Voltammetric study of secnidazole and its determination in pharmaceutical tablet using 1, 4-benzoquinone modified carbon paste electrode

2019 ◽  
Author(s):  
Chem Int
Keyword(s):  
Carbon Paste Electrode ◽  
Limit Of Detection ◽  
Modified Carbon Paste Electrode ◽  
Carbon Paste ◽  
Buffer Solution ◽  
Limit Of Quantification ◽  
Pharmaceutical Tablet ◽  
Relative Standard ◽  
Paste Electrode

In this study voltammetric behaviour of secnidazole (SCZ) at 1, 4-Benzoquinone Modified Carbon Paste Electrode (1,4-BQMCPE) was investigated in Britton Robinson buffer solution using cyclic voltammetric technique. A well-defined cathodic peak was observed for the SCZ in the entire pH range. The current increases steadily with scan rate and the results indicated that the process is irreversible reduction and adsorption controlled. The number of electrons transferred and different kinetic parameters like transfer coefficient and rate constant were calculated by using cyclic voltammetry technique. Differential pulse voltammetric method has been used for the determination of SCZ content in pharmaceutical tablet. This method enabled to determine SCZ in the concentration range 1.0 × 10-8 to 4.0 × 10-4 M. The limit of detection (LOD) and limit of quantification (LOQ) were found to be 2.13 × 10-9 and 2.85 × 10-9 respectively. The method was applied to determine the content of SCZ in different sample solutions of SCZ tablet with excellent recovery and relative standard deviation results (99.892±1.53 respectively) for spiked standard SCZ in tablet sample solutions. The selectivity of the method for SCZ was further studied in the presence of selected potential interferents such as fluconazole, azithromycin etc and confirmed the potential applicability of the developed method for the determination of SCZ in real pharmaceutical tablets.

scholarly journals Electrochemical Investigation of Catechol at Poly(niacinamide) Modified Carbon Paste Electrode: A Voltammetric Study

2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
A. B. Teradale ◽  
S. D. Lamani ◽  
B. E. Kumara Swamy ◽  
P. S. Ganesh ◽  
S. N. Das
Keyword(s):  
Carbon Paste Electrode ◽  
Limit Of Detection ◽  
Phosphate Buffer Solution ◽  
Modified Carbon Paste Electrode ◽  
Rate Variation ◽  
Carbon Paste ◽  
Buffer Solution ◽  
Limit Of Quantification ◽  
Paste Electrode

A polymeric thin film modified electrode, that is, poly(niacinamide) modified carbon paste electrode (MCPE), was developed for the electrochemical determination of catechol (CC) by using cyclic voltammetric technique. Compared to bare carbon paste electrode (BCPE), the poly(niacinamide) MCPE shows good electrocatalytic activity towards the oxidation of catechol in phosphate buffer solution (PBS) of physiological pH 7.4. All experimental parameters were optimized. Poly(niacinamide) modified carbon paste electrode gave a linear response between concentration of CC and its anodic peak current in the range within 20.6–229.0 μM. The limit of detection (3S/M) and limit of quantification (10S/M) were 1.497 μM and 4.99 μM, respectively. From the study of scan rate variation, the electrode process was found to be adsorption-controlled. The involvement of protons and electrons in the oxidation of CC was found to be equal. The probable electropolymerisation mechanism of niacinamide was proposed. Finally, this method can be used in development of a sensor for sensitive determination of CC.

scholarly journals Electrochemical analysis of indigo carmine using polyarginine modified carbon paste electrode

2021 ◽  
Author(s):  
D'Souza S. Edwin ◽  
Jamballi G. Manjunatha ◽  
Chenthattil Raril ◽  
Tigari Girish ◽  
Doddarasinakere K. Ravishankar ◽  
...  
Keyword(s):  
Carbon Paste Electrode ◽  
Limit Of Detection ◽  
Indigo Carmine ◽  
Electrochemical Analysis ◽  
Modified Carbon Paste Electrode ◽  
Carbon Paste ◽  
Limit Of Quantification ◽  
Selective Determination ◽  
Paste Electrode

