Interactions between Catanionic Vesicles and Oppositely Charged PolyelectrolytesPhase Behavior and Phase Structure

Detalhes bibliográficos
Autor(a) principal: Marques, Eduardo F.
Data de Publicação: 1999
Outros Autores: Regev, Oren, Khan, Ali, Miguel, Maria da Graça, Lindman, Björn
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
DOI: 10.1021/ma990350
Texto Completo: http://hdl.handle.net/10316/10458
https://doi.org/10.1021/ma990350+
Resumo: Structural and phase behavior effects resulting from the addition of a polyelectrolyte to a solution of oppositely charged vesicles are investigated in this work. Two cationic polyelectrolytes derived from hydroxyethylcellulose were used: JR400, a homopolymer, and Quatrisoft LM200, a polymer modified with alkyl side chains. The vesicles are composed of mixed anionic surfactant (sodium dodecyl sulfate) and cationic surfactant (didodecyldimethylammonium bromide), bearing 29 mol % of the cationic amphiphile. The phase behavior for the two mixed polymer−surfactant systems was investigated for polymer concentrations between 0.001 and 3 wt%. Three main regions were found in the two-phase maps, upon polymer addition: (i) a bluish solution phase; (ii) a wide region of phase separation, containing a precipitate and a solution; and (iii) a polymer−rich gel region, forming upon charge reversal of the system. Cryo-TEM imaging of the solution phase shows the formation of faceted vesicles and disklike aggregates, upon addition of JR400. For the LM200 system, besides the formation of faceted vesicles, clusters of vesicles and other bilayer structures are imaged. In the polymer−rich phase of JR400, membrane fragments, disklike aggregates, and vesicles are also found. These bilayer aggregates are likely to be involved with the polymer in highly connected networks, giving rise to the observed bluish gels. Electrostatic interactions, reinforced by hydrophobic interactions in the case of LM200, are the main driving force for the structural transitions observed.
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spelling Interactions between Catanionic Vesicles and Oppositely Charged PolyelectrolytesPhase Behavior and Phase StructureStructural and phase behavior effects resulting from the addition of a polyelectrolyte to a solution of oppositely charged vesicles are investigated in this work. Two cationic polyelectrolytes derived from hydroxyethylcellulose were used: JR400, a homopolymer, and Quatrisoft LM200, a polymer modified with alkyl side chains. The vesicles are composed of mixed anionic surfactant (sodium dodecyl sulfate) and cationic surfactant (didodecyldimethylammonium bromide), bearing 29 mol % of the cationic amphiphile. The phase behavior for the two mixed polymer−surfactant systems was investigated for polymer concentrations between 0.001 and 3 wt%. Three main regions were found in the two-phase maps, upon polymer addition: (i) a bluish solution phase; (ii) a wide region of phase separation, containing a precipitate and a solution; and (iii) a polymer−rich gel region, forming upon charge reversal of the system. Cryo-TEM imaging of the solution phase shows the formation of faceted vesicles and disklike aggregates, upon addition of JR400. For the LM200 system, besides the formation of faceted vesicles, clusters of vesicles and other bilayer structures are imaged. In the polymer−rich phase of JR400, membrane fragments, disklike aggregates, and vesicles are also found. These bilayer aggregates are likely to be involved with the polymer in highly connected networks, giving rise to the observed bluish gels. Electrostatic interactions, reinforced by hydrophobic interactions in the case of LM200, are the main driving force for the structural transitions observed.American Chemical Society1999-10-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/10458http://hdl.handle.net/10316/10458https://doi.org/10.1021/ma990350+engMacromolecules. 32:20 (1999) 6626-66370024-9297Marques, Eduardo F.Regev, OrenKhan, AliMiguel, Maria da GraçaLindman, Björninfo: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:RCAAP2020-05-25T13:15:38Zoai:estudogeral.uc.pt:10316/10458Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:30.703430Repositório 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 Interactions between Catanionic Vesicles and Oppositely Charged PolyelectrolytesPhase Behavior and Phase Structure
title Interactions between Catanionic Vesicles and Oppositely Charged PolyelectrolytesPhase Behavior and Phase Structure
spellingShingle Interactions between Catanionic Vesicles and Oppositely Charged PolyelectrolytesPhase Behavior and Phase Structure
Interactions between Catanionic Vesicles and Oppositely Charged PolyelectrolytesPhase Behavior and Phase Structure
Marques, Eduardo F.
