processes occurring on the titanium implant. Electrochemical impedance spectroscopy (EIS) data are presented as Nyquist and Bode plots. The results show the increasing reactivity of titanium implants in the presence of hydrogen peroxide, which is an oxygen-reactive compound that describes inflammatory conditions. The polarization resistance, which results from electrochemical impedance spectroscopy measurements, declined dramatically from the highest value registered in Hank's solution to smaller values registered in all solutions when different concentrations of hydrogen peroxide were tested. The EIS analysis provided insights into titanium's in vitro corrosion behavior as an implanted biomaterial, which could not be solely obtained through potentiodynamic polarization testing.

Influence of hydrogen peroxide on hatching of nauplii Artemia sp.

Nauplii of the brine shrimp Artemia sp. are the optimal starter food for many fish and crustaceans species. For this reason, technologies for their production are being improved, including the activation of cysts. The effect of different concentrations of hydrogen peroxide on hatching process a as activator was studied. Its optimal concentration has been determined; it amounts to 0.2-0.4 ml/l. The reasons for various impacts of hydrogen peroxide on different Artemia cysts are formulated. The dynamic of brine shrimp hatching with and without the activator was studied. It has been established that the addition of a hydrogen peroxide solution as an activator increases the hatching of Artemia nauplii, however, it does not impress on the rapidity of Artemia nauplii release from cysts.

Microstructural effect of different concentrations of hydrogen peroxide photoactivated with LED/laser

BackgroundThe use of different concentrations of hydrogen peroxide (HP) photoactivated with LED/laser sources is common however, their influence on tooth structure is not yet fully elucidated. This study aimed to evaluate the pH, microhardness and surface roughness of different bleaching protocols photoactivated with LED/laser. MethodsForty bovine incisors were sectioned (7 × 7 × 2 mm) and randomized into four groups for analysis of pH (n = 5), microhardness and roughness (n = 10): HP35, HP6_L, HP15_L, HP35_L. The pH analysis was performed in the initial and final minute of the bleaching protocol. Microhardness and roughness were evaluated before and 7 days after the last bleaching session. Results were obtained from two-way ANOVA for repeated measures and Bonferroni post-test at a significance level of 5%. ResultsHP6_L showed higher pH and greater stability between the initial and final evaluations, while the other groups showed similar pH with reduced values in the intragroup evaluation. No differences between groups in microhardness and roughness evaluations were observed. ConclusionsAlthough HP6_L showed higher alkalinity and pH stability, none of the protocols reduced the microhardness and surface roughness of bovine enamel.

Hydrogen Peroxide Stress Induced in the Marine Cyanobacterium Synechococcus aeruginosus and Phormidium valdarianum.

Biochemical markers against hydrogen peroxide-induced oxidative stress were developed in marine cyanobacteria under standard laboratory conditions. To find out the ability to cope with different concentrations of hydrogen peroxide, two species of marine cyanobacteria including unicellular and filamentous forms were exposed for shorter duration. Synechococcus aeruginosus and Phormidium valderianum tolerated hydrogen peroxide by showing the highest growth of Superoxide dismutase in Synechococcus aeruginosus and Phormidium valderianum, catalase in Synechococcus aeruginosus, peroxidase in Synechococcus aeruginosus and Phormidium valderianum, Glutathione S-transferase in Synechococcus aeruginosus and Phormidium valderianum which were identified as biochemical markers of oxidative stress against H2O2 in marine cyanobacteria. Synechococcus aeruginosus showed new isoforms for Superoxide dismutase, catalase, peroxidase, Glutathione peroxidase, and Glutathione S-transferase and Phormidium valderianum for Superoxide dismutase, peroxidase, and Glutathione S-transferase. Synechococcus aeruginosus is suggested as the indicator species for biochemical markers against hydrogen peroxide in marine cyanobacteria. Peroxidase is suggested as biochemical enzyme marker. The present investigated on these new isoenzymes were identified as biochemical markers for oxidative stress.