Suitable electro-catalytic technique is established for the selective determination of Indigo Carmine (IC) at poly(arginine) modified carbon paste electrode (PAMCPE). The surface morphological study of the electrode is done through Field Emission Scanning Electron Microscopy (FESEM). The different parameters such as concentration, pH and scan rate on the electrode response are studied. The individual and simultaneous performance of IC and Riboflavin (RF) is carried out through differential pulse voltammetry. The electrocatalytic response of the sensor varied with the concentration of IC in the range from 2×10-7 M to 1×10-6 M and 1.5×10-6 M to 3.5×10-6 M is observed. Limit of detection (LOD) and the limit of quantification (LOQ) is found 2.53×10-8 M and 8.43×10-8 M respectively. The developed PAMCPE successfully shows better electrochemical response towards IC when compared with BCPE. Preparation and characterization of both the electrodes is simple and easier. This has derived a standard method for the determination of IC in real samples.      

scholarly journals Electro-Polymerized Titan Yellow Modified Carbon Paste Electrode for the Analysis of Curcumin

Surfaces ◽  
2021 ◽  
Vol 4 (3) ◽  
pp. 191-204
Author(s):  
Edwin S. D’Souza ◽  
Jamballi G. Manjunatha ◽  
Chenthattil Raril ◽  
Girish Tigari ◽  
Huligerepura J. Arpitha ◽  
...  
Keyword(s):  
Carbon Paste Electrode ◽  
Limit Of Detection ◽  
Phosphate Buffer Solution ◽  
Modified Carbon Paste Electrode ◽  
Carbon Paste ◽  
Buffer Solution ◽  
Solution Ph ◽  
Real Sample Analysis ◽  
Titan Yellow ◽  
Paste Electrode

A modest, efficient, and sensitive chemically modified electrode was fabricated for sensing curcumin (CRC) through an electrochemically polymerized titan yellow (TY) modified carbon paste electrode (PTYMCPE) in phosphate buffer solution (pH 7.0). Cyclic voltammetry (CV) linear sweep voltammetry (LSV) and differential pulse voltammetry (DPV) approaches were used for CRC detection. PTYMCPE interaction with CRC suggests that the electrode exhibits admirable electrochemical response as compared to bare carbon paste electrode (BCPE). Under the optimized circumstances, a linear response of the electrode was observed for CRC in the concentration range 2 × 10−6 M to 10 × 10−6 M with a limit of detection (LOD) of 10.94 × 10−7 M. Moreover, the effort explains that the PTYMCPE electrode has a hopeful approach for the electrochemical resolution of biologically significant compounds. Additionally, the proposed electrode has demonstrated many advantages such as easy preparation, elevated sensitivity, stability, and enhanced catalytic activity, and can be successfully applied in real sample analysis.

Electrocatalytic performance of a zinc sulphide nanoparticles-modified carbon paste electrode for the simultaneous determination of acetaminophen, guanine and adenine

2018 ◽  
Vol 10 (11) ◽  
pp. 1362-1371 ◽  
Author(s):  
Mallappa Mahanthappa ◽  
Nagaraju Kottam ◽  
Shivaraj Yellappa
Keyword(s):  
Carbon Paste Electrode ◽  
Phosphate Buffer ◽  
Phosphate Buffer Solution ◽  
Zinc Sulphide ◽  
Modified Carbon Paste Electrode ◽  
Carbon Paste ◽  
Buffer Solution ◽  
Guanine And Adenine ◽  
Paste Electrode

The simultaneous electroanalysis of acetaminophen (AC), guanine (G) and adenine (A) was successfully achieved on the zinc sulphide nanoparticles-modified carbon paste electrode (ZnS NPs/CPE) in phosphate buffer solution (PBS).

