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A Sensor Array Based on Molecularly Imprinted Polymers and Machine Learning for the Analysis of Fluoroquinolone Antibiotics
[Image: see text] Fluoroquinolones (FQs) are one of the most important types of antibiotics in the clinical, poultry, and aquaculture industries, and their monitoring is required as the abuse has led to severe issues, such as antibiotic residues and antimicrobial resistance. In this study, we report...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706806/ https://www.ncbi.nlm.nih.gov/pubmed/36281963 http://dx.doi.org/10.1021/acssensors.2c01260 |
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author | Wang, Mingyue Cetó, Xavier del Valle, Manel |
author_facet | Wang, Mingyue Cetó, Xavier del Valle, Manel |
author_sort | Wang, Mingyue |
collection | PubMed |
description | [Image: see text] Fluoroquinolones (FQs) are one of the most important types of antibiotics in the clinical, poultry, and aquaculture industries, and their monitoring is required as the abuse has led to severe issues, such as antibiotic residues and antimicrobial resistance. In this study, we report a voltammetric electronic tongue (ET) for the simultaneous determination of ciprofloxacin, levofloxacin, and moxifloxacin in both pharmaceutical and biological samples. The ET comprises four sensors modified with three different customized molecularly imprinted polymers (MIPs) and a nonimprinted polymer integrated with Au nanoparticle-decorated multiwall carbon nanotubes (Au-fMWCNTs). MWCNTs were first functionalized to serve as a supporting substrate, while the anchored Au nanoparticles acted as a catalyst. Subsequently, MIP films were obtained by electropolymerization of pyrrole in the presence of the different target FQs. The sensors’ morphology was characterized by scanning electron microscopy and transmission electron microscopy, while the modification process was followed electrochemically step by step employing [Fe(CN)(6)](3–/4–) as the redox probe. Under the optimal conditions, the MIP(FQs)@Au-fMWCNT sensors exhibited different responses, limits of detection of ca. 1 μM, and a wide detection range up to 300 μM for the three FQs. Lastly, the developed ET presents satisfactory agreement between the expected and obtained values when used for the simultaneous determination of mixtures of the three FQs (R(2) ≥0.960, testing subset), which was also applied to the analysis of FQs in commercial pharmaceuticals and spiked human urine samples. |
format | Online Article Text |
id | pubmed-9706806 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-97068062022-11-30 A Sensor Array Based on Molecularly Imprinted Polymers and Machine Learning for the Analysis of Fluoroquinolone Antibiotics Wang, Mingyue Cetó, Xavier del Valle, Manel ACS Sens [Image: see text] Fluoroquinolones (FQs) are one of the most important types of antibiotics in the clinical, poultry, and aquaculture industries, and their monitoring is required as the abuse has led to severe issues, such as antibiotic residues and antimicrobial resistance. In this study, we report a voltammetric electronic tongue (ET) for the simultaneous determination of ciprofloxacin, levofloxacin, and moxifloxacin in both pharmaceutical and biological samples. The ET comprises four sensors modified with three different customized molecularly imprinted polymers (MIPs) and a nonimprinted polymer integrated with Au nanoparticle-decorated multiwall carbon nanotubes (Au-fMWCNTs). MWCNTs were first functionalized to serve as a supporting substrate, while the anchored Au nanoparticles acted as a catalyst. Subsequently, MIP films were obtained by electropolymerization of pyrrole in the presence of the different target FQs. The sensors’ morphology was characterized by scanning electron microscopy and transmission electron microscopy, while the modification process was followed electrochemically step by step employing [Fe(CN)(6)](3–/4–) as the redox probe. Under the optimal conditions, the MIP(FQs)@Au-fMWCNT sensors exhibited different responses, limits of detection of ca. 1 μM, and a wide detection range up to 300 μM for the three FQs. Lastly, the developed ET presents satisfactory agreement between the expected and obtained values when used for the simultaneous determination of mixtures of the three FQs (R(2) ≥0.960, testing subset), which was also applied to the analysis of FQs in commercial pharmaceuticals and spiked human urine samples. American Chemical Society 2022-10-25 2022-11-25 /pmc/articles/PMC9706806/ /pubmed/36281963 http://dx.doi.org/10.1021/acssensors.2c01260 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Wang, Mingyue Cetó, Xavier del Valle, Manel A Sensor Array Based on Molecularly Imprinted Polymers and Machine Learning for the Analysis of Fluoroquinolone Antibiotics |
title | A Sensor Array
Based on Molecularly Imprinted Polymers
and Machine Learning for the Analysis of Fluoroquinolone Antibiotics |
title_full | A Sensor Array
Based on Molecularly Imprinted Polymers
and Machine Learning for the Analysis of Fluoroquinolone Antibiotics |
title_fullStr | A Sensor Array
Based on Molecularly Imprinted Polymers
and Machine Learning for the Analysis of Fluoroquinolone Antibiotics |
title_full_unstemmed | A Sensor Array
Based on Molecularly Imprinted Polymers
and Machine Learning for the Analysis of Fluoroquinolone Antibiotics |
title_short | A Sensor Array
Based on Molecularly Imprinted Polymers
and Machine Learning for the Analysis of Fluoroquinolone Antibiotics |
title_sort | sensor array
based on molecularly imprinted polymers
and machine learning for the analysis of fluoroquinolone antibiotics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706806/ https://www.ncbi.nlm.nih.gov/pubmed/36281963 http://dx.doi.org/10.1021/acssensors.2c01260 |
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