0000000000023198

AUTHOR

Laurent Lemaire

showing 2 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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