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Articoli di riviste sul tema "Hydrogen peroxide"

Autore: Grafiati

Pubblicato: 4 giugno 2021

Ultima modifica: 25 luglio 2025

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1

Gaetani, GF, AM Ferraris, M. Rolfo, R. Mangerini, S. Arena, and HN Kirkman. "Predominant role of catalase in the disposal of hydrogen peroxide within human erythrocytes." Blood 87, no. 4 (1996): 1595–99. http://dx.doi.org/10.1182/blood.v87.4.1595.bloodjournal8741595.

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Purified enzymes were mixed to form a cell-free system that simulated the conditions for removal of hydrogen peroxide within human erythrocytes. Human glutathione peroxidase disposed of hydrogen peroxide (H2O2) at a rate that was only 17% of the rate at which human catalase simultaneously removed hydrogen peroxide. The relative rates observed were in agreement with the relative rates predicted from the kinetic constants of the two enzymes. These results confirm two earlier studies on intact erythrocytes, which refuted the notion that glutathione peroxidase is the primary enzyme for removal of

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2

VM, Aroutiounian. "Hydrogen Peroxide Gas Sensors." Physical Science & Biophysics Journal 5, no. 2 (2021): 1–22. http://dx.doi.org/10.23880/psbj-16000194.

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The results of studies of many types of semiconductor H 2 O 2 sensors are discussed in this review of 195 articles about hydrogen peroxide. The properties of electrochemical detectors, sensors based on organic and inorganic materials, graphene, and nano-sensors are analyzed. Optical and fluorescent sensors, detectors made of porous materials, quantum dots, fibers, and spheres are briefly discussed. The results of our studies in the YSU of hydrogen peroxide sensors made from solid solutions of carbon nanotubes with semiconducting metal oxides are also presented in the review. The fundamentals o

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3

Reva, I. V., T. T. Yamamoto, A. N. Gulkov, et al. "NEUROPROTECTIVE ROLE OF HYDROGEN PEROXIDE." International Journal of Applied and Fundamental Research (Международный журнал прикладных и фундаментальных исследований) 2, no. 12 2018 (2018): 346–52. http://dx.doi.org/10.17513/mjpfi.12537.

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4

Ajima, A., SG Cao, K. Takahashi, A. Matsushima, Y. Saito, and Y. Inada. "An attempt to determine lipid peroxides with polyethylene glycol‐modified hemin." Biotechnology and Applied Biochemistry 9, no. 1 (1987): 53–57. http://dx.doi.org/10.1111/j.1470-8744.1987.tb00462.x.

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Hemin, having two carboxyl groups, was coupled with alpha‐(3‐aminopropyl)‐omega‐methoxypoly(oxyethylene) through the acid‐amide bond formed with carbodiimide. The modified hemin catalyzed the peroxidase reaction in 1,1,1‐trichloroethane using benzoyl peroxide or peroxides in unsaturated fatty acids as the hydrogen acceptor and leuco crystal violet as the hydrogen donor. A basic study on quantitative microanalysis of the lipid peroxides was attempted.

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5

Calabria, Donato, Andrea Pace, Elisa Lazzarini, et al. "Smartphone-Based Chemiluminescence Glucose Biosensor Employing a Peroxidase-Mimicking, Guanosine-Based Self-Assembled Hydrogel." Biosensors 13, no. 6 (2023): 650. http://dx.doi.org/10.3390/bios13060650.

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Chemiluminescence is widely used for hydrogen peroxide detection, mainly exploiting the highly sensitive peroxidase-luminol-H2O2 system. Hydrogen peroxide plays an important role in several physiological and pathological processes and is produced by oxidases, thus providing a straightforward way to quantify these enzymes and their substrates. Recently, biomolecular self-assembled materials obtained by guanosine and its derivatives and displaying peroxidase enzyme-like catalytic activity have received great interest for hydrogen peroxide biosensing. These soft materials are highly biocompatible

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6

C., I. ANUNUSO. "Spectroscopic Evidence for the Generation of Singlet Oxygen Dimers." Journal of Indian Chemical Society Vol. 67, Nov 1990 (1990): 883–86. https://doi.org/10.5281/zenodo.6245055.

