Increase In Peroxide Concentration Research Articles

Salicylic acid induces apoptosis in colon carcinoma cells grown in-vitro: Influence of oxygen and salicylic acid concentration

In solid tumors the hypoxic environment can promote tumor progression and resistance to therapy. Recently, acetylsalicylic acid a major component of analgesic drugs and its metabolite salicylic acid (SA) have been shown to reduce the risk of colon cancer, but the mechanisms of action remain still unclear. Here we elucidate the effects of physiologically relevant concentrations of SA on colon carcinoma cells (CaCo-2) grown under normoxic and hypoxic conditions. Western blotting, caspase-3/7 apoptosis assays, MTS cell-proliferation assays, LDH cytotoxicity assays and hydrogen peroxide measurements were performed to investigate the effects of 1 and 10μM SA on CaCo-2 cells grown under normoxic conditions and cells exposed to hypoxia. Under normoxic conditions, SA did not influence cell proliferation or LDH release of CaCo-2 cells. However, caspase-3/7 activity was significantly increased. Under hypoxia, cell proliferation was reduced and LDH release and caspase-3/7 activities were increased. None of these parameters was altered by the addition of SA under hypoxic conditions. Hypoxia increased hydrogen peroxide concentrations 300-fold and SA significantly augmented the release of hydrogen peroxide under normoxic, but not under hypoxic conditions. Phosphorylation of the pro-survival kinases akt and erk1/2 was not changed by SA under hypoxic conditions, whereas under normoxia SA reduced phosphorylation of erk1/2 after 2 hours. We conclude that in colon carcinoma cells effects of SA on apoptosis and cellular signaling are dependent on the availability of oxygen.

Gelation time, homogeneity, and rupture testing of alginate‐calcium carbonate‐hydrogen peroxide gels for use as wound dressings

The care of chronic wounds carries a heavy financial burden on the healthcare industry, with billons being spent annually on their treatment. This, coupled with a decreased quality of life for sufferers, has led to a real urgency in developing inexpensive wound dressings that promote wound healing. Alginate gels for application as wound dressings were formed by varying alginate (0%-6% w/v), calcium carbonate (0%-1% w/v), hydrogen peroxide (0%-3.75% v/v), and hyaluronic acid (0-1.25 mg/L) content. The aging effects on the physical properties of the gels over a 14-day period were also investigated. The results indicated that the concentration of calcium carbonate and hydrogen peroxide, as well as sample age, all had a significant effect on the rupture characteristics and gelation time of the gels. Increased calcium carbonate content caused an increase in rupture force and rupture energy values, whereas increased hydrogen peroxide content and sample age resulted in a decrease in rupture force and rupture energy measurements. Increased calcium carbonate and hydrogen peroxide content produced a decrease in the time required for gel formation. Statistical models were also produced to provide a means of estimating rupture characteristics and gelation times for gels containing other concentrations of these components.

In Vitro Study of the Effect of Three Hydrogen Peroxide Concentrations on the Corrosion Behavior and Surface Topography of Alumina-Reinforced Dental Ceramic

This in vitro investigation studied the effect of three hydrogen peroxide (HP) concentrations (30%, 35%, 38% v/v) at two time intervals (1 and 2 hours) on the corrosion behavior and surface topography of a dental ceramic. A total of 62 Vitadur Alpha discs were constructed following manufacturer instructions. Specimens were divided into four main groups (n = 8). Group 1 (control): specimens were immersed in 4% acetic acid for 18 hours at 80°C. Groups 2, 3, and 4: specimens were immersed in 30%, 35%, and 38% HP concentrations, respectively. Each of the three groups was divided into two subgroups (a and b) according to the immersion time (1 and 2 hours, respectively). Specimens of subgroup a were further immersed in 4% acetic acid for 18 hours at 80°C and were designated as subgroup c. The corrosion behavior of the ceramic specimens were tested by solution analysis using the atomic absorption method, weight loss percent, and corrosion rate. Surface topography was investigated by surface roughness (Ra) measurements and scanning electron microscopy (SEM). Results were statistically analyzed. There was a significant increase for ions leached with the increase in time of immersion for all ions at 35% and 38% HP, while at 30% HP, ions of K(+) , Al(3+) , and Si(4+) did not increase significantly with time. The results also showed that at a fixed time of immersion, all ions released were dependent on the increase of HP concentration except for Al(3+) ions (p < 0.05). The combined treatment of specimens with HP followed by acetic acid had a significant effect on the increase of ions leached (p < 0.05). The surface roughness values for all specimens increased significantly with time of immersion as well as with the increase in concentration of HP (p < 0.05). These results were confirmed with SEM. The amount of released ions is directly proportional to HP concentration and time of immersion. Specimens exposed to both HP and acetic acid showed increased weight loss and a higher corrosion rate than those exposed to acetic acid only. Surface roughness values were time and HP concentration dependent.

