References of "Jérôme, Christine"
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See detailNew developments in electrografting of thin polymer films
Jérôme, Christine ULg

Conference (2006, June)

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See detailElectrografting of thermo-responsive polymer film on conductive substrate
Gabriel, Sabine ULg; Stach, M.; Zhang, T. et al

Poster (2006, May 18)

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See detailSynthesis of novel amphiphilic and pH-sensitive ABC miktoarm star copolymers
Van Butsele, Kathy; Stoffelbach, François; Jérôme, Robert ULg et al

Poster (2006, May 18)

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See detailA generic platform for SPM-based molecular recognition processes and stiluli-responsive probes
Gabriel, Sabine ULg; Jérôme, Christine ULg; Silva-Goncalves, Elsa et al

Poster (2006, May 18)

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See detailDesign of stealth nanoparticles for drug delivery based on new amphiphilic copolymers
Rieger, Jutta ULg; Passirani, Catherine; Dubois, Philippe et al

Conference (2006, May 18)

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See detailStructure and morphology of thin films of fulorinated copolymers
Awada, H.; Lenoir, Sandrine; Jérôme, Christine ULg et al

Poster (2006, May 18)

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See detailSynthèse de revêtement de nano-objets par électroréduction
Jérôme, Christine ULg

Poster (2006, May)

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See detailSurface modification of metallic cardiovascular stents by strongly adhering aliphatic polyester coatings
Jérôme, Christine ULg; Aqil, Abdelhafid ULg; Voccia, Samuel et al

in Journal of Biomedical Materials Research, Part A (2006), 76(3), 521-529

This article reports on a novel two-step strategy for the coating of cardiovascular stents by strongly adhering biocompatible and biodegradable aliphatic polyesters. First, a precoating of poly ... [more ▼]

This article reports on a novel two-step strategy for the coating of cardiovascular stents by strongly adhering biocompatible and biodegradable aliphatic polyesters. First, a precoating of poly(ethylacrylate) (PEA) was electrografted onto the metallic substrate by cathodic reduction of the parent monomer in dimethylformamide (DMF). The electrodeposition of PEA, in a good solvent of it, was confirmed by both Infra-red and Raman spectroscopies. The pendant ester groups of PEA were then chemically reduced into aluminum alkoxides, able to initiate the ring-opening polymerization (ROP) of either D,L-lactide (LA) or epsilon-caprolactone (CL). Growth of biodegradable PLA or PCL coatings from the adhering precoating was confirmed by both Infra-red and Raman spectroscopies, and directly observed by scanning electron microscopy (SEM). This type of coating can act as an anchoring layer for the subsequent casting of drug-loaded polyester films allowing the controlled release of antiproliferative agents for the treatment of in-stent restenosis. [less ▲]

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See detailElectrografting of thin polymer films: Three strategies for the tailoring of functional adherent coatings
Voccia, Samuel; Gabriel, Sabine ULg; Serwas, Harry et al

in Progress in Organic Coatings (2006), 55(2), 175-181

Cathodic electrografting is an efficient technique to impart adhesion to poly(meth)acrylate coatings onto inorganic conducting surfaces. Although this technique was restricted for many years to very few ... [more ▼]

Cathodic electrografting is an efficient technique to impart adhesion to poly(meth)acrylate coatings onto inorganic conducting surfaces. Although this technique was restricted for many years to very few monomers ((meth)acrylonitrile and (meth)acrylates) and to deposition of very thin polymer films, recent developments have overcome these limitations. First of all, classical controlled/living polymerization techniques have been combined with cathodic electrografting as a powerful strategy for tuning thickness, properties and reactivity of the chemisorbed organic films. Secondly, thanks to the successful electrografting of a new reactive monomer bearing an activated ester, electrografted surfaces are now available for further derivatization by a wide variety of nucleophiles. Finally, the electrografting process has been extended to the direct electrografting of reactive polymers, i.e. preformed polymers beating pendant acrylic functions, which opens the way to the grafting of, e.g., polycondensates. [less ▲]

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See detailCombination of electrografting and atom-transfer radical polymerization for making the stainless steel surface antibacterial and protein antiadhesive
Ignatova, Miléna; Voccia, Samuel; Gilbert, Bernard ULg et al

in Langmuir (2006), 22(1), 255-262

A two-step "grafting from" method has been successfully carried out, which is based on the electrografting of polyacrylate chains containing an initiator for the atom transfer radical polymerization (ATRP ... [more ▼]