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Department of Chemistry, School of Science. Federal University of Technology, P, N. B. 1526. Owerri, Nigeria <em>Manuscript received 13 December 1987, revised 29 June 1990, accepted 22 August 1990</em> Singlet oxygen dimers 2[<sup>1</sup> \(\bigtriangleup\)] and 2[<sup>1</sup> \(\sum\)] have been observed at 350, 630 and 725 nm on decomposition of organic peroxides. The intensity of emission decreases in the order, 2-methyl butanoyl peroxide > phenyl acetyl peroxide > hexanoyl peroxide, reflecting the structural features required for the decomposition of <em>p</em>- and sec-alkyl-pe

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7

Niimura, Youichi, Yoshitaka Nishiyama, Daisuke Saito, et al. "A Hydrogen Peroxide-Forming NADH Oxidase That Functions as an Alkyl Hydroperoxide Reductase in Amphibacillus xylanus." Journal of Bacteriology 182, no. 18 (2000): 5046–51. http://dx.doi.org/10.1128/jb.182.18.5046-5051.2000.

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ABSTRACT The Amphibacillus xylanus NADH oxidase, which catalyzes the reduction of oxygen to hydrogen peroxide with β-NADH, can also reduce hydrogen peroxide to water in the presence of free flavin adenine dinucleotide (FAD) or the small disulfide-containingSalmonella enterica AhpC protein. The enzyme has two disulfide bonds, Cys128-Cys131 and Cys337-Cys340, which can act as redox centers in addition to the enzyme-bound FAD (K. Ohnishi, Y. Niimura, M. Hidaka, H. Masaki, H. Suzuki, T. Uozumi, and T. Nishino, J. Biol. Chem. 270:5812–5817, 1995). The NADH-FAD reductase activity was directly depend

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8

Féliz-Matos, Leandro, Ninoska Abreu-Placeres, Luis Miguel Hernandez, Carlos Ruiz-Matuk, and Patricia Grau-Grullón. "Evaluation of In-office Vital Tooth Whitening Combined with Different Concentrations of At-home Peroxides: A Randomized Double-blind Clinical Trial." Open Dentistry Journal 13, no. 1 (2019): 377–82. http://dx.doi.org/10.2174/1874210601913010377.

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Background: The clinical evidence relate the effect of associating the in-office and at home vital tooth whitening, describing positive effects on tooth color change and reduction of dental sensitivity. Objective: The purpose of this randomized double-blind clinical trial was to evaluate the effect on the shortened application of in-office vital tooth whitening combined with different concentrations of at-home peroxides in the final tooth color change and dental sensitivity. Methods: Randomized double-blind clinical trial with 120 participants between 18-65 years, allocated in four tooth white

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9

Meizler, A., F. A. Roddick, and N. A. Porter. "Continuous enzymatic treatment of 4-bromophenol initiated by UV irradiation." Water Science and Technology 62, no. 9 (2010): 2016–20. http://dx.doi.org/10.2166/wst.2010.550.

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Horseradish peroxidase (HRP) can be used for the treatment of halogenated phenolic substances. In the presence of hydrogen peroxide phenols are oxidized to form polymers which undergo partial dehalogenation. However, when immobilized, the peroxidase is subject to inactivation due to blockage of the active sites by the growing polymers and to deactivation by elevated levels of hydrogen peroxide. When HRP immobilized on a novel glass-based support incorporating titanium dioxide is subjected to UV irradiation, hydrogen peroxide is produced and the nascent polymer is removed. In this work a reacto

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10

Cooper, William J., and Richard G. Zepp. "Hydrogen Peroxide Decay in Waters with Suspended Soils: Evidence for Biologically Mediated Processes." Canadian Journal of Fisheries and Aquatic Sciences 47, no. 5 (1990): 888–93. http://dx.doi.org/10.1139/f90-102.

