CROSSLINKED HYDROGELS
    3.
    发明公开
    CROSSLINKED HYDROGELS 有权
    交联水凝胶

    公开(公告)号:EP2219694A2

    公开(公告)日:2010-08-25

    申请号:EP08861332.8

    申请日:2008-12-16

    IPC分类号: A61L27/16

    CPC分类号: A61L27/16

    摘要: The present invention preferably provides for a method of forming and the resulting solid polymer gel composition comprising polyethylene imine and at least one hydrogen bonding polymer. The composition has a greater viscosity than either of the polyethylene imine or the hydrogen bonding polymer alone and is injectable immediately after mixing of the polyethylene imine and the at least one hydrogen bonding polymer. A method of tissue repair may include mixing about 9.25% (w/w) to about 13.65% (w/w) polyethylene imine and about 18.02% (w/w) to about 26.62% (w/w) polyvinyl alcohol to form an injectable composition; injecting the injectable composition into a cavity within a human body; and allowing the composition to solidify in situ. A kit may include a multi-barrel syringe at least one barrel is loaded with polyethylene imine and at least another barrel is loaded with at least one hydrogen bonding polymer.

    HYDROGEL BALLOON PROSTHESIS FOR NUCLEUS PULPOSUS
    4.
    发明公开
    HYDROGEL BALLOON PROSTHESIS FOR NUCLEUS PULPOSUS 有权
    HYDROGEL-BALLONPROTHESEFÜRNUCLEUS PULPOSUS

    公开(公告)号:EP1917050A2

    公开(公告)日:2008-05-07

    申请号:EP06813765.2

    申请日:2006-08-25

    申请人: Synthes GmbH

    IPC分类号: A61L27/52 A61F2/44

    摘要: A prosthesis for replacing or supplementing a nucleus pulposus of an intervertebral disk is an expandable container having flexible walls, the container being adapted to be inserted into a central cavity of an intervertebral disk through a narrow cannula, and the flexible walls are made from a biocompatible hydrogel. A preferred hydrogel is a cryogel formed from an aqueous solution of poly(vinyl alcohol) and poly(vinyl pyrrolidone). The prosthesis may be prepared by dip-coating a mandrel with an aqueous solution of a hydrogel-forming polymer or mixture of such polymers, gelling the coated solution by chilling, and subjecting the gelled coating to a series of repeated freeze-thaw treatments. In use, the prosthesis is inserted into a central cavity of an intervertebral disk and filled with biocompatible material, e.g., a biocompatible liquid, a biocompatible polymer, and a biocompatible hydrogel, particularly a thermogelling hydrogel.