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Core–shell nanocomposite of flower-like molybdenum disulfide nanospheres and molecularly imprinted polymers for electrochemical detection of anti COVID-19 drug favipiravir in biological samples

A novel electrochemical sensor is reported for the detection of the antiviral drug favipiravir based on the core–shell nanocomposite of flower-like molybdenum disulfide (MoS(2)) nanospheres and molecularly imprinted polymers (MIPs). The MoS(2)@MIP core–shell nanocomposite was prepared via the electr...

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Detalles Bibliográficos
Autores principales: Wang, Shuang, Wang, Chen, Xin, Yuxiao, Li, Qiuyun, Liu, Weilu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885316/
https://www.ncbi.nlm.nih.gov/pubmed/35229221
http://dx.doi.org/10.1007/s00604-022-05213-9
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author Wang, Shuang
Wang, Chen
Xin, Yuxiao
Li, Qiuyun
Liu, Weilu
author_facet Wang, Shuang
Wang, Chen
Xin, Yuxiao
Li, Qiuyun
Liu, Weilu
author_sort Wang, Shuang
collection PubMed
description A novel electrochemical sensor is reported for the detection of the antiviral drug favipiravir based on the core–shell nanocomposite of flower-like molybdenum disulfide (MoS(2)) nanospheres and molecularly imprinted polymers (MIPs). The MoS(2)@MIP core–shell nanocomposite was prepared via the electrodeposition of a MIP layer on the MoS(2) modified electrode, using o-phenylenediamine as the monomer and favipiravir as the template. The selective binding of target favipiravir at the MoS(2)@MIP core–shell nanocomposite produced a redox signal in a concentration dependent manner, which was used for the quantitative analysis. The preparation process of the MoS(2)@MIP core–shell nanocomposite was optimized. Under the optimal conditions, the sensor exhibited a wide linear response range of 0.01 ~ 100 nM (1.57*10(−6) ~ 1.57*10(−2) μg mL(−1)) and a low detection limit of 0.002 nM (3.14*10(−7) μg mL(−1)). Application of the sensor was demonstrated by detecting favipiravir in a minimum amount of 10 μL biological samples (urine and plasma). Satisfied results in the recovery tests indicated a high potential of favipiravir monitoring in infectious COVID-19 samples. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00604-022-05213-9.
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spelling pubmed-88853162022-03-01 Core–shell nanocomposite of flower-like molybdenum disulfide nanospheres and molecularly imprinted polymers for electrochemical detection of anti COVID-19 drug favipiravir in biological samples Wang, Shuang Wang, Chen Xin, Yuxiao Li, Qiuyun Liu, Weilu Mikrochim Acta Original Paper A novel electrochemical sensor is reported for the detection of the antiviral drug favipiravir based on the core–shell nanocomposite of flower-like molybdenum disulfide (MoS(2)) nanospheres and molecularly imprinted polymers (MIPs). The MoS(2)@MIP core–shell nanocomposite was prepared via the electrodeposition of a MIP layer on the MoS(2) modified electrode, using o-phenylenediamine as the monomer and favipiravir as the template. The selective binding of target favipiravir at the MoS(2)@MIP core–shell nanocomposite produced a redox signal in a concentration dependent manner, which was used for the quantitative analysis. The preparation process of the MoS(2)@MIP core–shell nanocomposite was optimized. Under the optimal conditions, the sensor exhibited a wide linear response range of 0.01 ~ 100 nM (1.57*10(−6) ~ 1.57*10(−2) μg mL(−1)) and a low detection limit of 0.002 nM (3.14*10(−7) μg mL(−1)). Application of the sensor was demonstrated by detecting favipiravir in a minimum amount of 10 μL biological samples (urine and plasma). Satisfied results in the recovery tests indicated a high potential of favipiravir monitoring in infectious COVID-19 samples. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00604-022-05213-9. Springer Vienna 2022-03-01 2022 /pmc/articles/PMC8885316/ /pubmed/35229221 http://dx.doi.org/10.1007/s00604-022-05213-9 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2022 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
Wang, Shuang
Wang, Chen
Xin, Yuxiao
Li, Qiuyun
Liu, Weilu
Core–shell nanocomposite of flower-like molybdenum disulfide nanospheres and molecularly imprinted polymers for electrochemical detection of anti COVID-19 drug favipiravir in biological samples
title Core–shell nanocomposite of flower-like molybdenum disulfide nanospheres and molecularly imprinted polymers for electrochemical detection of anti COVID-19 drug favipiravir in biological samples
title_full Core–shell nanocomposite of flower-like molybdenum disulfide nanospheres and molecularly imprinted polymers for electrochemical detection of anti COVID-19 drug favipiravir in biological samples
title_fullStr Core–shell nanocomposite of flower-like molybdenum disulfide nanospheres and molecularly imprinted polymers for electrochemical detection of anti COVID-19 drug favipiravir in biological samples
title_full_unstemmed Core–shell nanocomposite of flower-like molybdenum disulfide nanospheres and molecularly imprinted polymers for electrochemical detection of anti COVID-19 drug favipiravir in biological samples
title_short Core–shell nanocomposite of flower-like molybdenum disulfide nanospheres and molecularly imprinted polymers for electrochemical detection of anti COVID-19 drug favipiravir in biological samples
title_sort core–shell nanocomposite of flower-like molybdenum disulfide nanospheres and molecularly imprinted polymers for electrochemical detection of anti covid-19 drug favipiravir in biological samples
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885316/
https://www.ncbi.nlm.nih.gov/pubmed/35229221
http://dx.doi.org/10.1007/s00604-022-05213-9
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