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Synthesis, spectroscopic and computational characterization of charge transfer complex of remdesivir with chloranilic acid: Application to development of novel 96-microwell spectrophotometric assay

Remdesivir (REM) is an adenosine triphosphate analog antiviral drug that has received authorization from European Commission and approval from the U.S. Food and Drug Administration for treatment of coronavirus disease 2019 (Covid-19). This study, describes, for the first time, the synthesis of a nov...

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Autores principales: Darwish, Ibrahim A., Khalil, Nasr Y., Darwish, Hany W., Alzoman, Nourah Z., Al-Hossaini, Abdullah M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013485/
https://www.ncbi.nlm.nih.gov/pubmed/35465174
http://dx.doi.org/10.1016/j.molstruc.2022.133104
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author Darwish, Ibrahim A.
Khalil, Nasr Y.
Darwish, Hany W.
Alzoman, Nourah Z.
Al-Hossaini, Abdullah M.
author_facet Darwish, Ibrahim A.
Khalil, Nasr Y.
Darwish, Hany W.
Alzoman, Nourah Z.
Al-Hossaini, Abdullah M.
author_sort Darwish, Ibrahim A.
collection PubMed
description Remdesivir (REM) is an adenosine triphosphate analog antiviral drug that has received authorization from European Commission and approval from the U.S. Food and Drug Administration for treatment of coronavirus disease 2019 (Covid-19). This study, describes, for the first time, the synthesis of a novel charge transfer complex (CTC) between REM, as electron donor, with chloranilic acid (CLA), as π electron acceptor. The CTC was characterized using different spectroscopic and thermogravimetric techniques. UV–visible spectroscopy ascertained the formation of the CTC in methanol via formation of a new broad absorption band with maximum absorption peak (λ(max)) at 530 nm. The molar absorptivity (ε) of the complex was 3.33 × 10(3) L mol(−1) cm(−1) and its band gap energy was 1.91 eV. The stoichiometric ratio of REM:CLA was found to be 1:1. The association constant of the complex was 1.11 × 10(9) L mol(−1), and its standard free energy was 5.16 × 10(4) J mole(−1). Computational calculation for atomic charges of energy minimized REM was conducted, the site of interaction on REM molecule was assigned and the mechanism of the reaction was postulated. The solid-state CTC was further characterized by FT-IR and (1)H NMR spectroscopic techniques. Both FT-IR and (1)H NMR confirmed the formation of the CTC and its structure. The reaction was adopted as a basis for developing a novel 96-microwell spectrophotometric method (MW-SPA) for REM. The assay limits of detection and quantitation were 3.57 and 10.83 µg/well, respectively. The assay was validated, and all validation parameters were acceptable. The assay was implemented successfully with great precision and accuracy to the determination of REM in its bulk form and pharmaceutical formulation (injection). This assay is simple, economic, and more importantly, has high throughput property. Therefore, the assay can be valuable for routine in quality control laboratories for analysis of REM's bulk form and pharmaceutical injection.
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spelling pubmed-90134852022-04-18 Synthesis, spectroscopic and computational characterization of charge transfer complex of remdesivir with chloranilic acid: Application to development of novel 96-microwell spectrophotometric assay Darwish, Ibrahim A. Khalil, Nasr Y. Darwish, Hany W. Alzoman, Nourah Z. Al-Hossaini, Abdullah M. J Mol Struct Article Remdesivir (REM) is an adenosine triphosphate analog antiviral drug that has received authorization from European Commission and approval from the U.S. Food and Drug Administration for treatment of coronavirus disease 2019 (Covid-19). This study, describes, for the first time, the synthesis of a novel charge transfer complex (CTC) between REM, as electron donor, with chloranilic acid (CLA), as π electron acceptor. The CTC was characterized using different spectroscopic and thermogravimetric techniques. UV–visible spectroscopy ascertained the formation of the CTC in methanol via formation of a new broad absorption band with maximum absorption peak (λ(max)) at 530 nm. The molar absorptivity (ε) of the complex was 3.33 × 10(3) L mol(−1) cm(−1) and its band gap energy was 1.91 eV. The stoichiometric ratio of REM:CLA was found to be 1:1. The association constant of the complex was 1.11 × 10(9) L mol(−1), and its standard free energy was 5.16 × 10(4) J mole(−1). Computational calculation for atomic charges of energy minimized REM was conducted, the site of interaction on REM molecule was assigned and the mechanism of the reaction was postulated. The solid-state CTC was further characterized by FT-IR and (1)H NMR spectroscopic techniques. Both FT-IR and (1)H NMR confirmed the formation of the CTC and its structure. The reaction was adopted as a basis for developing a novel 96-microwell spectrophotometric method (MW-SPA) for REM. The assay limits of detection and quantitation were 3.57 and 10.83 µg/well, respectively. The assay was validated, and all validation parameters were acceptable. The assay was implemented successfully with great precision and accuracy to the determination of REM in its bulk form and pharmaceutical formulation (injection). This assay is simple, economic, and more importantly, has high throughput property. Therefore, the assay can be valuable for routine in quality control laboratories for analysis of REM's bulk form and pharmaceutical injection. Elsevier B.V. 2022-09-05 2022-04-17 /pmc/articles/PMC9013485/ /pubmed/35465174 http://dx.doi.org/10.1016/j.molstruc.2022.133104 Text en © 2022 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Darwish, Ibrahim A.
Khalil, Nasr Y.
Darwish, Hany W.
Alzoman, Nourah Z.
Al-Hossaini, Abdullah M.
Synthesis, spectroscopic and computational characterization of charge transfer complex of remdesivir with chloranilic acid: Application to development of novel 96-microwell spectrophotometric assay
title Synthesis, spectroscopic and computational characterization of charge transfer complex of remdesivir with chloranilic acid: Application to development of novel 96-microwell spectrophotometric assay
title_full Synthesis, spectroscopic and computational characterization of charge transfer complex of remdesivir with chloranilic acid: Application to development of novel 96-microwell spectrophotometric assay
title_fullStr Synthesis, spectroscopic and computational characterization of charge transfer complex of remdesivir with chloranilic acid: Application to development of novel 96-microwell spectrophotometric assay
title_full_unstemmed Synthesis, spectroscopic and computational characterization of charge transfer complex of remdesivir with chloranilic acid: Application to development of novel 96-microwell spectrophotometric assay
title_short Synthesis, spectroscopic and computational characterization of charge transfer complex of remdesivir with chloranilic acid: Application to development of novel 96-microwell spectrophotometric assay
title_sort synthesis, spectroscopic and computational characterization of charge transfer complex of remdesivir with chloranilic acid: application to development of novel 96-microwell spectrophotometric assay
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013485/
https://www.ncbi.nlm.nih.gov/pubmed/35465174
http://dx.doi.org/10.1016/j.molstruc.2022.133104
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