[HTML][HTML] Comparison of HPLC and UV spectrophotometric methods for quantification of favipiravir in pharmaceutical formulations

İ Bulduk - Iranian journal of pharmaceutical research: IJPR, 2021 - ncbi.nlm.nih.gov
There is no currently successful method to treat Covid-19 infection. Nevertheless, previously
licensed pharmaceuticals to treat other virus infections are used on an off-label basis either …

HPLC-UV method for quantification of favipiravir in pharmaceutical formulations

İ Bulduk - Acta Chromatographica, 2021 - akjournals.com
Favipiravir (FVP), a pyrazine analog, has shown antiviral activity against a wide variety of
viruses. It is considered to be worth further investigation as a potential candidate drug for …

[HTML][HTML] Development and validation of HPLC-UV method for the determination of favipiravir in human plasma

TN Komarov, PK Karnakova… - Drug development & …, 2022 - pharmjournal.ru
Abstract Introduction. Coronavirus disease (COVID-19) is an acute infectious disease
caused by SARS-CoV-2 (severe acute respiratory syndrome-related coronavirus 2) …

Development and validation of HPLC method for quantification of favipiravir in tablet

MS Kalshetti, SG Adlinge - Research journal of pharmacy and …, 2022 - indianjournals.com
Hplc method has been developed and validated for the quantification of Favipiravir in tablet
formulation The chromatographic separation was achieved by using Luna® Phenomenex …

[PDF][PDF] New FTIR method development and validation for quantitative analysis of favipiravir in bulk and pharmaceutical dosage forms

P Nithila, N Raghavendrababu, Y Padmavathi… - Int J Curr Pharm …, 2022 - academia.edu
Objective: A simple spectrophotometric method has been proposed for quantitative analysis
of favipiravir in bulk and pharmaceutical dosage form. Methods: New Fourier transform …

Bioanalytical method development and validation for the determination of favipiravir in spiked human plasma by using RP-HPLC

PV Duse, KG Baheti - Journal of Pharmaceutical …, 2021 - journal.submissionpages.com
A precise, simple and reproducible reverse phase liquid chromatography (RP-HPLC)
method was developed and validated for determination of Favipiravir by using …

[PDF][PDF] Stability-indicating RP HPLC method development for estimation of favipiravir in bulk and pharmaceutical dosage form

PA Balu, MS Paresh - World Journal …, 2021 - wjpr.s3.ap-south-1.amazonaws.com
Favipiravir is antiviral drug and nowadays it is part of treatment of covid 19. The aim of the
research work was to develop a validated simple, sensitive, precise and specific high …

New Analytical Methods for the Determination of New Anti-Viral Drug Favipiravir: A Potential Therapeutic Drug Against Covid-19 Virus, in Bulk and Dosage Forms

N Itigimatha, KS Chadchan, BC Yallur… - Pharmaceutical …, 2023 - Springer
Simple, accurate and robust analytical methods have been developed and validated for the
determination of favipiravir (FVPR) by RP-HPLC and UV spectroscopy techniques as per the …

Analytical method development and validation and forced degradation stability-indicating studies of Favipiravir by RP-HPLC and UV in bulk and pharmaceutical …

SNS Ali, L Mobina, M Mehfuza… - Journal of …, 2021 - info.euro-archives.com
Aims: To develop and validate a new, simple, rapid, precise, and accurate An Eco-friendly
RP-HPLC and UV-Method Development and Validation for an estimation of Favipiravir in …

Development and validation of a sensitive, fast and simple LC-MS/MS method for the quantitation of favipiravir in human serum

DE Onmaz, S Abusoglu, M Onmaz, FH Yerlikaya… - … of Chromatography B, 2021 - Elsevier
Favipiravir is a broad-spectrum inhibitor of viral RNA polymerase. It is currently used as a
possible treatment for coronavirus disease 2019 (COVID-19). Pre-clinical or clinical trials of …