A voltammetric biosensor based on poly(o-methoxyaniline)-gold nanocomposite modified electrode for the simultaneous determination of dopamine and folic acid

被引:35
|
作者
Sangamithirai, D. [1 ]
Munusamy, S. [2 ]
Narayanan, V [2 ]
Stephen, A. [1 ]
机构
[1] Univ Madras, Dept Nucl Phys, Mat Sci Ctr, Guindy Campus, Madras 600025, Tamil Nadu, India
[2] Univ Madras, Dept Inorgan Chem, Guindy Campus, Madras 600025, Tamil Nadu, India
关键词
Poly(o-methoxyaniline); Gold nanoparticles; Voltammetric sensor; Dopamine; Folic acid; Simultaneous determination; GOLD NANOPARTICLES; URIC-ACID; ELECTROCHEMICAL DETERMINATION; ELECTROCATALYTIC OXIDATION; METAL NANOPARTICLES; PASTE ELECTRODE; ASCORBIC-ACID; FABRICATION; SENSOR; POLYANILINE;
D O I
10.1016/j.msec.2018.05.070
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
Dopamine (DA) and Folic acid (FA) are co-existing compounds in biological fluids that plays a vital role in central nervous system and human metabolism. DA is an important neurotransmitter in the brain's neural circuits and its diminution often results in Parkinson's disease. Folate is another form of folic acid, which is known as one of the B vitamins. It is utilized as an additive by women during pregnancy in order to prevent the neural tube defects. The present study reports on the fabrication of electrochemical sensor for the simultaneous determination of DA and FA using poly(o-methoxyaniline)-gold (POMA-Au) nanocomposite. The POMA-Au nanocomposite was prepared via insitu chemical oxidative polymerization method and characterized using X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM) and X-ray photoelectron spectroscopy (XPS). The suitability of POMA-Au nanocomposite as a modifier for the electrocatalytic detection of DA and FA in aqueous solution was investigated by cyclic voltammetry (CV), differential pulse voltammetry (DPV) and chronoamperometry (CA) techniques. The fabricated POMA-Au/GCE sensor exhibited sharp and intense peaks towards the electro-oxidation of DA and FA as compared to bare electrode. The sensor exhibited the promising electron mediating behavior with well separated oxidation peaks with a potential difference of about 350.0 mV. The linear calibration plots of DA and FA were obtained from 10.0 to 300.0 mu M and 0.5 to 900.0 mu M with the detection limits of 0.062 mu M and 0.090 mu M, respectively. The reliability of this sensor was verified to be precise as well as sensitive for the determination of DA and FA in pharmaceutical samples and human urine samples.
引用
收藏
页码:512 / 523
页数:12
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