[引用][C] UV spectrophotometric determination of famciclovir

KV Subrahmanyam, P Mohanraj… - Asian Journal of …, 2007 - Asian Journal of Chemistry

[引用][C] Determination of ganciclovir and acyclovir in human serum using liquid chromatography-tandem mass spectrometry

JW Alffenaar, K van Hateren, AG Martson… - Journal of Applied …, 2018

[PDF][PDF] Development, validation and stability study of UV spectrophotometric method for determination of daclatasvirin bulk and pharmaceutical dosage forms

K Vikas, G Sachin, B Omprakash - Int J ChemTech Res, 2017 - researchgate.net
A simple, specific and economic UV spectrophotometric method has been developed using
as a solvent methanol: water (8: 2) to determine the daclatasvir content in bulk and …

[PDF][PDF] A New Stability Indicating Ultra Performance Liquid Chromatography-PDA Method for the Estimation of Valganciclovir in Bulk and Tablet Dosage Form.

S Mondal, GS Reddy, P Mondal… - Pharmaceutical …, 2018 - researchgate.net
Background: The present article described about the systemic development of ultra-
performance liquid chromatography (UPLC) method for the quantitative determination of …

Eco-Friendly and Green Assessment for the Quantification of Molnupiravir in Pharmaceutical Formulations and Biological Fluids: Study of Structural Elucidation and …

SA Abdel-Latif, AL El-Ansary, S Mohamed - papers.ssrn.com
The FDA-approved antiviral drug molnupiravir (MPV) was investigated for the first time using
a green spectrophotometric approach. With the help of UV-visible spectroscopy, Fourier …

[PDF][PDF] A NEW ROBUST ANALYTICAL METHOD DEVELOPMENT, VALIDATION, AND STRESS DEGRADATION STUDIES FOR ESTIMATING RITONAVIR BY UV …

N PARVEEN, T Routh, AK GOSWAMI, S MONDAL - Int J App Pharm, 2023 - academia.edu
Objective: To specify ritonavir and its commercial dosage form, the current study set out to
design and validate concise, precise, and efficient highperformance liquid chromatography …

Validated simultaneous spectrophotometric quantification of a new antiviral combination

SAN Abdel-Gawad - European Journal of Chemistry, 2017 - eurjchem.com
Simple, selective and precise spectrophotometric methods were applied for simultaneous
quantification of sofosbuvir (SFV) and ledipasvir (LDI) both in their raw and dosage forms. In …

A validated hptlc densitometric method for quantitative determination of zanamivir in bulk and pharmaceutical formulation

M Al Bratty, SF Saleh, HA Alhazmi… - European Journal of …, 2018 - eurjchem.com
The main purpose of the present study was to develop and validate a high performance thin
layer chromatographic (HPTLC) method for quantitative determination of an antiviral agent …

Determination of ganciclovir in human plasma by ultra performance liquid chromatography–UV detection

A Padullés, H Colom, Y Armendariz, G Cerezo… - Clinical …, 2012 - Elsevier
OBJECTIVES: Implement a sensitive UHPLC method for the assay of ganciclovir in human
plasma. DESIGN AND METHODS: We developed and validated a chromatographic method …

[PDF][PDF] Development and Validation of an Innovative Stability Indicating Method Using UV-Spectroscopy Techniques for Ritonavir in Bulk Drug and Pharmaceutical …

GSVNA Raj, S Mondal, S Chakraborty… - Int. J. Life Sci. Pharma … - researchgate.net
Ritonavir is a protease inhibitor used to treat HIV/AIDS. It is seldom employed for its antiviral
activity but instead as a booster for other protease inhibitors. Our study's significant objective …