Logotipo do repositório

Alginate-pectin microparticles embedding self-assembling antimicrobial peptides and resveratrol for antimicrobial and anti-inflammatory applications

dc.contributor.authorRoque-Borda, Cesar Augusto
dc.contributor.authorChávez-Morán, Marco Roberto
dc.contributor.authorPrimo, Laura Maria Duran Gleriani [UNESP]
dc.contributor.authorMontesinos, José C.E. Márquez
dc.contributor.authorCardoso, Vinicius Martinho Borges [UNESP]
dc.contributor.authorSaraiva, Mauro M.S. [UNESP]
dc.contributor.authorMarcos, Caroline Maria [UNESP]
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.authorAlbericio, Fernando
dc.contributor.authorde la Torre, Beatriz G.
dc.contributor.authorPavan, Fernando Rogério [UNESP]
dc.contributor.authorMeneguin, Andréia Bagliotti [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)pt
dc.date.accessioned2026-08-05T18:16:24Z
dc.date.issued2025-11-01
dc.description.abstractIntegrating antimicrobial peptides (AMPs) into alginate-pectin-based microstructured delivery systems enhances the controlled release and stability of bioactive like resveratrol. This study examines spray-dried microparticles utilizing alginate and pectin as primary carbohydrate polymers combined with aggregated AMPs for dual antioxidant and antimicrobial effects. The AMP was self-assembled into nanostructures upon interaction with alginate and pectin, which were subsequently incorporated into spray-dried microparticles, resulting in a stable delivery system. In silico modeling and in vitro release studies under simulated gastrointestinal conditions showed that AMP-containing microparticles provided a slower, sustained resveratrol release than peptide-free systems. The Weibull model best described the release, indicating a multi-phase behavior driven by diffusion and erosion. In gastric simulated conditions, the alginate-pectin matrices with AMP improved structural integrity, reducing release, while in intestinal ones, partial erosion enabled controlled release. In vivo infection studies using Galleria mellonella demonstrated significant reductions in inflammation and bacterial load 48 h post-infection. These results suggest that alginate-pectin microparticles with aggregated AMPs enhance the antioxidant release and maintain antimicrobial activity, making them promising for gastrointestinal applications. According to these promising findings, the next step studies will aim to enhance site-specific therapeutic performance through formulation refinement and targeted delivery strategies.
dc.description.affiliationVicerrectorado de Investigación, Universidad Católica de Santa María, Arequipa, Peru
dc.description.affiliationUniversidad Nacional de Frontera, Facultad de Industrias Alimentarias y Biotecnología, Piura, Peru
dc.description.affiliationSão Paulo State University (UNESP), Tuberculosis Research Laboratory, School of Pharmaceutical Sciences, Araraquara, Brazil
dc.description.affiliationCenter for Bioinformatics, Simulation and Modeling (CBSM), Universidad de Talca, Talca, 3460000, Chile
dc.description.affiliationCenter for Nanomedicine, Diagnostics and Drug Development (ND3), Molecular Physiology Laboratory, School of Medicine, University of Talca, Talca, Chile
dc.description.affiliationSão Paulo State University (UNESP), School of Agricultural and Veterinary Sciences, Jaboticabal, SP, Brazil
dc.description.affiliationPeptide Science Laboratory, School of Chemistry and Physics, University of KwaZulu-Natal, Durban, 4001, South Africa
dc.description.affiliationCIBER-BBN, Networking Centre on Bioengineering, Biomaterials and Nanomedicine, and Department of Organic Chemistry, University of Barcelona, 08028, Barcelona, Spain
dc.description.affiliationKRISP, School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu-Natal, Durban, 4041, South Africa
dc.description.affiliationUnespSão Paulo State University (UNESP), Tuberculosis Research Laboratory, School of Pharmaceutical Sciences, Araraquara, Brazil
dc.description.affiliationUnespSão Paulo State University (UNESP), School of Agricultural and Veterinary Sciences, Jaboticabal, SP, Brazil
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1187657999
dc.identifier.dimensionspub.1187657999
dc.identifier.doi10.1016/j.foodhyd.2025.111454
dc.identifier.issn0268-005X
dc.identifier.issn1873-7137
dc.identifier.orcid0000-0002-9262-0383
dc.identifier.orcid0000-0001-8439-3777
dc.identifier.orcid0000-0003-1875-4495
dc.identifier.orcid0000-0001-9306-7404
dc.identifier.orcid0000-0002-6698-0545
dc.identifier.orcid0000-0002-8946-0462
dc.identifier.orcid0000-0001-8521-9172
dc.identifier.orcid0000-0002-6969-3963
dc.identifier.orcid0000-0002-0227-5054
dc.identifier.orcid0000-0001-9284-2819
dc.identifier.urihttps://hdl.handle.net/11449/329094
dc.publisherElsevier
dc.relation.ispartofFood Hydrocolloids; v. 167; p. 111454
dc.rights.accessRightsAcesso abertopt
dc.rights.sourceRightsoa_all
dc.rights.sourceRightshybrid
dc.sourceDimensions
dc.titleAlginate-pectin microparticles embedding self-assembling antimicrobial peptides and resveratrol for antimicrobial and anti-inflammatory applications
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication3d807254-e442-45e5-a80b-0f6bf3a26e48
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery3d807254-e442-45e5-a80b-0f6bf3a26e48
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Agrárias e Veterinárias, Jaboticabalpt

Arquivos

Pacote original

Agora exibindo 1 - 1 de 1
Carregando...
Imagem de Miniatura
Nome:
1-s2.0-S0268005X2500414X-main.pdf
Tamanho:
9,06 MB
Formato:
Adobe Portable Document Format