0000000000343928

AUTHOR

Benjamin Nottelet

0000-0002-8577-9273

showing 3 related works from this author

MRI-visible nanoparticles from hydrophobic gadolinium poly(ε-caprolactone) conjugates

2015

International audience; In this work we report on the synthesis of two hydrophobic and degradable gadolinium poly(ε-caprolactone) conjugates and their use for the preparation of MRI-visible nanoparticles intended for diagnosis applications. Advantage has been taken from functional poly(ε-caprolactone)s (PCL) bearing propargyl (PCL-yne) or amine groups (P(CL-co-NH2VL)) to yield conjugates by following two strategies. In a first approach, an azido-chelate of gadolinium (Gd(III)) has been conjugated by CuAAC to PCL-yne to yield a polymeric chelate containing 2.6 wt% of Gd(III). In a second approach, a dianhydride Gd(III)-ligand was reacted with P(CL-co-NH2VL) to yield, after complexation with …

[CHIM.POLY] Chemical Sciences/PolymersMaterials sciencePolymers and PlasticsBiocompatibility[SDV.IB.IMA]Life Sciences [q-bio]/Bioengineering/ImagingGadoliniumchemistry.chemical_elementNanoparticle02 engineering and technologyConjugated system010402 general chemistry01 natural scienceschemistry.chemical_compoundNanoparticlePolymer chemistryMaterials ChemistrypolyesterChelationOrganic Chemistry021001 nanoscience & nanotechnology0104 chemical sciences[CHIM.POLY]Chemical Sciences/Polymers[SDV.IB.IMA] Life Sciences [q-bio]/Bioengineering/ImagingchemistryPropargylnanoparticlesAmine gas treating0210 nano-technologyCaprolactoneMRIPolymer
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MRI-Visible Poly(ε-caprolactone) with Controlled Contrast Agent Ratios for Enhanced Visualization in Temporary Imaging Applications

2013

International audience; Hydrophobic macromolecular contrast agents (MMCAs) are highly desirable to provide safe and efficient magnetic resonance (MR) visibility to implantable medical devices. In this study, we report on the synthesis and evaluation of novel biodegradable poly(ε-caprolactone)-based MMCAs. Poly(α-propargyl-ε-caprolactone-co-ε-caprolactone)s containing 2, 5, and 10 mol % of propargyl groups have been prepared by ring-opening copolymerization of ε-caprolactone and the corresponding propargylated lactone. In parallel, a diazido derivative of the clinically used diethylenetriaminepentaacetic acid (DTPA)/Gd3+ complex has been synthesized. Finally, MRI-visible poly(ε-caprolactone)…

Gadolinium DTPAPolymers and PlasticsMacromolecular SubstancesPolyestersContrast MediaBiocompatible MaterialsBioengineering02 engineering and technology010402 general chemistrybiomedical01 natural sciencesImagingBiomaterialsMicechemistry.chemical_compoundPoly(ε-caprolactone)Polymer chemistryMaterials ChemistryCopolymerAnimalsmacromolecularCell Proliferationchemistry.chemical_classificationMolecular Structure[CHIM.ORGA]Chemical Sciences/Organic chemistryMRI; Poly(ε-caprolactone); ImagingSpin–lattice relaxationFibroblastsHydrophobic[CHIM.ORGA] Chemical Sciences/Organic chemistry021001 nanoscience & nanotechnologyGraftingMagnetic Resonance ImagingvisibleCycloaddition0104 chemical sciencescopolymerizationchemistryPropargylDTPA0210 nano-technologyCaprolactoneLactoneMacromoleculeMRI
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Toward potent antibiofilm degradable medical devices: A generic method for the antibacterial surface modification of polylactide

2013

International audience; The effects of biomaterials on their environment must be carefully modulated in most biomedical applications. Among other approaches, this modulation can be obtained through the modification of the biomaterial surface. This paper proposes a simple and versatile strategy to produce non-leaching antibacterial polylactide (PLA) surfaces without any degradation of the polyester chains. The method is based on a one-pot procedure that provides a "clickable" PLA surface via anionic activation which is then functionalized with an antibacterial quaternized poly(2-(dimethylamino)ethyl methacrylate) (QPDMAEMA) by covalent immobilization on the surface. The anti-adherence and an…

Materials scienceBiocompatibilityCell SurvivalSurface PropertiesPolyestersBiomedical Engineering02 engineering and technologyBacterial Physiological PhenomenaPolylactide010402 general chemistryMethacrylate01 natural sciencesBiochemistryCell LineBiomaterialsMiceSurface modificationCoated Materials BiocompatibleAbsorbable ImplantsMaterials TestingPolymer chemistryAnimalsSurface modification Polylactide Antibacterial Biocompatibility BiofilmParticle SizeMolecular Biology[CHIM.ORGA]Chemical Sciences/Organic chemistryBiofilmtechnology industry and agricultureBiofilmBiomaterialGeneral Medicineequipment and supplies021001 nanoscience & nanotechnologyCombinatorial chemistryAnti-Bacterial Agents0104 chemical sciencesAntibacterialPolyesterNylonsCovalent bondBiofilmsMethacrylatesSurface modificationBiocompatibilityCrystallization0210 nano-technologyAntibacterial activityBiotechnologyActa Biomaterialia
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