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Membrane Vesicles for Nanoencapsulated Sulforaphane Increased Their Anti-Inflammatory Role on an In Vitro Human Macrophage Model

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dc.contributor.author Yepes-Molina, Lucía
dc.contributor.author Pérez-Jiménez, María-Isabel
dc.contributor.author Martínez-Esparza, María
dc.contributor.author Teruel, José-A
dc.contributor.author Ruiz-Alcaraz, Antonio-José
dc.contributor.author García-Penarrubia, Pilar
dc.contributor.author Carvajal, Micaela
dc.date.accessioned 2025-11-24T15:13:58Z
dc.date.available 2025-11-24T15:13:58Z
dc.date.issued 2022-02
dc.identifier.citation Yepes-Molina L, Pérez-Jiménez MI, Martínez-Esparza M, Teruel JA, Ruiz-Alcaraz AJ, García-Peñarrubia P, et al. Membrane Vesicles for Nanoencapsulated Sulforaphane Increased Their Anti-Inflammatory Role on an In Vitro Human Macrophage Model. IJMS. 9 de febrero de 2022;23(4):1940.
dc.identifier.issn 1661-6596
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/22369
dc.description.abstract At present, there is a growing interest in finding new non-toxic anti-inflammatory drugs to treat inflammation, which is a key pathology in the development of several diseases with considerable mortality. Sulforaphane (SFN), a bioactive compound derived from Brassica plants, was shown to be promising due to its anti-inflammatory properties and great potential, though its actual clinical use is limited due to its poor stability and bioavailability. In this sense, the use of nanocarriers could solve stability-related problems. In the current study, sulforaphane loaded into membrane vesicles derived from broccoli plants was studied to determine the anti-inflammatory potential in a human-macrophage-like in vitro cell model under both normal and inflammatory conditions. On the one hand, the release of SFN from membrane vesicles was modeled in vitro, and two release phases were stabilized, one faster and the other slower due to the interaction between SFN and membrane proteins, such as aquaporins. Furthermore, the anti-inflammatory action of sulforaphane-loaded membrane vesicles was demonstrated, as a decrease in interleukins crucial for the development of inflammation, such as TNF-?, IL-1? and IL-6, was observed. Furthermore, these results also showed that membrane vesicles by themselves had anti-inflammatory properties, opening the possibility of new lines of research to study these vesicles, not only as carriers but also as active compounds.
dc.language.iso eng
dc.publisher MDPI
dc.rights Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internacional 
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/4.0/es/  *
dc.subject.mesh Anti-Inflammatory Agents/pharmacology
dc.subject.mesh Brassica/metabolism
dc.subject.mesh Cell Line, Tumor
dc.subject.mesh Cells, Cultured
dc.subject.mesh HL-60 Cells
dc.subject.mesh Humans
dc.subject.mesh Inflammation/drug therapy
dc.subject.mesh Isothiocyanates/pharmacology
dc.subject.mesh Macrophages/drug effects
dc.subject.mesh Sulfoxides/pharmacology
dc.title Membrane Vesicles for Nanoencapsulated Sulforaphane Increased Their Anti-Inflammatory Role on an In Vitro Human Macrophage Model
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 35216054
dc.relation.publisherversion https://www.mdpi.com/1422-0067/23/4/1940
dc.identifier.doi 10.3390/ijms23041940
dc.journal.title International Journal of Molecular Sciences
dc.identifier.essn 1422-0067


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