scholarly journals Praseodymium ferrite nano-particles based modified electrode and its application in determination of dopamine

2020 ◽  
Vol 10 (4) ◽  
pp. 5855-5859

The present works report the graphite based electrochemical sensor modified by nano-sized praseodymium ferrite (np-PrFeO3) materials for the detection of dopamine. The combustion technique was used to synthesize these nanomaterials of np-PrFeO3 using praseodymium oxide and ferric nitrate as precursor materials. The nanomaterials were characterized by field emission scanning electron microscopy and transmission electron microscopy techniques. The crystallite sizes of synthesized nanoparticles (nps) were in the range from 40-45 nm with cubic crystal system. Cyclic voltammetry and Differential pulse voltammetry techniques were used to study the electrochemical property and were observed to be superior to earlier reports. The limit of detection of dopamine at PrFeO3/GP electrode was 600 nM with 5 to 200 µM for linearity range. The phosphate buffer solution of pH 6.0 was used for all experimental work with maintaining the scan rate 100mVs-1 and 50mVs-1 for cyclic voltammetry and Differential pulse voltammetry, respectively.

2020 ◽  
Vol 10 (5) ◽  
pp. 6182-6188

The perovskite type lanthanum ortho ferrite nano-particles (LaFeO3) based electrochemical sensor was developed and used to detect dopamine. For this work the lanthanum ortho ferrite nano-particles (LaFeO3) were synthesized by combustion technique using sugar and ethanolamine with lanthanum oxide and ferric nitrate. For the characterization of newly prepared lanthanum ortho ferrite nano-particles, techniques like FESEM, and TEM were used. The crystallite size was found to be 40 to 46 nm with cubic crystal structure. To check the electrochemical properties of a modified sensor electrode (LaFeO3/GP), the cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques were used. During the experiment, the phosphate buffer solution having pH 6.0 was employed, maintaining the scan rate 100mVs-1 and 50mVs-1 for cyclic voltammetry and Differential pulse voltammetry, respectively.


2020 ◽  
Vol 18 (4) ◽  
pp. 253-258
Author(s):  
Gamze Erdoğdu

A sensitive and simple modified sensor was prepared by electrodeposition of diphenylamine sulfonic acid (DPSA) to the glassy carbon electrode surface by cyclic voltammetry (CV) technique. The electrooxidation of epinephrine (EP) was accomplished by CV and differential pulse voltammetry at poly(DPSA) modified sensor. As a result of the findings, the current values were enhanced and both substances were separated at the modified sensor compared to the bare electrode. There was linearly between the oxidation current and concentration of EP from 0.2 to 100 μM in phosphate buffer solution at pH 7.0. The limit of detection was 5.0 nM and the sensitivity was 0.4205 μA/μM. The determination of EP was successfully and satisfactorily carried out in real samples such as human blood serum and urine at the poly(DPSA) sensor. To the best knowledge of this work, this is the first study that detect the EP in the presence of ascorbic acid at poly(DPSA) sensor in the literature.


2020 ◽  
Vol 16 (5) ◽  
pp. 591-600
Author(s):  
Şevket Zişan Yağcı ◽  
Ebru Kuyumcu Savan ◽  
Gamze Erdoğdu

Objective: In this study, it was aimed to prepare an electrochemical sensor capable of assigning Norepinephrine in the presence of an interference such as ascorbic acid. Methods: A sensitive modified sensor was prepared by electrodeposition of p-aminobenzenesulfonic acid (p-ABSA) to the glassy carbon electrode by cyclic voltammetry. The electrooxidation of Norepinephrine was accomplished by cyclic and differential pulse voltammetry. Results: The current values were enhanced and the peak potentials of Norepinephrine and ascorbic acid were separated at the sensor compared to the bare electrode. There was linearity between the oxidation current and concentration of Norepinephrine ranging from 0.5 to 99.8 μM in phosphate buffer solution at pH 7.0. The limit of detection was 10.0 nM and the sensitivity was 0.455 μA/μM. Conclusion: The determination of Norepinephrine was successfully performed in real samples such as blood serum and urine at the poly (p-ABSA) sensor. To the best of our knowledge, this is the first study to detect Norepinephrine in the presence of ascorbic acid at poly (p-ABSA) modified sensor in the literature.


Author(s):  
Fatma Ağin ◽  
Gökçe Öztürk ◽  
Dilek Kul

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.


2019 ◽  
Vol 9 (2) ◽  
pp. 113-123 ◽  
Author(s):  
Sayed Zia Mohammadi ◽  
Hadi Beitollahi ◽  
Tahereh Rohani ◽  
Hossein Allahabadi

Electrochemical characteristics of carvacrol were investigated on a screen-printed electrode (SPE) modified with La2O3/Co3O4 nanocomposite by using voltammetric techniques, which displayed a well-defined peak for sensitive carvacrol determination in phosphate buffer solution (PBS) at pH 7.0. La2O3/Co3O4 nanoparticles demonstrated suitable catalytic activity for carvacrol determination by differential pulse voltammetry (DPV) technique. Besides, determination of carvacrol in a real samples was recognized in the light of electrochemical findings and a validated voltammetric technique for quantitative analysis of carvacrol in a real formulation was proposed. The DPV peak currents were found to be linear in the concentration range of 10.0 to 800.0 μM. The limit of detection (LOD) was found to be 1.0 μM.


2015 ◽  
Vol 7 (20) ◽  
pp. 8673-8682 ◽  
Author(s):  
Nagaraj P. Shetti ◽  
Shweta J. Malode ◽  
Sharanappa T. Nandibewoor

Gold electrode was used for the oxidation of captopril in phosphate buffer solution pH 3.6 to study the influence of several physico-chemical parameters like potential, scan rate, pH and concentration by cyclic, linear sweep and differential pulse voltammetry.


2019 ◽  
Vol 14 (4) ◽  
pp. 216-223 ◽  
Author(s):  
Girish Tigari ◽  
J.G. Manjunatha ◽  
D.K. Ravishankar ◽  
G. Siddaraju

An electrogenerated Polyarginine modified carbon paste electrode (PAMCPE) was fabricated through a simple electropolymerization procedure. The devised electrode was characterized by cyclic voltammetry (CV) and Field Emission Scanning Electron Microscopy (FESEM). This electrode was utilized for electrocatalytic estimation of Riboflavin (RF) and its instantaneous resolution with ascorbic acid (AA) and folic acid (FA) in phosphate buffer solution (PBS) of pH 6.0 by differential pulse voltammetry (DPV). It was observed to be a very responsive electrode for the electrochemical detection and quantification of RF. It was revealed that PAMCPE generates higher current response towards RF contrast to the bare carbon paste electrode (BCPE). Under optimized condition, the RF oxidation current values were linearly reliant on the RF concentration increment with a limit of detection (LOD) of 9.3·10-8 M using DPV. The stable PAMCPE was effectively applied for estimation of RF in B-complex pill and complex human blood serum samples.


2013 ◽  
Vol 78 (6) ◽  
pp. 827-838 ◽  
Author(s):  
Maria-Laura Soare ◽  
Eleonora-Mihaela Ungureanu ◽  
Emilian Georgescu ◽  
Liviu Birzan

This work is devoted to the synthesis and characterization of new indolizine derivatives. Particular attention was paid to the electrochemical investigations by cyclic voltammetry and differential pulse voltammetry. The redox processes for each compound were established, analyzed and assessed to the particular functional groups at which they take place. This assessment was based on detailed comparison between the electrochemical behaviour of the compounds, similarities in their structure, as well as substituent effects.


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