Study of catalase reversibility during multiple injections of H2O2 using online measurement by FFT continuous cyclic voltammetry

This work presents a new method for the determination of catalase activation reversibility upon injection of different concentrations of hydrogen peroxide (H2O2) based on fast Fourier transformation continuous cyclic voltammetry (FFTCCV). The spectroscopic and cyclic voltammetric data demonstrated that catalase could rapidly decompose H2O2 at concentrations below 40 mM. Also, the catalase activity gradually decreased at higher concentrations of H2O2. In addition, the calculated kinetics model of suicide inhibition demonstrated that the catalase irreversibility was triggered at the concentration of 80 mM. FFTCCV data by multiple injections of H2O2 revealed that the catalase activity could be recovered at 10, 20, 40, and 60 mM after 6, 4, 3, and 2 injections of H2O2, respectively. H2O2 at concentrations above 40 mM was not fully decomposed and remained in the solution after the catalase reaction. The maximum reversibility of the catalase activity was observed for the concentration of 10 mM, when H2O2 concentration drastically decreased within a few seconds of the reaction. Our data shows that the FFTCCV method can be recruited to monitor and evaluate enzymatic reactions.

Effect the Different Concentrations of Hydrogen Peroxide and Addition Soil Amendments on Growth and Nutrient Balance in Ranunculus Asiaticus L. Grown under Salinity Conditions

An experiment was conducted in a greenhouse at research station (A) / College of Agricultural Engineering Sciences / University of Baghdad to study the impact of exogenous application of hydrogen peroxide and soil amendments (zeolite and Disper osmotic regulator) in the physiological traits of the Ranunculus asiaticus L. grown in saline soils. The experiment included three factors, soil (S) at two kinds (2.17, 5.8 dsm), soil amendments at includes 3 levels of zeolite (0,4,8 gm kg-1 soil), and two levels Disper Osmotic (1,2 gm l-1), hydrogen peroxide application (0,5,10 mmol l-1). results showed saline soils caused a significant decrease in vegetative and flowering growth, and the leaf content of N, P, K. While a significant increase in the leaf content of Na was observed, is an indicator of oxidative stress. The addition of soil amendments (M3) (1 gm l) to plants grown under salinity stress caused a significant increase in the leaf content of N, P, K and plant height, leaf area and all flowering growth characteristics. Exogenous application of hydrogen peroxide at a concentration (5 mmol l-1) had a significant effect on most of the vegetative and flowering growth characteristics.

Swimming behaviour as an alternative endpoint to assess differences in abiotic stress sensitivities between strains of Brachionus koreanus (Rotifera: Monogononta)

Brachionus plicatilis is a cosmopolitan rotifer used as a model organism in several research areas and as live food in aquaculture. Being a species complex, responses to stressors vary even among strains of the same species and, thus, the responses of one species are not representative of the whole complex. This study aimed to address the effects of extreme salinity ranges, and different concentrations of hydrogen peroxide, copper, cadmium, and chloramphenicol, in two strains of B. koreanus (MRS10 and IBA3) from B. plicatilis species complex, by assessing effects on their survival and swimming capacity. Neonates (0–4 h old) were exposed to the stressors in 48 well-microplates, for 24 and 6 h, to evaluate lethal and behavioural effects, respectively. Tested conditions of chloramphenicol did not show any effects on rotifers. The behavioural endpoint showed to be particularly sensitive to assess the effects of high salinity, hydrogen peroxide, and copper sulfate, as swimming capacity impairment was observed for both strains in the lowest concentrations used in lethal tests. Overall, results showed that IBA3 was more tolerant to the majority of stressors, comparing to MRS10, which may be due to differences in physiological characteristics, highlighting the importance of performing multiclonal experiments. Also, swimming capacity inhibition proved to be a good alternative to the classical lethality tests, being sensitive to lower concentrations and with shorter exposure periods.

Regeneration of granular activated carbon clogged in the treatment of leachates.

