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dc.rights.licenseopenen_US
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorAYDINLIOGLU, Esra
hal.structure.identifierEindhoven University of Technology [Eindhoven] [TU/e]
dc.contributor.authorABDELGHANI, Mona
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
hal.structure.identifierUnité Matériaux et Transformations - UMR 8207 [UMET]
dc.contributor.authorLE FER, Gaëlle
hal.structure.identifierEindhoven University of Technology [Eindhoven] [TU/e]
dc.contributor.authorVAN HEST, Jan C. M.
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorSANDRE, Olivier
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorLECOMMANDOUX, Sébastien
dc.date.accessioned2022-12-01T17:53:29Z
dc.date.available2022-12-01T17:53:29Z
dc.date.issued2022-11-30
dc.identifier.issn1022-1352en_US
dc.identifier.urioai:crossref.org:10.1002/macp.202200306
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/170447
dc.description.abstractEnTwo pairs of oppositely charged PEO-b-poly(amino acid) copolymers with neutral poly(ethylene oxide) block and polypeptide block composed of the hydrophobic l-phenylalanine (Phe) amino acid mixed with either negative l-glutamic acid (Glu) or positive l-lysine (Lys) units were synthesized. N-carboxyanhydride (NCA) ring opening polymerization (ROP) was performed with either PEO46-NH2 or PEO114-NH2 macroinitiators, leading respectively to PEO46-b-P(Glu100-co-Phe65) and PEO46-b-P(Lys100-co-Phe65), and PEO114-b-P(Glu60-co-Phe40) and PEO114-b-P(Lys60-co-Phe40). Polyion complexes (PIC) formed at near charge equilibrium led to vesicle formation (PICsomes), as shown by DLS, zetametry and TEM. The good stability of PICsomes, even in high salinity media, was interpreted by π-π stacking hydrophobic interactions between the Phe residues, playing the role of “physical cross-linking”. These PICsomes were successfully loaded with siRNA directed against firefly luciferase enzyme expression. They also exhibit minimal cell cytotoxicity while superior silencing efficacy was shown by cell bioluminescence assay as compared to free siRNA and a standard lipofectamine-siRNA complex. As such, self-assembly of oppositely charged PEO-b-poly(amino acids) block copolymers enabled forming PICsomes of high stability thanks to π-π interactions of the Phe co-monomer in the polypeptide block, with high potential as biocompatible nanocarriers for RNA interference.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-ShareAlike 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/us/*
dc.sourcecrossref
dc.subjectpoly(L-glutamic acid)
dc.subjectpoly(L-lysine)
dc.subjectpoly(L-phenylalanine)
dc.subjectN-carboxyanhydride (NCA)
dc.subjectring opening polymerization (ROP)
dc.subjectcircular dichroism
dc.subjectsmall interfering RNA (siRNA)
dc.subjectpolyionic complex (PIC) vesicles
dc.subject.enPEO-b-poly(amino acids) block copolymers
dc.subject.enPICsomes
dc.subject.ensiRNAsomes
dc.title.enRobust Polyion Complex Vesicles (PICsomes) based on PEO‐ b ‐Poly(Amino Acid) Copolymers Combining Electrostatic and Hydrophobic Interaction: Formation, siRNA Loading and Intracellular Delivery
dc.title.alternativeMacromol. Chem. Phys.en_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1002/macp.202200306en_US
dc.subject.halChimie/Polymèresen_US
dc.subject.halSciences du Vivant [q-bio]/Biochimie, Biologie Moléculaireen_US
bordeaux.journalMacromolecular Chemistry and Physicsen_US
bordeaux.page202200306en_US
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcedissemin
hal.identifierhal-03881535
hal.version1
hal.date.transferred2022-12-01T17:53:33Z
hal.exporttrue
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dc.rights.ccCC BY-NC-SAen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Macromolecular%20Chemistry%20and%20Physics&rft.date=2022-11-30&rft.spage=202200306&rft.epage=202200306&rft.eissn=1022-1352&rft.issn=1022-1352&rft.au=AYDINLIOGLU,%20Esra&ABDELGHANI,%20Mona&LE%20FER,%20Ga%C3%ABlle&VAN%20HEST,%20Jan%20C.%20M.&SANDRE,%20Olivier&rft.genre=article


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