Abstract: The invention relates to beads and a composition comprising an aqueous phase comprising a plurality of beads, the beads comprising or consisting in a hydrogel matrix comprising at least one carboxyalkyl chitosan having glucosamine units, N-acetyl-glucosamine units and glucosamine units substituted with a carboxyalkyl group, the carboxyalkyl chitosan being crosslinked by covalent bonds between the carboxyalkyl chitosan chains and/or co-crosslinked by covalent bonds with one or more other polymers. The invention also relates to processes for their preparation and applications thereof.

Abstract: The present invention relates to a crosslinked carboxyalkyl chitosan forming a matrix, compositions comprising same, a method for manufacturing same, and the different applications thereof, in particular in the field of therapy, rheumatology, ophthalmology, aesthetic medicine, plastic surgery, internal surgery, dermatology, gynecology or cosmetics. The invention relates in particular to a matrix comprising at least one carboxyalkyl chitosan having glucosamine units, N-acetylglucosamine units and glucosamine units substituted with a carboxyalkyl group, the carboxyalkyl chitosan having a degree of acetylation ranging from 40% to 80%, expressed as the number of moles of N-acetyl groups relative to the number of moles of total glucosamine units, the carboxyalkyl chitosan being crosslinked by covalent bonds between the chains of carboxyalkyl chitosan.

Abstract: A modified superabsorbent polymer (SAP) comprises a SAP matrix and urea in the form of crystals that is integrated into the SAP matrix. The SAP matrix and the urea are interpenetrated. A method for producing the modified SAP may comprise a) preparing a mixture comprising at least one urea solution and at least one SAP, b) swelling the SAP in the mixture, c) crystallizing the urea in the mixture obtained upon completion of step b), d) recovering the modified SAP in the mixture, and e) optionally, forming the modified SAP recovered at step d).

Abstract: The invention relates to a method for producing a biocompatible crosslinked gel consisting in crosslinking a determined quantity of at least one type of liquid biocompatible polymer by adding a quantity of crosslinking agent, in carrying out a crosslinking reaction, in adding an additional quantity of liquid polymer whose molecular mass is greater than 500,000 Da, in solving the reaction mixture in such a way that the total concentration of the liquid polymer is reduced, in crosslinking and in stopping the crosslinking reaction by removing the crosslinking agent. The inventive gel and the use thereof are also disclosed.

Abstract: The invention relates to an ocular device which permits the avoidance of the phenomenon of photophobia and the method for production thereof. The device comprises one or more chromophores which absorb light in the wavelengths between 400 and 575 nm (blue-green light) and which are dispersed, after the placement in or on the eye, in the surrounding body fluids in several weeks to several months depending on the concentration of the chromophores. The device is produced by conditioning of the non-colored ocular device in an aqueous solution of the chromophore(s) in the shade.

Abstract: The invention relates to a method for producing a biocompatible crosslinked gel consisting in crosslinking a determined quantity of at least one type of liquid biocompatible polymer by adding a quantity of crosslinking agent, in carrying out a crosslinking reaction, in adding an additional quantity of liquid polymer whose molecular mass is greater than 500,000 Da, in solving the reaction mixture in such a way that the total concentration of the liquid polymer is reduced, in crosslinking and in stopping the crosslinking reaction by removing the crosslinking agent. The inventive gel and the use thereof are also disclosed.

Abstract: A complex matrix is constituted by at least one biocompatible polymer of natural origin, cross linked and to which are grafted small chains of a molecular weight less than 50,000 Da with an amount of grafting of 10 to 40%, as well as a process for preparation of a biocompatible matrix that is partly degradable, constituted by at least one polymer of natural origin, consisting: on the one hand, grafting small chains of molecular weight less than 10,000 Da, with a grafting amount of 10 to 40%, on the other hand, cross linking the principal polymer chains to create a homogeneous matrix.