A two-step "grafting from" method has been successfully carried out, which is based on the electrografting of polyacrylate chains containing an initiator for the atom transfer radical polymerization (ATRP) of 2-(tert-butylamino)ethyl methacrylate (TBAEMA) or copolymerization of TBAEMA with either monomethyl ether of poly(ethylene oxide) methacrylate (PEOMA) or acrylic acid (AA) or styrene. The chemisorption of this type of polymer brushes onto stainless steel surfaces has potential in orthopaedic surgery. These films have been characterized by ATR-FTIR, Raman spectroscopy, atomic force microscopy (AFM), and measurement of contact angles of water. The polymer formed in solution by ATRP and that one detached on purpose from the surface have been analyzed by size exclusion chromathography (SEC) and H-1 NMR spectroscopy. The strong adherence of the films onto stainless steel has been assessed by peeling tests. AFM analysis has shown that addition of hydrophilic comonomers to the grafted chains decreases the surface roughness. According to dynamic quartz crystal microbalance experiments, proteins (e.g., fibrinogen) are more effectively repelled whenever copolymer brushes contain neutral hydrophilic (PEOMA) co-units rather than negatively charged groups (PAA salt). Moreover, a 2- to 3-fold decrease in the fibrinogen adsorption is observed when TBAEMA is copolymerized with either PEOMA or AA rather than homopolymerized or copolymerized with styrene. Compared to the bare stainless steel surface, brushes of polyTBAEMA, poly (TBAEMA-co-PEOMA) and poly(TBAEMA-co-AA) decrease the bacteria adhesion by 3 to 4 orders of magnitude as revealed by Gram-positive bacteria S. aureus adhesion tests. [less ▲]

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See detailMechanochemistry: targeted delivery of single molecules
Duwez, Anne-Sophie ULg; Cuenot, Stéphane; Jérôme, Christine ULg et al

in Nature Nanotechnology (2006), 1

The use of scanning probe microscopy-based techniques to manipulate single molecules(1) and deliver them in a precisely controlled manner to a specific target represents a significant nanotechnological ... [more ▼]

The use of scanning probe microscopy-based techniques to manipulate single molecules(1) and deliver them in a precisely controlled manner to a specific target represents a significant nanotechnological challenge(2,3). The ultimate physical limit in the design and fabrication of organic surfaces can be reached using this approach. Here we show that the atomic force microscope (AFM), which has been used extensively to investigate the stretching of individual molecules(4-12), can deliver and immobilize single molecules, one at a time, on a surface. Reactive polymer molecules, attached at one end to an AFM tip, are brought into contact with a modified silicon substrate to which they become linked by a chemical reaction. When the AFM tip is pulled away from the surface, the resulting mechanical force causes the weakest bond - the one between the tip and polymer - to break. This process transfers the polymer molecule to the substrate where it can be modified by further chemical reactions. [less ▲]

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See detailMechanochemistry: targeted delivery of single molecules
Duwez, Anne-Sophie ULg; Cuenot, Stéphane; Jérôme, Christine ULg et al

in Nature Nanotechnology (2006), 1

The use of scanning probe microscopy-based techniques to manipulate single molecules1 and deliver them in a precisely controlled manner to a specific target represents a significant nanotechnological ... [more ▼]

The use of scanning probe microscopy-based techniques to manipulate single molecules1 and deliver them in a precisely controlled manner to a specific target represents a significant nanotechnological challenge. The ultimate physical limit in the design and fabrication of organic surfaces can be reached using this approach. Here we show that the atomic force microscope (AFM), which has been used extensively to investigate the stretching of individual molecules, can deliver and immobilize single molecules, one at a time, on a surface. Reactive polymer molecules, attached at one end to an AFM tip, are brought into contact with a modified silicon substrate to which they become linked by a chemical reaction. When the AFM tip is pulled away from the surface, the resulting mechanical force causes the weakest bond — the one between the tip and polymer — to break. This process transfers the polymer molecule to the substrate where it can be modified by further chemical reactions [less ▲]

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See detailFirst Insights into Electrografted Polymers by AFM-Based Force Spectroscopy
Cuenot, Stéphane; Gabriel, Sabine ULg; Jérôme, Robert ULg et al

in Macromolecules (2006), 39

The very first characterization of the structural properties of polymer films obtained by electrografting is reported. AFM-based force spectroscopy was used to investigate poly-N-succinimidyl acrylate ... [more ▼]

The very first characterization of the structural properties of polymer films obtained by electrografting is reported. AFM-based force spectroscopy was used to investigate poly-N-succinimidyl acrylate (PNSA) layers electrografted directly from a silicon substrate. Quantitative analysis of compression profiles obtained in a good solvent and single molecule bridging interaction, in light of the Alexander-de Gennes model, gave access to the grafting density and degree of polymerization. A high swelling capacity has been evidenced. This report is the first evidence that polymers obtained by cathodic electrografting are in fact brush systems, and consequently the first evidence that a polymer brush can be obtained from a direct “grafting from” method, without any intermediate layer. [less ▲]

