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
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.
引用
收藏
页码:1337 / 1343
页数:7
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