Erythrocyte-derived liposomes for the treatment of inflammatory diseases

Detalhes bibliográficos
Autor(a) principal: Olival, Ana Sofia Martins
Data de Publicação: 2022
Outros Autores: Vieira, Sara Filipa Fontoura, Gonçalves, V. M. F., Cunha, C., Tiritan, M. E., Carvalho, A., Reis, R. L., Ferreira, Helena Susana Costa Machado, Neves, N. M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/1822/79335
Resumo: Effective and safe therapies to counteract persistent inflammation are necessary. We developed erythrocyte-derived liposomes (EDLs) with intrinsic anti-inflammatory activity. The EDLs were prepared using lipids extracted from erythrocyte membranes, which are rich in omega-3 fatty acids with several health benefits. Diclofenac, a widely used anti-inflammatory drug, was incorporated into EDLs in relevant therapeutic concentrations. The EDLs were also functionalised with folic acid to allow their active targeting of M1 macrophages, which are key players in inflammatory processes. In the presence of lipopolysaccharide (LPS)-stimulated macrophages, empty EDLs and EDLs incorporating diclofenac were able to reduce the levels of important pro-inflammatory cytokines, namely interleukin-6 (IL-6; ~85% and 77%, respectively) and tumour necrosis factor-alpha (TNF-a; ~64% and 72%, respectively). Strikingly, cytocompatible concentrations of EDLs presented similar effects to dexamethasone, a potent anti-inflammatory drug, in reducing IL-6 and TNF-a concentrations, demonstrating the EDLs potential to be used as bioactive carriers in the treatment of inflammatory diseases.
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spelling Erythrocyte-derived liposomes for the treatment of inflammatory diseasesActive targetingAnti-inflammatory activityDrug deliveryErythrocytesInflammatory diseasesLiposomesScience & TechnologyEffective and safe therapies to counteract persistent inflammation are necessary. We developed erythrocyte-derived liposomes (EDLs) with intrinsic anti-inflammatory activity. The EDLs were prepared using lipids extracted from erythrocyte membranes, which are rich in omega-3 fatty acids with several health benefits. Diclofenac, a widely used anti-inflammatory drug, was incorporated into EDLs in relevant therapeutic concentrations. The EDLs were also functionalised with folic acid to allow their active targeting of M1 macrophages, which are key players in inflammatory processes. In the presence of lipopolysaccharide (LPS)-stimulated macrophages, empty EDLs and EDLs incorporating diclofenac were able to reduce the levels of important pro-inflammatory cytokines, namely interleukin-6 (IL-6; ~85% and 77%, respectively) and tumour necrosis factor-alpha (TNF-a; ~64% and 72%, respectively). Strikingly, cytocompatible concentrations of EDLs presented similar effects to dexamethasone, a potent anti-inflammatory drug, in reducing IL-6 and TNF-a concentrations, demonstrating the EDLs potential to be used as bioactive carriers in the treatment of inflammatory diseases.Authors acknowledge the financial support from the Fundação para a Ciência e a Tecnologia (FCT) to the PhD grant PD/BD/ 135246/2017, CEECIND/03628/2017 and CEECIND/04058/2018 and the project Cells4_IDs (PTDC/BTM-SAL/28882/2017), and the NORTE 2020 Structured Project, cofunded by Norte2020 (NORTE 01-0145-FEDER-000021). The authors would also like to acknow ledge the additional support provided by FCT (UIDB/50026/2020 and UIDP/50026/2020). Authors would also like to thank CEF Taipas for the blood donations.Taylor & FrancisUniversidade do MinhoOlival, Ana Sofia MartinsVieira, Sara Filipa FontouraGonçalves, V. M. F.Cunha, C.Tiritan, M. E.Carvalho, A.Reis, R. L.Ferreira, Helena Susana Costa MachadoNeves, N. M.2022-042022-04-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/1822/79335engOlival A., Vieira S. F., Gonçalves V. M. F., Cunha C., Tiritan M. E., Carvalho A., Reis R. L., Ferreira H., Neves N. M. Erythrocyte-derived liposomes for the treatment of inflammatory diseases, Journal of Drug Targeting, doi:10.1080/1061186X.2022.2066107, 20221029-233010.1080/1061186X.2022.20661073541428510.1080/1061186X.2022.2066107info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-05-11T07:26:26Zoai:repositorium.sdum.uminho.pt:1822/79335Portal AgregadorONGhttps://www.rcaap.pt/oai/openairemluisa.alvim@gmail.comopendoar:71602024-05-11T07:26:26Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Erythrocyte-derived liposomes for the treatment of inflammatory diseases
