scholarly journals Electrochemically Activated Screen-Printed Carbon Electrode for Determination of Ibuprofen

2021 ◽  
Vol 11 (21) ◽  
pp. 9908
Author(s):  
Katarzyna Tyszczuk-Rotko ◽  
Jędrzej Kozak ◽  
Anna Węzińska
Keyword(s):  
Supporting Electrolyte ◽  
Pharmaceutical Formulations ◽  
Differential Pulse ◽  
Acetate Buffer Solution ◽  
Carbon Electrode ◽  
Buffer Solution ◽  
Screen Printed Carbon Electrode ◽  
Relative Errors ◽  
Screen Printed

In this study, we present a simple, sensitive and selective analytical procedure for the ibuprofen (IBP) analysis using the commercially available screen-printed carbon electrode electrochemically activated (aSPCE) by cyclic voltammetry in 0.1 M NaOH. The quantitative determinations of IBP were carried out in 0.25 M acetate buffer solution of pH 4.5 ± 0.1 using the differential-pulse voltammetry (DPV). Different experimental parameters for DPV analysis were optimized, including pH and concentration of supporting electrolyte, amplitude (ΔEA), scan rate (ν) and modulation time (tm). The linear ranges of calibration curve were from 0.50–20.0 and 20.0–500.0 µM. The detection and quantification limits were estimated to be 0.059 and 0.20 µM. The aSPCE displayed satisfactory repeatability, reproducibility, and selectivity. Furthermore, the DPV procedure with the use of aSPCE was used to determination of IBP in pharmaceutical formulations. The results achieved by DPV show satisfactory agreement with those obtained by manufacturers (the relative errors are in the range of 3.1–4.7%).

A Renewable Amperometric Immunosensor for hs-CRP Based on Functionalized Fe3O4@Au Magnetic Nanoparticles Attracted on Fe (III) Phthlocyanine/Chitosan-Membrane Modified Screen-Printed Carbon Electrode by a Magnet

2011 ◽  
Vol 110-116 ◽  
pp. 519-526 ◽  
Author(s):  
Ning Gan ◽  
Ling Hua Meng ◽  
Fu Tao Hu ◽  
Yu Ting Cao ◽  
Yuan Zhao Wu ◽  
...  
Keyword(s):  
Magnetic Nanoparticles ◽  
Rapid Determination ◽  
Phosphate Buffer Solution ◽  
Carbon Electrode ◽  
Buffer Solution ◽  
Chitosan Membrane ◽  
Screen Printed Carbon Electrode ◽  
Hs Crp ◽  
Screen Printed

A novel disposable screen-printed immunosensor for rapid determination of highly sensitive C reactiveprotein (hs-CRP) in human serum has been developed in the experiment. The sensor was constructed on one screen-printed carbon electrode (SPCE) with HRP labeled anti-hs-CRP antibody functionalized Fe3O4@Au magnetic nanoparticles (HRP labeled anti hs-CRP/ Fe3O4@Au) as the biorecognition probes attracted on the surface of Fe (III) phthalocyanine (FePc)/ chitosan membrane modified screen-printed carbon electrode (SPCE|FePc/Chit/chitosan) by external magnetic field. FePc was acted as electron immediate. The modified electrode shows an excellent electrocatalytic activity for hs-CRP in phosphate buffer solution (pH=7.0). After the immunosensor is incubated with hs-CRP antigen solution at 37°C for 20 min, the access of activity center of the HRP to electrode is partly inhibited, which leads to a linear decrease of the catalytic efficiency of the HRP to the reduction of immobilized FePc by H2O2 at –50 mV in hs-CRP’s concentration ranges from 1.2 to 200 ng/mL. The detection limit was 0.5ng/mL. The immunosensor was successfully utilized for determination of hs-CRP in real serum samples of heart disease patients, whose results were consistent with that by ELISA method. The accuracy and precision of the assay were 91.5-104.4% and 15.8-24.4%, respectively. The immunosensor was reusable once constructed and can be regenerated by adding new nanoprobes on the surface of basal electrode through magnet on its bottom. It can greatly reduce the detection cost which is valuable for the early diagnosis of tumors.

