Amperometric biosensor for ascorbic acid

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Autor principal: I. N. Tomita
Formato: Artículo científico
Lenguaje:en
Publicado: Universidade Estadual Paulista Júlio de Mesquita Filho 2005
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author I. N. Tomita
author_facet I. N. Tomita
contents Amperometric biosensor for ascorbic acid I. N. Tomita A. Manzoli F. L. Fertonani H. Yamanaka Química biosensor ascorbic acid flow injection analysis A L-ascorbic acid biosensor based on ascorbate oxidase has been developed. The enzyme wasextracted from the mesocarp of cucumber (Cucumis sativus) by using 0.05 mol L-1 phosphate buffer, pH5.8 containing 0.5 mol L-1 NaCl. After the dialysis versus phosphate buffer0.05 mol L-1 pH 5.8, the enzyme was immobilized onto nylon net through glutaraldehyde covalentbond. The membrane was coupled to an O2 electrode and the yielding reaction monitored by oxygendepletion at -600 mV using flow injection analysis optimized to 0.1 mol L-1 phosphate buffer pH 5.8, as thecarrier solution and flow-rate of 0.5 mL min-1. The ascorbic acid calibration curve was linear from 1.2x10-4 to1.0x10-3 mol L-1. The evaluation of biosensor lifetime leads to 500 injections. Commercial pharmaceuticalsamples were analyzed with the proposed method and the results were compared with those obtained byhigh-performance liquid chromatography (HPLC). 2005 artículo científico 0100-4670 https://www.redalyc.org/articulo.oa?id=42930205 en http://www.redalyc.org/revista.oa?id=429 Eclética Química application/pdf Universidade Estadual Paulista Júlio de Mesquita Filho Eclética Química (Brasil) Num.2 Vol.30
format Artículo científico
id redalyc_42930205
institution Redalyc
language en
publishDate 2005
publisher Universidade Estadual Paulista Júlio de Mesquita Filho
spellingShingle Amperometric biosensor for ascorbic acid
I. N. Tomita
Química
biosensor
ascorbic acid
flow injection analysis
Amperometric biosensor for ascorbic acid I. N. Tomita A. Manzoli F. L. Fertonani H. Yamanaka Química biosensor ascorbic acid flow injection analysis A L-ascorbic acid biosensor based on ascorbate oxidase has been developed. The enzyme wasextracted from the mesocarp of cucumber (Cucumis sativus) by using 0.05 mol L-1 phosphate buffer, pH5.8 containing 0.5 mol L-1 NaCl. After the dialysis versus phosphate buffer0.05 mol L-1 pH 5.8, the enzyme was immobilized onto nylon net through glutaraldehyde covalentbond. The membrane was coupled to an O2 electrode and the yielding reaction monitored by oxygendepletion at -600 mV using flow injection analysis optimized to 0.1 mol L-1 phosphate buffer pH 5.8, as thecarrier solution and flow-rate of 0.5 mL min-1. The ascorbic acid calibration curve was linear from 1.2x10-4 to1.0x10-3 mol L-1. The evaluation of biosensor lifetime leads to 500 injections. Commercial pharmaceuticalsamples were analyzed with the proposed method and the results were compared with those obtained byhigh-performance liquid chromatography (HPLC). 2005 artículo científico 0100-4670 https://www.redalyc.org/articulo.oa?id=42930205 en http://www.redalyc.org/revista.oa?id=429 Eclética Química application/pdf Universidade Estadual Paulista Júlio de Mesquita Filho Eclética Química (Brasil) Num.2 Vol.30
title Amperometric biosensor for ascorbic acid
topic Química
biosensor
ascorbic acid
flow injection analysis
url https://www.redalyc.org/articulo.oa?id=42930205