Increased encapsulation efficiency of methotrexate in liposomes for rheumatoid arthritis therapy
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/1822/71034 |
Resumo: | Methotrexate (MTX) is a common drug used to treat rheumatoid arthritis. Due to the excessive side effects, encapsulation of MTX in liposomes is considered an effective delivery system, reducing drug toxicity, while maintaining its efficacy. The ethanol injection method is an interesting technique for liposome production, due to its simplicity, fast implementation, and reproducibility. However, this method occasionally requires the extrusion process, to obtain suitable size distribution, and achieve a low level of MTX encapsulation. Here, we develop a novel pre-concentration method, based on the principles of the ethanol injection, using an initial aqueous volume of 20% and 1:1 ratio of organic:aqueous phase (v/v). The liposomes obtained present small values of size and polydispersity index, without the extrusion process, and a higher MTX encapsulation (efficiency higher than 30%), suitable characteristics for in vivo application. The great potential of MTX to interact at the surface of the lipid bilayer was shown by nuclear magnetic resonance (NMR) studies, revealing mutual interactions between the drug and the main phospholipid via hydrogen bonding. In vivo experiments reveal that liposomes encapsulating MTX significantly increase the biological benefit in arthritic mice. This approach shows a significant advance in MTX therapeutic applications. |
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Increased encapsulation efficiency of methotrexate in liposomes for rheumatoid arthritis therapyliposomesmethotrexateencapsulationpre-concentration ethanol injection methodrheumatoid arthritisScience & TechnologyMethotrexate (MTX) is a common drug used to treat rheumatoid arthritis. Due to the excessive side effects, encapsulation of MTX in liposomes is considered an effective delivery system, reducing drug toxicity, while maintaining its efficacy. The ethanol injection method is an interesting technique for liposome production, due to its simplicity, fast implementation, and reproducibility. However, this method occasionally requires the extrusion process, to obtain suitable size distribution, and achieve a low level of MTX encapsulation. Here, we develop a novel pre-concentration method, based on the principles of the ethanol injection, using an initial aqueous volume of 20% and 1:1 ratio of organic:aqueous phase (v/v). The liposomes obtained present small values of size and polydispersity index, without the extrusion process, and a higher MTX encapsulation (efficiency higher than 30%), suitable characteristics for in vivo application. The great potential of MTX to interact at the surface of the lipid bilayer was shown by nuclear magnetic resonance (NMR) studies, revealing mutual interactions between the drug and the main phospholipid via hydrogen bonding. In vivo experiments reveal that liposomes encapsulating MTX significantly increase the biological benefit in arthritic mice. This approach shows a significant advance in MTX therapeutic applications.This work has received funding from the European Union Horizon 2020 research and innovation programme under grant agreement NMP-06-2015-683356 FOLSMART. This study was also supported by the Portuguese Foundation for Science and Technology (FCT) under the scope of the strategic funding of UIDB/04469/2020 unit and BioTecNorte operation (NORTE-01-0145-FEDER-000004) funded by the European Regional Development Fund under the scope of Norte2020—Programa Operacional Regional do Norte. Diana Guimarães (SFRH/BD/140321/2018) and Jennifer Noro (SFRH/BD/121673/2016) hold a scholarship from FCT.info:eu-repo/semantics/publishedVersionMDPIUniversidade do MinhoGuimarães, Diana Isabel PereiraNoro, Jennifer MartinsLoureiro, Ana Isabel SáLager, FranckRenault, GillesCavaco-Paulo, ArturNogueira, Eugénia2020-12-182020-12-18T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/71034engGuimarães, Diana Isabel Pereira; Jennifer Noro; Loureiro, Ana; Lager, Franck; Renault, Gilles; Cavaco-Paulo, Artur; Nogueira, E., Increased encapsulation efficiency of methotrexate in liposomes for rheumatoid arthritis therapy. Biomedicines, 8(12), 630, 20202227-905910.3390/biomedicines8120630https://www.mdpi.com/2227-9059/8/12/630info: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:RCAAP2023-07-21T12:46:36Zoai:repositorium.sdum.uminho.pt:1822/71034Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:44:36.363835Repositório 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 |