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See detailMulti-biomaterial for controlled release of active substances
Zalfen, Alina; Nizet, Dominique; Jérôme, Christine ULg et al

Poster (2006)

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See detailControlled synthesis of an ABC miktoarm star-shaped copolymer by sequential ring-opening polymerization of ethylene oxide, benzyl beta-malolactonate, and epsilon-caprolactone
Rieger, Jutta ULg; Coulembier, Olivier; Dubois, Philippe ULg et al

in Macromolecules (2005), 38(26), 10650-10657

This paper reports on the synthesis of an amphiphilic miktoarm ABC star-shaped copolymer, s[(PEO)(PMLABz)(PCL)], consisting of biocompatible/bioresorbable arms. Indeed, PEO is a hydrophilic biocompatible ... [more ▼]

This paper reports on the synthesis of an amphiphilic miktoarm ABC star-shaped copolymer, s[(PEO)(PMLABz)(PCL)], consisting of biocompatible/bioresorbable arms. Indeed, PEO is a hydrophilic biocompatible poly(ethylene oxide) arm, PMLABz is a poly(benzyl beta-malolactonate) arm precursor of a pH-sensitive bioresorbable poly(beta-malic acid) block, and PCL is a hydrophobic bioresorbable poly(epsilon-caprolactone) arm. Each constitutive arm was prepared by ring-opening polymerization. A double-headed PEO macroinitiator [PEO-(OH)-COO-K+] was first prepared by selective hydrolysis of the alpha-lactone (2-oxepanone) end group of PEO chains end-capped by a omega-methoxy group. The anionic polymerization of benzyl beta-malolactonate (MLABz) was selectively initiated by the alpha-potassium carboxylate end group of PEO in the presence of 18-crown-6 ether. The polymerization of epsilon-caprolactone (epsilon-CL) was initiated by the hydroxyl group left at the junction of the two blocks of the as-prepared PEO-b-PMLABz diblock copolymer, in the presence of tin(II) bis(2-ethylhexanoate) (Sn(Oct)(2)). The macroinitiator, the intermediate diblock, and the final miktoarm. star-shaped copolymer were analyzed by H-1 NMR spectroscopy and size exclusion chromatography. [less ▲]

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See detailCombination of ring-opening polymerization and "click" chemistry towards functionalization of aliphatic polyesters
Riva, Raphaël ULg; Schmeits, Stephanie ULg; Stoffelbach, François et al

in Chemical Communications (2005), (42), 5334-5336

Azide pendent groups of aliphatic polyesters have been derivatized into tertiary amines, ammonium salts and poly(ethylene oxide) grafts. The experimental conditions have been optimized (organic solvent ... [more ▼]

Azide pendent groups of aliphatic polyesters have been derivatized into tertiary amines, ammonium salts and poly(ethylene oxide) grafts. The experimental conditions have been optimized (organic solvent, 35 degrees C), such that the aliphatic polyesters are not degraded, including even poly(lactide) which is very sensitive to attack by weak nucleophiles. [less ▲]

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See detailTailoring of thin polymer films chemisorbed onto conductive surfaces by electrografting
Jérôme, Christine ULg; Jérôme, Robert ULg

in Urban, Marek W (Ed.) Stimuli-responsive polymeric films and coatings (2005)

Cathodic electrografting is an efficient technique to impart adhesion to poly(meth)acrylate coatings onto inorganic conducting surfaces. Although this technique was restricted for many years to very few ... [more ▼]

Cathodic electrografting is an efficient technique to impart adhesion to poly(meth)acrylate coatings onto inorganic conducting surfaces. Although this technique was restricted for many years to very few monomers ((meth)acrylonitrile) and to deposition of very thin polymer films, recent developments have overcome these limitations. First of all, the judicious choice of the solvent has proved to be a powerful lever to increase the range of the chemisorbed polymers, including functional polymers. Quite interestingly, classical controlled polymerization techniques have been combined with cathodic electrografting as a powerful strategy for tuning thickness, properties and reactivity of the chemisorbed organic films. At the time being, cathodic electrografting has contributed to substantial progress in very demanding applications, such as protection against corrosion, food packaging, biomaterials, sizing of reinforcing agents in polymer composites and sensoring devices. [less ▲]

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See detailAn easy and economically viable route for the decoration of carbon nanotubes by magnetite nanoparticles, and their orientation in a magnetic field
Stoffelbach, François; Aqil, Abdelhafid ULg; Jérôme, Christine ULg et al

in Chemical Communications (2005), (36), 4532-4533

A simple, cheap and tunable approach for the decoration of carbon nanotubes by magnetite nanoparticles and their orientation in a magnetic field is reported.

Detailed reference viewed: 20 (3 ULg)