Sensitive anodic voltammetric determination of methylergometrine maleate in bulk and pharmaceutical dosage forms using differential pulse voltammetry

2015 ◽  
Vol 749 ◽  
pp. 53-61 ◽  
Author(s):  
Mohamed Rizk ◽  
Hassan A.M. Hendawy ◽  
Maha M. Abou El‐Alamin ◽  
Mervat I. Moawad
Keyword(s):  
Differential Pulse Voltammetry ◽  
Differential Pulse ◽  
Dosage Forms ◽  
Voltammetric Determination ◽  
Pharmaceutical Dosage Forms ◽  
Pulse Voltammetry

Polarographic and voltammetric determination of 6-mercaptopurine and 6-thioguanine

1986 ◽  
Vol 51 (11) ◽  
pp. 2466-2472 ◽  
Author(s):  
Jiří Barek ◽  
Antonín Berka ◽  
Ludmila Dempírová ◽  
Jiří Zima
Keyword(s):  
Detection Limit ◽  
Differential Pulse Voltammetry ◽  
Detection Limits ◽  
Differential Pulse ◽  
Voltammetric Determination ◽  
Differential Pulse Polarography ◽  
Hanging Mercury Drop Electrode ◽  
Pulse Polarography ◽  
Pulse Voltammetry

Conditions were found for the determination of 6-mercaptopurine (I) and 6-thioguanine (II) by TAST polarography, differential pulse polarography and fast-scan differential pulse voltammetry at a hanging mercury drop electrode. The detection limits were 10-6, 8 . 10-8, and 6 . 10-8 mol l-1, respectively. A further lowering of the detection limit to 2 . 10-8 mol l-1 was attained by preliminary accumulation of the determined substances at the surface of a hanging mercury drop.

The voltammetric determination of 4-nitrobiphenyl

1991 ◽  
Vol 56 (3) ◽  
pp. 595-601 ◽  
Author(s):  
Jiří Barek ◽  
Gulamustafa Malik ◽  
Jiří Zima
Keyword(s):  
Differential Pulse Voltammetry ◽  
Differential Pulse ◽  
Voltammetric Determination ◽  
Hanging Mercury Drop Electrode ◽  
Optimum Conditions ◽  
Mercury Drop Electrode ◽  
Working Electrode ◽  
Pulse Voltammetry ◽  
Unstirred Solution

Optimum conditions were found for the determination of 4-nitrobiphenyl by fast scan differential pulse voltammetry at a hanging mercury drop electrode in the concentration range 1 . 10-5 to 2 . 10-7 mol l-1. A further increase in sensitivity was attained by adsorptive accumulation of this substance on the surface of the working electrode, permitting determination in the concentration range (2 – 10) . 10-8 mol l-1 with one minute accumulation of the substance in unstirred solution or (2 – 10) . 10-9 mol l-1 with three-minute accumulation in stirred solution. Linear scan voltammetry can be used to determine 4-nitrobiphenyl in the concentration range (2 – 10) . 10-9 mol l-1 with five-minute accumulation in stirred solution, with the advantage of a smoother baseline and smaller interference from substances that yield only tensametric peaks.

scholarly journals Determination of methiocarb pesticide using differential pulse voltammetry with a boron-doped diamond electrode

2015 ◽  
Vol 7 (11) ◽  
pp. 4671-4677 ◽  
Author(s):  
J. Chýlková ◽  
M. Tomášková ◽  
I. Švancara ◽  
L. Janíková ◽  
R. Šelešovská
Keyword(s):  
Differential Pulse Voltammetry ◽  
Rapid Method ◽  
Differential Pulse ◽  
Voltammetric Determination ◽  
Boron Doped Diamond ◽  
Diamond Electrode ◽  
Boron Doped ◽  
Boron Doped Diamond Electrode ◽  
Pulse Voltammetry

In this article, a simple and rapid method is described for voltammetric determination of methiocarb (MTC, a pesticide of the carbamate type).

