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Development of a highly sensitive bioanalytical assay for the quantification of favipiravir.
Favipiravir (FAV; T-705) has been approved for use as an anti-influenza therapeutic and has reports against a wide range of viruses (e.g., Ebola virus, rabies and norovirus). Most recently FAV has been reported to demonstrate activity against SARS-CoV-2. Repurposing opportunities have been intensive...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7872349/ https://www.ncbi.nlm.nih.gov/pubmed/33564761 http://dx.doi.org/10.1101/2021.02.03.429628 |
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author | Curley, Paul Neary, Megan Arshad, Usman Tatham, Lee Pertinez, Henry Box, Helen Rajoli, Rajith KR Valentijn, Anthony Sharp, Joanne Rannard, Steve P Owen, Andrew |
author_facet | Curley, Paul Neary, Megan Arshad, Usman Tatham, Lee Pertinez, Henry Box, Helen Rajoli, Rajith KR Valentijn, Anthony Sharp, Joanne Rannard, Steve P Owen, Andrew |
author_sort | Curley, Paul |
collection | PubMed |
description | Favipiravir (FAV; T-705) has been approved for use as an anti-influenza therapeutic and has reports against a wide range of viruses (e.g., Ebola virus, rabies and norovirus). Most recently FAV has been reported to demonstrate activity against SARS-CoV-2. Repurposing opportunities have been intensively studied with only limited success to date. If successful, repurposing will allow interventions to become more rapidly available than development of new chemical entities. Pre-clinical and clinical investigations of FAV require robust, reproducible and sensitive bioanalytical assay. Here, a liquid chromatography tandem mass spectrometry assay is presented which was linear from 0.78–200 ng/mL Accuracy and precision ranged between 89% and 110%, 101% and 106%, respectively. The presented assay here has applications in both pre-clinical and clinical research and may be used to facilitate further investigations into the application of FAV against SARS-CoV-2. |
format | Online Article Text |
id | pubmed-7872349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-78723492021-02-10 Development of a highly sensitive bioanalytical assay for the quantification of favipiravir. Curley, Paul Neary, Megan Arshad, Usman Tatham, Lee Pertinez, Henry Box, Helen Rajoli, Rajith KR Valentijn, Anthony Sharp, Joanne Rannard, Steve P Owen, Andrew bioRxiv Article Favipiravir (FAV; T-705) has been approved for use as an anti-influenza therapeutic and has reports against a wide range of viruses (e.g., Ebola virus, rabies and norovirus). Most recently FAV has been reported to demonstrate activity against SARS-CoV-2. Repurposing opportunities have been intensively studied with only limited success to date. If successful, repurposing will allow interventions to become more rapidly available than development of new chemical entities. Pre-clinical and clinical investigations of FAV require robust, reproducible and sensitive bioanalytical assay. Here, a liquid chromatography tandem mass spectrometry assay is presented which was linear from 0.78–200 ng/mL Accuracy and precision ranged between 89% and 110%, 101% and 106%, respectively. The presented assay here has applications in both pre-clinical and clinical research and may be used to facilitate further investigations into the application of FAV against SARS-CoV-2. Cold Spring Harbor Laboratory 2021-02-05 /pmc/articles/PMC7872349/ /pubmed/33564761 http://dx.doi.org/10.1101/2021.02.03.429628 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Curley, Paul Neary, Megan Arshad, Usman Tatham, Lee Pertinez, Henry Box, Helen Rajoli, Rajith KR Valentijn, Anthony Sharp, Joanne Rannard, Steve P Owen, Andrew Development of a highly sensitive bioanalytical assay for the quantification of favipiravir. |
title | Development of a highly sensitive bioanalytical assay for the quantification of favipiravir. |
title_full | Development of a highly sensitive bioanalytical assay for the quantification of favipiravir. |
title_fullStr | Development of a highly sensitive bioanalytical assay for the quantification of favipiravir. |
title_full_unstemmed | Development of a highly sensitive bioanalytical assay for the quantification of favipiravir. |
title_short | Development of a highly sensitive bioanalytical assay for the quantification of favipiravir. |
title_sort | development of a highly sensitive bioanalytical assay for the quantification of favipiravir. |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7872349/ https://www.ncbi.nlm.nih.gov/pubmed/33564761 http://dx.doi.org/10.1101/2021.02.03.429628 |
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