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      Simultaneous Determination of Ascorbic Acid, L-Dopa, Uric Acid, Insulin, and Acetylsalicylic Acid on Reactive Blue 19 and Multi-Wall Carbon Nanotube Modified Glassy Carbon Electrode

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          Abstract

          A trifunctional electrochemical sensor was fabricated for simultaneous determination of ascorbic acid (AA), levodopa (LD), and insulin. This was done by modifying a glassy carbon electrode (GCE) with multi-walled carbon nanotubes and reactive blue 19 (RB-MWCNT-GCE). Cyclic voltammetry was used to investigate the redox properties of this modified electrode. The electro-catalytic activity of the modified electrode was studied for the oxidation of AA, LD, and insulin. By differential pulse voltammetry (DPV), the detection limits of AA, LD, and insulin were estimated to be 0.45 µmol L -1, 0.37 µmol L-1, and 0.25 µmol L-1, respectively. In DPV measurements, the RB-MWCNT-GCE could separate the oxidation peak potentials of AA, LD, uric acid (UA), insulin, and acetylsalicylic acid (ASA) in a mixture. The practical utility of this modified electrode was demonstrated by detecting AA, LD, UA, insulin, and ASA in real samples.

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          Electrochemical Methods Fundamentals and Applications

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            Directed aggregation and fusion of lipid vesicles induced by DNA-surfactants

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              Increased oxidative stress with aging reduces chondrocyte survival: correlation with intracellular glutathione levels.

              To examine the role of oxidative stress in mediating cell death in chondrocytes isolated from the articular cartilage of young and old adult human tissue donors. Cell death induced by the oxidant SIN-1 was evaluated in the alginate bead culture system using fluorescent probes to assess membrane integrity. Generation of peroxynitrite by the decomposition of SIN-1 was confirmed by positive immunostaining of treated cells for 3-nitrotyrosine. Determinations of oxidized glutathione (GSSG) and reduced glutathione (GSH) were performed in monolayer cultures using an enzyme- recycling assay. Cells were depleted of intracellular glutathione either by the addition of DL-buthionine-(S,R)-sulfoximine or by removal of L-cystine from the culture media. The activity of cellular antioxidant enzymes was determined spectrophotometrically by the decay of substrate from the reaction mixture. More chondrocytes (>2-fold) from old donors (>/=50 years) died after exposure to 1 mM SIN-1 relative to those derived from young donors (18-49 years). Although autocrine production of insulin-like growth factor 1 (IGF-1) promotes chondrocyte survival, pretreatment with IGF-1 could not prevent the cell death induced by SIN-1 exposure. Cells isolated from old donors had a higher ratio of GSSG to GSH. Glutathione reductase is the principal enzyme involved in the regeneration of GSH from GSSG. Treatment of chondrocytes with SIN-1 to induce oxidative stress in vitro resulted in the decreased activity of glutathione reductase and thioredoxin reductase, but not catalase. Cells depleted of intracellular glutathione were more susceptible to cell death induced by SIN-1. These results provide evidence that increased oxidative stress with aging makes chondrocytes more susceptible to oxidant-mediated cell death through the dysregulation of the glutathione antioxidant system. This may represent an important contributing factor to the development of osteoarthritis in older adults.
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                Author and article information

                Contributors
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Journal
                jbchs
                Journal of the Brazilian Chemical Society
                J. Braz. Chem. Soc.
                Sociedade Brasileira de Química (São Paulo )
                1678-4790
                April 2015
                : 26
                : 4
                : 713-722
                Affiliations
                [1 ] Islamic Azad University Iran
                Article
                S0103-50532015000400713
                10.5935/0103-5053.20150031
                7f4324c2-893d-450d-8bdd-6a2a06c5bf74

                http://creativecommons.org/licenses/by/4.0/

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                SciELO Brazil

                Self URI (journal page): http://www.scielo.br/scielo.php?script=sci_serial&pid=0103-5053&lng=en
                Categories
                CHEMISTRY, MULTIDISCIPLINARY

                General chemistry
                trifunctional,ascorbic acid,L-dopa,uric acid,insulin
                General chemistry
                trifunctional, ascorbic acid, L-dopa, uric acid, insulin

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