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Desenvolvimento e aplica??o de um sensor voltam?trico para an?lise simult?nea de dopamina, ?cido asc?rbico e ?cido ?rico empregando um eletrodo modificado com naftoquinona adsorvida sobre nanotubos de carbono

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Previous issue date: 2013-02-21 / Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior (Capes) / Funda??o de Amparo ? Pesquisa do estado de Minas Gerais (FAPEMIG) / O presente trabalho descreve o desenvolvimento de um sensor voltam?trico altamente seletivo e sens?vel para dopamina (DA), ?cido asc?rbico (AA) e ?cido ?rico (AU) utilizando um eletrodo de grafite pirol?tico de plano basal modificado com 1,4-naftoquinona adsorvida sobre nanotubos de carbono de paredes m?ltiplas (EGPPB/NTCPM/NQ). Imagens de Microscopia Eletr?nica de Varredura foram utilizadas para caracterizar os materiais. Os processos de oxida??o de DA, AA e AU foram investigados por Voltametria C?clica (VC) e Voltametria de Pulso Diferencial (VPD). O eletrodo modificado apresentou excelente atividade catal?tica para oxida??o de DA, AA e AU, fornecendo tr?s picos voltam?tricos bem definidos em aproximadamente ? 0,050, 0,145 e 0,270 V vs. Ag/AgCl, respectivamente, por VPD. Ap?s a otimiza??o dos par?metros experimentais (solu??o 0,1 mol L-1 de tamp?o fosfato pH 7,5), obteve-se as curvas anal?ticas para DA, AA e AU, cujas faixas de linearidade foram 10,0-70,0 nmol L-1, 40,0-280,0 ?mol L-1 e 2,0-14,0 ?mol L-1, respectivamente. Os limites de detec??o e sensibilidade foram, respectivamente, 0,126 nmol L-1 e 0,653 ?A/ nmol L-1 para DA, 2,136 ?mol L-1 e 0,076 ?A/ ?mol L-1 para AA e 0,018 ?mol L-1 e 9,888 ?A/ ?mol L-1 para AU. O sensor foi aplicado com sucesso em amostras de urina humana e os resultados mostraram que o mesmo n?o sofre interfer?ncia da matriz biol?gica. Estudos de adi??o e recupera??o dos analitos foram realizados para avaliar a exatid?o do m?todo e obteve-se uma porcentagem de recupera??o entre 95,14% e 101,49% para DA, 96,10% e 103,47% para AA e 97,90% e 102,32% para AU. / Disserta??o (Mestrado) ? Programa de P?s-Gradua??o em Qu?mica, Universidade Federal dos Vales do Jequitinhonha e Mucuri, 2012. / The present work describes the development of a highly selective and sensitive voltammetric sensor for dopamine (DA), ascorbic acid (AA) and uric acid (AU) using a basal plane pyrolytic graphite electrode modified with 1,4-naphthoquinone adsorbed on multi-walled carbon nanotubes (EGPPB/NTCPM/NQ). Images of Scanning Electron Microscopy were used to characterize the materials. Oxidation process of DA, AA and AU were investigated by Cyclic Voltammetry (VC) and Differential Pulse Voltammetry (VPD). The modified electrode showed an excellent catalytic activity towards the oxidations of DA, AA and AU, providing three well-defined voltammetric peaks at ? 0.050, 0.145 e 0.270 V vs. Ag/AgCl, respectively, by VPD. After optimization of experimental parameters (0.1 mol L-1 phosphate buffer solution pH 7.5), the calibration plots were obtained for DA, AA and AU, in the range from 10.0 up to 70.0 nmol L-1, 40.0 up to 280.0 ?mol L-1 and 2.0 up to 14.0 ?mol L-1, respectively. The detection limit and sensitivity were, respectively, 0.126 nmol L-1 and 0.653 ?A/ nmol L-1 for DA, 2.136 ?mol L-1 and 0.076 ?A/ ?mol L-1 for AA and 0.018 ?mol L-1 and 9.888 ?A/ ?mol L-1 for AU. The sensor developed has been successfully applied in human urine samples and the results showed that the matrix biological does not affect the response of the sensor. Studies of addition and recovery for DA, AA and AU were carried out to evaluate the error of the method and was verified a recovery percentage between 95.14% and 101.49% for DA, 96.10% and 103.47% for AA and 97.90% and 102.32% for AU.

Identiferoai:union.ndltd.org:IBICT/oai:acervo.ufvjm.edu.br/jspui:1/546
Date January 2012
CreatorsOliveira, Ananda Xavier
ContributorsDamos, Fl?vio Santos, Malagutti, Andr?a Renata, Te?filo, Reinaldo Francisco, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), Luz, Rita de C?ssia Silva
Source SetsIBICT Brazilian ETDs
LanguagePortuguese
Detected LanguageEnglish
Typeinfo:eu-repo/semantics/publishedVersion, info:eu-repo/semantics/masterThesis
Sourcereponame:Repositório Institucional da UFVJM, instname:Universidade Federal dos Vales do Jequitinhonha e Mucuri, instacron:UFVJM
Rightsinfo:eu-repo/semantics/openAccess

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