Electrochemical Determination of Albendazole at Glassy Carbon Electrode

2016 ◽  
Vol 99 (6) ◽  
pp. 1522-1526 ◽  
Author(s):  
Jayant I Gowda ◽  
Rahul B Kantikar ◽  
Devaraddi G Harakuni ◽  
Kirankumar Y Jadhav ◽  
Vinay C Chanagoudar ◽  
...  

Abstract In this article, the electrochemical behavior on a glassy carbon electrode (GCE) was investigated and the electrochemical parameters of albendazole (ALB) were calculated. ALB effectively accumulated on the GCE surface and caused a pair of redox peaks at around 1.095 V and 1.028 V and an oxidation peak at 0.844 V (versus saturated calomel electrode) in 0.2 M phosphate buffer solution (pH 3.0). Under optimized conditions, the anodic peak current was linear to the ALB concentration the range of 1.5 × 10−7 M to 4.0 × 10−5 M. The regression equation was: Ipa (10−6 A) = 0.79 [ALB] (μM) + 0.84 (R2 = 0.982). The detection limit 6.08 × 10−8 M was obtained. The proposed method was successfully used to determine ALB content in tablet samples, with satisfactory results.

2013 ◽  
Vol 78 (5) ◽  
pp. 701-711 ◽  
Author(s):  
Addisu Kitte ◽  
Desalegn Assresahegn ◽  
Refera Soreta

We report here the modification of glassy carbon electrode (GCE) with palladium nanoparticles and palladium film. The response to hydrogen peroxide on the modified electrode was examined using cyclic voltammetry and amperometry (at -0.2 V vs Ag/AgCl reference electrode in the phosphate buffer solution pH 7.4). The palladium film and palladium nanoparticle modified GCE showed a linear response to hydrogen peroxide in the concentration range between 10 ?M to 14 mM and 1 ?M to 14 mM with detection limit of 6.79 ?M and 0.33 ?M, respectively.


2014 ◽  
Vol 955-959 ◽  
pp. 1160-1166
Author(s):  
Shao Hua Li ◽  
Ying Ying Zhao ◽  
Jun Qing Yang ◽  
Guo Yan Zhang ◽  
Ju Rui Qi

A novel multi-walled carbon nanotubes (MWCNTs)-modified glassy carbon electrode (GCE) with excellent stability, repeatability and anti-interference was synthesized and it exhibited an electrocatalytic signal for hydroquinone (HQ) compared to bare GCE, which suggested that the presence of MWCNTs efficiently enhances electron transfer. Various parameters such as pH, modifier volume, and scan rate were optimized using cyclic voltammetry (CV) and differential pulse voltammetry (DPV) methods. Under optimum conditions, linear responses for HQ in 0.1mol·L-1 phosphate buffer solution of pH 6.0 were obtained in the range of 5×10-6 mol·L-1 to 2×10-4 mol·L-1 with detection limits of 2.7×10-6 mol·L-1 (signal-to-noise ratio of 3). Such MWCNTs-modified GCE was successfully applied for the determination of hydroquinone in simulated water samples and can be developed for the the detection of HQ.


2015 ◽  
Vol 7 (3) ◽  
pp. 1147-1153 ◽  
Author(s):  
Hualing Xiao ◽  
Lingen Sun ◽  
Hongling Yan ◽  
Wen Wang ◽  
Jiali Liu ◽  
...  

Nicotine is determined at a glassy carbon electrode modified with partially electroreduced carboxylated graphene by cyclic voltammetry and semi-derivative treatment after enrichment at −1.1 V in 0.1 M pH 7.0 phosphate buffer solution.


2019 ◽  
Vol 2019 ◽  
pp. 1-10
Author(s):  
Miao Zhang ◽  
Chuang-ye Ge ◽  
Ya-feng Jin ◽  
Liang-bin Hu ◽  
Hai-zhen Mo ◽  
...  

Hydroquinone (HQ) and catechol (CT) are considered as environmental pollutants with high toxicity. We have developed a simple electrochemical sensor using an anodized glassy carbon electrode modified with a stable 2-(phenylazo) chromotropic acid- (CH-) conducting polymer (PCH/AGCE). The PCH/AGCE sensor showed good electrocatalytic activity and reversibility towards the redox of HQ and CT in phosphate buffer solution (PBS, pH 7.0). The cyclic voltammetry (CV) in mixed solution of HQ and CT showed that the oxidation peaks of them became well resolved with a peak separation of 0.1 V. The detection limits of HQ and CT were 0.044 and 0.066 μM, respectively, in a wide linear response range of 1–300 μM for both. Moreover, the sensor displayed an excellent selectivity in the presence of common interferences. This study provided a simple, sensitive, and high recovery method for simultaneous and quantitative determination of HQ and CT in aqueous medium.


