%0 Journal Article %@holdercode {isadg {BR SPINPE} ibi 8JMKD3MGPCW/3DT298S} %@nexthigherunit 8JMKD3MGPCW/3ESR3H2 %@archivingpolicy denypublisher denyfinaldraft24 %@resumeid %@resumeid %@resumeid 8JMKD3MGP5W/3C9JHU3 %@usergroup administrator %@usergroup simone %3 Voltammetric detection.pdf %X This paper describes the electrochemical behavior of the nitrofurazone (NFZ), in predominantly aqueous medium, in the absence and presence of glutathione (reduced form) (GSH), L-Cysteine (Cys) and O-2 using a highly boron doped diamond electrode (HBDDE). In presence of [Thiol] >= 3.7 x 10(-2) mol L-1 NFZ is directly reduced to RNO-Thiol adducts in an electrochemical process involving two electrons and two protons. On the other side, 02 acts as a RNO2 center dot- scavenger and the velocity constant for the reaction, kO(2), is 60 L mol(-1) s(-1). The process is catalytic and can be used to the analytical determination of NFZ in the range of 9.9 x 10(-7) <= [NFZ] <= 1.1 x 10(-5) mol L-1 at pH 8.0, with sensitivity of 2.2 x 10(6) mu A mol(-1) cm(-2) and detection limit of 3.4 x 10(-7) mol L-1. The analytical parameters were similar to those obtained at pH 4.0 using the direct reduction of NFZ to the respective amine derivative in a process involving six electrons and six protons. The characterization of NFZ global reduction process in aqueous medium and at relative low scan rate, 100 mV s(-1), was only possible due the intrinsic superficial characteristics of the HBDDE, which stabilize the RNO2 center dot- free radical, allowing to work in a large potential window, without losing the RNO2 center dot- oxidation signal. %8 July %N 24 %T Voltammetric detection of the interactions between RNO2 circle- and electron acceptors in aqueous medium at highly boron doped diamond electrode (HBDDE) %@secondarytype PRE PI %K highly boron doped diamond electrode (HBDDE), nitrofurazone free radical, electronic acceptors, voltammetry and catalytic reaction, NITRO RADICAL-ANION, DNA BASES, DERIVATIVES, NITROIMIDAZOLE, GLUTATHIONE, REACTIVITY, REDUCTION, DRUGS. %@group %@group %@group LAS-INPE-MCT-BR %@secondarykey INPE-14427-PRE/9511 %@copyholder SID/SCD %@issn 0013-4686 %2 sid.inpe.br/mtc-m16@80/2006/11.23.11.31.58 %@affiliation Univ Sao Paulo (USP) %@affiliation Univ Estadual Vale Acarau %@affiliation Instituto Nacional de Pesquisas Espaciais (INPE) %@affiliation Univ Sao Paulo (USP) %B Electrochimica Acta %P 5080-5086 %4 sid.inpe.br/mtc-m16@80/2006/11.23.11.31 %D 2006 %V 51 %A Julião, Murilo S. S., %A I., Ferreira Elizabeth, %A Ferreira, Neidenêi Gomes, %A Serrano, S. H. P., %@dissemination WEBSCI %@area FISMAT