Differential pulse voltammetric determination of 7-hydroxycoumarin in human urine

1993 ◽  
Vol 11 (6) ◽  
pp. 443-446 ◽  
Author(s):  
Eithne Dempsey ◽  
Ciara O'Sullivan ◽  
Malcolm R. Smyth ◽  
Denise Egan ◽  
Richard O'Kennedy ◽  
...  
2015 ◽  
Vol 7 (16) ◽  
pp. 6755-6763 ◽  
Author(s):  
K. Cinková ◽  
N. Zbojeková ◽  
M. Vojs ◽  
M. Marton ◽  
A. Samphao ◽  
...  

In this paper, a novel voltammetric method for the determination of 1,3-dimethylxanthine alkaloid theophylline is elaborated using differential pulse (DPV) and square-wave voltammetric (SWV) modes on a boron-doped diamond electrode.


RSC Advances ◽  
2015 ◽  
Vol 5 (129) ◽  
pp. 107058-107063 ◽  
Author(s):  
D. Stanković ◽  
T. Dimitrijević ◽  
D. Kuzmanović ◽  
M. P. Krstić ◽  
B. B. Petković

Differential pulse voltammetric determination of antipsychotic drug trifluoperazine on boron-doped diamond electrode.


2018 ◽  
Vol 14 (3) ◽  
pp. 271-276 ◽  
Author(s):  
Isaac Yves Lopes de Macedo ◽  
Morgana Fernandes Alecrim ◽  
Luane Ferreira Garcia ◽  
Aparecido Ribeiro de Souza ◽  
Wallans Torres Pio dos Santos ◽  
...  

1986 ◽  
Vol 51 (11) ◽  
pp. 2466-2472 ◽  
Author(s):  
Jiří Barek ◽  
Antonín Berka ◽  
Ludmila Dempírová ◽  
Jiří Zima

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.


1991 ◽  
Vol 56 (3) ◽  
pp. 595-601 ◽  
Author(s):  
Jiří Barek ◽  
Gulamustafa Malik ◽  
Jiří Zima

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.


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