title Erythrocyte-derived liposomes for the treatment of inflammatory diseases
spellingShingle Erythrocyte-derived liposomes for the treatment of inflammatory diseases
Olival, Ana Sofia Martins
Active targeting
Anti-inflammatory activity
Drug delivery
Erythrocytes
Inflammatory diseases
Liposomes
Science & Technology
title_short Erythrocyte-derived liposomes for the treatment of inflammatory diseases
title_full Erythrocyte-derived liposomes for the treatment of inflammatory diseases
title_fullStr Erythrocyte-derived liposomes for the treatment of inflammatory diseases
title_full_unstemmed Erythrocyte-derived liposomes for the treatment of inflammatory diseases
title_sort Erythrocyte-derived liposomes for the treatment of inflammatory diseases
author Olival, Ana Sofia Martins
author_facet Olival, Ana Sofia Martins
Vieira, Sara Filipa Fontoura
Gonçalves, V. M. F.
Cunha, C.
Tiritan, M. E.
Carvalho, A.
Reis, R. L.
Ferreira, Helena Susana Costa Machado
Neves, N. M.
author_role author
author2 Vieira, Sara Filipa Fontoura
Gonçalves, V. M. F.
Cunha, C.
Tiritan, M. E.
Carvalho, A.
Reis, R. L.
Ferreira, Helena Susana Costa Machado
Neves, N. M.
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Olival, Ana Sofia Martins
Vieira, Sara Filipa Fontoura
Gonçalves, V. M. F.
Cunha, C.
Tiritan, M. E.
Carvalho, A.
Reis, R. L.
Ferreira, Helena Susana Costa Machado
Neves, N. M.
dc.subject.por.fl_str_mv Active targeting
Anti-inflammatory activity
Drug delivery
Erythrocytes
Inflammatory diseases
Liposomes
Science & Technology
topic Active targeting
Anti-inflammatory activity
Drug delivery
Erythrocytes
Inflammatory diseases
Liposomes
Science & Technology
description Effective and safe therapies to counteract persistent inflammation are necessary. We developed erythrocyte-derived liposomes (EDLs) with intrinsic anti-inflammatory activity. The EDLs were prepared using lipids extracted from erythrocyte membranes, which are rich in omega-3 fatty acids with several health benefits. Diclofenac, a widely used anti-inflammatory drug, was incorporated into EDLs in relevant therapeutic concentrations. The EDLs were also functionalised with folic acid to allow their active targeting of M1 macrophages, which are key players in inflammatory processes. In the presence of lipopolysaccharide (LPS)-stimulated macrophages, empty EDLs and EDLs incorporating diclofenac were able to reduce the levels of important pro-inflammatory cytokines, namely interleukin-6 (IL-6; ~85% and 77%, respectively) and tumour necrosis factor-alpha (TNF-a; ~64% and 72%, respectively). Strikingly, cytocompatible concentrations of EDLs presented similar effects to dexamethasone, a potent anti-inflammatory drug, in reducing IL-6 and TNF-a concentrations, demonstrating the EDLs potential to be used as bioactive carriers in the treatment of inflammatory diseases.
publishDate 2022
dc.date.none.fl_str_mv 2022-04
2022-04-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://hdl.handle.net/1822/79335
url https://hdl.handle.net/1822/79335
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Olival A., Vieira S. F., Gonçalves V. M. F., Cunha C., Tiritan M. E., Carvalho A., Reis R. L., Ferreira H., Neves N. M. Erythrocyte-derived liposomes for the treatment of inflammatory diseases, Journal of Drug Targeting, doi:10.1080/1061186X.2022.2066107, 2022
1029-2330
10.1080/1061186X.2022.2066107
35414285
10.1080/1061186X.2022.2066107
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Taylor & Francis
publisher.none.fl_str_mv Taylor & Francis
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv mluisa.alvim@gmail.com
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