Synthesis of nickel oxides nanoparticles on glassy carbon as an electron transfer facilitator for horseradish peroxidase: Direct electron transfer and H2O2 determination

被引:31
|
作者
Mohammadi, Ali [2 ,3 ]
Moghaddam, Abdolmajid Bayandori [1 ]
Kazemzad, Mahmood [4 ]
Dinarvand, Rassoul [2 ]
Badraghi, Jalil [5 ]
机构
[1] Univ Tehran, Nanosci & Nanotechnol Res Ctr, Tehran, Iran
[2] Univ Tehran Med Sci, Fac Pharm, Med Nanotechnol Res Ctr, Tehran, Iran
[3] Univ Tehran Med Sci, Fac Pharm, Dept Drug & Food Control, Tehran, Iran
[4] Mat & Energy Res Ctr, Dept Energy, Tehran, Iran
[5] Shaheed Beheshti Univ, Res Inst Appl Sci ACECR, Tehran, Iran
来源
MATERIALS SCIENCE & ENGINEERING C-BIOMIMETIC AND SUPRAMOLECULAR SYSTEMS | 2009年 / 29卷 / 05期
关键词
Horseradish peroxidase; Atomic force microscopy; Bioelectrochemistry; Nanoparticle; Hydrogen peroxide; MODIFIED GOLD ELECTRODE; SOL-GEL FILM; DIRECT ELECTROCHEMISTRY; HYDROGEN-PEROXIDE; MYOGLOBIN; NANOCOMPOSITE; VOLTAMMETRY; BIOSENSOR; BIOELECTROCATALYSIS; ELECTROCATALYSIS;
D O I
10.1016/j.msec.2009.01.029
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In this study, horseradish peroxidase/nickel oxides nanoparticles/glassy carbon (HRP/NiO NPs/GC) electrode was prepared by first applying nickel oxides nanoparticles on glassy carbon surface and then horseradish peroxidase immobilized on the NiO NPs. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) have been used as a diagnostic tools to identify the synthesized NiO NPs. Immobilized HRP showed an electrochemical redox behavior pertained to HRP(Fe(III)-Fe(II)) by direct electron transfer between protein and nanoparticles with a formal potential (E-o') of -55.5 mV (vs. Ag/AgCl and 141.5 mV vs. NHE) in 50 mM phosphate buffer solution (PBS). The anodic charge transfer coefficient (alpha) and heterogeneous electron transfer rate constant (k(s)) were 0.42 and 0.75 s(-1), respectively. Biocatalytic activity of HRP/NiO NPs/GC electrode for reduction of hydrogen peroxide and application to hydrogen peroxide determination was exemplified. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1752 / 1758
页数:7
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