Investigation of the antibacterial and photocatalytic properties of the zeolitic nanosized AgBr/TiO2 composites

Zeolite-based Ag/AgBr and Ag/AgBr/TiO2 photocatalysts were prepared by sol–gel and deposition methods and were characterized. Their photocatalytic activities were evaluated by inactivation of Escherichia (E.) coli and the photodegradation of Acid Blue 92 and potassium permanganate. The composites containing Ag/AgBr showed the antibacterial activity in the dark by releasing Ag+ ions into the medium. The results for inactivation of E. coli indicated that Ag/AgBr/TiO2 modified photocatalyst had better antibacterial activity than Ag/AgBr/zeolite, while zeolite and TiO2/zeolite did not show any antibacterial activity under visible light and dark conditions. Photodecolarization rate was affected differently in the presence of H2O2 depending upon the illumination source. Under visible light the photodecolorization rate is decreased while with UV light it is increased initially and then decreased by increasing hydrogen peroxide concentration. A mechanism for KMnO4 photodegradation is proposed. The effects of catalyst concentration, initial dye concentration and temperature were also studied.

Pressure leaching of metals from waste printed circuit boards using sulfuric acid

Printed circuit boards (PCBs) are essential components of electronic equipments which contain various metallic values. This paper reports a hydrometallurgical recycling process for waste PCBs, which consists of the novel pretreatment consisting of organic swelling of PCBs followed by sulfuric acid leaching of metals from waste PCBs. To recycle the waste PCBs, experiments were carried out for the recovery of copper from the crushed and organic swelled materials of waste PCBs using sulfuric acid leaching in presence of hydrogen peroxide under atmospheric and pressure condition. The leaching of PCBs at 90°C, pulp density 100 g/L under atmospheric condition, using 6M sulfuric acid resulted in the dissolution of a minor amount of copper due to the presence of plastic coating on the surface of metallic layers. On the other hand, when the liberated metal sheets from organic swelled PCBs were treated with dilute sulfuric acid of concentration 2M along with hydrogen peroxide in an autoclave under oxygen atmosphere, the percentage recovery of copper was found to increase from 59.63% to 97.01% with an increase in hydrogen peroxide concentration from 5 to 15% (v/v) keeping constant pulp density 30 g/L.

Cross-linking kinetics study and high temperature mechanical properties of ethylene–octene copolymer (EOC)/dicumylperoxide(DCP) system

Ethylene–octene copolymer (EOC) was cross-linked by dicumyl peroxide (DCP) at various temperatures (150–200 °C). Six concentrations of DCP in range 0.2–0.7 wt.% were investigated. Cross-linking was studied by rubber process analyzer (RPA). From RPA data analysis real part modulus s′, tan(delta) and reaction rate constant K were investigated as a function of peroxide content and temperature. The highest s′ max and the lowest tan(delta) were found for 0.7% of DCP at 150 °C. The quantitative analysis confirmed that the DCP–EOC cross-linking was occurring as first order reaction. The highest cross-linking kinetics constant K was found for 0.6% of peroxide at 200 °C. The activation energy of cross-linking E A obtained by Arrhenius plot had maximum at 0.5–0.6% of peroxide. While at 190–200 °C temperature range there was no detectable degradation for 0.2% of peroxide, for 0.4–0.7% of peroxide there was increasing level of degradation with increasing peroxide content. Generally, at low temperatures (150–180 °C) the increasing peroxide content caused increase in cross-linking kinetics. However at higher temperatures (190–200 °C) increase in kinetics (for 0.2–0.5% of peroxide) was followed by decrease. Especially in 0.6–0.7% peroxide level range the cross-linking is in competition with degradation which lowers the overall cross-linking kinetics. Gel content of the cross-linked EOC samples was found to be increasing with increase in peroxide content, which is caused by the increased cross-link network. Cross-linked samples were subjected to creep studies at elevated temperature (150 °C) and the result was found in agreement with the gel content and RPA results. Storage modulus and tan(delta) values obtained by Dynamic Mechanical Analysis (DMA) also support the RPA results.