A Facile In-Situ Development of L-Valine Film onto the Surface of Carbon Paste Electrode Towards the Detection of Environmentally Hazardous 4-Amino Phenol

2019 ◽  
Vol 0 (0) ◽  
Author(s):  
T. Venu Gopal ◽  
Tukiakula Madhusudana Reddy ◽  
P. Shaikshavali ◽  
G. Venkataprasad ◽  
P. Gopal
Keyword(s):  
Cyclic Voltammetry ◽  
Carbon Paste Electrode ◽  
Electrochemical Impedance ◽  
Limit Of Detection ◽  
Small Scale ◽  
Carbon Paste ◽  
Relative Standard ◽  
Paste Electrode

Abstract A small scale of environmentally hazardous 4-aminophenol can show significant impact on human health. Hence, in the present work, we have designed L-Valine film (Vf) modified carbon paste electrode (Vf/CPE) for the determination of 4-aminophenol. Herein, a facile in-situ L-Valine film was developed by electrochemical polymerization method onto the surface of bare carbon paste electrode (BCPE) with the help of cyclic voltammetry (CV) technique. A two-folds of electrochemical peak current enhancement was achieved at Vf/CPE in comparison with BCPE towards the determination of 4-aminophenol in optimum pH 7.0 of phosphate buffer solution (PBS). This was achieved due to the large surface area and conductive nature of Vf/CPE, which was concluded through the techniques of cyclic voltammetry and electrochemical impedance spectroscopy (EIS). The effect of pH of buffer and scan rate studies were successfully studied. Morphological changes of BCPE and Vf/CPE was studied with the help of scanning electron microscopy (SEM). The formation of Vf on CPE was also analyzed by Fourier transform infrared (FTIR) spectra. Under the optimized conditions, the limit of detection (LOD) and limit of quantification (LOQ) values of 4-aminophenol were estimated with the aid of chronoamperometry (CA) technique and was found to be 9.8 μM and 32 μM, respectively. Finally the proposed method was found to have satisfactory repeatability, reproducibility and stability results with low relative standard deviation (RSD) values.

Enhanced Electrochemical Determination Of Riboflavin In Biological And Pharmaceutical Samples At Poly (Arginine) Modified Carbon Paste Electrode

2019 ◽  
Vol 14 (4) ◽  
pp. 216-223 ◽  
Author(s):  
Girish Tigari ◽  
J.G. Manjunatha ◽  
D.K. Ravishankar ◽  
G. Siddaraju
Keyword(s):  
Carbon Paste Electrode ◽  
Limit Of Detection ◽  
Phosphate Buffer Solution ◽  
Differential Pulse ◽  
Modified Carbon Paste Electrode ◽  
Current Response ◽  
Carbon Paste ◽  
Serum Samples ◽  
Buffer Solution ◽  
Paste Electrode

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.

scholarly journals Square wave anodic stripping voltammetric determination of Hg(II) with N-p- chlorophenylcinnamohydroxamic acid modified carbon paste electrode

2020 ◽  
Vol 34 (1) ◽  
pp. 25-39
Author(s):  
Denekew Alemayehu ◽  
Bhagwan Singh Chandravanshi Chandravanshi ◽  
Tesfu Hailu ◽  
Merid Tessema
Keyword(s):  
Carbon Paste Electrode ◽  
Anodic Stripping Voltammetry ◽  
Open Circuit ◽  
Modified Carbon Paste Electrode ◽  
Carbon Paste ◽  
Square Wave ◽  
Relative Standard ◽  
Anodic Stripping ◽  
Paste Electrode

A new method has been developed for the electrochemical determination of Hg(II) with N-p-chlorophenylcinnamohydroxamic acid (CPCHA) modified carbon paste electrode by square wave anodic stripping voltammetry (SWASV). Hg(II) was accumulated on the electrode surface by the formation of the complex in an open circuit and the resulting surface was characterized by electrochemical reduction and stripping. The optimum voltammetric response was observed using a carbon paste composition of 7.5% (w/w) CPCHA and preconcentration time of 210 s in 0.1 M sodium acetate at pH 8 followed by electrochemical SWASV in 0.3 M NH4Cl solution at pH 4 at a reduction potential of -0.6 V. The voltammetric signals were linear in the range of 1-25 µM Hg(II) with a detection limit of 12.9 nM. The voltammetric response for six replicate measurements of 15 µM Hg(II) was reproduced with 3.8% relative standard deviation (RSD). Many coexisting metal ions had little or no effect on the determination of Hg(II). Five spiked samples of water were evaluated by using the developed method giving recoveries of Hg(II) in the range 98-105%.   Bull. Chem. Soc. Ethiop. 2020, 34(1), 25-39. DOI: https://dx.doi.org/10.4314/bcse.v34i1.3

scholarly journals Electroanalysis Of Paracetamol By A Carbon Paste Electrode Modified By Zinc: Analytical Application In Human Blood

