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Vincent Darcos

Vincent Darcos

Research engineer, Faculty of pharmacy, University of Montpellier

Vincent is a CNRS Research Engineer at the Institute of Biomolecules Max Mousseron (IBMM). After defending his PhD in the field of organic chemistry (2000, University of Bordeaux), he joined the group of Prof. Dave Haddleton at the University of Warwick in UK (Marie-Curie Fellowship, 2000-2002). Then, he moved for a one-year post-doctoral fellow at the University of Bordeaux (LCPO) in the group of Dr. Yves Gnanou (Rhodia funding). In 2004, he joined the IBMM and defended his HDR in 2017. His research interests focus in the field of macromolecular engineering in order to develop original polymeric biomaterials for health applications.
His research interests focus in the field of macromolecular engineering in order to develop original polymeric biomaterials for health applications. Some of his current projects focus on the development of new drug delivery systems, implantable medical devices for bone reconstruction, or bioconjugates for medical diagnosis. He is the co-author of 42 publications and 2 patents in the field of polymer chemistry.
He’s in charge of the “polymer” facility of the SynBio3 platform (IBISA label & ISO9001 certification) dedicated to assist the development of research programs in life science providing biomolecules and polymers of biological and pharmaceutical interest.


(+33) 0411759704

5 recent publications:

El Habnouni, S.; Darcos, V.; Coudane, J., Synthesis and Ring Opening Polymerization of a New Functional Lactone, alpha-Iodo-epsilon-caprolactone: A Novel Route to Functionalized Aliphatic Polyesters. Macromolecular Rapid Communications 2009, 30 (3), 165-169.

Bakkour, Y.; Darcos, V.; Li, S. M.; Coudane, J., Diffusion ordered spectroscopy (DOSY) as a powerful tool for amphiphilic block copolymer characterization and for critical micelle concentration (CMC) determination. Polymer Chemistry 2012, 3 (8), 2006-2010.

Coumes, F.; Huang, C. Y.; Huang, C. H.; Coudane, J.; Domurado, D.; Li, S. M.; Darcos, V.; Huang, M. H., Design and Development of Immunomodulatory Antigen Delivery Systems Based on Peptide/PEG-PLA Conjugate for Tuning Immunity. Biomacromolecules 2015, 16 (11), 3666-3673.

Younis, M.; Darcos, V.; Paniagua, C.; Ronjat, P.; Lemaire, L.; Nottelet, B.; Garric, X.; Bakkour, Y.; El Nakat, J. H.; Coudane, J., MRI-visible polymer based on poly(methyl methacrylate) for imaging applications. Rsc Advances 2016, 6 (7), 5754-5760.

Coumes, F.; Beaute, L.; Domurado, D.; Li, S.; Lecommandoux, S.; Coudane, J.; Darcos, V., Self-assembly of well-defined triblock copolymers based on poly(lactic acid) and poly(oligo(ethylene glycol) methyl ether methacrylate) prepared by ATRP. RSC Advances 2016, 6 (58), 53370-53377

Star-poly(lactide)-peptide hybrid networks as bioactive materials


European Polymer Journal Volume 139, 5 October 2020, 109990

L.V. Arsenie, C. Pinese, A. Bethry, L. Valot, P. Verdie, B. Nottelet, G. Subra, V. Darcos, X. Garric


Abstract Poly(lactide) (PLA) is a widely used biomaterial in many biomedical applications. However, it is inert and therefore lacks bioactivity, which is a major drawback in addressing tissue regeneration issues. This work aims to develop new implantable biomaterials composed of PLAs functionalized with bioactive peptides. For that purpose, we set up an original synthesis based on star-PLA bearing triethoxysilyl propyl groups (PLA-PTES) and bifunctional silylated peptides that react together via sol-gel process to create a bioactive network. We demonstrate that the molecular weight of the PLA and the quantity of peptide have a large influence on the crosslinking efficiency, the mechanical properties and the biodegradability of the resulting materials. The presence of peptide increases the crosslinking efficiency of the networks resulting in more rigid networks with stable mechanical properties up to 8 weeks. At last, the potential of this new type of hybrid biomaterials for soft tissue engineering was demonstrated through cells adhesion assays that showed a significant enhancement of fibroblasts adhesion

Star-poly(lactide)-peptide hybrid networks as bioactive materials

Star-poly(lactide)-peptide hybrid networks as bioactive materials

Well-defined polyester-grafted silica nanoparticles for biomedical applications: Synthesis and quantitative characterization

Polymer, 2020, 211, 123048

Lagarrigue P., Soulié J., Grossin D., Dupret-Bories A., Combes C., Darcos V.


