Evidence map›Paper›PMID 42601612›Full record

ArticleVirology journal2026

In silico, in vitro, and in vivo evaluation of the antiviral potential of glycyrrhizic acid and chitosan nanoparticles against foot and mouth disease virus.

Asmaa R F Eweis, Khodeir M Hassan, Sahar A H Shoman, Hoda A Taha, Ehab E Ibrahim, Tahsin Shoala

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Article in Virology journal, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Asmaa R F EweisMicrobiology Department, Faculty of Science, Ain Shams University, Cairo, Egypt. asmaaawis@sci.asu.edu.eg.
Khodeir M HassanAgriculture Research Center (ARC), Veterinary Serum and Vaccine Research Institute (VSVRI), Abasia, Cairo, Egypt.
Sahar A H ShomanMicrobiology Department, Faculty of Science, Ain Shams University, Cairo, Egypt.
Hoda A TahaMicrobiology Department, Faculty of Science, Ain Shams University, Cairo, Egypt.
Ehab E IbrahimAgriculture Research Center (ARC), Veterinary Serum and Vaccine Research Institute (VSVRI), Abasia, Cairo, Egypt.
Tahsin ShoalaCollege of Biotechnology, Misr University for Science and Technology, 6th of October City, Giza, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFoot-and-mouth disease (FMD) considers as one of the extremely infectious diseases with major economic impact on cloven-hoofed animals globally. The causative agent of the disease, Foot and Mouth Disease Virus (FMDV), comprises seven serotypes designated as; O, A, SAT1, SAT2, SAT3, C, and Asia1. Over the past decades, studies have shown that glycyrrhizic acid, the primary bioactive compound of licorice root, and chitosan, as a biodegradable and biocompatible natural polymer derived from crustacean shells, are potent candidates for inhibition of FMDV activity. The current work evaluated the potential antiviral efficacy of glycyrrhizic acid nanoparticles (GA-NPs) and chitosan nanoparticles (Ch-NPs) against different FMDV serotypes through computational (molecular docking), in vitro and in vivo assays. MATERIALS AND

methodsThe study included the use of field isolates from local FMD viral outbreaks (O PanAsia-2, A Iran 05, A Africa 2020, A Africa G IV Egypt 2022, A Venezuela, and SAT2/EGY/2012); Glycyrrhizic acid and chitosan nanoparticles were prepared and characterized; antiviral activity was assessed by molecular docking analysis, BHK-21 cell assays, and experimental animal studies using representative FMDV serotypes.

resultsMolecular docking showed that GA-NPs exhibited stronger binding affinity toward the FMDV RNA-dependent RNA polymerase (3D

conclusionThese findings highlighted that GA-NPs and Ch-NPs possess broad-spectrum antiviral activity against six FMDV serotypes, supporting their further development as nanoparticle-based antiviral agents for the control of FMD.

Indexed as

Antiviral AgentsChitosanFoot-and-Mouth DiseaseFoot-and-Mouth Disease VirusGlycyrrhizic AcidNanoparticlesAnimalsCell LineComputer SimulationMolecular Docking SimulationVirus ReplicationAntiviral AgentsChitosanGlycyrrhizic AcidAntiviralCh-NPsFMDGA-NPs

Identifiers

PMID42601612
PMCPMC13476927

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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.