Optimization of modified carbon paste electrode with multiwalled carbon nanotube/ionic liquid/cauliflower-like gold nanostructures for simultaneous determination of ascorbic acid, dopamine and uric acid

被引:43
作者
Afraz, Ahmadreza [1 ]
Rafati, Amir Abbas [1 ]
Najafi, Mojgan [2 ]
机构
[1] Bu Ali Sina Univ, Fac Chem, Dept Phys Chem, Hamadan, Iran
[2] Hamedan Univ Technol, Dept Mat Engn, Hamadan 65169, Iran
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2014年 / 44卷
关键词
Carbon paste electrode; Multiwalled carbon nanotube; Ionic liquid; Gold nanostructure; IONIC LIQUID ELECTRODE; GRAPHENE-MODIFIED ELECTRODE; ELECTROCATALYTIC OXIDATION; ELECTROCHEMICAL SENSOR; SILVER NANOPARTICLES; TRYPTOPHAN; NANOCOMPOSITE; HEMOGLOBIN; SURFACES; OXIDE;
D O I
10.1016/j.msec.2014.07.065
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
We describe the modification of a carbon paste electrode (CPE) with multiwalled carbon nanotubes (MWCNTs) and an ionic liquid (IL). Electrochemical studiesby using a D-optimal mixture design in Design-Expert software revealed an optimized composition of 60% graphite, 14.2% paraffin, 10.8% MWCNT and 15% IL. The optimal modified CPE shows good electrochemical properties that are well matched with model prediction parameters. In the next step, the optimized CPE was modified with gold nanostructures by applying a double-pulse electrochemical technique. The resulting electrode was characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction, and electrochemical impedance spectroscopy. It gives three sharp and well-separated oxidation peaks for ascorbic acid (AA), dopamine (DA), and uric acid (UA). The sensor enables simultaneous determination of AA, DA and UA with linear responses from 03 to 285, 0.08 to 200, and 0.1 to 450 mu M, respectively, and with 120,30 and 30 nM detection limits (at an S/N of 3). The method was successfully applied to the determination of AA, DA, and UA in spiked samples of human serum and urine. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:58 / 68
页数:11
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