References of "Jérôme, Christine"
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See detailPAI Annual Meeting
Ouhib, Farid ULg; Aqil, Abdelhafid ULg; Dirani, Ali et al

Poster (2016, September 12)

Detailed reference viewed: 13 (1 ULg)
See detailOrganocobalt complexes as source of radicals for the controlled polymerization of unconjugated monomers
Demarteau, Jérémy ULg; Cordella, Daniela ULg; Kermagoret, Anthony et al

Poster (2016, September 12)

Detailed reference viewed: 15 (3 ULg)
See detailPolyphosphoester containing amphiphilic block copolymers as drug nanocarriers
Ergül, Zeynep ULg; Vanslambrouck, Stéphanie; Thiry, Justine ULg et al

Poster (2016, September 12)

The design of drug delivery systems often requires biodegradable and biocompatible materials that allow safe retention and controlled release of the drug. In this respect, supramolecularly self-assembled ... [more ▼]

The design of drug delivery systems often requires biodegradable and biocompatible materials that allow safe retention and controlled release of the drug. In this respect, supramolecularly self-assembled amphiphilic block copolymers into spherical micelles are appropriate carriers for poorly soluble drugs. In that framework, we have designed novel functional poly(ethylene oxide)-b-polyphosphoester amphiphilic block copolymers able to cross-linked under UV and degrade in response to a reduction of the pH from neutral conditions. Therefore, an unsaturated alkene side-chain was introduced on the cyclic phosphate monomer according to a one-step reaction followed by its organocatalyzed polymerization initiated by a poly(ethylene oxide) macroinitiator. After self-assembly into water, the micelles were cross-linked by UV irradiation. Then, these cross-linked micelles have been loaded by doxorubicin, i.e. a drug used in cancer therapy. We observed that the doxorubicin loading increased with the number of double bonds on the polyphosphate block of non-cross-linked micelles. This diblock amphiphilic copolymer bearing pendant unsaturations appears thus particularly promising candidate to build micellar drug delivery systems for intravenous injection. [less ▲]

Detailed reference viewed: 36 (2 ULg)
See detailSynthesis and characterizations of non-isocyanate polyurethane (NIPU) hydrogels
Gennen, Sandro ULg; Grignard, Bruno ULg; Thomassin, Jean-Michel ULg et al

Poster (2016, September 12)

Polyurethane (PU) is on of the most used polymers for the preparation of hydrogels due to its good biocompatibility, biodegradation and excellent mechanical properties. PU hydrogels are found in lot of ... [more ▼]

Polyurethane (PU) is on of the most used polymers for the preparation of hydrogels due to its good biocompatibility, biodegradation and excellent mechanical properties. PU hydrogels are found in lot of applications such as wound dressing, soft contact lenses, drug delivery and scaffolds for tissue engineering. Classicaly, PU is produced by a step-growth polymerization between diols and diisocyanates. However, in order to avoid the use of harmful isocyanates compounds and because of regulations which tend to ban the use of isocyanates, we developed hydrogels based on a non-isocyanate polyurethane (NIPU) chemistry by valorizing CO2-sourced cyclic carbonates and amines. Precisely, NIPU hydrogels were prepared by a solvent-free copolymerization between bifunctional hydrophilic polyethylene glycol cyclic carbonates and diamines in presence of a triamine as a crosslinker, followed by a water swelling of the obtained cross-linked gel. Parameters such as the cross-linking ratio and diamine’s nature were optimized. Different clay contents (cloiste 30B) as nanofiller were dispersed in the ideal cyclic carbonate/diamine/triamine formulation prior polymerization in order to reinforce the compression properties of NIPU hydrogels. Finaly, we were able to prepare NIPU hydrogels with water content up to 80 % and good compression properties using low clay content. [less ▲]

Detailed reference viewed: 98 (7 ULg)
See detailSynthesis of cross-linked nanoparticles in supercritical carbon dioxide for protein delivery
Parilti, Rahmet ULg; Jérôme, Christine ULg; Howdle, Steven M.

