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Volume 6, Issue 9, Pages 3640-3648 (September 2010)


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Fabrication of porous polysaccharide-based scaffolds using a combined freeze-drying/cross-linking process

Aude Autissierab, Catherine Le Visagea, Cécile Pouzetc, Frédéric Chaubetab, Didier LetourneurabCorresponding Author Informationemail address

Received 23 December 2009; received in revised form 22 February 2010; accepted 2 March 2010. published online 08 March 2010.

Abstract 

Biocompatible three-dimensional (3-D) porous scaffolds are of great interest for tissue engineering applications. We here present a novel combined freeze-drying/cross-linking process to prepare porous polysaccharide-based scaffolds. This process does not require an organic solvent or porogen agent. We unexpectedly found that cross-linking of biomacromolecules such as pullulan and dextran with sodium trimetaphosphate could be performed during freeze-drying. We have demonstrated that the freeze-drying pressure modulates the degree of porosity. High freeze-drying pressure scaffolds presented pores with a mean diameter of 55±4μm and a porosity of 33±12%, whereas low freeze-drying pressure scaffolds contained larger pores with a mean diameter of 243±14μm and a porosity of 68±3%. Porous scaffolds of the desired shape could be easily obtained and were stable in culture medium for weeks. In vitro viable mesenchymal stem cells were found associated with porous scaffolds in higher proportions than with non-porous scaffolds. Moreover, cells penetrated deeper into scaffolds with larger pores. This novel combined freeze-drying/cross-linking processing of polysaccharides enabled the fabrication of biocompatible scaffolds with controlled porosity and architectures suitable for 3-D in vitro culture and biomedical applications.

a INSERM, U698, Bio-ingénierie Cardiovasculaire, Hôpital Bichat, 46 Rue H. Huchard, F-75877 Paris Cedex 18, France

b Institut Galilée, Université Paris 13, 99 Avenue Jean-Baptiste Clément, F-93430 Villetaneuse, France

c IFR2, Institut Claude Bernard, Faculté de Médecine Paris 7 Diderot, Hôpital Bichat, 46 Rue H. Huchard, F-75870 Paris Cedex 18, France

Corresponding Author InformationCorresponding author. Address: INSERM, U698, Bio-ingénierie Cardiovasculaire, Hôpital Bichat, 46 Rue H. Huchard, F-75877 Paris Cedex 18, France. Tel.: +33 140258600; fax: +33 140258602.

PII: S1742-7061(10)00130-3

doi:10.1016/j.actbio.2010.03.004


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