Polyester-based composites with silica nanoparticles fillers are promising candidates as biomaterials due to improved mechanical and biological properties. However, nanofillers use generally leads to an inhomogeneous distribution inside the polymer matrix because of agglomeration, decreasing composites overall performances. To improve nanofillers dispersion, the aim of this study is to prepare and characterize poly(D,L lactide) grafted silica nanoparticles using “grafting to” method and to quantify the amount of grafted poly(D,L lactide). Firstly, well-defined N hydroxysuccinimide ester poly(D,L lactide)s were synthetized through a new pathway. Then, amino-functionalized silica nanoparticles were grafted with those customized polyesters yielding an amide covalent bond between both reagents. Such PDLLA grafted nanoparticles were precisely characterized and the grafting amount was quantified using a dual approach based on TGA and FTIR analysis. The synthesis and the characterization methods developed constitute a robust and reproducible way to design well-defined polymer grafted silica nanoparticles that could be used as nanofillers in polymer matrix nanocomposites for biomedical


Self-assembly of well-defined triblock copolymers based on poly(lactic acid) and poly(oligo(ethylene glycol) methyl ether methacrylate) prepared by ATRP

 RSC Adv. 6, 53370–53377 (2016)

Coumes, F., Beaute, L., Domurado, D., Li, S., Lecommandoux, S., Coudane, J. & Darcos, V.


Self-assembly of a series of amphiphilic poly(oligo(ethylene glycol) methyl ether methacrylate)-block-poly(lactic acid)-block-poly(oligo(ethylene glycol) methyl ether methacrylate) (P(OEGMA)-b-PLLA-b-P(OEGMA)) copolymers was investigated. The copolymers were synthesized by a combination of ring-opening polymerization (ROP) of L-lactide and atom transfer radical polymerization (ATRP) of oligo ethylene glycol methyl ether methacrylate (OEGMA). The resulting brush-like triblock copolymers were characterized by 1H NMR and size exclusion chromatography. Self-assembly behavior of the copolymers in deionized water was investigated by fluorescence spectroscopy, dynamic light scattering (DLS), and transmission electron microscopy (TEM). The critical aggregation concentration ranged from 50 to 160 mg L−1 depending on the composition. The diameter of the nanoparticles (NPs) was determined by DLS and TEM. Images showed that these nano-sized objects displayed spherical and worm-like morphology with a length increasing with the hydrophilic content. Preliminary studies of drug loading and drug release with a water-insoluble model drug, namely curcumin, showed that these NPs are potential candidates for drug delivery carriers.

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MRI-visible polymer based on poly(methyl methacrylate) for imaging applications

RSC Adv. 6, 5754–5760 (2016).

Younis, M., Darcos, V., Paniagua, C., Ronjat, P., Lemaire, L., Nottelet, B., Garric, X., Bakkour, Y., El Nakat, J. H. & Coudane, J.



Macromolecular contrast agents are very attractive to afford efficient magnetic resonance imaging (MRI) visualization of implantable medical devices. In this work, we report on the grafting of a Gd-based DTPA contrast agent onto a poly(methyl methacrylate) derivative backbone by combining free radical polymerization and copper-catalyzed azide-alkyne cycloaddition (CuAAC). Using free radical polymerization, poly(methyl methacrylate-co-propargyl methacrylate) copolymers were prepared with a control of the ratio in propargyl methacrylate monomer units. The synthesis of a new azido mono-functionalized DTPA ligand was also reported and characterized by 1H NMR and mass spectroscopy. After complexation with gadolinium, this ligand has been grafted on the polymer backbone by click chemistry reaction. The obtained macromolecular contrast agent was then coated on a polypropylene mesh using the airbrushing technique and the mesh was assessed for MRI visualization at 7 teslas. The polymeric contrast agent was also tested for cytocompatibility and stability to assess its suitability for biomedical applications.

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