2017
DOI: 10.1039/c7ay01455d
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Versatility of a carbon paste electrode coupled to differential pulse voltammetry for determination of lisinopril with its associations (hydrochlorothiazide and amlodipine)

Abstract: This work describes two analytical methods for the determination of pairs of antihypertensives using a carbon paste electrode coupled with differential pulse voltammetry.

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Cited by 7 publications
(4 citation statements)
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“…According to the results, the change in I pa causes the shift of E p to more positive values by increasing the scan rate values from 10 to 450 mV/s. The linear corrolation between I pa and υ also indicates that the electrochemical behavior of AML and HCTZ at the surface of AlV 3 O 9 /CNT/CPE is affected by the diffusion process. , The resulting linear relation is presented below (Figures c and c): …”
Section: Resultsmentioning
confidence: 96%
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“…According to the results, the change in I pa causes the shift of E p to more positive values by increasing the scan rate values from 10 to 450 mV/s. The linear corrolation between I pa and υ also indicates that the electrochemical behavior of AML and HCTZ at the surface of AlV 3 O 9 /CNT/CPE is affected by the diffusion process. , The resulting linear relation is presented below (Figures c and c): …”
Section: Resultsmentioning
confidence: 96%
“…To survey the influence of potential scan rate (υ) on the electrochemical behavior of AML and HCTZ at the surface of AlV 3 O 9 /CNT/ CPE, cyclic voltammograms of these two drugs with a concentration of 0.01 M were recorded in phosphate buffer (0.1 M, pH = 7.0) at different values of scan rate of 10, 30, 50, 80, and υ also indicates that the electrochemical behavior of AML and HCTZ at the surface of AlV 3 O 9 /CNT/CPE is affected by the diffusion process. 14,33 The resulting linear relation is presented below (Figures 8c and 9c): In addition, there is a relation between E p and the logarithm of the scan rates (log υ) in both AML and HCTZ, which is described as follows (see Figures 8c and 9c): Linear deviation determined by the error bar is 0.2%. According to the Laviron equation for irreversible electrode processes, the slope value E p versus log υ for the anodic peak is obtained from the relation 2.303RT/(1 − α)nF.…”
Section: Methodsmentioning
confidence: 95%
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“…Various analytical methods for determining lisinopril have been reported, including spectrofluorimetry [12], chemiluminescence [13], potentiometric titration [14], capillary zone electrophoresis [15], reverse phase-high-performance liquid chromatography [16] micellar electrokinetic chromatography [17] spectrophotometry [18] differential pulse voltammetry [19], and fluorescence [20]. In this work oxidative coupling method is proposed to determine Lisinopril in Pharmaceutical Preparations by coupling reaction with 4aminonaphthalene-1-sulfonic acid in presence of potassium peroxydisulfate as oxidation agent to form a green color product dissolved in water.…”
Section: Introductionmentioning
confidence: 99%