Compounds for functionalizing biomaterials

The present invention provides compounds suitable for functionalizing biomaterials, in particular prosthetics and implant materials, functionalized biomaterials, and methods for synthesizing the compound. The compounds contain an anchoring group, a group for covalent binding to modified osteoblast precursor cells and a group for binding to endothelial cells or precursor cells

Tuning the Properties of Hydrogel Microspheres by Adding Chemical Cross-linking Functionality to Sodium Alginate

The production of hydrogel microspheres (MS) for cell immobilization, maintaining the favorable properties of alginate gels but presenting enhanced performance in terms of in vivo durability and physical properties, is desirable to extend the therapeutic potential of cell transplantation. A novel type of hydrogel MS was produced by straightforward functionalization of sodium alginate (Na-alg) with heterotelechelic poly(ethylene glycol) (PEG) derivatives equipped with either end thiol or 1,2-dithiolane moieties. Activation of the hydroxyl moieties of the alginate backbone in the form of imidazolide intermediate allowed for fast conjugation to PEG oligomers through a covalent carbamate linkage. Evaluation of the modified alginates for the preparation of MS combining fast ionic gelation ability of the alginate carboxylate groups and slow covalent cross-linking provided by the PEG-end functionalities highlighted the influence of the chemical composition of the PEG-grafting units on the physical characteristics of the MS. The mechanical properties of the MS (resistance and shape recovery) and durability of PEG-grafted alginates in physiological environment can be adjusted by varying the nature of the end functionalities and the length of the PEG chains. In vitro cell microencapsulation studies and preliminary in vivo assessment suggested the potential of these hydrogels for cell transplantation applications

Functionalization of microstructured open-porous bioceramic scaffolds with human fetal bone cells.

Bone substitute materials allowing trans-scaffold migration and in-scaffold survival of human bone-derived cells are mandatory for development of cell-engineered permanent implants to repair bone defects. In this study, we evaluated the influence on human bone-derived cells of the material composition and microstructure of foam scaffolds of calcium aluminate. The scaffolds were prepared using a direct foaming method allowing wide-range tailoring of the microstructure for pore size and pore openings. Human fetal osteoblasts (osteo-progenitors) attached to the scaffolds, migrated across the entire bioceramic depending on the scaffold pore size, colonized, and survived in the porous material for at least 6 weeks. The long-term biocompatibility of the scaffold material for human bone-derived cells was evidenced by in-scaffold determination of cell metabolic activity using a modified MTT assay, a repeated WST-1 assay, and scanning electron microscopy. Finally, we demonstrated that the osteo-progenitors can be covalently bound to the scaffolds using biocompatible click chemistry, thus enhancing the rapid adhesion of the cells to the scaffolds. Therefore, the different microstructures of the foams influenced the migratory potential of the cells, but not cell viability. Scaffolds allow covalent biocompatible chemical binding of the cells to the materials, either localized or widespread integration of the scaffolds for cell-engineered implants

Surface functionalization of alumina ceramic foams with organic ligands.

Different anchoring groups have been studied with the aim of covalently binding organic linkers to the surface of alumina ceramic foams. The results suggested that a higher degree of functionalization was achieved with a pyrogallol derivative - as compared to its catechol analogue - based on the XPS analysis of the ceramic surface. The conjugation of organic ligands to the surface of these alumina materials was corroborated by DNP-MAS NMR measurements

Role of habitat and landscape in structuring small mammal assemblages in hedgerow networks of contrasted farming landscapes in Brittany, France.

International audienceIn this study, we investigated the environmental factors driving small mammal (rodents and shrews) assemblages in permanent habitat patches in response to a gradient of agricultural intensification. Small mammals were sampled using a trapping standard method in the hedgerow networks of three contrasted landscapes differing by their level of landuse intensity and hedgerow network density (BOC1: slightly intensified; BOC2: moderately intensified and POL: highly intensified). We hypothesized that habitat and landscape characteristics have to be considered to understand the structure of local community. In that way, we carried out a multi-scale study using environmental variables ranging from local habitat (structure and composition of the hedgerows) to hedgerows neighbourhoods in a radius of 300 m (land cover and connectivity around hedges) and to landscape units (three sites). During 1 year, 24 hedgerows were sampled seven times, representing a total of 1,379 captures (86% of rodents and 14% of shrews) and eight species, dominated by the wood mouse (Apodemus sylvaticus) and the bank vole (Clethrionomys glareolus). Inter-site variability was significant and accounted for 18% of total variation in small mammal species abundances. But intra-site variability was also highlighted: species abundance profiles may differ greatly among hedgerows within a site. The more explanatory variables were identified at the different scales of the study: the landscape unit POL was shown to be an important factor in structuring the community, but the predominant factors explaining differences of abundances among hedgerows were about local habitat. In fact, the width of hedges and the tree species richness appeared to be significant and explaining the greatest part of the total variation of the small mammal community composition