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Facile preparation of magnetic core-shell Fe3O4@Au nanoparticle/myoglobin biofilm for direct electrochemistry
被引:91
|作者:
Qiu, Jian-Ding
[1
]
Peng, Hua-Ping
[1
]
Liang, Ru-Ping
[1
]
Xia, Xing-Hua
[2
]
机构:
[1] Nanchang Univ, Dept Chem, Nanchang 330031, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, Nanjing 210093, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Fe3O4@Au nanoparticles;
Myoglobin;
Direct electrochemistry;
Magnetic glassy carbon electrode;
Biosensor;
BY-LAYER FILMS;
DIRECT ELECTRON-TRANSFER;
TEMPERATURE IONIC LIQUIDS;
MESOPOROUS SILICA MATRIX;
DISK ENZYME ELECTRODE;
SOL-GEL DEPOSITION;
GOLD NANOPARTICLES;
HEME-PROTEINS;
BIOELECTROCATALYTIC PROCESSES;
ACTIVE FILMS;
D O I:
10.1016/j.bios.2009.10.043
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
In this work, the magnetic core-shell Fe3O4@Au nanoparticles attached to the surface of a magnetic glassy carbon electrode (MGCE) were applied to the immobilization/adsorption of myoglobin (Mb) for fabricating Mb/Fe3O4@Au biofilm. The morphology, structure, and electrochemistry of the nanocomposite were characterized by transmission electron microscope, UV-vis spectroscopy, electrochemical impedance spectroscopy, and cyclic voltammetry, respectively. The resultant Fe3O4@Au NPs not only have the magnetism of Fe3O4 NPs that make them easily manipulated by an external magnetic field, but also have the good conductivity and excellent biocompatibility of Au layer which can maintain the bioactivity and facilitate the direct electrochemistry of Mb in the biofilm. The modified electrode based on this Mb/Fe3O4@Au biofilm displayed good electrocatalytic activity to the reduction of H2O2 with a linear range from 1.28 to 283 mu M. The proposed method simplified the immobilization methodology of proteins and showed potential application for fabricating novel biosensors and bioelectronic devices. (c) 2009 Elsevier B.V. All rights reserved.
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页码:1447 / 1453
页数:7
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