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Genipin-Cross-Linked Layer-by-Layer Assemblies: Biocompatible Microenvironments To Direct Bone Cell Fate

Year: 2014

Journal: Biomacromolecules, 2014, 15 (5), pp 1602–1611, 20141007

Authors: Fabien Gaudière †, Sandrine Morin-Grognet †,Laurent Bidault ‡, Pierre Lembré ‡, Emmanuel Pauthe ‡, Jean-Pierre Vannier †, Hassan Atmani †,Guy Ladam †, and Béatrice Labat †

Last authors: Béatrice Labat

Organizations: † Laboratoire de Biophysique et Biomatériaux (La2B),MERCI EA 3829, University of Rouen, Centre Universitaire d’Évreux, 1 rue du 7ème Chasseurs, 27002 Évreux Cedex, France ‡ ERRMECe EA 1391, University of Cergy-Pontoise, 2 avenue Adolphe Chauvin, 95302 Cergy-Pontoise Cedex, France

Country: France

The design of biomimetic coatings capable of improving the osseointegration of bone biomaterials is a current challenge in the field of bone repair. Toward this end, layer-by-layer (LbL) films composed of natural components are suitable candidates. Chondroitin sulfate A (CSA), a natural glycosaminoglycan (GAG), was used as the polyanionic component because it promotes osteoblast maturation in vivo. In their native state, GAG-containing LbL films are generally cytophobic because of their low stiffness. To stiffen our CSA-based LbL films, genipin (GnP) was used as a natural cross-linking agent, which is much less cytotoxic than conventional chemical cross-linkers. GnP-cross-linked films display an original combination of microscale topography and tunable mechanical properties. Structural characterization was partly based on a novel donor/acceptor Förster resonance energy transfer (FRET) couple, namely, FITC/GnP, which is a promising approach for further inspection of any GnP-cross-linked system. GnP-cross-linked films significantly promote adhesion, proliferation, and early and late differentiation of preosteoblasts.