PEG-coated vesicles from Pluronic/lipid mixtures for the carrying of photoactive erythrosine derivatives
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , , , |
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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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:29462024-08-05T18:11:12.100670Repositório 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 |
|
_version_ |
1808128906096541696 |