PEG-coated vesicles from Pluronic/lipid mixtures for the carrying of photoactive erythrosine derivatives

Detalhes bibliográficos
Autor(a) principal: de Freitas, Camila Fabiano
Data de Publicação: 2019
Outros Autores: Calori, Italo Rodrigo, da Silva, Ana Claudia Pedrozo, de Castro, Lidiane Vizioli, Sato, Francielle, Silva Pellosi, Diogo [UNESP], Tessaro, André Luiz, Caetano, Wilker, Hioka, Noboru
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.colsurfb.2018.12.031
http://hdl.handle.net/11449/221228
Resumo: Liposomes are very attractive membrane models and excellent drug delivery systems. Concerning their drug delivery aspects, the mixing liposomes with biocompatible copolymers allows for stability and the incorporation of several drugs. We developed PEG coated vesicles from the mixture of DPPC and F127 Pluronic copolymer to obtain long-circulating nanoparticles (mixed vesicles). We employed an innovative process previously developed by us: a small amount of F127 mixed in DPPC, thin film preparation, followed by hydration (lipids plus F127) using a bath sonicator cleaner type, forming unilamellar spherical vesicles with diameter ∼100 nm. The formed PEG coated vesicles were incorporated with the xanthene dye Erythrosine B (ERY), and its ester derivatives as photosensitizers (PS) for photodynamic proposes. The F127/DPPC mixed vesicles promoted a higher PS incorporation, and with better thermal and kinetic stability, at least 60 days, when compared to conventional DPPC liposome. The binding constant and quenching analysis revealed that with a higher PS hydrophobicity, PS affinity increases toward the nanoparticle and results in a deeper PS location inside the lipid bilayer. An increment in the fluorescence quantum yield was observed, while the PS singlet oxygen generations remained high. Dialysis studies demonstrated that PS were released based on their hydrophobicity. Permeation analysis showed that all PS can reach the deeper regions of the skin. The Decyl Ester derivative/nanoparticle exhibited high photoactivity against Caco-2 cancer cells (in vitro studies). The PEG coated from F127/DPPC mixed vesicles are very promising nanocarriers for erythrosine and its derivatives.
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spelling PEG-coated vesicles from Pluronic/lipid mixtures for the carrying of photoactive erythrosine derivativesMixed vesiclesPhotodynamicPluronicsStealth liposomeXanthenesLiposomes are very attractive membrane models and excellent drug delivery systems. Concerning their drug delivery aspects, the mixing liposomes with biocompatible copolymers allows for stability and the incorporation of several drugs. We developed PEG coated vesicles from the mixture of DPPC and F127 Pluronic copolymer to obtain long-circulating nanoparticles (mixed vesicles). We employed an innovative process previously developed by us: a small amount of F127 mixed in DPPC, thin film preparation, followed by hydration (lipids plus F127) using a bath sonicator cleaner type, forming unilamellar spherical vesicles with diameter ∼100 nm. The formed PEG coated vesicles were incorporated with the xanthene dye Erythrosine B (ERY), and its ester derivatives as photosensitizers (PS) for photodynamic proposes. The F127/DPPC mixed vesicles promoted a higher PS incorporation, and with better thermal and kinetic stability, at least 60 days, when compared to conventional DPPC liposome. The binding constant and quenching analysis revealed that with a higher PS hydrophobicity, PS affinity increases toward the nanoparticle and results in a deeper PS location inside the lipid bilayer. An increment in the fluorescence quantum yield was observed, while the PS singlet oxygen generations remained high. Dialysis studies demonstrated that PS were released based on their hydrophobicity. Permeation analysis showed that all PS can reach the deeper regions of the skin. The Decyl Ester derivative/nanoparticle exhibited high photoactivity against Caco-2 cancer cells (in vitro studies). The PEG coated from F127/DPPC mixed vesicles are very promising nanocarriers for erythrosine and its derivatives.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Department of Chemistry Universidade Estadual de Maringá, Av. Colombo, 5.790Department of Chemistry Universidade Estadual de São Paulo, Campus Diadema, Unidade José de Filippi, R. Prof. Artur Riedel, 275 - Jd. EldoradoDepartment of Chemistry Universidade Tecnológica Federal do Paraná, Campus Apucarana, R. Marcílio Dias, 635 - Jardim ParaisoDepartment of Chemistry Universidade Estadual de São Paulo, Campus Diadema, Unidade José de Filippi, R. Prof. Artur Riedel, 275 - Jd. EldoradoUniversidade Estadual de Maringá (UEM)Universidade Estadual Paulista (UNESP)Universidade Tecnológica Federal do Paranáde Freitas, Camila FabianoCalori, Italo Rodrigoda Silva, Ana Claudia Pedrozode Castro, Lidiane VizioliSato, FrancielleSilva Pellosi, Diogo [UNESP]Tessaro, André LuizCaetano, WilkerHioka, Noboru2022-04-28T19:26:55Z2022-04-28T19:26:55Z2019-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article530-544http://dx.doi.org/10.1016/j.colsurfb.2018.12.031Colloids and Surfaces B: Biointerfaces, v. 175, p. 530-544.1873-43670927-7765http://hdl.handle.net/11449/22122810.1016/j.colsurfb.2018.12.0312-s2.0-85058645951Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengColloids and Surfaces B: Biointerfacesinfo:eu-repo/semantics/openAccess2022-04-28T19:26:55Zoai:repositorio.unesp.br:11449/221228Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462022-04-28T19:26:55Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv PEG-coated vesicles from Pluronic/lipid mixtures for the carrying of photoactive erythrosine derivatives
