Abstract: A family of infection resistant and biocidal polymeric materials incorporates an infection resistant biguanide such as chlorhexidine or polyhexanide pendant to the polymer chain, chemically linked to the polymer through the biguanide group secondary nitrogen atoms. The disclosure extends to the use of such polymeric materials in articles of manufacture and particularly in medical devices, and the preparation of the materials as polymer resins from which articles can be made, as solutions and emulsions which can be used for coating performed articles, and in situ on the surface of preformed polymeric articles.

Abstract: Polymers having non-thrombogenic properties can be prepared by copolymerizing monomers of at least three classes selected from (a) monomers having sulphate groups, (b) monomers having sulphonate groups, (c) monomers having sulphamate groups, (d) monomers having polyoxyalkylene ether groups, and (e) monomers having zwitterionic groups. The polymers can additionally be provided with anti-thrombogenic properties by including an additional comonomer having a pendant heparin (or hirudin, warfarin or hyaluronic acid) group. The polymers can be used as coating materials for medical devices, such as tubing or connectors, in order to provide them with non-thrombogenic, and optionally anti-thrombogenic, properties.

Abstract: The invention provides a medical device which comprises a polymer coating. The polymer coating comprises a polymer comprising a polymer backbone and having at least two pendant groups selected from: (a) a polyoxyalkylene ether group, (b) a sulphate group, (c) a sulphonate group, or (d) a sulphamate group, and the polymer is produced by polymerizing monomers having such groups.

Abstract: A biocompatible, lubricious, hydrophilic material useful for coating medical devices or for blending into polymer compositions intended for making medical devices comprises a terpolymer of 5 to 25 mole percent of a polymerisable monomer (1) having a polyethylene oxide unit with an average degree of polymerisation from 5 to 18 and a polymerisable carbon-carbon double bond, 5 to 30 mole percent of a polymerisable monomer (2) having a polyethylene oxide unit with an average degree of polymerisation from 19 to 65 and polymerisable carbon-carbon double bond, and 45 to 90 mole percent of an alkyl methacrylate (3): (1) CH2═C(R)—CO—[—O—CH2—CH2—]n1—O—R where n1 is from 5 to 18, and each R is independently H or CH3; (2) CH2═C(R)—CO—[—O—CH2—CH2—]n2—O—R where n2 is from 19 to 65 and each R is independently H or CH3; (3) CH2═C(CH3)—CO2—(CH2)m—CH3 where m is from 3 to 17, whic

Abstract: Polymers having non-thrombogenic properties can be prepared by copolymerizing monomers of at least three classes selected from (a) monomers having sulphate groups, (b) monomers having sulphonate groups, (c) monomers having sulphamate groups, (d) monomers having polyoxyalkylene ether groups, and (e) monomers having zwitterionic groups. The polymers can additionally be provided with anti-thrombogenic properties by including an additional comonomer having a pendant heparin (or hirudin, warfarin or hyaluronic acid) group. The polymers can be used as coating materials for medical devices, such as tubing or connectors, in order to provide them with non-thrombogenic, and optionally anti-thrombogenic, properties.