Landfill leachates are highly contaminated liquids and complex to treat. Two of the processes which are promising for the treatment are the advanced oxidation and adsorption methods. With the combination of the Fenton and adsorption methods, practically all the organic load of leachates can be removed; however, this combination of processes is limited due to the soon clogging of adsorbent material, which leads to high operation costs. In the present work, the results of the regeneration of clogged activated carbon are shown after the application of the Fenton/adsorption process in leachates. This research consisted of four stages: sampling and leachate characterization, clogging of the carbon through the Fenton/adsorption process, carbon regeneration through the oxidative Fenton process, and lastly, evaluation of regenerated carbon adsorption through jar and column tests. In the experiments, HCl 3M was used, and different concentration of hydrogen peroxide (0.15M, 0.2M, 0.25M) were tested at different times (16h and 30h). The activated carbon regeneration through the Fenton process and the optimal peroxide dosage was 0.15M for 16h. The regeneration efficiency was obtained from comparing the adsorption efficiency between regenerated and virgin carbon, reaching 98.27% and can be applied up to 4 times without losing regeneration efficiency. These results prove that it is possible to restore the clogged activated carbon adsorption capacity during the Fenton/adsorption process.

The mechanism of oxidative stress in keloid fibroblasts and the experimental study of early application of angiotensin-converting enzyme inhibitor.

Objective To investigate the protective effects of an angiotensin-converting enzyme inhibitor after inducing oxidative stress on keloid fibroblasts. Methods Primary keloid fibroblasts were isolated and cultured by enzyme digestion combined with the tissue adhesion method in vitro, and the third to fifth generations of cells were selected for the experiment. For 24 hours, keloid fibroblasts were treated with different concentrations of hydrogen peroxide. Different concentrations of angiotensin-converting enzyme inhibitor were added to the keloid fibroblast culture medium, and then the cells were treated with hydrogen peroxide for 24 hours. Results With the increase of hydrogen peroxide concentration, the growth of keloid fibroblasts was inhibited and the levels of malondialdehyde, superoxide dismutase, and reactive oxygen species increased gradually, accompanied by an increase in the expression of nicotinamide adenine dinucleotide phosphate oxidase and collagen I mRNA. The expression of nicotinamide adenine dinucleotide phosphate oxidase-mRNA in keloid fibroblasts and the formation of reactive oxygen species in keloid fibroblasts were induced by different concentrations of angiotensin II, and the most significant effect was at 10-5 mmol/mL. The effects of diphenyleneiodonium chloride (NOX inhibitor), N-acetylcysteine (reactive oxygen species inhibitor) and nicotinamide adenine dinucleotide phosphate oxidase (NADPH oxidase) RNA treatment on angiotensin II-induced nicotinamide adenine dinucleotide phosphate oxidase and collagen I increased significantly. Hydrogen peroxide and angiotensin II alone or combined can induce NADPH oxidase and reactive oxygen species expression in keloid fibroblasts. When the angiotensin-converting enzyme inhibitor was added, the expression of NADPH oxidase and reactive oxygen species in keloid induced by hydrogen peroxide and angiotensin II could be inhibited. Conclusion Oxidative stress can lead to increased expression of reactive oxygen species, NADPH oxidase and collagen I in keloid fibroblasts, suggesting oxidative stress mediates the migration of human keloid fibroblasts and extracellular matrix synthesis.

Effect of Hydrogen Peroxide on the Soil Microbial Community Structure and Growth of Malus hupehensis Rehd. Seedlings under Replant Conditions.

Apple replant disease (ARD) is common in apple production, which seriously affects the growth and development of apples. In this study, hydrogen peroxide with a bactericidal effect was used to treat the replanted soil, and the effects of different concentrations of hydrogen peroxide on replanted seedlings and soil microbiology were investigated in order to seek a green, clean way to control ARD. Five treatments were set up in this study: replanted soil (CK1), replanted soil with methyl bromide fumigation (CK2), replanted soil + 1.5% hydrogen peroxide (H1), replanted soil + 3.0% hydrogen peroxide (H2), and replanted soil + 4.5% hydrogen peroxide (H3). The results showed that hydrogen peroxide treatment improved replanted seedling growth and also inactivated a certain number of Fusarium, while the Bacillus, Mortierella, and Guehomyces also became more abundant in relative terms. The best results were obtained with replanted soil + 4.5% hydrogen peroxide (H3). Consequently, hydrogen peroxide applied to the soil can effectively prevent and control ARD.