title PEG-coated vesicles from Pluronic/lipid mixtures for the carrying of photoactive erythrosine derivatives
spellingShingle PEG-coated vesicles from Pluronic/lipid mixtures for the carrying of photoactive erythrosine derivatives
de Freitas, Camila Fabiano
Mixed vesicles
Photodynamic
Pluronics
Stealth liposome
Xanthenes
title_short PEG-coated vesicles from Pluronic/lipid mixtures for the carrying of photoactive erythrosine derivatives
title_full PEG-coated vesicles from Pluronic/lipid mixtures for the carrying of photoactive erythrosine derivatives
title_fullStr PEG-coated vesicles from Pluronic/lipid mixtures for the carrying of photoactive erythrosine derivatives
title_full_unstemmed PEG-coated vesicles from Pluronic/lipid mixtures for the carrying of photoactive erythrosine derivatives
title_sort PEG-coated vesicles from Pluronic/lipid mixtures for the carrying of photoactive erythrosine derivatives
author de Freitas, Camila Fabiano
author_facet de Freitas, Camila Fabiano
Calori, Italo Rodrigo
da Silva, Ana Claudia Pedrozo
de Castro, Lidiane Vizioli
Sato, Francielle
Silva Pellosi, Diogo [UNESP]
Tessaro, André Luiz
Caetano, Wilker
Hioka, Noboru
author_role author
author2 Calori, Italo Rodrigo
da Silva, Ana Claudia Pedrozo
de Castro, Lidiane Vizioli
Sato, Francielle
Silva Pellosi, Diogo [UNESP]
Tessaro, André Luiz
Caetano, Wilker
Hioka, Noboru
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual de Maringá (UEM)
Universidade Estadual Paulista (UNESP)
Universidade Tecnológica Federal do Paraná
dc.contributor.author.fl_str_mv de Freitas, Camila Fabiano
Calori, Italo Rodrigo
da Silva, Ana Claudia Pedrozo
de Castro, Lidiane Vizioli
Sato, Francielle
Silva Pellosi, Diogo [UNESP]
Tessaro, André Luiz
Caetano, Wilker
Hioka, Noboru
dc.subject.por.fl_str_mv Mixed vesicles
Photodynamic
Pluronics
Stealth liposome
Xanthenes
topic Mixed vesicles
Photodynamic
Pluronics
Stealth liposome
Xanthenes
description Liposomes are very attractive membrane models and excellent drug delivery systems. Concerning their drug delivery aspects, the mixing liposomes with biocompatible copolymers allows for stability and the incorporation of several drugs. We developed PEG coated vesicles from the mixture of DPPC and F127 Pluronic copolymer to obtain long-circulating nanoparticles (mixed vesicles). We employed an innovative process previously developed by us: a small amount of F127 mixed in DPPC, thin film preparation, followed by hydration (lipids plus F127) using a bath sonicator cleaner type, forming unilamellar spherical vesicles with diameter ∼100 nm. The formed PEG coated vesicles were incorporated with the xanthene dye Erythrosine B (ERY), and its ester derivatives as photosensitizers (PS) for photodynamic proposes. The F127/DPPC mixed vesicles promoted a higher PS incorporation, and with better thermal and kinetic stability, at least 60 days, when compared to conventional DPPC liposome. The binding constant and quenching analysis revealed that with a higher PS hydrophobicity, PS affinity increases toward the nanoparticle and results in a deeper PS location inside the lipid bilayer. An increment in the fluorescence quantum yield was observed, while the PS singlet oxygen generations remained high. Dialysis studies demonstrated that PS were released based on their hydrophobicity. Permeation analysis showed that all PS can reach the deeper regions of the skin. The Decyl Ester derivative/nanoparticle exhibited high photoactivity against Caco-2 cancer cells (in vitro studies). The PEG coated from F127/DPPC mixed vesicles are very promising nanocarriers for erythrosine and its derivatives.
publishDate 2019
dc.date.none.fl_str_mv 2019-03-01
2022-04-28T19:26:55Z
2022-04-28T19:26:55Z
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://dx.doi.org/10.1016/j.colsurfb.2018.12.031
Colloids and Surfaces B: Biointerfaces, v. 175, p. 530-544.
1873-4367
0927-7765
http://hdl.handle.net/11449/221228
10.1016/j.colsurfb.2018.12.031
2-s2.0-85058645951
url http://dx.doi.org/10.1016/j.colsurfb.2018.12.031
http://hdl.handle.net/11449/221228
identifier_str_mv Colloids and Surfaces B: Biointerfaces, v. 175, p. 530-544.
1873-4367
0927-7765
10.1016/j.colsurfb.2018.12.031
2-s2.0-85058645951
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Colloids and Surfaces B: Biointerfaces
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 530-544
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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