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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Catalytic spectrofluorimetric determination of superoxide anion radical and superoxide dismutase activity using N,N-dimethylaniline as the substrate for horseradish peroxidase (HRP)
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Catalytic spectrofluorimetric determination of superoxide anion radical and superoxide dismutase activity using N,N-dimethylaniline as the substrate for horseradish peroxidase (HRP)

机译:N,N-二甲基苯胺作为辣根过氧化物酶(HRP)的底物催化荧光光谱法测定超氧化物阴离子自由基和超氧化物歧化酶活性

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摘要

The coupled reaction of N,N-dimethylaniline (DMA) with 4-aminoantipyrine (4-AAP) using superoxide anion radical (02) as oxidizing agent under the catalysis of horseradish peroxidase (HRP) was studied. Based on the reaction, O-2(-) produced by irradiating Vitamin B-2, (V-B2) was spectrophotometricly determined at 554 nm. The linear range of this method was 1.8 X 10(-6) - 1.2 x 10(-4) mol l(-1) with a detection limit of 5.3 x 10(-7) mol l(-1). The effect of interferences on the determination of O-2(-) was investigated. The proposed method was successfully applied to the determination of superoxide dismutase (SOD) activity in human blood and mouse blood. (C) 2002 Elsevier Science B.V. All rights reserved. [References: 10]
机译:以辣根过氧化物酶(HRP)为催化剂,研究了N,N-二甲基苯胺(DMA)与4-氨基安替比林(4-AAP)在超氧阴离子自由基(02)的作用下的偶联反应。基于该反应,通过分光光度法在554nm下测定了通过照射维生素B-2(V-B2)而产生的O-2(-)。该方法的线性范围为1.8 X 10(-6)-1.2 x 10(-4)mol l(-1),检测极限为5.3 x 10(-7)mol l(-1)。研究了干扰对O-2(-)测定的影响。该方法成功地用于测定人血和小鼠血液中的超氧化物歧化酶(SOD)活性。 (C)2002 Elsevier Science B.V.保留所有权利。 [参考:10]

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