Electroanalytical Determination of Some Sulfonamides on Overoxidized Polypyrrole Electrodes

2011 ◽  
Vol 64 (7) ◽  
pp. 965 ◽  
Author(s):  
Sabriye Percin Ozkorucuklu ◽  
Levent Ozcan ◽  
Yucel Sahin ◽  
Guleren Alsancak
Keyword(s):  
Correlation Coefficients ◽  
Differential Pulse ◽  
Pencil Graphite Electrode ◽  
Buffer Solution ◽  
Graphite Electrodes ◽  
Buffer Solutions ◽  
Pharmaceutical Tablet ◽  
Overoxidized Polypyrrole ◽  
Pulse Voltammetry

The electrochemical behaviours of five sulfonamides (sulfanilamide, sulfadiazine, sulfamerazine, sulfamonomethoxine, sulfamethoxazole) were investigated with overoxidized polypyrrole (OPPy) modified pencil graphite electrodes. The performance of the OPPy electrode was evaluated by differential pulse voltammetry in Britton–Robinson buffer solutions prepared in different ratio of acetonitrile-water binary mixture, between pH 1.5 and 7.0. The highest anodic signals of sulfonamides were obtained in Britton–Robinson buffer solution prepared in 50% (v/v) acetonitrile-water at pH 2.5 and 3.0. The OPPy electrodes exhibited good performance for sulfonamides with wide linear ranges (≈10–5–10–3 M), highly reproducible responses (RSD% ≤0.92) and correlation coefficients (≥0.9990). The calculated limits of detection were ~10–6 or 10–7 M at 3σ. In order to verify the reliability of the OPPy electrode as a sensor, it is used for determination of sulfamethoxazole in a pharmaceutical tablet. The recovery was found as 95.96% with the RSD% of 0.68. The overoxidized polypyrrole modified pencil graphite electrode showed a stable and reproducible response without any influence of interferent commonly existing in pharmaceutical containing sulfamethoxazole.

scholarly journals Utility of Activated Glassy Carbon and Pencil Graphite Electrodes for Voltammetric Determination of Nalbuphine Hydrochloride in Pharmaceutical and Biological Fluids

2016 ◽  
Vol 2016 ◽  
pp. 1-9 ◽  
Author(s):  
Hoda M. Elqudaby ◽  
Hassan A. M. Hendawy ◽  
Eglal R. Souaya ◽  
Gehad G. Mohamed ◽  
Ghada M. G. Eldin
Keyword(s):  
Glassy Carbon ◽  
Biological Fluids ◽  
Differential Pulse ◽  
Pencil Graphite Electrode ◽  
Buffer Solution ◽  
Graphite Electrodes ◽  
Diffusion Controlled ◽  
Pulse Voltammetry ◽  
Voltammetric Peak

This work compares voltammetric response of nalbuphine hydrochloride (NP·HCl) at both activated glassy carbon and pencil graphite electrodes. The electrochemical oxidation of the drug was studied using cyclic voltammetry (CV), differential pulse voltammetry (DPV), and square wave voltammetry (SWV) techniques. For analytical purpose a well-resolved irreversible diffusion controlled voltammetric peak was established in Britton-Robinson (B-R) buffer solution of pH 6.00 using pencil graphite electrode (PGE). Using activated glassy carbon electrode (GCE) a well-resolved irreversible diffusion controlled voltammetric peak was obtained at pH 7.00 using the same buffer solution. According to the linear relationship between the peak current and NP·HCl concentration, DPV and SWV methods were developed for their quantitative determination in pharmaceutical and human biological fluids. The linear response was obtained in the range from1.6×10-5to1.5×10-4 mol L−1using PGE and from12.5×10-6to13.75×10-5 mol L−1using a GC electrode, respectively. Precision and accuracy of the developed method were checked by recovery studies.

Sensitive Determination of Epinephrine in the Presence of Ascorbic Acid at Poly(diphenylamine sulfonic acid) Modified Sensor

2020 ◽  
Vol 18 (4) ◽  
pp. 253-258
Author(s):  
Gamze Erdoğdu
Keyword(s):  
Ascorbic Acid ◽  
Sulfonic Acid ◽  
Limit Of Detection ◽  
Phosphate Buffer Solution ◽  
Differential Pulse ◽  
Buffer Solution ◽  
Sensitive Determination ◽  
Pulse Voltammetry ◽  
Modified Sensor

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.

Electrochemical Sensor for Acetaminophen Based on a Poly(diphenylamine sulfonic acid) Modified Sensor

2020 ◽  
Vol 18 (10) ◽  
pp. 739-744
Author(s):  
Gamze Erdogdu
Keyword(s):  
Sulfonic Acid ◽  
Limit Of Detection ◽  
Differential Pulse ◽  
Carbon Electrode ◽  
Buffer Solution ◽  
Real Samples ◽  
Oxidation Current ◽  
Pulse Voltammetry ◽  
Modified Sensor

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 Acetaminophen (AC) 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 AC from 0.0 to 100 μM in phospate buffer solution at pH 7.0. The limit of detection was 3.0 nM and the sensitivity was 0.4108 μA/μM. The determination of AC 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 AC in the presence of ascorbic acid at poly(DPSA) sensor in the literature.

