Interactions between Catanionic Vesicles and Oppositely Charged PolyelectrolytesPhase Behavior and Phase Structure
Autor(a) principal: | |
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Data de Publicação: | 1999 |
Outros Autores: | , , , |
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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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 |
format |
article |
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 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
American Chemical Society |
publisher.none.fl_str_mv |
American Chemical Society |
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 |
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 |
|
_version_ |
1822218374276448256 |
dc.identifier.doi.none.fl_str_mv |
10.1021/ma990350 |