Voltammetric analysis of ephedrine in pharmaceutical dosage forms and urine using poly(Nile blue A) modified glassy carbon electrode

2020 ◽  
Vol 23 ◽  
Author(s):  
Fatma Ağin ◽  
Gökçe Öztürk ◽  
Dilek Kul
Keyword(s):  
Differential Pulse Voltammetry ◽  
Glassy Carbon ◽  
Limit Of Detection ◽  
Nile Blue ◽  
Differential Pulse ◽  
Dosage Forms ◽  
Buffer Solution ◽  
Pharmaceutical Dosage Forms ◽  
Nile Blue A ◽  
Pulse Voltammetry

Objective: The electrochemical analysis of ephedrine which is a sympathometric drug has been studied using poly(Nile blue A) modified glassy carbon electrodes using cyclic voltammetry, differential pulse voltammetry and square wave voltammetry. Methods: The modified electrodes were prepared by potential cycling electropolymerization of Nile blue A in 0.1 M phosphate buffer solution at pH 6.0. The redox behavior of ephedrine was investigated in different buffer solutions at pH values between 5.5 and 9.0. Results: Scan rate studies showed that the electron transfer reaction of ephedrine was diffusion controlled. A linear response was obtained between the peak current and the ephedrine concentration in the range of 0.6 to 100 μM with a limit of detection of 2.91×10-3 µM for differential pulse voltammetry in Britton-Robinson buffer solution at pH 9.0. The linearity range of ephedrine in human urine was between 1.0 and 100 μM with a detection limit of 8.16 nM. Conclusion: The recovery studies in both pharmaceutical dosage forms and urine showed that the proposed method ensured good selectivity, precision and accuracy without any interference from inactive excipients.

Simultaneous determination of nifedipine and atenolol in combined dosage forms using a boron-doped diamond electrode with differential pulse voltammetry

2018 ◽  
Vol 96 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Jessica Scremin ◽  
Elen Romão Sartori
Keyword(s):  
Differential Pulse Voltammetry ◽  
Differential Pulse ◽  
Dosage Forms ◽  
Current Response ◽  
Boron Doped Diamond ◽  
Diamond Electrode ◽  
Boron Doped ◽  
Boron Doped Diamond Electrode ◽  
Pulse Voltammetry

Combinations of nifedipine (NIF) and atenolol (ATN) are used for the treatment of arterial hypertension. Dosages values different from those presented on the label of pharmaceuticals can significantly impact a consumer’s health. To control the quality of the pharmaceuticals effectively, a method for the simultaneous determination of these both drugs using an anodically pretreated boron-doped diamond electrode coupled to differential pulse voltammetry technique was developed. The influence of supporting electrolyte, pH and scan rate on the current response of these both antihypertensives was examined to select the optimum experimental conditions. It was found that NIF and ATN provided two well-shaped and reproducible oxidation peaks at 0.97 V and 1.36 V (vs. Ag/AgCl electrode), respectively, in TRIS buffer solution (pH 8.0). At optimized differential pulse voltammetric parameters, the current response of NIF and ATN was proportionally linear in the concentration range of 3.98–107 μmol L–1 and 1.99–47.2 μmol L–1, with detection limit of 0.612 and 0.999 μmol L−1, respectively. The proposed method was successfully applied in analysis of several commercial combined dosage forms, whose accuracy was attested by good agreement of the results (paired t test at a 95% confidence level) with those obtained using high performance liquid chromatography.

Ultrasensitive Electrochemical Determination of Phosphate in water by Hydrophilic TiO2 modified Glassy Carbon Electrodes

2021 ◽  
Author(s):  
Yan Jin ◽  
Tong QI ◽  
Yuqing Ge ◽  
Jin Chen ◽  
Li juan Liang ◽  
...  
Keyword(s):  
Differential Pulse Voltammetry ◽  
Glassy Carbon ◽  
Differential Pulse ◽  
Electrochemical Determination ◽  
Carbon Electrodes ◽  
Glassy Carbon Electrodes ◽  
Time Differential ◽  
Pulse Voltammetry ◽  
First Time

In this paper, ultrasensitive electrochemical determination of phosphate in water is achieved by hydrophilic TiO2 modified glassy carbon electrodes for the first time. Differential pulse voltammetry (DPV) method is proposed...

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