Facile Electrochemical Pretreatment of Multiwalled Carbon Nanotube - Polydimethylsiloxane Paste Electrode for Enhanced Detection of Dopamine and Uric Acid

被引:1
作者
Buenaventura, Angelo Gabriel E. [1 ,2 ]
Yago, Allan Christopher C. [1 ,2 ]
机构
[1] Univ Philippines, Nat Sci Res Inst, Diliman, Philippines
[2] Univ Philippines, Inst Chem, Diliman, Philippines
来源
3RD INTERNATIONAL CONFERENCE ON THE SCIENCE AND ENGINEERING OF MATERIALS (ICOSEM 2017) | 2018年 / 1958卷
关键词
ASCORBIC-ACID; DISEASE;
D O I
10.1063/1.5034560
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A facile electrochemical pretreatment via anodization was done on Carbon Paste Electrodes (CPEs) composed of Multiwalled Carbon Nanotubes (MWCNTs) and Polydimethylsiloxane (PDMS) binder to produce 'anodized' CPEs (ACPE). Cyclic Voltammetry (CV) technique was used to anodize the CPEs. The anodization step, performed in various solutions (0.2 M NaOH(aq), 0.06 M BR Buffer at pH 7.0, and 0.2 M HNO3(aq)), were found to enhance the electrochemical properties of the ACPEs compared to non-anodized CPE. Electrochemical Impedance Spectroscopy (EIS) measurements revealed a significantly lower charge transfer resistance (Rct) for the ACPEs (4.01-6.25 k Omega) as compared to CPE (25.9 k Omega). Comparison of the reversibility analysis for Fe(CN)(6)(3-/4-) redox couple showed that the ACPEs have peak current ratio (Ia/Ic) at range of 0.97-1.10 while 1.92 for the CPE; this result indicated better electrochemical reversible behavior for Fe(CN)(6)(3-/4-) redox couple using the ACPEs. CV Anodization process was further optimized by varying solution and CV parameters (i.e. pH, composition, number of cycles, and potential range), and the resulting optimized ACPE was used for enhanced detection of Dopamine (DA) and Uric Acid (UA) in the presence of excess Ascorbic Acid (AA). Employing Differential Pulse Voltammetry technique, enhanced voltammetric signal for DA and significant peak separation between DA and UA was obtained. The anodic peak currents for the oxidation of DA and UA appeared at 0.263V and 0.414 V, respectively, and it was observed to be linearly increasing with increasing concentrations of biomolecules (25-100 mu M). The detection limit was determined to be 3.86 mu M for DA and 5.61 mu M for UA. This study showed a quick and cost-effective pretreatment for CPEs based on MWCNT-PDMS composite which lead to significant enhancement on its electrochemical properties.
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页数:11
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