Melatonin protects against clomiphene citrate-induced generation of hydrogen peroxide and morphological apoptotic changes in rat eggs

The present study was aimed to determine whether clomiphene citrate-induces generation of hydrogen peroxide in ovary, if so, whether melatonin could scavenge hydrogen peroxide and protect against clomiphene citrate-induced morphological apoptotic changes in rat eggs. For this purpose, forty five sexually immature female rats were given single intramuscular injection of 10 IU pregnant mare's serum gonadotropin for 48 h followed by single injections of 10 IU human chorionic gonadotropin and clomiphene citrate (10 mg/kg bw) with or without melatonin (20 mg/kg bw) for 16 h. The histology of ovary, ovulation rate, hydrogen peroxide concentration and catalase activity in ovary and morphological changes in ovulated eggs were analyzed. Co-administration of clomiphene citrate along with human chorionic gonadotropin significantly increased hydrogen peroxide concentration and inhibited catalase activity in ovary, inhibited ovulation rate and induced egg apoptosis. Supplementation of melatonin reduced hydrogen peroxide concentration and increased catalase activity in the ovary, delayed meiotic cell cycle progression in follicular oocytes as well as in ovulated eggs since extrusion of first polar body was still in progress even after ovulation and protected against clomiphene citrate-induced egg apoptosis. These results clearly suggest that the melatonin reduces oxidative stress by scavenging hydrogen peroxide produced in the ovary after clomiphene citrate treatment, slows down meiotic cell cycle progression in eggs and protects against clomiphene citrate-induced apoptosis in rat eggs.

Characterization of stress processes ofPhaffia rhodozymastress-resistant mutant

A carotenoid-less Phaffia rhodozyma mutant (MCP 325) exhibited significantly higher resistance to oxidative stressors such as menadione, H2O2 and K2Cr2O7 than its astaxanthin-producing parental strain (MCP 324). The absence of carotenoids in the mutant did not explain this phenomenon. The cause of the decreased superoxide, hydroxyl radical and glutathione contents, the increased peroxide concentration and the elevated specific activity of catalase under uninduced conditions may be a second mutation. Peroxide treatment induced specific catalase activity in the mutant but not in the parental strain. Regulation of these processes led to the result that, in spite of the mutations, the two strains exhibited the same multiplication rate and generation time.

The depolymerization of sodium alginate by oxidative degradation

Alginate has been extensively used as a carrier for macromolecules and as gene delivery vehicle. Both properties are molecular weight (Mw) dependent. Herein, we investigated factors affecting the oxidative depolymerization of alginate. The depolymerization process occurred mainly in the first 1 h. The Mw of the depolymerized alginate was influenced by the reaction temperature. At temperature 20 and 30°C, Mw of the alginate fragment kept constant and further Mw decrease was observed at 40°C. Along with the increase of hydrogen peroxide concentration, the Mw of the fragments decreased gradually. Influence of alginate initial concentration was marginal. A linear decrease of Mw was observed when the system pH was in the range of 5–7, whereas no further change was found when the system pH decreased from 7 to 8. Fourier transformed infrared spectroscopy spectra revealed that degradation undergoes by the breakage of the glycosidic bonds of polymers. No structural change was observed during the depolymerization process by UV spectroscopy. Cloud point pH increase was found for alginate 30 k. In summary, this method is an effective and convenient approach for preparing low Mw oligosaccharides from sodium alginate and may be potentially useful for the drug delivery system design with alginate.

