Elise Guégain

ORCID: 0000-0002-9620-8038
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About
Contact & Profiles
Research Areas
  • Advanced Polymer Synthesis and Characterization
  • biodegradable polymer synthesis and properties
  • Dendrimers and Hyperbranched Polymers
  • Nanoparticle-Based Drug Delivery
  • Antimicrobial agents and applications
  • Polymer Surface Interaction Studies
  • Graphene and Nanomaterials Applications
  • Chemical Synthesis and Reactions
  • Synthetic Organic Chemistry Methods
  • Chemical Synthesis and Analysis
  • Luminescence and Fluorescent Materials
  • Lanthanide and Transition Metal Complexes
  • Orthopaedic implants and arthroplasty
  • Nanoplatforms for cancer theranostics
  • Polymer composites and self-healing
  • RNA Interference and Gene Delivery
  • Molecular Sensors and Ion Detection
  • Photopolymerization techniques and applications
  • Radioactive element chemistry and processing
  • Polyoxometalates: Synthesis and Applications

MedinCell (France)
2023

Centre National de la Recherche Scientifique
2015-2019

Institut Galien Paris-Saclay
2015-2019

Centro de Investigacion Principe Felipe
2019

Centro Médico Sanitas Valencia
2019

Université Paris-Sud
2015-2018

Pharmac
2015-2018

Laboratoire d'Énergétique Moléculaire et Macroscopique, Combustion
2015-2018

Radical copolymerization of donor-acceptor (D-A) monomer pairs has served as a versatile platform for the development alternating copolymers. However, due to use conventional radical polymerization, resulting copolymers have generally been limited nondegradable vinyl polymers. By combining D-A with ring-opening polymerization (rROP), we synthesized an copolymer high incorporation degradable backbone units. Copolymerization N-ethyl maleimide (NEtMI) cyclic ketene acetal (CKA)...

10.1021/acsmacrolett.7b00572 article EN ACS Macro Letters 2017-09-15

Radical ring-opening copolymerization-induced self-assembly (rROPISA) was performed by copolymerizing benzyl methacrylate and cyclic ketene acetals (CKA), such as 2-methylene-4-phenyl-1,3-dioxolane or 5,6-benzo-2-methylene-1,3-dioxepane, in heptane at 90 °C reversible addition-fragmentation chain transfer (RAFT) polymerization from a poly(lauryl methacrylate) macro-RAFT agent. The lengths of both the solvophilic agent solvophobic block, together with initial amount CKA, were independently...

10.1021/acs.macromol.9b00161 article EN Macromolecules 2019-05-06

The review focus on branched polymers as promising delivery systems with immunomodulatory properties against cancer and infectious diseases. It covers their physicochemical how those can be tailored to modulate the immune system.

10.1039/c9mh00628a article EN Materials Horizons 2019-01-01

The efficient and reliable synthesis of 2-methylene-4-phenyl-1,3-dioxolane (MPDL) was reported MPDL used as a controlling comonomer for nitroxide-mediated polymerization methyl methacrylate to give degradable copolymers.

10.1039/c6py00778c article EN Polymer Chemistry 2016-01-01

Polymer prodrug nanoparticles with aggregation-induced emission properties were readily prepared by a “grafting from” approach, leading to excellent imaging ability and cytotoxicity cancer cells.

10.1039/c6cc09052d article EN Chemical Communications 2017-01-01

Two libraries of well-defined, degradable vinyl copolymers opposite solubility, based either on methyl methacrylate (MMA) or oligo(ethylene glycol) ether (OEGMA), and containing various amount 2-methylene-4-phenyl-1,3-dioxolane (MPDL), were synthesized by nitroxide-mediated radical ring-opening polymerization. A comprehensive degradation study (long-term hydrolytic degradation, thick thin films, water uptake, enzymatic degradation) was then performed, results compared with those from...

10.1021/acs.macromol.7b02655 article EN Macromolecules 2018-02-02

2 Methylene-4-phenyl-1,3-dioxolane (MPDL) was used as a controlling comonomer in NMP with oligo(ethylene glycol) methyl ether methacrylate (MeOEGMA) to prepare well-defined and degradable PEG-based P(MeOEGMA-<italic>co</italic>-MPDL) copolymers.

10.1039/c5cc04610f article EN cc-by-nc Chemical Communications 2015-01-01

Degradable polymer prodrugs were synthesized by ‘drug-initiated’ nitroxide-mediated radical ring-opening copolymerization and led to either nanoparticles or soluble with adjustable cytotoxicity on two different cancer cell lines.

10.1039/c8sc02256a article EN cc-by-nc Chemical Science 2018-01-01

Polymer prodrugs based on cladribine (CdA) as an anticancer drug have been prepared by growing short, well-defined polyisoprene (PI) chains (with number-average molar mass = 1420–4980 g mol–1 and dispersity 1.09–1.20) from CdA-bearing alkoxyamine nitroxide-mediated polymerization. Nanoparticles were formed nanoprecipitation into water of the resulting CdA-PI conjugates exhibited long-term colloidal stability in different media, tunable characteristics, release profiles, activities vitro,...

10.1021/acs.chemmater.6b02502 article EN Chemistry of Materials 2016-08-22

Facile derivatization of paclitaxel (Ptx) and subsequent “drug-initiated” synthesis well-defined Ptx-polymer prodrugs was performed from nitroxide-mediated polymerization or reversible addition–fragmentation chain transfer polymerization.

10.1039/c7py01918a article EN Polymer Chemistry 2018-01-01

Investigation on the reactivity and controlling ability of a series amide-functionalized alkoxyamines based SG1 nitroxide is reported.

10.1039/c5py00283d article EN cc-by-nc Polymer Chemistry 2015-01-01

Front Cover: Nitroxide-mediated polymerization (NMP) of methacrylic esters is still a great challenge in the field polymer science. This Feature Article will first discuss reasons why this class monomers–the most representative one being methyl methacrylate–is usually poorly controlled by NMP, and then present successful strategies to control their polymerization. NMP-derived materials comprising uncontrolled methacrylate segments also be covered. Further details can found article E....

10.1002/marc.201570051 article EN Macromolecular Rapid Communications 2015-07-01
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