Development of a highly sensitive bioanalytical assay for the quantification of favipiravir.
COVID-19
Favipiravir
LC-MS/MS
SARS-CoV-2
plasma
Journal
bioRxiv : the preprint server for biology
Titre abrégé: bioRxiv
Pays: United States
ID NLM: 101680187
Informations de publication
Date de publication:
05 Feb 2021
05 Feb 2021
Historique:
pubmed:
11
2
2021
medline:
11
2
2021
entrez:
10
2
2021
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 33564761
doi: 10.1101/2021.02.03.429628
pmc: PMC7872349
pii:
doi:
Types de publication
Preprint
Langues
eng
Subventions
Organisme : NIAID NIH HHS
ID : R01 AI134091
Pays : United States
Organisme : NIAID NIH HHS
ID : R24 AI118397
Pays : United States
Déclaration de conflit d'intérêts
Conflicts of interest statement AO and SR have received research funding from AstraZeneca and ViiV and consultancies from Gilead; AO has additionally received funding from Merck and Janssen and consultancies from ViiV and Merck not related to the current paper. No other conflicts are declared by the authors.