Kinetic Modelling of Phenol Oxidation in a Bioremediation Medium Using Fenton's Reagent

The present study is aimed at kinetic modeling of phenol oxidation using Fenton’s reagent in a medium suitable for bioremediation of organic pollutants. Batch experiments were conducted to study the effects of H2O2 concentration (29.26 to 146.31 mM), temperature (5 to 35°C), and to compare the oxidation of phenol in a bioremediation medium to that in pure water. The reaction mechanism used for kinetic modeling is based on the intermediate oxidation products identified in this study using LC-MS and ion chromatography. Progress of the chemical oxidation by Fenton’s reagent was monitored by determining the residual phenol concentration and concentrations of evolved intermediate compounds (catechol and hydroquinone) at regular time intervals. The rate of phenol oxidation and ultimate conversion of phenol were found to increase with increase in hydrogen peroxide concentration. The increase in temperatures has a positive effect on phenol oxidation and the rate of phenol oxidation was found to increase with temperature in the range of 5-35°C. Kinetic parameters, namely rate constants and activation energies for reactions involved, were determined by best-fitting the experimental data to the proposed reaction model. The values of the rate constants for oxidation of phenol and intermediate compounds, k1 (phenol to catechol), k2 (phenol to hydroquinone), k3 (catechol to maleic acid), k4 (hydroquinone to maleic acid) at 25°C were found to be 7.02x10-5±4.63x10-5, 7.22x10-4±6.09x10-4, 1.82x10-4±1.08x10-4, 1.68x10-3±1.29x10-3 L/mM min, respectively.

Mesoporous silica iron-doped as stable and efficient heterogeneous catalyst for the degradation of C.I. Acid Orange 7 using sono–photo-Fenton process

Iron-containing mesostructured silica (Fe 2O 3/SBA-15) was prepared and used as heterogeneous catalyst in the integrated sono–photo-Fenton process. The effect of hydrogen peroxide concentration, initial pH, Fe 2O 3/SBA-15 loading, ultrasonic power, and initial solution concentration on the decolorization of C.I. Acid Orange 7 (AO7) by the integrated heterogeneous sono–photo-Fenton process was investigated in order to optimize process efficiency. The results showed that the decolorization efficiency increased with the increase of hydrogen peroxide concentration, ultrasonic power, Fe 2O 3/SBA-15 loading, but decreased with the increase of initial pH and initial dye concentration. Catalyst stability was evaluated by measuring iron leaching in solution. The particles size distribution of spent catalyst evidenced a remarkable size reduction during reaction, leading to more reactive surface and higher mass transfer rate. The main reaction intermediates were separated and identified using GC–MS and a possible degradation pathway was proposed.

Effect of americium-241 on luminous bacteria. Role of peroxides

The effect of americium-241 ( 241Am), an alpha-emitting radionuclide of high specific activity, on luminous bacteria Photobacterium phosphoreum was studied. Traces of 241Am in nutrient media (0.16–6.67 kBq/L) suppressed the growth of bacteria, but enhanced luminescence intensity and quantum yield at room temperature. Lower temperature (4 °C) increased the time of bacterial luminescence and revealed a stage of bioluminescence inhibition after 150 h of bioluminescence registration start. The role of conditions of exposure the bacterial cells to the 241Am is discussed. The effect of 241Am on luminous bacteria was attributed to peroxide compounds generated in water solutions as secondary products of radioactive decay. Increase of peroxide concentration in 241Am solutions was demonstrated; and the similarity of 241Am and hydrogen peroxide effects on bacterial luminescence was revealed. The study provides a scientific basis for elaboration of bioluminescence-based assay to monitor radiotoxicity of alpha-emitting radionuclides in aquatic solutions.

Novel nanoporous silver particles for electro-reduction of hydrogen peroxide in alkaline media

Silver nanoparticles (nanoAg) were hydrothermally prepared through the reduction of the complex Ag+–EDTA by polyethylene glycol as the reduction agent and deposited on the titanium surface to form a nanoporous network texture which possesses considerable numbers of active sites. Electrocatalytic activity of the nanoAg electrode towards hydrogen peroxide reduction in 1molL−1 NaOH solution was assessed utilizing cyclic voltammetry (CV), linear scanning voltammetry (LSV), chronoamperometry (CA), and electrochemical impedance spectroscopy (EIS). At the nanoAg electrode, hydrogen peroxide reduction in 1molL−1 NaOH took place at a potential of −0.05V (vs. SCE) and presented considerable large current density of hydrogen peroxide reduction. Cyclic voltammetric responses of the nanoAg electrode showed a fast electro-reduction process of hydrogen peroxide at the initial stage of hydrogen peroxide reduction activation region. Chronoamperometric data on the nanoAg electrode presented stable reduction currents of hydrogen peroxide which exhibited a linear increment with the increasing hydrogen peroxide concentration in the range of 0–0.1molL−1. Further, EIS data were obtain at various hydrogen peroxide concentrations and showed significantly low charge transfer resistances for hydrogen peroxide reduction on the nanoAg electrode. Results reveal that the nanoAg electrode of the present investigation is a highly efficient and stable electrocatalyst for hydrogen peroxide reduction in alkaline media.