2011 ◽  
Vol 239-242 ◽  
pp. 328-333
Author(s):  
Jing Jie Cui ◽  
De Hui Sun ◽  
Hong Liu ◽  
Guan Cong Wang ◽  
Hong Shi Zhao ◽  
...  

The electrochemical behavior of nucleobases has been studied in 0.1 M phosphate buffer solution (PBS), pH 7.4 without removing oxygen, using glassy carbon electrode (GCE). Cyclic voltammetry (CV), electrochemical impedance experiment (EIS) and square wave voltammetry (SWV) were employed in the measurements of the nucleobases electrochemical signals at GCEs. Guanine (G) and adenine (A) produced well-defined oxidation peaks at about +0.66 and +0.96 V under the CV sweep at 100 mV/s, respectively. SWV was particularly useful in investigating the electrochemical behaviour of pyrimidine bases. In the SWV detection, thymine (T) clearly appeared an oxidation peak at 1.1 V, while cytosine (C) and uracil (U) did a complex oxidation peak at 1.3 V. Nucleobases possess an irreversible and adsorption-controlled electrochemical process at GCEs in 0.1 M PBS (pH 7.4). The average surface concentrations (Γ) of G and A on the surface of the GCE were estimated to be about 1.6515×10−10and 8.8232×10−11mol/cm2, respectively. Due to the selective interactions of nucleobases with each other, the nucleobase oxidation peaks shift and new oxidation peaks appeared. The new oxidation peaks at +1.62 and 1.55 V may correspond to the oxidation of GC pairs and AT pairs, respectively. The detection of the electrochemical behaviour and selective binding of nucleobases in a physiological PBS at pH 7.4 is of particular interest for electrochemical sensor applications in physiological media.


2017 ◽  
Vol 70 (10) ◽  
pp. 1118 ◽  
Author(s):  
Gaopeng Dai ◽  
Jingwen Xie ◽  
Cheng Li ◽  
Suqin Liu

A simple and highly sensitive method for the determination of hydrogen peroxide was developed by electrodepositing Cu and MnO2 onto a g-C3N4 coated glassy carbon electrode in a one-step procedure. The morphology of the fabricated electrode material was characterized by scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX). The electrochemical properties were measured using cyclic voltammetry (CV) and chronoamperometry. The modified sensor exhibits high catalytic activity towards electrochemical oxidation of hydrogen peroxide in a neutral phosphate buffer solution. Within the concentration ranges of 0.01–20 mM and 20–400 mM, the fabricated sensor shows a good linear relationship with the oxidation peak current, the detection limit is 0.85 × 10−6 M. Furthermore, the sensor exhibits high selectivity, good stability, and reproducibility. We successfully applied the sensor to detect hydrogen peroxide residues in food samples with satisfactory results, providing a new approach for food security evaluation.


2012 ◽  
Vol 602-604 ◽  
pp. 239-242
Author(s):  
Zhuo Cai ◽  
Wei Chao Yue ◽  
Jing Ni Gan ◽  
Yue Peng ◽  
Xiao Liang He

A multi-wall carbon nanotube modified glassy carbon electrode (MWCNTs/GCE) has been prepared. The electrochemical behavior of scutellarin at the modified electrode and its electroanalytical method have been studied. It was showed that in 0.20 mol/L Na2HPO4-NaH2PO4 buffer solution (pH=7.4) MWCNTs/GCE exhibited excellent catalytic and enhancement effect on the electrochemical oxidation of scutellarin, the sensitivity increaced 23 times compared with that at bare GCE. The measurement parameters were optimized. Under the optimal conditions, the linear range of scutellarin concentration was 4.0×10-6-1.0×10-4 mol/L (R=0.9991) with a detection limit of 8.2×10-7 mol/L(S/N =3), and the RSD for 4.0×10-5 mol/L scutellarin solution was 1.8% (n=11). This method was successfully used in the determination of scutellarin in injection and tablets.


2019 ◽  
Vol 11 (30) ◽  
pp. 3866-3873 ◽  
Author(s):  
R. Karthikeyan ◽  
D. James Nelson ◽  
S. Abraham John

Selective and sensitive determination of one of the purine nucleotides, inosine (INO) using a low cost carbon dot (CD) modified glassy carbon (GC) electrode in 0.2 M phosphate buffer solution (pH 7.2) was demonstrated in this paper.


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