2000
DOI: 10.1016/s0013-4686(99)00388-6
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First electrochemical investigation of the redox properties of DOPA–melanins by means of a carbon paste electrode

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Cited by 44 publications
(35 citation statements)
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“…An electrochemical investigation of redox properties of an enzymically prepared eumelanin was reported by Serpentini et al (2000). A two-electron oxidation process was observed with the corresponding potentials being +460 and +525 mV versus SCE.…”
Section: Electron Exchange Propertiesmentioning
confidence: 99%
“…An electrochemical investigation of redox properties of an enzymically prepared eumelanin was reported by Serpentini et al (2000). A two-electron oxidation process was observed with the corresponding potentials being +460 and +525 mV versus SCE.…”
Section: Electron Exchange Propertiesmentioning
confidence: 99%
“…Figure 1 shows a first redox pair in +217 and +386 mV and one shoulder in +628 mV and one reduction signal in -69 mV versus Ag/AgCl. This difference between oxidation and reduction peaks (386 -217 mV) of 169 mV suggests that redox system is irreversible 12 . Some authors 8 described that anodic peaks presented on the cyclic voltammogram cannot be assigned totally to L-dopa oxidation.…”
Section: Resultsmentioning
confidence: 97%
“…Many studies have been done about the melanins polymerization mechanism to understand its biosynthesis 9 . Some chromatographic, electrochemical and spectro-electrochemical studies [10][11][12] , besides capillary electrophoresis 13 and photoelectron spectroscopy (XPS) studies 14 have been employed to determine the melanin formation mechanism. The L-dopa (3, 4-dihydroxiphenilalanine) was used as a model compound because its structure is similar to monomers found into natural melanin structure 15 allowing the biomimetic studies about it 8,16 .…”
Section: Introductionmentioning
confidence: 99%
“…In this work we utilized the carbon paste (CP) electrode, which was previously used for studying melanin electrochemistry [6,15]. Dry melanin ghosts were crushed lightly to a powder with a clean glass rod and mixed by weight with CP (Bioanalytical Systems, BAS, West Lafayette, IN) at melanin /CP ratios of 10:90, 20:80 and 30:70.…”
Section: Electrodesmentioning
confidence: 99%
“…Dry melanin ghosts were crushed lightly to a powder with a clean glass rod and mixed by weight with CP (Bioanalytical Systems, BAS, West Lafayette, IN) at melanin /CP ratios of 10:90, 20:80 and 30:70. The melanin/CP mixtures were packed into electrode housings (BAS) as previously described [6,15]. The packed electrodes were stored in sterile, pH 7, 50 mM/L, phosphate buffered saline (PBS) at 25°C for at least one week to allow the melanin to hydrate.…”
Section: Electrodesmentioning
confidence: 99%