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Hydrogen peroxide decay studies have been conducted in suspensions of several well-characterized soils and in natural water samples. Kinetic and product studies indicated that the decay was biologically-mediated, and could be described by pseudo first-order rate expressions. At an initial H2O2 concentration of 0.5 μM, the hydrogen peroxide half-life varied from 1 to 8 h. The decay was inhibited by thermal and chemical sterilization of the soils. Peroxidase activity was inferred in several natural water samples, where the suspended particles catalyzed the oxidation of p-anisidine by hydrogen pe

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11

Gutowicz, Marzena. "Antioxidant and detoxycative mechanisms in central nervous system." Postępy Higieny i Medycyny Doświadczalnej 74 (February 19, 2020): 1–11. http://dx.doi.org/10.5604/01.3001.0013.8548.

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Since the brain contains a large amount of polyunsaturated fatty acids, consumes up to 20% of oxygen used by the whole body and exhibits low antioxidants activity, it seems to be especially vulnerable to oxidative stress. The most important antioxidant enzymes are superoxide dismutase (SOD), which catalyze the dismutation of superoxide anion to hydrogen peroxide, catalase (CAT), which converts toxic hydrogen peroxide to water and oxygen, and glutathione peroxidase (Se-GSHPx), which reduces hydrogen peroxide and organic peroxides with glutathione as the cofactor. Among other detoxifying enzymes

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12

Mikashinowich, Z. I., and Ye V. Olempieva. "State of antioxidant blood system at physiological pregnancy and pregnancy complicated with bleeding." Bulletin of Siberian Medicine 7, no. 2 (2008): 101–5. http://dx.doi.org/10.20538/1682-0363-2008-2-101-105.

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The task of our investigation was the analysis of enzyme activity of antioxidant defense in women blood at physiological pregnancy and pregnancy complicated with hypertension. It was established that hyper production of hydrogen peroxide and glutathione peroxidase activation at physiological pregnancy improved microcirculation due to vasodilatation effect of hydrogen peroxide. It was established that activation of superoxiddysmutase and myeloperoxidase at pregnancy complicated with hypertension developed endothelial dysfunction owing to citotoxic effects of hydrogen peroxide.

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13

Moy, Terence I., Eleftherios Mylonakis, Stephen B. Calderwood, and Frederick M. Ausubel. "Cytotoxicity of Hydrogen Peroxide Produced by Enterococcus faecium." Infection and Immunity 72, no. 8 (2004): 4512–20. http://dx.doi.org/10.1128/iai.72.8.4512-4520.2004.

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ABSTRACT Although the opportunistic bacterial pathogen Enterococcus faecium is a leading source of nosocomial infections, it appears to lack many of the overt virulence factors produced by other bacterial pathogens, and the underlying mechanism of pathogenesis is not clear. Using E. faecium-mediated killing of the nematode worm Caenorhabditis elegans as an indicator of toxicity, we determined that E. faecium produces hydrogen peroxide at levels that cause cellular damage. We identified E. faecium transposon insertion mutants with altered C. elegans killing activity, and these mutants were alte

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14

Jacob, Peter, Bernhard Wehling, Wieland Hill, and Dieter Klockow. "Feasibility Study of Raman Spectroscopy as a Tool to Investigate the Liquid-Phase Chemistry of Aliphatic Organic Peroxides." Applied Spectroscopy 51, no. 1 (1997): 74–80. http://dx.doi.org/10.1366/0003702971938795.