Poster (2016, September 09)

Polymeric nanoparticles have been extensively investigated for their biomedical applications especially as drug carriers. There has been much research on multifunctional polymeric nanoparticles for the ... [more ▼]

Polymeric nanoparticles have been extensively investigated for their biomedical applications especially as drug carriers. There has been much research on multifunctional polymeric nanoparticles for the controlled release and targeted delivery of hydrophobic drugs. However, efficient encapsulation and delivery of hydrophilic therapeutics especially peptides/proteins still presents significant challenges. This project aims to develop a novel one-pot strategy to obtain well-defined cross-linked nanoparticles able to carry peptides/proteins in their core, as along with targeting and/or imaging agents on their surface. In addition to this objective, the polymerisations will be carried out in supercritical carbon dioxide (scCO2), which confers environmentally benign features to the process. Here, we investigate the feasibility of free radical dispersion polymerizations of 2-hydroxyethyl methacrylate (HEMA) in scCO2. In order to ensure the successful dispersion in scCO2 novel diblock CO2-philic surfactants are employed. These diblock surfactants are formed from two different segments, a CO2-phobic block which has an affinity to the growing particles and a second CO2-philic block that ensures surfactant solubility. [less ▲]

Detailed reference viewed: 26 (3 ULg)
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Peer Reviewed
See detailMacro- and near-mesoporous monoliths by medium internal phase emulsion polymerization: a systematic study
Mathieu, Kevin ULg; Jérôme, Christine ULg; Debuigne, Antoine ULg

in Polymer (2016), 99

The synthesis of a series of poly(ethylene oxide)-b-polystyrene copolymers with different block lengths was performed by radical addition fragmentation chain transfer. These amphiphilic copolymers were ... [more ▼]

The synthesis of a series of poly(ethylene oxide)-b-polystyrene copolymers with different block lengths was performed by radical addition fragmentation chain transfer. These amphiphilic copolymers were tested as stabilizers for water-in-oil medium internal phase emulsion (MIPE) templating polymerization and the formation of polyMIPEs with controlled morphology. Aside from the structure of the emulsion stabilizer, several parameters susceptible to influence the size of the cavities and the interconnectivity of the porous monoliths were probed including the choice of the comonomers, treatment of the emulsion by ultrasound, the use of controlled radical polymerization method for the network formation as well as interfacial initiation. Interconnected cellular monoliths were produced. The polymerization of the ultrasonicated water-in-ethylhexylacrylate/divinylbenzene MIPE notably led to near-mesoporous open-cell material. Mechanical properties and specific surface areas of the polyMIPEs were also investigated and discussed. [less ▲]

Detailed reference viewed: 41 (18 ULg)
See detailValorization of CO2 for the preparation of advanced materials
Gennen, Sandro ULg; Grignard, Bruno ULg; Thomassin, Jean-Michel ULg et al

Conference (2016, July 07)

Detailed reference viewed: 29 (6 ULg)
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Peer Reviewed
See detailAnionic flow polymerizations toward functional polyphosphoesters in microreactors: Polymerization and UV-modification
Baeten, Evelien; Vanslambrouck, Stéphanie; Jérôme, Christine ULg et al

in European Polymer Journal (2016), 80

The polymerization of cyclic phosphates to poly(phosphoester)s, PPEs, is optimized for chip- based microreactors under continuous flow conditions. The anionic ring-opening polymerization of 2-isobutyoxy-2 ... [more ▼]

The polymerization of cyclic phosphates to poly(phosphoester)s, PPEs, is optimized for chip- based microreactors under continuous flow conditions. The anionic ring-opening polymerization of 2-isobutyoxy-2-oxo-1,3,2-dioxaphospholane (iBP) via the use of two organocatalytic systems allowed to polymerize to nearly quantitative monomer conversion within 10 or 3 minutes, respectively at a reaction temperature of 40 °C. Further, the optimized polymerization protocol was applied to 2-butenoxy-2-oxo-1,3,2-dioxaphospholane (BP) which yields a polymer that carries an alkene functionality per monomer repeating unit. This material can be postmodified in an UV-induced radical thiol-ene reaction, which was also shown to proceed with very high efficiency under UV-flow conditions. Eventually, both reactions were coupled in a two-stage reactor setup, showing that the thermally-activated polymerization can be coupled with high efficiency to the UV-activated post-polymerization modification reaction. The introduced reactor setup can in the future be used to produce and screen a broad variety of functional PPE materials with various functionalities and physical properties. [less ▲]

Detailed reference viewed: 82 (31 ULg)