Graphene-loaded nanofiber-modified electrodes for the ultrasensitive determination of dopamine

被引:50
|
作者
Rodthongkum, Nadnudda [1 ]
Ruecha, Nipapan [2 ]
Rangkupan, Ratthapol [1 ,3 ]
Vachet, Richard W. [4 ]
Chailapakul, Orawon [5 ]
机构
[1] Chulalongkorn Univ, Met & Mat Sci Res Inst, Bangkok 10330, Thailand
[2] Chulalongkorn Univ, Fac Sci, Program Macromol Sci, Bangkok 10330, Thailand
[3] Chulalongkorn Univ, Ctr Innovat Nanotechnol, Bangkok 10330, Thailand
[4] Univ Massachusetts, Dept Chem, Amherst, MA 01002 USA
[5] Chulalongkorn Univ, Fac Sci, Dept Chem, Electrochem & Opt Spect Res Unit, Bangkok 10330, Thailand
关键词
Graphene; Polyaniline; Polystyrene; Nanofiber; Electrospinning; Dopamine; ASCORBIC-ACID; URIC-ACID; SELECTIVE DETECTION; CARBON NANOTUBES; ELECTROCHEMICAL DETECTION; COMPOSITE FILM; NANOCOMPOSITE; CONDUCTIVITY; MOVEMENT; PLATFORM;
D O I
10.1016/j.aca.2013.09.057
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel and highly sensitive electrochemical system based on electrospun graphene/polyaniline/polystyrene (G/PANI/PS) nanofiber-modified screen-printed carbon electrodes has been developed for dopamine (DA) determination. A dramatic increase (9 times) in the current signal for the redox reaction of a standard, ferri/ferrocyanide [Fe(CN)(6)](3-/4) couple was found when compared to an unmodified electrode. This modified electrode also exhibited favorable electron transfer kinetics and excellent electrocatalytic activity toward the oxidation of DA. When used together with square wave voltammetry (SWV), DA can be selectively determined in the presence of the common interferents (i.e. ascorbic acid and uric acid). Under optimal conditions, a very low limit of detection (0.05 nM) and limit of quantification (0.30 nM) were achieved for DA. In addition, a wide dynamic range of 0.1 nM to 100 p,M was found for this electrode system. Finally, the system can be successfully applied to determine DA in complex biological environment (e.g. human serum, urine) with excellent reproducibility. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:84 / 91
页数:8
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