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Sensitive Determination of SARS-COV-2 and the Anti-hepatitis C Virus Agent Velpatasvir Enabled by Novel Metal–Organic Frameworks
[Image: see text] Herein, we report on the electrochemical determination of velpatasvir (VLP) as the main constituent of Epclusa, a SARS-COV-2 and anti-hepatitis C virus (HCV) agent, using a novel metal–organic framework (MOF). The NH(2)-MIL-53(Al) MOF was successfully modified with 5-bromo-salicyla...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515823/ https://www.ncbi.nlm.nih.gov/pubmed/34661033 http://dx.doi.org/10.1021/acsomega.1c04525 |
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author | Saleh, Mahmoud A. Mohamed, Mona A. Shahat, Ahmed Allam, Nageh K. |
author_facet | Saleh, Mahmoud A. Mohamed, Mona A. Shahat, Ahmed Allam, Nageh K. |
author_sort | Saleh, Mahmoud A. |
collection | PubMed |
description | [Image: see text] Herein, we report on the electrochemical determination of velpatasvir (VLP) as the main constituent of Epclusa, a SARS-COV-2 and anti-hepatitis C virus (HCV) agent, using a novel metal–organic framework (MOF). The NH(2)-MIL-53(Al) MOF was successfully modified with 5-bromo-salicylaldehyde to synthesize 5-BSA=N-MIL-53(Al) MOF. The synthesized MOF has been characterized using Fourier transform infrared spectroscopy, X-ray powder diffraction, scanning electron microscopy, cyclic voltammetry, square wave voltammetry, and electrochemical impedance spectroscopy. The modified MOF showed higher electrochemical activity and response than the bare NH(2)-MIL-53(Al) MOF. Compared to the bare carbon paste electrode (CPE), the 5-BSA=N-MIL-53(Al)/CPE platform was shown to enhance the electrochemical oxidation and detection of the anti-SARS-COV-2 and anti-HCV agent. Under optimized conditions, the 5-BSA=N-MIL-53(Al)/CPE platform showed a linear range of 1.11 × 10(–6) to 1.11 × 10(–7) and 1.11 × 10(–7) to 25.97 × 10(–6) M Britton–Robinson buffer (pH 7) with a detection limit and limit of quantification of 8.776 × 10(–9) and 2.924 × 10(–8) M, respectively. Repeatability, storage stability, and reproducibility in addition to selectivity studies and interference studies were conducted to illustrate the superiority of the electrode material. The study also included a highly accurate platform for the determination of VLP concentrations in both urine and plasma samples with reasonable recovery. |
format | Online Article Text |
id | pubmed-8515823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-85158232021-10-15 Sensitive Determination of SARS-COV-2 and the Anti-hepatitis C Virus Agent Velpatasvir Enabled by Novel Metal–Organic Frameworks Saleh, Mahmoud A. Mohamed, Mona A. Shahat, Ahmed Allam, Nageh K. ACS Omega [Image: see text] Herein, we report on the electrochemical determination of velpatasvir (VLP) as the main constituent of Epclusa, a SARS-COV-2 and anti-hepatitis C virus (HCV) agent, using a novel metal–organic framework (MOF). The NH(2)-MIL-53(Al) MOF was successfully modified with 5-bromo-salicylaldehyde to synthesize 5-BSA=N-MIL-53(Al) MOF. The synthesized MOF has been characterized using Fourier transform infrared spectroscopy, X-ray powder diffraction, scanning electron microscopy, cyclic voltammetry, square wave voltammetry, and electrochemical impedance spectroscopy. The modified MOF showed higher electrochemical activity and response than the bare NH(2)-MIL-53(Al) MOF. Compared to the bare carbon paste electrode (CPE), the 5-BSA=N-MIL-53(Al)/CPE platform was shown to enhance the electrochemical oxidation and detection of the anti-SARS-COV-2 and anti-HCV agent. Under optimized conditions, the 5-BSA=N-MIL-53(Al)/CPE platform showed a linear range of 1.11 × 10(–6) to 1.11 × 10(–7) and 1.11 × 10(–7) to 25.97 × 10(–6) M Britton–Robinson buffer (pH 7) with a detection limit and limit of quantification of 8.776 × 10(–9) and 2.924 × 10(–8) M, respectively. Repeatability, storage stability, and reproducibility in addition to selectivity studies and interference studies were conducted to illustrate the superiority of the electrode material. The study also included a highly accurate platform for the determination of VLP concentrations in both urine and plasma samples with reasonable recovery. American Chemical Society 2021-09-30 /pmc/articles/PMC8515823/ /pubmed/34661033 http://dx.doi.org/10.1021/acsomega.1c04525 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Saleh, Mahmoud A. Mohamed, Mona A. Shahat, Ahmed Allam, Nageh K. Sensitive Determination of SARS-COV-2 and the Anti-hepatitis C Virus Agent Velpatasvir Enabled by Novel Metal–Organic Frameworks |
title | Sensitive Determination of SARS-COV-2 and the
Anti-hepatitis C Virus Agent Velpatasvir Enabled by Novel Metal–Organic
Frameworks |
title_full | Sensitive Determination of SARS-COV-2 and the
Anti-hepatitis C Virus Agent Velpatasvir Enabled by Novel Metal–Organic
Frameworks |
title_fullStr | Sensitive Determination of SARS-COV-2 and the
Anti-hepatitis C Virus Agent Velpatasvir Enabled by Novel Metal–Organic
Frameworks |
title_full_unstemmed | Sensitive Determination of SARS-COV-2 and the
Anti-hepatitis C Virus Agent Velpatasvir Enabled by Novel Metal–Organic
Frameworks |
title_short | Sensitive Determination of SARS-COV-2 and the
Anti-hepatitis C Virus Agent Velpatasvir Enabled by Novel Metal–Organic
Frameworks |
title_sort | sensitive determination of sars-cov-2 and the
anti-hepatitis c virus agent velpatasvir enabled by novel metal–organic
frameworks |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515823/ https://www.ncbi.nlm.nih.gov/pubmed/34661033 http://dx.doi.org/10.1021/acsomega.1c04525 |
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