Electrocatalytical oxidation and sensitive determination of acetaminophen on glassy carbon electrode modified with graphene-chitosan composite

被引:84
|
作者
Zheng, Meixia [1 ]
Gao, Feng [1 ]
Wang, Qingxiang [1 ]
Cai, Xili [1 ]
Jiang, Shulian [2 ]
Huang, Lizhang [2 ]
Gao, Fei [1 ]
机构
[1] Zhangzhou Normal Univ, Dept Chem & Environm Sci, Zhangzhou 363000, Peoples R China
[2] Zhangzhou Prod Qual Supervis & Inspect Inst, Zhangzhou 363000, Peoples R China
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2013年 / 33卷 / 03期
关键词
Graphene-chitosan composite; Acetaminophen; Electrochemistry; Determination; ELECTROCHEMICAL-BEHAVIOR; GLUCOSE-OXIDASE; NANOPARTICLES; PARACETAMOL; SENSOR; NANOTUBES; SAMPLES; FILM; DNA;
D O I
10.1016/j.msec.2012.12.055
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
The electrochemical behaviors of acetaminophen (ACOP) on a graphene-chitosan (GR-CS) nanocomposite modified glassy carbon electrode (GCE) were investigated by cyclic voltammetry (CV), chronocoulometry (CC) and differential pulse voltammetry (DPV). Electrochemical characterization showed that the GR-CS nanocomposite had excellent electrocatalytic activity and surface area effect. As compared with bare GCE, the redox signal of ACOP on GR-CS/GCE was greatly enhanced. The values of electron transfer rate constant (k(s)), diffusion coefficient (D) and the surface adsorption amount (I*) of ACOP on GR-CS/GCE were determined to be 025 s(-1), 3.61 x 10(-5) cm(2) s(-1) and 1.09 x 10(-9) mol cm(-2), respectively. Additionally, a 2e(-)/2H(+) electrochemical reaction mechanism of ACOP was deduced based on the acidity experiment. Under the optimized conditions, the ACOP could be quantified in the range from 1.0 x 10(-6) to 1.0 x 10(-4) M with a low detection limit of 3.0 x 10(-7) M based on 3S/N. The interference and recovery experiments further showed that the proposed method is acceptable for the determination of ACOP in real pharmaceutical preparations. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1514 / 1520
页数:7
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