Ageing in embryos from wheat grains stored at different temperatures: oxidative stress and antioxidant response.

In the present work we studied oxidative stress as an important cause of seed deterioration during ageing in embryos from durum wheat grains stored at room temperature and at low temperature (10°C). The protective role of low temperature on seed viability was confirmed. The increase of hydrogen peroxide content during dry storage was strongly correlated with the decrease of germinability. Ascorbate and glutathione showed a good correlation with grain germinability and significantly increased upon imbibition, in particular in embryos from viable grains. Ascorbate peroxidase (APX), dehydroascorbate reductase (DHAR), glutathione reductase (GR), glutathione peroxidase (GPX) and catalase (CAT) were studied quantitatively (enzymatic assays). APX, GR, and GPX were also studied qualitatively by native PAGE. The enzymes were active in dry, still viable, embryos whereas no activity was detected in non-viable embryos. With the exception of APX, all enzymatic activities decreased upon imbibition. The study of grains stored in different conditions indicated a negative correlation between the efficiency of the antioxidant enzymatic machinery and the age of the grain. The differences detected in differently stored materials confirmed that both germination parameters and the length of storage period are important in determining grain condition.

Photocatalyzed destruction of organic dyes using microwave/UV/O 3/H 2O 2/TiO 2 oxidation system

Photocatalytic decomposition characteristics of three different single-component organic dyes and their mixture using microwave/UV/O 3/H 2O 2/TiO 2 photocatalysts hybrid process system were investigated in this study. The decomposition rates of all organic dyes were higher in single-component experiments than in mixed solution experiments. The decomposition rates of all organic dyes increased with the ozone injection rate. The decomposition rate increased with increasing hydrogen peroxide concentration until it reached a maximum point beyond which it decreased with increasing hydrogen peroxide concentration. The result demonstrates that combination of elemental techniques that have little effect when used alone can make a synergy effect.

Is the microtubule disruption-induced alteration of peroxide concentration a factor inhibiting the assembly of ribonucleoprotein stress granules?

It has been examined whether the destruction of cell microtubules affects the increase in the intracellular hydrogen peroxide concentration caused by sodium arsenite, which induces the formation of stress ribonucleoprotein granules. As expected, sodium arsenite caused a 50% increase in hydrogen peroxide concentration in HeLa cells; on the other hand, another stress granule inducer tert-buthylhydroquinone did not affect the peroxide concentration. The disruption of microtubules by nocodazole or vinblastine also resulted in some increase in the intracellular peroxide concentration,y taxol did not affect it. The combined treatment of cells with and the microtubule stabilization by taxol did not affect it. The combined treatment of cells with arsenite and antimicrotubule drugs caused an additive effect, and the peroxide concentration increased twice or more. Thus, the inhibition of stress granule formation after microtubule disruption cannot be explained by a decrease in peroxide concentration as compared with the affect of arsenite.