Increased encapsulation efficiency of methotrexate in liposomes for rheumatoid arthritis therapy |
title |
Increased encapsulation efficiency of methotrexate in liposomes for rheumatoid arthritis therapy |
spellingShingle |
Increased encapsulation efficiency of methotrexate in liposomes for rheumatoid arthritis therapy Guimarães, Diana Isabel Pereira liposomes methotrexate encapsulation pre-concentration ethanol injection method rheumatoid arthritis Science & Technology |
title_short |
Increased encapsulation efficiency of methotrexate in liposomes for rheumatoid arthritis therapy |
title_full |
Increased encapsulation efficiency of methotrexate in liposomes for rheumatoid arthritis therapy |
title_fullStr |
Increased encapsulation efficiency of methotrexate in liposomes for rheumatoid arthritis therapy |
title_full_unstemmed |
Increased encapsulation efficiency of methotrexate in liposomes for rheumatoid arthritis therapy |
title_sort |
Increased encapsulation efficiency of methotrexate in liposomes for rheumatoid arthritis therapy |
author |
Guimarães, Diana Isabel Pereira |
author_facet |
Guimarães, Diana Isabel Pereira Noro, Jennifer Martins Loureiro, Ana Isabel Sá Lager, Franck Renault, Gilles Cavaco-Paulo, Artur Nogueira, Eugénia |
author_role |
author |
author2 |
Noro, Jennifer Martins Loureiro, Ana Isabel Sá Lager, Franck Renault, Gilles Cavaco-Paulo, Artur Nogueira, Eugénia |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade do Minho |
dc.contributor.author.fl_str_mv |
Guimarães, Diana Isabel Pereira Noro, Jennifer Martins Loureiro, Ana Isabel Sá Lager, Franck Renault, Gilles Cavaco-Paulo, Artur Nogueira, Eugénia |
dc.subject.por.fl_str_mv |
liposomes methotrexate encapsulation pre-concentration ethanol injection method rheumatoid arthritis Science & Technology |
topic |
liposomes methotrexate encapsulation pre-concentration ethanol injection method rheumatoid arthritis Science & Technology |
description |
Methotrexate (MTX) is a common drug used to treat rheumatoid arthritis. Due to the excessive side effects, encapsulation of MTX in liposomes is considered an effective delivery system, reducing drug toxicity, while maintaining its efficacy. The ethanol injection method is an interesting technique for liposome production, due to its simplicity, fast implementation, and reproducibility. However, this method occasionally requires the extrusion process, to obtain suitable size distribution, and achieve a low level of MTX encapsulation. Here, we develop a novel pre-concentration method, based on the principles of the ethanol injection, using an initial aqueous volume of 20% and 1:1 ratio of organic:aqueous phase (v/v). The liposomes obtained present small values of size and polydispersity index, without the extrusion process, and a higher MTX encapsulation (efficiency higher than 30%), suitable characteristics for in vivo application. The great potential of MTX to interact at the surface of the lipid bilayer was shown by nuclear magnetic resonance (NMR) studies, revealing mutual interactions between the drug and the main phospholipid via hydrogen bonding. In vivo experiments reveal that liposomes encapsulating MTX significantly increase the biological benefit in arthritic mice. This approach shows a significant advance in MTX therapeutic applications. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-12-18 2020-12-18T00:00:00Z |
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 |
http://hdl.handle.net/1822/71034 |
url |
http://hdl.handle.net/1822/71034 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Guimarães, Diana Isabel Pereira; Jennifer Noro; Loureiro, Ana; Lager, Franck; Renault, Gilles; Cavaco-Paulo, Artur; Nogueira, E., Increased encapsulation efficiency of methotrexate in liposomes for rheumatoid arthritis therapy. Biomedicines, 8(12), 630, 2020 2227-9059 10.3390/biomedicines8120630 https://www.mdpi.com/2227-9059/8/12/630 |
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 |
MDPI |
publisher.none.fl_str_mv |
MDPI |
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 |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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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 |
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1799133007383101440 |