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First Screen-Printed Sensor (Electrochemically Activated Screen-Printed Boron-Doped Diamond Electrode) for Quantitative Determination of Rifampicin by Adsorptive Stripping Voltammetry

In this paper, a screen-printed boron-doped electrode (aSPBDDE) was subjected to electrochemical activation by cyclic voltammetry (CV) in 0.1 M NaOH and the response to rifampicin (RIF) oxidation was used as a testing probe. Changes in surface morphology and electrochemical behaviour of RIF before a...

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Autores principales: Kozak, Jędrzej, Tyszczuk-Rotko, Katarzyna, Wójciak, Magdalena, Sowa, Ireneusz, Rotko, Marek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8347414/
https://www.ncbi.nlm.nih.gov/pubmed/34361425
http://dx.doi.org/10.3390/ma14154231
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author Kozak, Jędrzej
Tyszczuk-Rotko, Katarzyna
Wójciak, Magdalena
Sowa, Ireneusz
Rotko, Marek
author_facet Kozak, Jędrzej
Tyszczuk-Rotko, Katarzyna
Wójciak, Magdalena
Sowa, Ireneusz
Rotko, Marek
author_sort Kozak, Jędrzej
collection PubMed
description In this paper, a screen-printed boron-doped electrode (aSPBDDE) was subjected to electrochemical activation by cyclic voltammetry (CV) in 0.1 M NaOH and the response to rifampicin (RIF) oxidation was used as a testing probe. Changes in surface morphology and electrochemical behaviour of RIF before and after the electrochemical activation of SPBDDE were studied by scanning electron microscopy (SEM), CV and electrochemical impedance spectroscopy (EIS). The increase in number and size of pores in the modifier layer and reduction of charge transfer residence were likely responsible for electrochemical improvement of the analytical signal from RIF at the SPBDDE. Quantitative analysis of RIF by using differential pulse adsorptive stripping voltammetry in 0.1 mol L(−1) solution of PBS of pH 3.0 ± 0.1 at the aSPBDDE was carried out. Using optimized conditions (E(acc) of −0.45 V, t(acc) of 120 s, ΔE(A) of 150 mV, ν of 100 mV s(−1) and t(m) of 5 ms), the RIF peak current increased linearly with the concentration in the four ranges: 0.002–0.02, 0.02–0.2, 0.2–2.0, and 2.0–20.0 nM. The limits of detection and quantification were calculated at 0.22 and 0.73 pM. The aSPBDDE showed satisfactory repeatability, reproducibility, and selectivity towards potential interferences. The applicability of the aSPBDDE for control analysis of RIF was demonstrated using river water samples and certified reference material of bovine urine.
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spelling pubmed-83474142021-08-08 First Screen-Printed Sensor (Electrochemically Activated Screen-Printed Boron-Doped Diamond Electrode) for Quantitative Determination of Rifampicin by Adsorptive Stripping Voltammetry Kozak, Jędrzej Tyszczuk-Rotko, Katarzyna Wójciak, Magdalena Sowa, Ireneusz Rotko, Marek Materials (Basel) Article In this paper, a screen-printed boron-doped electrode (aSPBDDE) was subjected to electrochemical activation by cyclic voltammetry (CV) in 0.1 M NaOH and the response to rifampicin (RIF) oxidation was used as a testing probe. Changes in surface morphology and electrochemical behaviour of RIF before and after the electrochemical activation of SPBDDE were studied by scanning electron microscopy (SEM), CV and electrochemical impedance spectroscopy (EIS). The increase in number and size of pores in the modifier layer and reduction of charge transfer residence were likely responsible for electrochemical improvement of the analytical signal from RIF at the SPBDDE. Quantitative analysis of RIF by using differential pulse adsorptive stripping voltammetry in 0.1 mol L(−1) solution of PBS of pH 3.0 ± 0.1 at the aSPBDDE was carried out. Using optimized conditions (E(acc) of −0.45 V, t(acc) of 120 s, ΔE(A) of 150 mV, ν of 100 mV s(−1) and t(m) of 5 ms), the RIF peak current increased linearly with the concentration in the four ranges: 0.002–0.02, 0.02–0.2, 0.2–2.0, and 2.0–20.0 nM. The limits of detection and quantification were calculated at 0.22 and 0.73 pM. The aSPBDDE showed satisfactory repeatability, reproducibility, and selectivity towards potential interferences. The applicability of the aSPBDDE for control analysis of RIF was demonstrated using river water samples and certified reference material of bovine urine. MDPI 2021-07-29 /pmc/articles/PMC8347414/ /pubmed/34361425 http://dx.doi.org/10.3390/ma14154231 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kozak, Jędrzej
Tyszczuk-Rotko, Katarzyna
Wójciak, Magdalena
Sowa, Ireneusz
Rotko, Marek
First Screen-Printed Sensor (Electrochemically Activated Screen-Printed Boron-Doped Diamond Electrode) for Quantitative Determination of Rifampicin by Adsorptive Stripping Voltammetry
title First Screen-Printed Sensor (Electrochemically Activated Screen-Printed Boron-Doped Diamond Electrode) for Quantitative Determination of Rifampicin by Adsorptive Stripping Voltammetry
title_full First Screen-Printed Sensor (Electrochemically Activated Screen-Printed Boron-Doped Diamond Electrode) for Quantitative Determination of Rifampicin by Adsorptive Stripping Voltammetry
title_fullStr First Screen-Printed Sensor (Electrochemically Activated Screen-Printed Boron-Doped Diamond Electrode) for Quantitative Determination of Rifampicin by Adsorptive Stripping Voltammetry
title_full_unstemmed First Screen-Printed Sensor (Electrochemically Activated Screen-Printed Boron-Doped Diamond Electrode) for Quantitative Determination of Rifampicin by Adsorptive Stripping Voltammetry
title_short First Screen-Printed Sensor (Electrochemically Activated Screen-Printed Boron-Doped Diamond Electrode) for Quantitative Determination of Rifampicin by Adsorptive Stripping Voltammetry
title_sort first screen-printed sensor (electrochemically activated screen-printed boron-doped diamond electrode) for quantitative determination of rifampicin by adsorptive stripping voltammetry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8347414/
https://www.ncbi.nlm.nih.gov/pubmed/34361425
http://dx.doi.org/10.3390/ma14154231
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