Structural Elucidation of Alkali Degradation Impurities of Favipiravir from the Oral Suspension: UPLC-TQ-ESI-MS/MS and NMR

A novel stability-indicating, reversed-phase, high-performance liquid chromatography (RP-HPLC) method was developed and validated for the determination of favipiravir in an oral suspension. The effective separation of favipiravir and its degradation products was achieved on a Zorbax Eclipse Plus C18...

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Detalles Bibliográficos
Autores principales: Patel, Ravi, Dube, Abhishek, Solanki, Ravisinh, Khunt, Dignesh, Parikh, Shalin, Junnuthula, Vijayabhaskarreddy, Dyawanapelly, Sathish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9457609/
https://www.ncbi.nlm.nih.gov/pubmed/36080375
http://dx.doi.org/10.3390/molecules27175606

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9457609/
https://www.ncbi.nlm.nih.gov/pubmed/36080375
http://dx.doi.org/10.3390/molecules27175606

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