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Voltammetric sensor based on bimetallic nanocomposite for determination of favipiravir as an antiviral drug

A novel and sensitive voltammetric nanosensor was developed for the first time for trace level monitoring of favipiravir based on gold/silver core–shell nanoparticles (Au@Ag CSNPs) with conductive polymer poly (3,4-ethylene dioxythiophene) polystyrene sulfonate (PEDOT:PSS) and functionalized multi c...

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Autores principales: Mehmandoust, Mohammad, Khoshnavaz, Yasamin, Tuzen, Mustafa, Erk, Nevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626286/
https://www.ncbi.nlm.nih.gov/pubmed/34837114
http://dx.doi.org/10.1007/s00604-021-05107-2
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author Mehmandoust, Mohammad
Khoshnavaz, Yasamin
Tuzen, Mustafa
Erk, Nevin
author_facet Mehmandoust, Mohammad
Khoshnavaz, Yasamin
Tuzen, Mustafa
Erk, Nevin
author_sort Mehmandoust, Mohammad
collection PubMed
description A novel and sensitive voltammetric nanosensor was developed for the first time for trace level monitoring of favipiravir based on gold/silver core–shell nanoparticles (Au@Ag CSNPs) with conductive polymer poly (3,4-ethylene dioxythiophene) polystyrene sulfonate (PEDOT:PSS) and functionalized multi carbon nanotubes (F-MWCNTs) on a glassy carbon electrode (GCE). The formation of Au@Ag CSNPs/PEDOT:PSS/F-MWCNT composite was confirmed by various analytical techniques, including X-ray diffraction (XRD), ultraviolet–visible spectroscopy (UV–Vis), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), and field-emission scanning electron microscopy (SEM). Under the optimized conditions and at a typical working potential of + 1.23 V (vs. Ag/AgCl), the Au@Ag CSNPs/PEDOT:PSS/F-MWCNT/GCE revealed linear quantitative ranges from 0.005 to 0.009 and 0.009 to 1.95 µM with a limit of detection 0.46 nM (S/N = 3) with acceptable relative standard deviations (1.1-4.9 %) for pharmaceutical formulations, urine, and human plasma samples without applying any sample pretreatment (1.12–4.93%). The interference effect of antiviral drugs, biological compounds, and amino acids was negligible, and the sensing system demonstrated outstanding reproducibility, repeatability, stability, and reusability. The findings revealed that this assay strategy has promising applications in diagnosing FAV in clinical samples, which could be attributed to the large surface area on active sites and high conductivity of bimetallic nanocomposite. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00604-021-05107-2.
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spelling pubmed-86262862021-11-29 Voltammetric sensor based on bimetallic nanocomposite for determination of favipiravir as an antiviral drug Mehmandoust, Mohammad Khoshnavaz, Yasamin Tuzen, Mustafa Erk, Nevin Mikrochim Acta Original Paper A novel and sensitive voltammetric nanosensor was developed for the first time for trace level monitoring of favipiravir based on gold/silver core–shell nanoparticles (Au@Ag CSNPs) with conductive polymer poly (3,4-ethylene dioxythiophene) polystyrene sulfonate (PEDOT:PSS) and functionalized multi carbon nanotubes (F-MWCNTs) on a glassy carbon electrode (GCE). The formation of Au@Ag CSNPs/PEDOT:PSS/F-MWCNT composite was confirmed by various analytical techniques, including X-ray diffraction (XRD), ultraviolet–visible spectroscopy (UV–Vis), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), and field-emission scanning electron microscopy (SEM). Under the optimized conditions and at a typical working potential of + 1.23 V (vs. Ag/AgCl), the Au@Ag CSNPs/PEDOT:PSS/F-MWCNT/GCE revealed linear quantitative ranges from 0.005 to 0.009 and 0.009 to 1.95 µM with a limit of detection 0.46 nM (S/N = 3) with acceptable relative standard deviations (1.1-4.9 %) for pharmaceutical formulations, urine, and human plasma samples without applying any sample pretreatment (1.12–4.93%). The interference effect of antiviral drugs, biological compounds, and amino acids was negligible, and the sensing system demonstrated outstanding reproducibility, repeatability, stability, and reusability. The findings revealed that this assay strategy has promising applications in diagnosing FAV in clinical samples, which could be attributed to the large surface area on active sites and high conductivity of bimetallic nanocomposite. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00604-021-05107-2. Springer Vienna 2021-11-27 2021 /pmc/articles/PMC8626286/ /pubmed/34837114 http://dx.doi.org/10.1007/s00604-021-05107-2 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Paper
Mehmandoust, Mohammad
Khoshnavaz, Yasamin
Tuzen, Mustafa
Erk, Nevin
Voltammetric sensor based on bimetallic nanocomposite for determination of favipiravir as an antiviral drug
title Voltammetric sensor based on bimetallic nanocomposite for determination of favipiravir as an antiviral drug
title_full Voltammetric sensor based on bimetallic nanocomposite for determination of favipiravir as an antiviral drug
title_fullStr Voltammetric sensor based on bimetallic nanocomposite for determination of favipiravir as an antiviral drug
title_full_unstemmed Voltammetric sensor based on bimetallic nanocomposite for determination of favipiravir as an antiviral drug
title_short Voltammetric sensor based on bimetallic nanocomposite for determination of favipiravir as an antiviral drug
title_sort voltammetric sensor based on bimetallic nanocomposite for determination of favipiravir as an antiviral drug
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626286/
https://www.ncbi.nlm.nih.gov/pubmed/34837114
http://dx.doi.org/10.1007/s00604-021-05107-2
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