scholarly journals Voltammetric Determination of Flunixin on Molecularly Imprinted Polypyrrole Modified Glassy Carbon Electrode

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Abd-Elgawad Radi ◽  
Nadia Abd El-Ghany ◽  
Tarek Wahdan

A novel electrochemical sensing approach, based on electropolymerization of a molecularly imprinted polypyrrole (MIPpy) film onto a glassy carbon electrode (GCE) surface, was developed for the detection of flunixin (FXN). The sensing conditions and the performance of the constructed sensor were assessed by cyclic, differential pulse and (DPV) square wave voltammetry (SWV). The sensor exhibited high sensitivity, with linear responses in the range of 5.0 to 50.0 µM with detection limits of 1.5 and 1.0 µM for DPV and SWV, respectively. In addition, the sensor showed high selectivity towards FXN in comparison to other interferents. The sensor was successfully utilized for the direct determination of FXN in buffalo raw milk samples.

2019 ◽  
Vol 2019 ◽  
pp. 1-12 ◽  
Author(s):  
Hajer Hrichi ◽  
Lotfi Monser ◽  
Nafaâ Adhoum

A simple and efficient new electrochemical sensor based on molecularly imprinted polymer has been developed for selective detection of an anticancer agent Etoposide (ETP). The sensor was prepared by electropolymerization via cyclic voltammetry (CV) of pyrrole onto a glassy carbon electrode (GCE) in the presence of ETP molecules. The extraction of ETP molecules embedded in the polymeric matrix was carried out by overoxidation in sodium hydroxide medium using CV. Various important parameters affecting the performance of the imprinted film (MIP) coated sensor were studied and optimized using differential pulse voltammetry (DPV). Under optimal conditions, the sensor response exhibited a linear dependence on ETP concentration (R2= 0.999) over the range 5.0×10−7M – 1.0×10−5M with a LOD (3σ/m) of 2.8×10−9M. The precision (% RSD, n=6) of the proposed sensor for intra- and interdays was found to be 0.84 and 2.46%, respectively. The selectivity of MIP/GCE sensor toward ETP was investigated in the presence of different interfering molecules including excipients and ETP metabolites. The developed sensor showed great recognition ability toward ETP and was successfully applied for its determination in injectable dosage forms and biological human fluids.


2005 ◽  
Vol 70 (2) ◽  
pp. 178-187 ◽  
Author(s):  
Wanyun Qu ◽  
Hong Wang ◽  
Kangbing Wu

An electrochemical method for the direct determination of mitomycin c (MMC), based on a multi wall carbon nanotube (MWNT)-modified electrode, has been developed. A well-shaped and highly sensitive oxidation peak at 0.79 V was observed on the MWNT-modified electrode for MMC. Further studies show strong evidence that MWNT-modified electrode significantly enhances the sensitivity of determination of MMC since the oxidation peak current of MMC increases remarkably, compared with that with a bare glassy carbon electrode. All the experimental parameters such as pH, scan rate, accumulation conditions, have been examined. A sensitive linear voltammetric response for MMC was obtained over the concentration range of 2.5 × 10-7-1.0 × 10-4 mol/l; the detection limit is 8 × 10-8 mol/l. Compared with other methods, this new-proposed method possesses advantages such as high sensitivity, fast response, low cost and simplicity. Eventually, the proposed method has been successfully employed to detect MMC in urine samples.


Author(s):  
Bhagyashri Kamble ◽  
Kalyanrao M. Garadkar ◽  
Kirankumar K. Sharma ◽  
Pravin Kamble ◽  
Shivaji Tayade ◽  
...  

In order to raise possible ways of MoO3 synthesis and improve its existing applications, MoO3 nanomaterial was successfully synthesized through the solvo-hydrothermal route by utilizing a mixture of ionic liquid (1-butyl-3-methylimidazolium bromide) as a solvent, and water as co-solvent in 1:1 ratio. The morphology and structural parameters of IL-as­sisted MoO3 product were examined by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), and scanning electron microscopy (SEM). Additionally, the surface wettability and particle size distribution were inspected using the contact angle and dynamic light scattering (DLS) analysis. Glassy carbon electrode (GCE) surface was then modified by IL-assisted MoO3. The formed IL-MoO3/GCE was employed as an electro­chemical sensor for determination of 4-nitrophenol (4-NP), which is very toxic and important pollutant. The redox behavior of 4-NP at the surface of IL-MoO3/GCE was investigated by cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques. Limits of detection (LOD) and limits of quantification (LOQ) determined from CV were found to be 6.76 and 22.5 mM, while from DPV recordings, 5.41 and 18.0 mM are found. The obtained results clearly reveal possible application of MoO3 for selective and sensitive sensing of 4-NP. The decorated electrode was successfully employed for determination of 4-NP in the river water real samples.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Pattan-Siddappa Ganesh ◽  
Ganesh Shimoga ◽  
Seok-Han Lee ◽  
Sang-Youn Kim ◽  
Eno E. Ebenso

Abstract Background A simple and simultaneous electrochemical sensing platform was fabricated by electropolymerization of allura red on glassy carbon electrode (GCE) for the interference-free detection of dihydroxy benzene isomers. Methods The modified working electrode was characterized by electrochemical and field emission scanning electron microscopy methods. The modified electrode showed excellent electrocatalytic activity for the electrooxidation of catechol (CC) and hydroquinone (HQ) at physiological pH of 7.4 by cyclic voltammetric (CV) and differential pulse voltammetric (DPV) techniques. Results The effective split in the overlapped oxidation signal of CC and HQ was achieved in a binary mixture with peak to peak separation of 0.102 V and 0.103 V by CV and DPV techniques. The electrode kinetics was found to be adsorption-controlled. The oxidation potential directly depends on the pH of the buffer solution, and it witnessed the transfer of equal number of protons and electrons in the redox phenomenon. Conclusions The limit of detection (LOD) for CC and HQ was calculated to be 0.126 μM and 0.132 μM in the linear range of 0 to 80.0 μM and 0 to 110.0 μM, respectively, by ultra-sensitive DPV technique. The practical applicability of the proposed sensor was evaluated for tap water sample analysis, and good recovery rates were observed. Graphical abstract Electrocatalytic interaction of ALR/GCE with dihydroxy benzene isomers.


1997 ◽  
Vol 9 (12) ◽  
pp. 952-955 ◽  
Author(s):  
Agustina Guiberteau Cabanillas ◽  
Teresa Galeano Díaz ◽  
Francisco Salinas ◽  
Juan Manuel Ortiz ◽  
Jean Michel Kauffmann

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