Morphology and oxidative physiology of sulphur-deficient mulberry plants

The aim of the study was to induce S deficiency symptoms and to relate the generation of reactive oxygen species (ROS) and altered cellular redox environment with the effects of S deficiency in mulberry ( Morus alba L.) cv. Kanva-2 plants. A study of antioxidant responses, malondialdehyde (MDA) content as an indicator of oxidative damage and ratio of dehydroascorbate (DHA) to ascorbic acid (AsA) as an index of cellular redox environment in S-deficient mulberry plants was undertaken. The S deficiency effects appeared as paling of the youngest emerging leaves. Soon, the leaves, as they expanded, became devoid of the green pigment and turned completely yellow. These leaves showed upward curling of the leaf margins and prominent wrinkles in the lamina tissues. Sulphur-deficient plants showed improved leaf water status, as indicated by increases in the degree of succulence (DS), specific water content (SWC), relative water content (RWC) and water potential ( Ψ) of leaves, contained less tissue S concentration, less chloroplastic pigments, decreased tissue Fe and Cu and had improved tissue Mn concentrations. Increased hydrogen peroxide concentration under deficiency of S did not induce oxidative damage as indicated by decreased MDA concentration. The S-deficient plants exhibited significant decreases in the concentrations of DHA and total ascorbate. The ratio DHA/AsA decreased in these plants. While the activity of catalase (EC 1.11.1.6) decreased in S-deficient plants, activities of peroxidase (EC 1.11.1.7), superoxide dismutase (EC 1.15.1.1), and ascorbate peroxidase (EC 1.11.1.11) were increased. The results suggest that deficiency of S induced oxidative stress, however, because of low tissue Fe and Cu and enhanced antioxidant enzymes activities other than catalase, provided ample protection against oxidative challenge to the S-deficient mulberry plants.

Comparison of influence of carmustine and new proline analog of nitrosourea on antioxidant system in breast carcinoma cells (MCF-7)

The high toxicity and low selectivity of carmustine restrict its application in anticancer therapy. Therefore, proline analogs of nitrosourea have been synthesized to obtain compounds whose action on neoplastic cells is characterized by higher selectivity. The present studies have aimed at examining the influence of carmustine and a new proline analog of nitrosourea on the redox system of fibroblasts and breast cancer cells (MCF-7). Carmustine and the proline analog of nitrosourea caused an increase in hydrogen peroxide concentration both in fibroblasts and MCF-7 cells. Moreover, administration of carmustine and the new analog of nitrosourea caused a decrease in the activity of antioxidant enzymes. Observed changes in the antioxidant system correlated with an increase in concentration of dityrosine, as well as a decrease in tryptophan concentration. Changes in the antioxidant system were also accompanied by intensification of the lipid peroxidation process. In conclusion, carmustine and proline analog of nitrosourea produce similar changes in the antioxidant system in normal and cancer cells and are responsible for oxidative stress.

Structural and spectroscopic ellipsometry characterization for electrodeposited ZnO growth at different hydrogen peroxide concentration

This work deals with textural and optical characterization of zinc oxide (ZnO) layers obtained by potentiostatic electroplating at various hydrogen peroxide concentrations (from 0 up to 5 mM). The electrodeposition process was studied by cyclic voltametry and chronoamperometry. The [002] preferred growth orientation of hexagonal phase is obtained for the lowest hydrogen peroxide concentration (1 mM), while additionally X-ray diffraction peaks are observed for hydrogen peroxide concentration ranging from 3 to 5 mM. The optical constants and the thickness of films were determined by spectroscopic ellipsometry measurements. The refractive index of all thin films shows normal dispersion behavior. It was also found that refractive index values decrease with increasing hydrogen peroxide concentration. Further, it was revealed that the changes in the optical properties are correlated to the changes in the surface structure .

Proline Analogue of Nitrosourea as a New Cytotoxic Prodrug

Carmustine is frequently used as anticancer drug. High toxicity and low selectivity reduces the application of this drug. Though, there is a necessity to find new compounds characterized by similar therapeutic effects but a higher selectivity and safety. As a result, the proline analogue of nitrosourea, N-[N'-(2-bromophenyl)-N'-nitrosocarbamoyl]proline (AC), has been synthesized. The aim of this study was to compare the influence of carmustine and the proline analogue of nitrosourea on the antioxidant abilities of fibroblasts and leukemia cells, MOLT4. It was shown that carmustine as well as AC cause an increase in hydrogen peroxide concentration in normal and neoplastic cells. Incubation with both compounds led to a diminution of the activity of antioxidant enzymes such as superoxide dismutase, glutathione peroxidase, and reductase. Changes in activity / level of antioxidant parameters were accompanied by augmentation of lipid and oxidative protein modifications. In conclusion, carmustine and AC cause changes in the antioxidative system of normal and MOLT4 cells and are a reason of oxidative stress formation.