Marques, Eduardo F.
title_short Interactions between Catanionic Vesicles and Oppositely Charged PolyelectrolytesPhase Behavior and Phase Structure
title_full Interactions between Catanionic Vesicles and Oppositely Charged PolyelectrolytesPhase Behavior and Phase Structure
title_fullStr Interactions between Catanionic Vesicles and Oppositely Charged PolyelectrolytesPhase Behavior and Phase Structure
Interactions between Catanionic Vesicles and Oppositely Charged PolyelectrolytesPhase Behavior and Phase Structure
title_full_unstemmed Interactions between Catanionic Vesicles and Oppositely Charged PolyelectrolytesPhase Behavior and Phase Structure
Interactions between Catanionic Vesicles and Oppositely Charged PolyelectrolytesPhase Behavior and Phase Structure
title_sort Interactions between Catanionic Vesicles and Oppositely Charged PolyelectrolytesPhase Behavior and Phase Structure
author Marques, Eduardo F.
author_facet Marques, Eduardo F.
Marques, Eduardo F.
Regev, Oren
Khan, Ali
Miguel, Maria da Graça
Lindman, Björn
Regev, Oren
Khan, Ali
Miguel, Maria da Graça
Lindman, Björn
author_role author
author2 Regev, Oren
Khan, Ali
Miguel, Maria da Graça
Lindman, Björn
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Marques, Eduardo F.
Regev, Oren
Khan, Ali
Miguel, Maria da Graça
Lindman, Björn
description Structural and phase behavior effects resulting from the addition of a polyelectrolyte to a solution of oppositely charged vesicles are investigated in this work. Two cationic polyelectrolytes derived from hydroxyethylcellulose were used: JR400, a homopolymer, and Quatrisoft LM200, a polymer modified with alkyl side chains. The vesicles are composed of mixed anionic surfactant (sodium dodecyl sulfate) and cationic surfactant (didodecyldimethylammonium bromide), bearing 29 mol % of the cationic amphiphile. The phase behavior for the two mixed polymer−surfactant systems was investigated for polymer concentrations between 0.001 and 3 wt%. Three main regions were found in the two-phase maps, upon polymer addition: (i) a bluish solution phase; (ii) a wide region of phase separation, containing a precipitate and a solution; and (iii) a polymer−rich gel region, forming upon charge reversal of the system. Cryo-TEM imaging of the solution phase shows the formation of faceted vesicles and disklike aggregates, upon addition of JR400. For the LM200 system, besides the formation of faceted vesicles, clusters of vesicles and other bilayer structures are imaged. In the polymer−rich phase of JR400, membrane fragments, disklike aggregates, and vesicles are also found. These bilayer aggregates are likely to be involved with the polymer in highly connected networks, giving rise to the observed bluish gels. Electrostatic interactions, reinforced by hydrophobic interactions in the case of LM200, are the main driving force for the structural transitions observed.
publishDate 1999
dc.date.none.fl_str_mv 1999-10-05
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/10458
http://hdl.handle.net/10316/10458
https://doi.org/10.1021/ma990350+
url http://hdl.handle.net/10316/10458
https://doi.org/10.1021/ma990350+
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Macromolecules. 32:20 (1999) 6626-6637
0024-9297
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dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
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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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dc.identifier.doi.none.fl_str_mv 10.1021/ma990350