scholarly journals Determination of Mercury (II) Ion on Aryl Amide-Type Podand-Modified Glassy Carbon Electrode

2011 ◽  
Vol 2011 ◽  
pp. 1-6 ◽  
Author(s):  
Sevgi Güney ◽  
Gülcemal Yıldız ◽  
Gönül Yapar
Keyword(s):  
Glassy Carbon Electrode ◽  
Modified Electrode ◽  
Glassy Carbon ◽  
Reference Electrode ◽  
Differential Pulse ◽  
Acetate Buffer Solution ◽  
Carbon Electrode ◽  
Modified Glassy Carbon Electrode ◽  
Buffer Solution

A new voltammetric sensor based on an aryl amide type podand, 1,8-bis(o-amidophenoxy)-3,6-dioxaoctane, (AAP) modified glassy carbon electrode, was described for the determination of trace level of mercury (II) ion by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). A well-defined anodic peak corresponding to the oxidation of mercury on proposed electrode was obtained at 0.2 V versus Ag/AgCl reference electrode. The effect of experimental parameters on differential voltammetric peak currents was investigated in acetate buffer solution of pH 7.0 containing 1 × 10−1 mol L−1NaCl. Mercury (II) ion was preconcentrated at the modified electrode by forming complex with AAP under proper conditions and then reduced on the surface of the electrode. Interferences of Cu2+, Pb2+, Fe3+, Cd2+, and Zn2+ions were also studied at two different concentration ratios with respect to mercury (II) ions. The modified electrode was applied to the determination of mercury (II) ions in seawater sample.

scholarly journals Quantitative Determination of Lercanidipine Enantiomers in Commercial Formulations by Capillary Electrophoresis

2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
Luciana Pereira Lourenço ◽  
Fernando Armani Aguiar ◽  
Anderson Rodrigo Moraes de Oliveira ◽  
Cristiane Masetto de Gaitani
Keyword(s):  
Capillary Electrophoresis ◽  
Background Electrolyte ◽  
Pharmaceutical Formulations ◽  
Acetate Buffer Solution ◽  
Buffer Solution ◽  
Long Duration ◽  
Accuracy And Precision ◽  
Relative Errors ◽  
Optimum Separation

An enantioselective method based on capillary electrophoresis (CE) using cyclodextrin (CD) as chiral selector was developed and validated for determination of lercanidipine (LER) enantiomers, a drug calcium channel blocker which exerts antihypertensive effects of long duration, in a pharmaceutical formulation. Optimum separation of LER enantiomers was obtained on a 50 cm × 50 μm id capillary using a sodium acetate buffer solution 200 mmol/L pH 4.0 containing 10 mmol/L of 2,3,6-o-methyl-β-cyclodextrin (TM-β-CD) as background electrolyte. The capillary temperature and voltage were 15°C and 25 kV, respectively, hydrodynamic injection and detection at 237 nm. Linearity was obtained in the range 12.5–100 μg/mL for both enantiomers (r≥0.995). The RSD (%) and relative errors (E, %) obtained in precision and accuracy studies (intraday and interday) were lower than 5%. After validation, the method was applied to quantify the enantiomers of LER in commercial tablets and the results were satisfactory in terms of accuracy and precision, both less than 5%. Therefore, this method was found to be appropriate for enantioselective quality control of LER enantiomers in pharmaceutical formulations.

scholarly journals Carvacrol electrochemical reaction characteristics on screen printed electrode modified with La2O3/Co3O4 nanocomposite

2019 ◽  
Vol 9 (2) ◽  
pp. 113-123 ◽  
Author(s):  
Sayed Zia Mohammadi ◽  
Hadi Beitollahi ◽  
Tahereh Rohani ◽  
Hossein Allahabadi
Keyword(s):  
Limit Of Detection ◽  
Phosphate Buffer Solution ◽  
Differential Pulse ◽  
Co3o4 Nanoparticles ◽  
Electrochemical Characteristics ◽  
Screen Printed Electrode ◽  
Buffer Solution ◽  
Voltammetric Techniques ◽  
Screen Printed

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.

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