Evidence map›Paper›PMID 41917043›Full record

ArticleScientific reports2026

Novel green UPLC method with life cycle assessment for determination of favipiravir and molnupiravir drugs and environmental water samples.

Khadiga Mohamed Kelani, Menna S Elsherbiny, Sherif M Eid, Maha F Abdel Ghany, Mahmoud M Abbas

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Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Khadiga Mohamed KelaniAnalytical Chemistry Department, Faculty of Pharmacy, Cairo University, El-Kasr El-Aini Street, Cairo, 11562, Egypt. khadigakelani@gmail.com.
Menna S ElsherbinyAnalytical Chemistry Department, Faculty of Pharmacy, Modern University for Technology and Information, Cairo, Egypt.
Sherif M EidAnalytical Chemistry Department, Faculty of Pharmacy, October 6 University, 6 October City, Giza, Egypt.
Maha F Abdel GhanyPharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Ain Shams University, Abbassia, Cairo, 11566, Egypt.
Mahmoud M AbbasPharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Ain Shams University, Abbassia, Cairo, 11566, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A novel green UPLC–SPE analytical method was developed for the simultaneous determination of Favipiravir (FVP) and Molnupiravir (MPV) in pharmaceutical and environmental water samples. The method was designed to address the analytical gap surrounding concurrent antiviral monitoring given their co-administration while minimizing solvent consumption, waste generation, and environmental impact. Water samples preparation employed a solid-phase extraction strategy optimized through systematic evaluation of sorbent type, conditioning, washing, and elution steps. Chromatographic separation was achieved using a mobile phase consisting of 0.01 M potassium dihydrogen phosphate buffer (pH 3.5) and 50% methanol (85:15, v/v), delivered at a flow rate of 0.2 mL/min with a 10 µL injection volume. This method produced sharp, well-resolved peaks with a total run time of less than 5 min. The method exhibited excellent linearity (r² ≥ 0.999), accuracy (98.56–101.19%), precision (RSD ≤ 1.8%), and recoveries of (98.97- 100.74%) across tap water, Nile River water, and pharmaceutical wastewater. Greenness was assessed using the Multi-Color Assessment (MA) platform, yielding a final whiteness score of 85.7%, which indicates a well-balanced integration of environmental, practical, analytical, and innovative attributes and supports the method’s suitability for routine application. The Analytical Eco-Scale score (77) and AGREE pictogram score (0.84) further confirm the strong environmental compatibility of the proposed method. Life cycle assessment (LCA) revealed substantial reductions in energy consumption and waste generation compared with conventional HPLC methods. Overall, the proposed UPLC–SPE approach, integrated with LCA and comprehensive greenness evaluation, represents a pioneering and environmentally informed strategy for antiviral analysis and provides a sustainable platform for future pharmaceutical residue monitoring.

Indexed as

AmidesAntiviral AgentsGreen Chemistry TechnologyPyrazinesWater Pollutants, ChemicalChromatography, High Pressure LiquidSolid Phase ExtractionAmidesAntiviral AgentsfavipiravirPyrazinesWater Pollutants, ChemicalFavipiravirGreen Analytical ChemistryLife Cycle AssessmentMolnupiravirSolid-Phase ExtractionUPLC

Identifiers

PMID41917043
PMCPMC13044257

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.