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Antiviral Activity of Liposomes Containing Natural Compounds Against CHIKV

dc.contributor.authorCalmon, Marília Freitas [UNESP]
dc.contributor.authorGusmão, Luiza Araújo
dc.contributor.authorRuiz, Thalles Fernando Rocha
dc.contributor.authorCampos, Guilherme Rodrigues Fernandes
dc.contributor.authorAyusso, Gabriela Miranda
dc.contributor.authorCarvalho, Tamara
dc.contributor.authordo Vale Francisco Bortolato, Isabella [UNESP]
dc.contributor.authorConceição, Pâmela Joyce Previdelli [UNESP]
dc.contributor.authorTaboga, Sebastião Roberto [UNESP]
dc.contributor.authorJardim, Ana Carolina Gomes [UNESP]
dc.contributor.authorMerits, Andres
dc.contributor.authorRahal, Paula [UNESP]
dc.contributor.authorTedesco, Antonio Claudio
dc.date.accessioned2026-06-22T14:01:25Z
dc.date.issued2025-09-22
dc.description.abstract<b>Background/Objectives:</b> Chikungunya virus (CHIKV), a mosquito-borne single-stranded RNA virus belonging to the genus <i>Alphavirus</i> (family <i>Togaviridae</i>), causes large-scale outbreaks. However, no specific treatment for CHIKV infections is currently available. Berberine and emodin are plant-derived compounds with anti-CHIKV activities. This study aimed to evaluate the antiviral efficacy of liposomes containing berberine (LB) or emodin (LE) against CHIKV in vitro, since nanocarriers incorporating zwitterionic polymers are known to enhance the biostability, biocompatibility, and therapeutic efficacy of drug candidates. <b>Methods:</b> Liposomes were synthesized and characterized, and cell viability was assessed to determine appropriate concentrations for subsequent assays. Confocal microscopy, antiviral assays, and western blotting were performed in BHK-21 and Huh7 cells. <b>Results:</b> In BHK-21 and Huh7 cells, LB and LE were well tolerated at concentrations of 5 and 10 µM, respectively. In both cell types, liposomes were internalized; LE was predominantly localized in the cytoplasm, whereas LB was also detected in the nucleus. EGCG, used as a standard drug against CHIKV in antiviral assays, exhibited virucidal activity and inhibited RNA replication and multiple stages of the CHIKV replication cycle in BHK-21 and Huh7 cells. Both the nanoformulations and EGCG consistently suppressed the expression of CHIKV replicase and virion proteins. <b>Conclusions:</b> These findings highlight the potential of berberine- and emodin-loaded liposomes as antiviral agents against CHIKV infection.
dc.description.affiliationInstitute of Biosciences, Letters and Exact Sciences, São Paulo State University (UNESP), São José do Rio Preto 15054-000, SP, Brazil;, thalles.ruiz@unesp.br, (T.F.R.R.);, gabriela.ayusso@unesp.br, (G.M.A.);, tamara.carvalho@unesp.br, (T.C.);, isabella.bortolato@unesp.br, (I.d.V.F.B.);, pamela.joyce@unesp.br, (P.J.P.C.);, sebastiao.taboga@unesp.br, (S.R.T.);, jardim@ufu.br, (A.C.G.J.);, p.rahal@unesp.br, (P.R.)
dc.description.affiliationCenter of Nanotechnology and Tissue Engineering, Photobiology and Photomedicine Research Group, Faculty of Philosophy, Sciences and Letters of Ribeirão Preto, University of São Paulo, Ribeirão Preto 14040-901, SP, Brazil;, luizaaraujo@usp.br
dc.description.affiliationLaboratório de Pesquisas em Virologia (LPV), Faculdade de Medicina de São José do Rio Preto (FAMERP), São José do Rio Preto 15054-000, SP, Brazil;, guilherme.campos@unesp.br
dc.description.affiliationLaboratory of Antiviral Research, Institute of Biomedical Science, ICBIM/UFU, Uberlândia 38405-302, MG, Brazil
dc.description.affiliationInstitute of Bioengineering, University of Tartu, 50090 Tartu, Estonia;, andres.merits@ut.ee
dc.description.affiliationUnespInstitute of Biosciences, Letters and Exact Sciences, São Paulo State University (UNESP), São José do Rio Preto 15054-000, SP, Brazil;, thalles.ruiz@unesp.br, (T.F.R.R.);, gabriela.ayusso@unesp.br, (G.M.A.);, tamara.carvalho@unesp.br, (T.C.);, isabella.bortolato@unesp.br, (I.d.V.F.B.);, pamela.joyce@unesp.br, (P.J.P.C.);, sebastiao.taboga@unesp.br, (S.R.T.);, jardim@ufu.br, (A.C.G.J.);, p.rahal@unesp.br, (P.R.)
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1193156788
dc.identifier.dimensionspub.1193156788
dc.identifier.doi10.3390/pharmaceutics17091229
dc.identifier.issn1999-4923
dc.identifier.orcid0000-0001-5203-0103
dc.identifier.orcid0000-0003-2480-2684
dc.identifier.orcid0000-0003-0544-8325
dc.identifier.orcid0000-0002-6008-634X
dc.identifier.orcid0000-0002-0114-8379
dc.identifier.orcid0000-0001-8314-6870
dc.identifier.orcid0000-0002-0970-4288
dc.identifier.orcid0000-0002-6348-7923
dc.identifier.orcid0000-0001-8193-0071
dc.identifier.orcid0000-0001-5693-6148
dc.identifier.orcid0000-0003-4198-9321
dc.identifier.pmcidPMC12473542
dc.identifier.pmid41012564
dc.identifier.urihttps://hdl.handle.net/11449/326347
dc.publisherMDPI
dc.relation.ispartofPharmaceutics; n. 9; v. 17; p. 1229
dc.rights.accessRightsAcesso abertopt
dc.rights.sourceRightsoa_all
dc.rights.sourceRightsgold
dc.sourceDimensions
dc.titleAntiviral Activity of Liposomes Containing Natural Compounds Against CHIKV
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication43c38943-bd6f-4fb6-a9a5-8482a1f632c0
relation.isOrgUnitOfPublication.latestForDiscovery43c38943-bd6f-4fb6-a9a5-8482a1f632c0
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Letras e Ciências Exatas, São José do Rio Pretopt

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