共 37 条
In situ electrodepo sited nanoparticles for facilitating electron transfer across self-assembled monolayers in biosensor design
被引:25
作者:
Du, Dan
[1
]
Ding, Jiawang
[1
]
Cai, Jie
[2
]
Zhang, Jianming
[1
]
Liu, Li
[1
]
机构:
[1] Cent China Normal Univ, Coll Chem, Key Lab Pesticide & Chem Biol, Minist Educ, Wuhan 430079, Peoples R China
[2] Wuhan Iron & Steel Co, Ctr Technol, Wuhan 430080, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
electrodeposition;
gold nanoparticles;
self-assembled monolayers;
organophosphate pesticides;
biosensor;
GLASSY-CARBON ELECTRODES;
GOLD NANOPARTICLES;
REDUCTIVE DESORPTION;
SURFACE;
ELECTROCHEMISTRY;
FILMS;
ACETYLCHOLINESTERASE;
IMMOBILIZATION;
INSECTICIDE;
COMPOSITE;
D O I:
10.1016/j.talanta.2007.09.003
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Gold nanoparticles (AuNPs) were synthesized in situ and electrodeposited onto An substrate. The AuNPs modified interface facilitates electron transfer across self-assembled monolayers (SAMs) of 11-mercaptoundecanoic acid (MUA). After activation of surface carboxyl groups with 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide and N-hydroxysuccinimide, the interface displayed good stability for immobilization of biomolecules. These modification processes were characterized by contact angle measurement, cyclic voltammetry and electrochemical impedance spectra. The immobilized acetyleholinesterase (AChE), as a model, showed excellent activity to its substrate, leading to a stable AChE biosensor. Under the optimal experimental conditions, the inhibition of malathion on AChE biosensor was proportional to its concentration in two ranges, from 0.001 to 0.1 mu g mL(-1) and from 0.1 to 25 mu g mL(-1), with detection limit of 0.001 mu g mL(-1). The simple method showed good reproducibility and acceptable stability, which had potential application in biosensor design. (c) 2007 Elsevier B.V. All rights reserved.
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页码:1337 / 1343
页数:7
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