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The described investigations are focused on peroxides occurring as products in atmospheric chemical processes, namely, hydrogen peroxide, methylhydroperoxide, hydroxymethylhydroperoxide, bis-(hydroxymethyl)peroxide, 1-hydroxyethylhydroperoxide, bis-(hydroxyethyl)peroxide, and hydroxymethylmethylperoxide. The compounds are identified and determined through the position and intensity of their characteristic O–O stretching bands in the range between 767 and 878 cm−1. Time-resolved Raman spectroscopy of peroxide solutions permits the in situ investigation of pathways and kinetics of reactions betw

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15

&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1377 (2011): 21. http://dx.doi.org/10.2165/00128415-201113770-00068.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1380 (2011): 22–23. http://dx.doi.org/10.2165/00128415-201113800-00079.

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17

&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1385 (2012): 22. http://dx.doi.org/10.2165/00128415-201213850-00076.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1393 (2012): 23. http://dx.doi.org/10.2165/00128415-201213930-00078.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1180 (2007): 19. http://dx.doi.org/10.2165/00128415-200711800-00053.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1183 (2008): 17. http://dx.doi.org/10.2165/00128415-200811830-00053.

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21

&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1189 (2008): 20–21. http://dx.doi.org/10.2165/00128415-200811890-00061.

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22

&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1134 (2007): 15–16. http://dx.doi.org/10.2165/00128415-200711340-00052.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1140 (2007): 12. http://dx.doi.org/10.2165/00128415-200711400-00041.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1365 (2011): 24. http://dx.doi.org/10.2165/00128415-201113650-00086.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1368 (2011): 21. http://dx.doi.org/10.2165/00128415-201113680-00074.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1369 (2011): 23. http://dx.doi.org/10.2165/00128415-201113690-00082.

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27

&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 474 (1993): 6. http://dx.doi.org/10.2165/00128415-199304740-00027.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 647 (1997): 9. http://dx.doi.org/10.2165/00128415-199706470-00024.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1407 (2012): 26. http://dx.doi.org/10.2165/00128415-201214070-00091.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1407 (2012): 27. http://dx.doi.org/10.2165/00128415-201214070-00096.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1093 (2006): 18. http://dx.doi.org/10.2165/00128415-200610930-00061.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1118 (2006): 12–13. http://dx.doi.org/10.2165/00128415-200611180-00036.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1280 (2009): 26. http://dx.doi.org/10.2165/00128415-200912800-00085.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1228 (2008): 21. http://dx.doi.org/10.2165/00128415-200812280-00057.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1325 (2010): 18–19. http://dx.doi.org/10.2165/00128415-201013250-00061.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1304 (2010): 20. http://dx.doi.org/10.2165/00128415-201013040-00065.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1307 (2010): 27. http://dx.doi.org/10.2165/00128415-201013070-00085.

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38

&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1016 (2004): 10. http://dx.doi.org/10.2165/00128415-200410160-00033.

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39

&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1041 (2005): 12–13. http://dx.doi.org/10.2165/00128415-200510410-00034.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1339 (2011): 23. http://dx.doi.org/10.2165/00128415-201113390-00068.

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&NA;. "Hydrogen peroxide." Reactions Weekly &NA;, no. 1351 (2011): 24. http://dx.doi.org/10.2165/00128415-201113510-00080.

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42

Cina, Stephen J., James C. U. Downs, and Sandra E. Conradi. "Hydrogen Peroxide." American Journal of Forensic Medicine and Pathology 15, no. 1 (1994): 44–50. http://dx.doi.org/10.1097/00000433-199403000-00011.

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43

Faraci, Frank M. "Hydrogen Peroxide." Arteriosclerosis, Thrombosis, and Vascular Biology 26, no. 9 (2006): 1931–33. http://dx.doi.org/10.1161/01.atv.0000238355.56172.b3.

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44

Saitoh, Shu-ichi, Cuihua Zhang, Johnathan D. Tune, et al. "Hydrogen Peroxide." Arteriosclerosis, Thrombosis, and Vascular Biology 26, no. 12 (2006): 2614–21. http://dx.doi.org/10.1161/01.atv.0000249408.55796.da.

