Source:http://linkedlifedata.com/resource/pubmed/id/12699814
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
2003-4-17
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pubmed:abstractText |
Glassy carbon (GC) electrode is modified with an electropolymerized film of N,N-dimethylaniline (DMA). This polymer (PDMA) film-coated GC electrode is used to electrochemically detect dopamine (DA) in the presence of ascorbic acid (AA). Polymer film has the positive charge in its backbone, and in neutral solution DA exists as the positively charged species whereas AA exists as the negatively charged one. In cyclic voltammetric measurements, favorable ionic interaction (i.e., electrostatic attraction) between AA and PDMA film causes a large negative shift of the oxidation potential for AA compared to that at the bare electrode. Oxidation potential for DA is positively shifted due to the electrostatic repulsion. The PDMA film shows hydrophobicity by incorporating uncharged hydroquinone molecule within the film. DA is also incorporated into the film due to hydrophobic attraction even though DA has a positive charge. The responses of DA and AA at polymer-modified electrodes largely change with the concentration of the monomer (i.e., 0.2, 0.1 and 0.05 M DMA) used in electropolymerization and thus with the film thickness. Hydrophobicity of the polymer film shows great influence on the voltammetric responses of both DA and AA. In square wave voltammetric measurements, the PDMA film-coated electrode can separate the DA and AA oxidation potentials by about 300 mV and can detect DA at its low concentration (e.g., 0.2 microM) in the presence of 1000 times higher concentration of AA, which is close to the physiological level. AA oxidizes at more negative potential than DA. The electrode response is not affected by the oxidized product of AA. So unlike the bare electrode, the fouling effect as well as the catalytic oxidation of AA by the oxidized form of DA are eliminated at the PDMA film-coated GC electrode. The electrode exhibits the stable and sensitive response to DA.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1567-5394
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
59
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
11-9
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:12699814-Aniline Compounds,
pubmed-meshheading:12699814-Ascorbic Acid,
pubmed-meshheading:12699814-Dopamine,
pubmed-meshheading:12699814-Electrochemistry,
pubmed-meshheading:12699814-Electrodes,
pubmed-meshheading:12699814-Hydrophobic and Hydrophilic Interactions,
pubmed-meshheading:12699814-Oxidation-Reduction,
pubmed-meshheading:12699814-Polymers
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pubmed:year |
2003
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pubmed:articleTitle |
Simultaneous electroanalysis of dopamine and ascorbic acid using poly (N,N-dimethylaniline)-modified electrodes.
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pubmed:affiliation |
Department of Electronic Chemistry, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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