A facile one-pot green synthesis of gold nanoparticle-graphene-PEDOT: PSS nanocomposite for selective electrochemical detection of dopamine

被引:31
|
作者
Pananon, Paweena [1 ]
Sriprachuabwong, Chakrit [1 ,2 ]
Wisitsoraat, Anurat [2 ]
Chuysinuan, Piyachat [3 ]
Tuantranont, Adisorn [2 ]
Saparpakorn, Patchareenart [4 ]
Dechtrirat, Decha [1 ,5 ]
机构
[1] Kasetsart Univ, Dept Mat Sci, Fac Sci, Bangkok, Thailand
[2] Natl Sci & Technol Dev Agcy, Natl Elect & Comp Technol Ctr NECTEC, Pathum Thani, Thailand
[3] Chulabhorn Res Inst, Lab Organ Synth, Bangkok, Thailand
[4] Kasetsart Univ, Fac Sci, Dept Chem, Bangkok, Thailand
[5] Kasetsart Univ, Fac Sci, Specialized Ctr Rubber & Polymer Mat Agr & Ind RP, Bangkok, Thailand
来源
RSC ADVANCES | 2018年 / 8卷 / 23期
关键词
GLASSY-CARBON ELECTRODE; SODIUM DODECYL-SULFATE; URIC-ACID; ASCORBIC-ACID; SENSOR; OXIDE; POLY(3,4-ETHYLENE-DIOXYTHIOPHENE); DEFICIENCY; GRAPHITE;
D O I
10.1039/c8ra01564c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A facile one-pot and green method was developed to prepare a nanocomposite of gold nanoparticle (AuNP), graphene (GP) and poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS). Graphene was first electro-exfoliated in a polystyrene sulfonate solution, followed by a one-step simultaneous in situ formation of gold nanoparticle and PEDOT. The as-synthesized aqueous dispersion of AuNP-GP-PEDOT:PSS was thereafter used to modify the glassy carbon electrode (GCE). For the first time, the quaternary composite between AuNP, GP, PEDOT and PSS was used for selective determination of dopamine (DA) and uric acid (UA) in the presence of ascorbic acid (AA). In comparison to a bare GCE, the nanocomposite electrode shows considerably higher electrocatalytic activities toward the oxidation of DA and UA due to a synergistic effect between AuNP, GP, PEDOT and PSS. Using differential pulse voltammetry (DPV), selective determination of DA and UA in the presence of AA could be achieved with a peak potential separation of 110mV between DA and UA. The sensor exhibits wide linear responses for DA and UA in the ranges of 1 nM to 300 M and 10 M to 1 mM with detection limits (S/N = 3) of 100 pM and 10 M, respectively. Furthermore, the proposed sensor was also successfully used to determine DA in a real pharmaceutical injection sample as well as DA and UA in human serum with satisfactory recovery results.
引用
收藏
页码:12724 / 12732
页数:9
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