Prosthesis with improved biocompatibility

Prosthesis (i.e. – artificial body members) – parts thereof – or ai – Implantable prosthesis

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623 8, A61F 202

Patent

active

051163713

ABSTRACT:
An implantable prosthesis comprises a hydrogel enclosed within a flexible envelope. The hydrogel contains both hydrophilic and hydrophobic domains. It is prepared by copolymerizing a hydrophilic monomer such as water soluble N-vinylpyrrolidone, acrylates or methacrylates with non-water soluble monomers such as acrylates, methacrylates, N-vinyl carbazole, its derivatives, or a non-water soluble derivative of N-vinylpyrrolidone. The flexible envelope may be either porous or non-porous. The hydrogel may be either solid or composed of particles of a size greater than the porosity of the envelope.

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K. Kliment, et al; Use of Spongy Hydron in Plastic Surgery; 1968 J. Biomed. Mater. Res. vol. 2, pp. 237-243.
J. S. Calnan, et al; Clinical and Experimental Studies of Polyhydroxyehtylmethacrylate Gel ("Hydron") for Reconstructive Surgery; British J. Plastic Surg. vol. 24, pp. 113-124.

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