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dc.rights.licenseembargoen_US
hal.structure.identifierNorwegian University of Science and Technology [Trondheim] [NTNU]
dc.contributor.authorSOLBERG, Amalie
hal.structure.identifierNorwegian University of Science and Technology [Trondheim] [NTNU]
dc.contributor.authorMO, Ingrid V.
hal.structure.identifierNorwegian University of Science and Technology [Trondheim] [NTNU]
dc.contributor.authorAACHMANN, Finn L.
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorSCHATZ, Christophe
hal.structure.identifierNorwegian University of Science and Technology [Trondheim] [NTNU]
dc.contributor.authorCHRISTENSEN, Bjørn E.
dc.date.accessioned2022-01-04T18:43:09Z
dc.date.available2022-01-04T18:43:09Z
dc.date.issued2021-09-09
dc.identifier.issn1759-9954en_US
dc.identifier.urioai:crossref.org:10.1039/d1py00727k
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/124315
dc.description.abstractEnRenewable resources can provide a range of different polysaccharide blocks that can be used to prepare new types of stimuli-responsive polysaccharide-based block copolymers. Alginates are natural polysaccharides widely used as biomaterials. Functional properties depend on the content and distribution of the two 4-linked monomers (β-D-mannuronate (M) and α-L-guluronate (G)). Blocks of L-guluronate (Gn) are responsible for cooperative binding of calcium ions and hydrogel formation. Incorporation of such blocks in block polysaccharide copolymers would represent a new class of engineered, Ca-sensitive biomacromolecules. Dioxyamines and dihydrazides have recently been shown to be well suited for preparation of block polysaccharide structures. Here we first show that when applied to alginate blocks (Gn and Mn) the two types are both very reactive, but the detailed distribution of acyclic (E)- and (Z)-forms and cyclic N-pyranosides, reaction kinetics, conjugate stability, and the rate of Schiff base reduction with α-picoline borane differ considerably, also compared to other polysaccharides. Hence, alginate specific protocols were developed. The linkers introduce a highly flexible joint in otherwise semiflexible Gn-based diblocks. This was demonstrated by SEC-MALS using a symmetrical Gn-b-Gn diblock, which in solution can best be described according to a broken rod model. Ca-Induced self-assembly of Gn-b-dextran diblocks was studied by dynamic light scattering, demonstrating that well defined nanoparticles could be prepared for certain combinations of chain lengths. Taken together, this approach provides a new class of engineered, stimuli-responsive block polysaccharide copolymers solely based on natural resources.
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.title.enAlginate-based diblock polymers: preparation, characterization and Ca-induced self-assembly
dc.typeArticle de revueen_US
dc.identifier.doi10.1039/d1py00727ken_US
dc.subject.halChimie/Polymèresen_US
bordeaux.journalPolymer Chemistryen_US
bordeaux.page5412-5425en_US
bordeaux.volume12en_US
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629en_US
bordeaux.issue38en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcedissemin
hal.identifierhal-03511278
hal.version1
hal.date.transferred2022-01-04T18:43:13Z
hal.exporttrue
workflow.import.sourcedissemin
dc.rights.ccCC BY-NC-SAen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Polymer%20Chemistry&rft.date=2021-09-09&rft.volume=12&rft.issue=38&rft.spage=5412-5425&rft.epage=5412-5425&rft.eissn=1759-9954&rft.issn=1759-9954&rft.au=SOLBERG,%20Amalie&MO,%20Ingrid%20V.&AACHMANN,%20Finn%20L.&SCHATZ,%20Christophe&CHRISTENSEN,%20Bj%C3%B8rn%20E.&rft.genre=article


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