2021 ◽  
Vol 16 (1) ◽  
pp. 25-31
Author(s):  
Hayat EL Ouafy ◽  
Tarik EL Ouafy ◽  
Mustapha Oubenali ◽  
Mohamed Mbarki ◽  
Malika Echajia ◽  
...  
Keyword(s):  
Human Blood ◽  
Carbon Paste Electrode ◽  
Catalytic Effect ◽  
Limit Of Detection ◽  
Detection Sensitivity ◽  
Modified Carbon Paste Electrode ◽  
Potential Range ◽  
Carbon Paste ◽  
Relative Standard ◽  
Paste Electrode

The present work describes the catalytic effect of zinc particles for electroanalysis the paracetamol (PAR). The working electrode was prepared by mixing the zinc with the carbon powder. The voltammetric behavior of paracetamol was studied when an anodic peak to appear at 0.35 V in 0.1 M Na2SO4 solution (pH 12). The peak resulting from the irreversible oxidation of paracetamol on the zinc modified carbon paste electrode (Zn/CPE). The catalytic effect was evaluated by cyclic voltammetry (CV) and square wave voltammetry (SWV). The electrocatalytic behavior of the zinc particles is allotted to its chemical and physical properties. This electrode has a good performance for the electroanalysis of paracetamol. To obtain an electrochemical analysis of paracetamol oxidation at the surface of Zn/CPE, the voltammograms are used in a potential range of - 1.5 V to 1.5 V. More, Zn/CPE can be utilized successfully to ameliorate the electroanalysis of paracetamol at very feeble concentration and with high detection sensitivity. The limit of detection (LD) and quantification (LQ) obtained are respectively 7.52·10-8 mol L-1 and 2.6·10-7 mol L-1. Then the relative standard deviation (RSD) at 2.0·10-5 mol L-1 PAR concentration was 2.88 % for nine repetitions. Afterward, the presented method was used to electroanalysis paracetamol in human blood samples with satisfying results.

scholarly journals MODIFICATION OF CARBON PASTE ELECTRODE WITH CROWN ETHER (DIBENZO-18-CROWN-6) FOR ASCORBIC ACID ANALYSIS USING DIFFERENTIAL PULSE VOLTAMMETRY METHOD

2016 ◽  
Vol 11 (2) ◽  
pp. 175
Author(s):  
Irdhawati Irdhawati ◽  
Manuntun Manurung ◽  
Anisha Maulinasari
Keyword(s):  
Ascorbic Acid ◽  
Crown Ether ◽  
Carbon Paste Electrode ◽  
Limit Of Detection ◽  
Differential Pulse ◽  
Modified Carbon Paste Electrode ◽  
Range Limit ◽  
Carbon Paste ◽  
Paste Electrode

In this research, the modified carbon paste electrode with crown ether (dibenzo-18-crown-6) has been prepared, for determination of ascorbic acid. Some of parameters observed were optimization of crown ether composition in carbon paste, pH of solution, linear concentration range, limit of detection, reproducibility, and recovery. The optimum performance of the prepared electrode was applied for determination of commercialsampleswhich contain of ascorbic acid. The result of this research showsthat the optimum composition of crown ether in carbon paste is 0.6 % at pH 4. Linear range of concentration obtained is from 2 - 200 μM. The detection limit and percentage of recovery are 1.243 μM and 101.31 %, respectively. The modified electrode has HorRat value less than 2, it indicates a good reproducibility. Analysis of 4 commercial samples which contain of ascorbic acid were in agreement with the content listed in the label with the suitability of 94 - 100 %.

Sign in / Sign up

Export Citation Format

Share Document