De-bundled single-walled carbon nanotube-modified sensors for simultaneous differential pulse voltammetric determination of ascorbic acid, dopamine, and uric acid

被引:28
作者
Thirumalai, Dinakaran [1 ]
Subramani, Devaraju [2 ]
Yoon, Jang-Hee [3 ]
Lee, Jaewon [4 ]
Paik, Hyun-jong [2 ]
Chang, Seung-Cheol [5 ]
机构
[1] Pusan Natl Univ, Grad Dept Chem Mat, Busan 46241, South Korea
[2] Pusan Natl Univ, Dept Polymer Sci & Engn, Busan 46241, South Korea
[3] Korea Basic Sci Inst, Busan Ctr, Busan 46742, South Korea
[4] Pusan Natl Univ, Mol Inflammat Res Ctr Aging Intervent, Coll Pharm, Busan 46241, South Korea
[5] Pusan Natl Univ, Inst Biophysio Sensor Technol, Busan 46241, South Korea
基金
新加坡国家研究基金会;
关键词
TRANSPARENT CONDUCTIVE FILMS; GRAPHENE OXIDE; MODIFIED ELECTRODE; FABRICATION; NANOPARTICLES; NANOMATERIALS; TRYPTOPHAN; DISPERSION; BIOSENSORS; OXIDATION;
D O I
10.1039/c7nj04371f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new approach based on differential pulse voltammetry (DPV) was developed for the simultaneous determination of ascorbic acid (AA), dopamine (DA), and uric acid (UA) using a modified glassy carbon electrode (GCE). The sensor was constructed by a simple "one-step" technique, wherein de-bundled single-walled carbon nanotubes (SWCNTs) were drop-cast onto the GCE. Without de-bundling, the SWCNTs were poorly dispersed in aqueous solution and were ineffective for the one-step procedure. De-bundling of the SWCNTs was achieved using a small amount (0.1 wt%) of the synthesized polymer dispersant, sulfonated poly(ether sulfone) (SPES); the de-bundled SWCNTs had a high aspect ratio (length = 2.5 +/- 1.0 mu m; height = 2 +/- 1 nm, as determined using transmission electron microscopy and atomic force microscopy). The de-bundled SWCNTs also led to enhanced electrocatalytic activity and selectivity of the modified sensor for the simultaneous determination of AA, DA, and UA in DPV measurements: the peak-to-peak separation values were 221, 119, and 340 mV (vs. Ag/AgCl) for DA-AA, UA-DA, and AA-UA, respectively. The dynamic linear ranges for AA, DA, and UA were 0.2-1.6 mM, 5.0-50 mu M, and 5.0-60 mu M, and the detection limits were 10.6 mu M, 15 nM, and 113 nM (S/N = 3), respectively. The analytical performance of the developed sensor was demonstrated in the determination of AA and DA in commercial pharmaceutical samples (vitamin C tablets and DA injection). The characteristics of the modified sensor make it promising for the individual or simultaneous determination of AA, DA, and UA.
引用
收藏
页码:2432 / 2438
页数:7
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