Some remarks concerning polarographic determination of sulphur-containing herbicides

1984 ◽  
Vol 49 (5) ◽  
pp. 1282-1288 ◽  
Author(s):  
Věra Stará ◽  
Miloslav Kopanica
Keyword(s):  
Differential Pulse Voltammetry ◽  
Concentration Dependence ◽  
Acidic Medium ◽  
Differential Pulse ◽  
Hanging Mercury Drop Electrode ◽  
Voltammetric Curve ◽  
Buffer Solution ◽  
Peak Current ◽  
Pulse Voltammetry

The herbicide methomyl (2-methylthio-propionaldehyde-o-methylcarbamoyloxime) can be determined using fast scan differential pulse voltammetry with hanging mercury drop electrode by the measurement of the peak at -1.30 V (S.C.E.) which caused by the presence of methomyl in the ammoniacal buffer solution containing cobalt(II) salt. The peak current vs methomyl concentration dependence is linear over the concentration range 0.5 to 20.0 μg . l-1. The herbicide aldicarb (2-methyl-2(methylthio)propionaldehyde-o-methylcarbamoyloxime) is determined by its influence on the differential pulse voltammetric curve of copper(II) recorded in electrochemically enriched solution in acidic medium. The corresponding peak current at the potential + 0.08 V (S.C.E.) depends linearly on the aldicarb concentration in the range 0.07 to 5.00 μg ml-1.

Electrochemical Determination of Norepinephrine at Poly (p-aminobenzenesulfonic Acid) Modified Sensor

2020 ◽  
Vol 16 (5) ◽  
pp. 591-600
Author(s):  
Şevket Zişan Yağcı ◽  
Ebru Kuyumcu Savan ◽  
Gamze Erdoğdu
Keyword(s):  
Ascorbic Acid ◽  
Limit Of Detection ◽  
Phosphate Buffer Solution ◽  
Differential Pulse ◽  
Electrochemical Determination ◽  
Buffer Solution ◽  
Oxidation Current ◽  
Pulse Voltammetry ◽  
Modified Sensor

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.

An Integrative Medical Perspective on Novel Dopamine Detection Method

2018 ◽  
Vol 69 (1) ◽  
pp. 277-281
Author(s):  
Dragos Cristian Stefanescu ◽  
Anton Alexandru Ciucu ◽  
Andreea Alexandra Rabinca ◽  
Mihaela Buleandra ◽  
Anca Pantea Stoian ◽  
...  
Keyword(s):  
Detection Method ◽  
Graphite Electrode ◽  
Differential Pulse ◽  
Pencil Graphite Electrode ◽  
Dopamine Detection ◽  
Pharmaceutical Sample ◽  
Pulse Voltammetry ◽  
Voltammetric Assay ◽  
Medical Perspective

Dopamine is very important neurotransmitter and the rapid and effective methods for its determination are of great importance in fundamental medical research. A rapid voltammetric assay for dopamine (DA) detection in presence of ascorbic acid (AA) based on an electrochemically pretreated pencil graphite electrode has been investigated. Differential pulse voltammetry results showed two well-distinguished oxidation peaks for DA and AA at 0.369 V and 0.142 V, respectively, and the method was applied for DA determination without previous separation. The obtained detection limit for DA was 5.17 � 10-8 M. The method has been successfully applied for determination of DA in a pharmaceutical sample.

Graphene Modified Molecular Imprinting Electrochemical Sensor for Determining the Content of Dopamine

2019 ◽  
Vol 15 (6) ◽  
pp. 628-634
Author(s):  
Rong Liu ◽  
Jie Li ◽  
Tongsheng Zhong ◽  
Liping Long
Keyword(s):  
Electrochemical Sensor ◽  
Molecular Imprinting ◽  
Neurological Disorders ◽  
Room Temperature ◽  
Low Cost ◽  
Differential Pulse ◽  
Current Response ◽  
Specific Selectivity ◽  
Pulse Voltammetry

Background: The unnatural levels of dopamine (DA) result in serious neurological disorders such as Parkinson’s disease. Electrochemical methods which have the obvious advantages of simple operation and low-cost instrumentation were widely used for determination of DA. In order to improve the measurement performance of the electrochemical sensor, molecular imprinting technique and graphene have always been employed to increase the selectivity and sensitivity. Methods: An electrochemical sensor which has specific selectivity to (DA) was proposed based on the combination of a molecular imprinting polymer (MIP) with a graphene (GR) modified gold electrode. The performance and effect of MIP film were investigated by differential pulse voltammetry (DPV) and cyclic voltammetry (CV) in the solution of 5.0 ×10-3 mol/L K3[Fe(CN)6] and K4[Fe(CN)6] with 0.2 mol/L KCl at room temperature. Results: This fabricated sensor has well repeatability and stability, and was used to determine the dopamine of urine. Under the optimized experiment conditions, the current response of the imprinted sensor was linear to the concentration of dopamine in the range of 1.0×10-7 ~ 1.0×10-5 mol/L, the linear equation was I (µA) = 7.9824+2.7210lgc (mol/L) with the detection limit of 3.3×10-8 mol/L. Conclusion: In this work, a highly efficient sensor for determination of DA was prepared with good sensitivity by GR and great selectivity of high special recognization ability by molecular imprinting membrane. This proposed sensor was used to determine the dopamine in human urine successfully.

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.

Sign in / Sign up

Export Citation Format

Share Document