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Synthesis and Characterization of Conjugated Hyaluronic Acids. Application to Stability Studies of Chitosan-Hyaluronic Acid Nanogels Based on Fluorescence Resonance Energy Transfer
dc.rights.license | open | en_US |
dc.contributor.author | MALYTSKYI, Volodymyr | |
dc.contributor.author | MOREAU, Juliette | |
dc.contributor.author | CALLEWAERT, Maite | |
dc.contributor.author | HENOUMONT, Celine | |
dc.contributor.author | CADIOU, Cyril | |
hal.structure.identifier | Chimie et Biologie des Membranes et des Nanoobjets [CBMN] | |
dc.contributor.author | FEUILLIE, Cecile | |
dc.contributor.author | LAURENT, Sophie | |
dc.contributor.author | MOLINARI, Michael | |
dc.contributor.author | CHUBURU, Francoise | |
dc.date.accessioned | 2024-09-19T07:49:57Z | |
dc.date.available | 2024-09-19T07:49:57Z | |
dc.date.issued | 2022-03-15 | |
dc.identifier.issn | 2310-2861 | en_US |
dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/201673 | |
dc.description.abstractEn | Hyaluronic acid (HA) was functionalized with a series of amino synthons (octylamine, polyethylene glycol amine, trifluoropropyl amine, rhodamine). Sodium hyaluronate (HAs) was first converted into its protonated form (HAp) and the reaction was conducted in DMSO by varying the initial ratio (−NH2 (synthon)/COOH (HAp)). HA derivatives were characterized by a combination of techniques (FTIR, 1H NMR, 1D diffusion-filtered 19F NMR, DOSY experiments), and degrees of substitution (DSHA) varying from 0.3% to 47% were determined, according to the grafted synthon. Nanohydrogels were then obtained by ionic gelation between functionalized hyaluronic acids and chitosan (CS) and tripolyphosphate (TPP) as a cross-linker. Nanohydrogels for which HA and CS were respectively labeled by rhodamine and fluorescein which are a fluorescent donor-acceptor pair were subjected to FRET experiments to evaluate the stability of these nano-assemblies. | |
dc.language.iso | EN | en_US |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 United States | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/us/ | * |
dc.subject.en | Nanohydrogels–hyaluronic acid–HA-mPEG2000 | |
dc.subject.en | Fluorinated and fluorescent HA conjugates–hyaluronic acid degree of substitution–diffusion ordered spectroscopy (DOSY)–1D diffusion-filtered 19F NMR–atomic force microscopy–FRET experiments–hyaluronidase–nanohydrogel stability | |
dc.title.en | Synthesis and Characterization of Conjugated Hyaluronic Acids. Application to Stability Studies of Chitosan-Hyaluronic Acid Nanogels Based on Fluorescence Resonance Energy Transfer | |
dc.type | Article de revue | en_US |
dc.identifier.doi | 10.3390/gels8030182 | en_US |
dc.subject.hal | Chimie/Matériaux | en_US |
dc.description.sponsorshipEurope | European Regional Development Fund | en_US |
bordeaux.journal | Gels | en_US |
bordeaux.volume | 8 | en_US |
bordeaux.hal.laboratories | CBMN : Chimie & de Biologie des Membranes & des Nano-objets - UMR 5248 | en_US |
bordeaux.issue | 3 | en_US |
bordeaux.institution | Université de Bordeaux | en_US |
bordeaux.institution | Bordeaux INP | en_US |
bordeaux.institution | CNRS | en_US |
bordeaux.peerReviewed | oui | en_US |
bordeaux.inpress | non | en_US |
hal.popular | non | en_US |
hal.audience | Internationale | en_US |
hal.export | false | |
dc.rights.cc | CC BY-NC-ND | en_US |
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