Simple Electrochemical Chloramphenicol Assay at a Disposable Pencil Graphite Electrode by Square Wave Voltammetry and Linear Sweep Voltammetry

2021 ◽  
pp. 1-18
Author(s):  
Iulia Gabriela David ◽  
Mihaela Buleandră ◽  
Dana Elena Popa ◽  
Ana Maria Bercea ◽  
Anton Alexandru Ciucu
2020 ◽  
Author(s):  
Guilherme Figueira Alves ◽  
Thalles Pedrosa Lisboa ◽  
Lucas Vinícius Faria ◽  
Davi Marques Farias ◽  
Maria Auxiliadora Costa Matos ◽  
...  

2001 ◽  
Vol 66 (3) ◽  
pp. 434-444 ◽  
Author(s):  
Šebojka Komorsky-Lovrić ◽  
Milivoj Lovrić ◽  
Fritz Scholz

Drops of nitrobenzene and 1,2-dichloroethane with 0.1 M decamethylferrocene (dmfc) are attached to the surface of a paraffin-impregnated graphite electrode and immersed into various aqueous electrolytes. The oxidation of dmfc and the reduction of dmfc+ cation are enabled by simultaneous transfers of anions between the aqueous electrolyte and the organic solvents. Square-wave voltammetry of this reaction is reported. A linear relationship was observed between the peak potentials of dmfc and the standard Galvani potential differences of the anions. The influence of the anion concentration on this relation is explained.


2009 ◽  
Vol 74 (10) ◽  
pp. 1455-1466 ◽  
Author(s):  
Sławomira Skrzypek ◽  
Agnieszka Nosal-Wiercińska ◽  
Witold Ciesielski

Although ganciclovir (gan) as a purine analogue is a compound of biological interest (antiviral drug), it has been rarely electrochemically studied. In this paper surface catalytic electrode mechanism based on the hydrogen evolution reaction is analyzed under conditions of square-wave voltammetry and differential capacity curves of double layer measurements. The electrode mechanism is assumed to involve a preceding chemical reaction in which the adsorbed catalyst (ganads) is protonated at the electrode surface, i.e., ganads + H+aq → ganH+ads. The protonated form of the catalyst (ganH+ads) is irreversibly reduced at potential about –1.35 V vs Ag|AgCl, yielding the initial form of the catalyst and atomic hydrogen, i.e., ganH+ads + e → ganads + Haq. Changes of zero charge potential and surface tension point to the adsorption of ganciclovir molecule directed with guanine group to the mercury surface and suggests that ganciclovir molecules are not placed flat on the mercury surface. The effect of adsorption on mercury electrode was studied in detail in respect to analytical usefulness of the obtained results. A new catalytic method for voltammetric determination of ganciclovir was developed. The detection and quantification limits were 1.3 × 10–7 and 4.3 × 10–7 mol l–1 for square-wave voltammetry, and 1.4 × 10–7 and 4.7 × 10–7 mol l–1 for linear-sweep voltammetry.


2010 ◽  
Vol 22 (24) ◽  
pp. 2879-2883 ◽  
Author(s):  
Eva Vrublová ◽  
Jitka Ulrichová ◽  
Vilím Šimánek ◽  
Miroslav Fojta ◽  
Jan Vacek

2018 ◽  
Vol 69 (10) ◽  
pp. 2858-2862
Author(s):  
Mihaela Buleandra ◽  
Anton Alexandru Ciucu ◽  
Dragos Cristian Stefanescu

A novel voltammetric assay for captopril (CAP) determination by using an electrochemically pretreated pencil graphite electrode (PGE*) is presented. The electrochemical oxidation reaction of CAP was investigated with PGE* by using cyclic voltammetry and linear sweep voltammetry techniques. CAP was electrochemically inactive at the non-pretreated pencil graphite electrode surface, while a sharp anodic wave with an anodic peak potential at around 200 mV resulted by using the PGE*. According to kinetic studies upon the electrode behavior, a new reaction mechanism for electrochemical oxidation of captopril is proposed. The sensor was examined as a selective, simple and precise new electrochemical disposable electrode for the determination of CAP in pharmaceutical samples in complex medical cases associated with sleep apnea, with good results.


2020 ◽  
Vol 16 (3) ◽  
pp. 341-348
Author(s):  
Surinya Traipop ◽  
Suchada Chuanuwatanakul ◽  
Orawon Chailapakul ◽  
Eakkasit Punrat

Background: Recently, Derris scandens, a Thai herbal medicine with anti-inflammatory activity, is widely used as beverage and supplementary food. When the traditional medicine is a choice for health therapy, the simple and reliable equipment is required to control the suitable consuming amount of the active component. Objective: To develop the electrochemical sensor for genistein determination in Derris scandens with high sensitivity and rapid operation. Methods: An in-house screen-printed electrochemical sensor consisting of a three-electrode system was developed for genistein determination. A silver/silver chloride (Ag/AgCl) reference electrode, a carbon counter electrode and a carbon working electrode were prepared on a 0.3-mm-thick plastic substrate by the screen-printing technique using conductive ink. The dimensions of each sensor were 2.5×1.0 cm. Only 50 µL of sample solution was required on this device for the determination of genistein concentration by rapid response square wave voltammetry. Results: The oxidation peak of genistein appeared with good response in acidic media at a peak potential of 0.6 V. Moreover, the signal was enhanced by modifying the conductive carbon ink with cobalt( II) phthalocyanine. Under the optimized conditions, the linear range was found to be 2.5-150 µM and the detection limit was 1.5 µM. Moreover, the small volume extraction was successfully developed without any further pre-concentration. This proposed method was applied to determine genistein in Derris scandens with satisfying results. Conclusion: The proposed method is promising as an alternative method for genistein determination with facile and fast analysis.


2009 ◽  
Vol 74 (10) ◽  
pp. 1489-1501 ◽  
Author(s):  
Marina Zelić ◽  
Milivoj Lovrić

Isopotential points in square-wave voltammetry are described for the first time. Model calculations and real measurements (performed with UO22+ and Eu3+ in perchlorate and bromide solutions, respectively) indicate that such an intersection could be observed when backward components of the net response, resulting from an increase in frequency or reactant concentration, are presented together. The electrode reaction should be fully reversible because quasireversible or slower electron transfer processes give the isopoints only at increasing reactant concentrations but not at increasing square-wave frequencies. The effect could be used as an additional diagnostic criterion for recognition of reversible electrode reactions where products remain dissolved in the electrolyte solution.


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