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Accueil > Les équipes > Chimie des Polymères (LCP) > Séminaires

17 10 06 Prof. Byeong-Su KIM

publié le , mis à jour le

Ulsan National Institute of Science and Technology (UNIST), Corée

"C-O-C Chemistry : Functional Epoxide Monomers for Novel Polyethers toward Smart Drug Delivery Applications"
vendredi 6 octobre 2017 à 10h30

Campus Jussieu
Barre 43-53, 5e étage, salle 522

Abstract :
Poly(ethylene glycol) (PEG) is by far the most well-known synthetic biocompatible polymer for its widespread use in the food, cosmetics, and biomedical applications. However, its limited functionality combined with its complicated synthetic nature often poses challenges for advanced material design and synthesis. In this talk, our recent effort in the development of novel functional epoxide monomers with multifunctionality will be highlighted. Specifically, we will cover the design and the synthesis of well-defined stimuli-responsive polyethers such as pH- and redox-stimuli for biocompatible and biodegradable smart drug delivery systems.
In the first part of the talk, the design and the synthesis of novel hydrophobic, pH-responsive epoxide monomer, pyranyl glycidyl ether (PGE) will be discussed. Anionic ring-opening polymerization affords the controlled synthesis of a series of its homopolymers (PPGE) and amphiphilic polymers, poly(ethylene glycol)-block-poly(pyranyl glycidyl ether) (PEG-b-PPGE). Interestingly, these block copolymers with cyclic PGE moieties showed superior stability in biological media, high loading capacity, tunable release, and controllable degradation compared to its acyclic analogue, 1-ethoxy glycidyl ether (EEGE), widely employed in the polyether, which satisfy all the required design principles and address the challenges in drug delivery systems.
In the second part of the talk, the redox-degradable hyperbranched polyglycerols (PSSG) based on a glycerol monomer containing a disulfide bond, i.e., 2-((2-(oxiran-2-ylmethoxy)ethyl)disulfanyl)ethan-1-ol (SSG) will be presented. The polymerization through anionic ring-opening multibranching polymerization to yield a series of redox-degradable hyperbranched polyglycerols (PSSGs) with controlled molecular weights and relatively low molecular weight distributions. Furthermore, the redox-responsive degradation of the polymers upon treatment with a reducing agent resulted in selective degradation of the polymers in small segments. With its high biocompatibility, we anticipate that these novel redox-degradable and will find applications in a variety of emerging biomedical fields.