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AssigneeGliatech, Inc.
InventorsDikla Roufa, Adrian Harel, Robert C. A. Frederickson, George T. Coker, III
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The present invention relates to the discovery that biocompatible anionic polymers can effectively inhibit fibrosis, scar formation, and surgical adhesions. The invention is predicated on the discovery that anionic polymers effectively inhibit invasion of cells associated with detrimental healing processes, and in particular, that he effectiveness of an anionic polymer at inhibiting cell invasion correlates with the anionic charge density of the polymer. Thus the present invention provides a large number of materials for use in methods of inhibiting fibrosis and fibroblast invasion. Anionic polymers for use in the invention include but are not limited to natural proteoglycans, and the glycosaminoglycan moieties of proteoglycans. Additionally, anionic carbohydrates and other anionic polymers may be used. The anionic polymers dextran sulfate and pentosan polysulfate are preferred. In a more preferred embodiment, dextran sulfate, in which the sulfur content is greater than about 10% by weight, may be used. In a more preferred embodiment, the average molecular weight is about 40,000 to 500,000 Daltons. The present invention provides compositions and methods to inhibit fibrosis and scarring associated with surgery. The invention further provides compositions and methods to inhibit glial cell invasion, detrimental bone growth and neurite outgrowth. In a preferred embodiment, the inhibitory compositions further comprise an adhesive protein.
A composition comprising:
A method for inhibiting fibrosis at a site of a lesion in a mammal comprising administering to a site of a lesion in a mammal a composition comprising an amount of dextran sulfate effective to inhibit fibrosis at the site of administration, in which the average molecular weight of the dextran sulfate is in the range of about 40,000 to 2,000,000 Daltons.
A method for inhibiting fibrosis at the site of a lesion in a mammal comprising the following steps:
A method of inhibiting peridural fibrosis in a mammal following laminectomy, comprising administering a composition comprising an amount of dextran sulfate effective to inhibit peridural fibrosis at the site of administration, to a laminectomy site in a mammal, in which the average molecular weight of the dextran sulfate is in the range of about 40,000 to 2,000,000 Daltons.
A composition comprising an amount of dextran sulfate effective to inhibit fibrosis in a mammal, in which the average molecular weight of the dextran sulfate is in the range of about 40,000 to 2,000,000 Daltons, and a pharmaceutically acceptable implant, which implant comprises denatured collagen.
A composition comprising an amount of dextran sulfate effective to inhibit fibrosis in a mammal, in which the average molecular weight of the dextran sulfate is in the range of about 40,000 to 2,000,000 Daltons, and a pharmaceutically acceptable implant, which implant comprises dextran.
A composition comprising (a) a solution in which the concentration of dextran sulfate is in the 2-20 mg/ml, and (b) denatured collagen, in which the sulfur content of the dextran sulfate is greater than about 10% by weight, and in which the average molecular weight of the dextran sulfate is about 40,000 Daltons.
A method for inhibiting fibrosis at the site of a lesion in a mammal comprising administering a composition produced from a solution in which the concentration of dextran sulfate is in the range of about 2-20 mg/ml, to a site of a lesion in a mammal, said composition being effective to inhibit fibrosis at the site of administration, in which the sulfur content of the dextran sulfate is greater than about 10% by weight, and in which the average molecular weight of the dextran sulfate is about 40,000 Daltons.
A method of inhibiting peridural fibrosis in a mammal following laminectomy or discectomy, comprising administering a composition comprising an amount of dextran sulfate effective to inhibit peridural fibrosis at the site of administration, to a laminectomy or discectomy site in a mammal, in which the average molecular weight of the dextran sulfate is in the range of about 40,000 to 2,000,000 Daltons.
A method for inhibiting fibrosis around an implant in a mammal comprising administering a pharmaceutically acceptable polymer implant to a mammal, which polymer implant contains or is coated by an amount of dextran sulfate effective to inhibit fibrosis at the site of administration in the mammal, which implant is selected from the group consisting of nephrostomy tube, peritoneal drainage tube, artificial hip joint, artificial heart valve, peripheral nerve repair prosthesis and other prostheses, and in which the average molecular weight of the dextran sulfate is in the range of about 40,000 to 2,000,000 Daltons.
A composition comprising a solution in which the concentration of dextran sulfate is in the range of about 2-20 mg/ml, in which the sulfur content of the dextran sulfate is greater than about 10% by weight, and a pharmaceutically acceptable surgical implant, which implant consists essentially of a polymer.
A composition comprising a denatured collagen gel, said gel comprising an amount of dextran sulfate effective to inhibit fibrosis in a mammal, in which the average molecular weight of the dextran sulfate is in the range of about 40,000 to 2,000,000 Daltons.
A composition comprising a dextran gel, said gel comprising an amount of dextran sulfate effective to inhibit fibrosis in a mammal.
Dependencies are inferred from the claim text.