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dc.contributor.author장동표-
dc.date.accessioned2018-03-15T12:24:11Z-
dc.date.available2018-03-15T12:24:11Z-
dc.date.issued2014-01-
dc.identifier.citationJournal of Electroanalytical Chemistry, Vol. 717?718, 15 March 2014, Pages 157-164en_US
dc.identifier.issn1572-6657-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S1572665714000277-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/47466-
dc.description.abstractThe oxidation of dopamine (DA) around +0.6 V potential in anodic sweep and its reduction around -0.1 V in cathodic sweep at a relatively fast scanning rate (300 V/s or greater) have been used for identification of DA oxidation in fast-scan cyclic voltammetry (FSCV). However, compared to the oxidation peak of DA, the reduction peak has not been fully examined in analytical studies, although it has been used as one of the representative features to identify DA. In this study, the reduction process of DA was investigated using paired pulse voltammetry (PPV), which consists of two identical triangle-shaped waveforms, separated by a short interval at the holding potential. Especially, the discrepancies between the magnitude of the oxidation and reduction peaks of DA were investigated based on three factors: (I) the instant desorption of the DA oxidation product (dopamine-o-quinone: DOQ) after production, (2) the effect of the holding potential on the reduction process, and (3) the rate-limited reduction process of DA. For the first test, the triangle waveform FSCV experiment was performed on DA with various scan-rates (from 400 to 1000 V/s) and durations of switching potentials of the triangle waveform (from 0.0 to 6.0 ms) in order to vary the duration between the applied oxidation potential at +0.6 V and the reduction potential at -0.2 V. As a result, the ratio of reduction over oxidation peak current response decreased as the duration became longer. To evaluate the effect of holding potentials during the reduction process, FSCV experiments were conducted with holding potential from 0.0 V to -0.8 V. We found that more negative holding potentials lead to larger amount of reduction process. For evaluation of the rate-limited reduction process of DA, PPV with a 1 Hz repetition rate and various delays (2, 8, 20, 40 and 80 ms) between the paired scans were utilized to determine how much reduction process occurred during the holding potential (-0.4 V). These tests showed that relatively large amounts of DOQ are reduced to DA during the holding potential. The rate-limited reduction process was also confirmed with the increase of reduction in a lower pH environment. In addition to the mechanism of the reduction process of DA, we found that the differences between the responses of primary and secondary pulses in PPV were mainly dependent on the ratelimited reduction process during the holding potential. In conclusion, the reduction process may be one of the important factors to be considered in the kinetic analysis of DA and other electroactive species in brain tissue and in the design of new types of waveform in FSCV. (C) 2014 Elsevier B.V. All rights reserved.en_US
dc.description.sponsorshipThis research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (2012R1A1A2006597) and in part by NIH (R01 Ns75013).en_US
dc.language.isoenen_US
dc.publisherELSEVIER SCIENCE SA, PO BOX 564, 1001 LAUSANNE, SWITZERLANDen_US
dc.subjectFast-scan cyclic voltammetry (FSCV)en_US
dc.subjectPaired pulse voltammetry (PPV)en_US
dc.subjectRate-limited reduction processen_US
dc.subjectKinetic analysis of DAen_US
dc.subjectRedox ratioen_US
dc.subjectCARBON-FIBER MICROELECTRODESen_US
dc.subjectSCAN CYCLIC VOLTAMMETRYen_US
dc.subjectREAL-TIME MEASUREMENTen_US
dc.subjectADSORPTIONen_US
dc.subjectBRAINen_US
dc.subjectSENSITIVITYen_US
dc.subjectADENOSINEen_US
dc.subjectSURFACEen_US
dc.subjectRATSen_US
dc.titleInvestigation of the reduction process of dopamine using paired pulse voltammetryen_US
dc.typeArticleen_US
dc.relation.volume717-
dc.identifier.doi10.1016/j.jelechem.2014.01.020-
dc.relation.page157-164-
dc.relation.journalJOURNAL OF ELECTROANALYTICAL CHEMISTRY-
dc.contributor.googleauthorKim, Do Hyoung-
dc.contributor.googleauthorOh, Yoonbae-
dc.contributor.googleauthorShin, Hojin-
dc.contributor.googleauthorBlaha, Charles D.-
dc.contributor.googleauthorBennet, Kevin E.-
dc.contributor.googleauthorLee, Kendall H.-
dc.contributor.googleauthorKim, In Young-
dc.contributor.googleauthorJang, Dong Pyo-
dc.relation.code2014033027-
dc.sector.campusS-
dc.sector.daehakGRADUATE SCHOOL OF BIOMEDICAL SCIENCE AND ENGINEERING[S]-
dc.identifier.piddongpjang-
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