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hal.structure.identifierUniv Mons, Belgique, Serv Chim Mat Nouveaux
dc.contributor.authorOUARTI, Nadia
hal.structure.identifierUniv Mons, Belgique, Serv Chim Mat Nouveaux
dc.contributor.authorVIVILLE, Pascal
hal.structure.identifierUniv Mons, Belgique, Serv Chim Mat Nouveaux
dc.contributor.authorLAZZARONI, Roberto
hal.structure.identifierUniv Fed Santa Catarina, Dept Quim
dc.contributor.authorMINATTI, Edson
hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
dc.contributor.authorSCHAPPACHER, Michel
hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorDEFFIEUX, Alain
hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorBORSALI, Redouane
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2005
dc.identifier.issn0743-7463
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20686
dc.description.abstractEnWe have studied the effect of polystyrene (PS) homopolymer addition on the morphology of self-assembled block copolymer micelles made from linear or cyclic poly(styrene-b-isoprene), PS-b-PI, in a selective solvent for the PI block (heptane). Both copolymers have the same composition: the degree of polymerization is 290 for the PS block, and 110 for the PI block, and we focused on the influence of the addition of small amounts of PS homopolymer on the micellar morphology. For the copolymer concentrations considered, the linear copolymer self-organizes into spherical micelles while the cyclic copolymer forms cylindrical micelles. PS and PI chains constitute the core and the corona of these micelles, respectively, due to the different affinity of the blocks for heptane. Consequently, the PS homopolymer added is "solubilized" into the micellar core. Dynamic light scattering (DLS) data combined with atomic force microscopy (AFM) results show that the addition of PS homopolymer induces a drastic change in the micellar organization. Indeed, a morphological transition, from spheres to cylinders for the linear copolymer, and from cylinders to vesicles for the cyclic copolymer, is observed. These results highlight the fact that a small incorporation of PS homopolymer is clearly sufficient to modify the morphology (size and shape) of the micelles. This approach could be a key parameter for the design/control of micelles for specific applications in nanotechnology.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enSURFACTANTS
dc.subject.enACID)
dc.subject.enDILUTE-SOLUTION
dc.subject.enPHASE-BEHAVIOR
dc.subject.enANGLE NEUTRON-SCATTERING
dc.subject.enDIBLOCK COPOLYMERS
dc.subject.enMULTIPLE MORPHOLOGIES
dc.subject.enDRUG-DELIVERY
dc.subject.enWORMLIKE MICELLES
dc.subject.enVESICLES
dc.title.enControl of the morphology of linear and cyclic PS-b-PI block copolymer micelles via PS addition
dc.typeArticle de revue
dc.identifier.doi10.1021/la048944f
dc.subject.halChimie/Polymères
bordeaux.journalLangmuir
bordeaux.page1180-1186
bordeaux.volume21
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue4
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00394136
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00394136v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Langmuir&rft.date=2005&rft.volume=21&rft.issue=4&rft.spage=1180-1186&rft.epage=1180-1186&rft.eissn=0743-7463&rft.issn=0743-7463&rft.au=OUARTI,%20Nadia&VIVILLE,%20Pascal&LAZZARONI,%20Roberto&MINATTI,%20Edson&SCHAPPACHER,%20Michel&rft.genre=article


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