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45

"Peroxidase activity of hemoglobin and heme destruction in the presence of hydrogen peroxide and CT-DNA." Glasnik hemicara i tehnologa Bosne i Hercegovine, no. 55 (December 29, 2020). http://dx.doi.org/10.35666/ghtbh.2020.55.04.

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The aim of this study was to investigate the peroxidase activity of Hb with different concentrations of hydrogen peroxide and compare it with hypochlorous acid effect on Hb. Hypochlorous acid at higher concentrations decomposed Hb and heme, releasing fee iron ion from the metal center. High concentrations of hydrogen peroxide switched the peroxidase activity of Hb towards the partial Hb and heme destruction. Heme alone was degraded showing that the Hb conformation and protein environment protects Hb from the distraction in the presence of highly increased hydrogen peroxide concentration that o

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46

Stols, E., and Jacques M. Berner. "Ozone leads to an increase of hydrogen peroxide levels and peroxidase activity in two maize varieties." Suid-Afrikaanse Tydskrif vir Natuurwetenskap en Tegnologie 31, no. 1 (2012). http://dx.doi.org/10.4102/satnt.v31i1.300.

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The goal of this study was to determine whether ozone induce hydrogen peroxide concentrations and peroxidase activity in two maize cultivars. Hydrogen peroxide levels as well as peroxidase activity was higher in both the ozone treated cultivars.

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47

Giura, A., O. Slusanschi, R. Oancea, I. C. Popa, and C. Funieru. "Dental Bleaching Techniques: Hydrogen Peroxide Application vs Laser. Which is More Efficient?" Medicine in Evolution, March 31, 2024, 58–64. http://dx.doi.org/10.70921/medev.v30i1.901.

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Teeth whitening is a clinical procedure that can be done in many ways usually using gels with carbamide or hydrogen peroxides. The main objective of this study is to compare two methods of teeth whitening: conventional (with 40% hydrogen peroxide gel) and laser method (with 45% hydrogen peroxide gel activated by diode laser). We analysed two groups of 10 patients, one for each method. The results lead to the conclusion that hydrogen peroxide activated by laser seems to be more efficient but it also brings more dental hypersensitivity at the end.

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48

"Semiconductor gas sensors detecting hydrogen peroxide." Advances in Nanoscience and Nanotechnology 5, no. 1 (2021). http://dx.doi.org/10.33140/ann.05.01.04.

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The results of studies of many types of semiconductor H2 O2 sensors are discussed in this review of 185 articles about hydrogen peroxide. The properties of electrochemical detectors, sensors based on organic and inorganic materials, graphene, and nano-sensors are analyzed. Optical and fluorescent sensors, detectors made of porous materials, quantum dots, fibers, and spheres are briefly discussed. The results of our studies in the YSU of hydrogen peroxide sensors made from solid solutions of carbon nanotubes with semiconducting metal oxides are also presented in the review. The fundamentals of

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49

Boonpoempoon, Tuchpongpuch, Wanida Wonsawat, and Takashi Kaneta. "Long-term stabilization of hydrogen peroxide by poly(vinyl alcohol) on paper-based analytical devices." Scientific Reports 9, no. 1 (2019). http://dx.doi.org/10.1038/s41598-019-49393-6.

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Abstract Stabilizing reagents that can be deposited onto paper is an important issue for researchers who depend on paper-based analytical devices (PADs), because long-term stability of the devices is essential in point-of-care testing. Here, we found that poly(vinyl alcohol) (PVA) would stabilize hydrogen peroxide placed on a paper substrate following exposure to air. Horseradish peroxidase was employed as a sample in colorimetric measurements of PADs after hydrogen peroxide and 3,3′,5,5′-tetramethylbenzidine were deposited as substrates in an enzymatic reaction. The addition of PVA to hydroge

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"Hydrogen peroxide." Reactions Weekly 1853, no. 1 (2021): 227. http://dx.doi.org/10.1007/s40278-021-95093-1.

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