US2007254833A1PendingUtilityA1
Compositions and methods for treating diverticular disease
Est. expiryNov 10, 2023(expired)· nominal 20-yr term from priority
A61P 43/00A61P 9/00A61B 17/12109A61L 2300/412A61L 27/54A61B 17/11A61B 17/1219A61K 38/363A61K 38/39A61L 2300/00A61L 2430/38A61B 17/12099A61B 17/12022A61B 17/1214A61F 2250/0067A61B 17/12168A61L 31/16A61P 19/00A61B 17/68A61K 38/38A61K 45/06A61K 38/4833A61P 1/00A61B 17/12186
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Claims
Abstract
Agents, compositions, and implants are provided herein for treating diverticular disease (e.g., diverticulosis and diverticulitis). In particular, fibrosis-inducing agents, hemostatic agents, and/or anti-infective agents, or compositions containing one or more of these agents are provided for use in methods for treating diverticular disease.
Claims
exact text as granted — not AI-modified1 . A method of treating a diverticular disease, comprising introducing into a diverticulum in a host, a therapeutically effective amount of a composition comprising a fibrosing agent and a polymer, wherein the fibrosing agent induces a fibrotic response within the diverticulum, thereby treating diverticular disease in the host.
2 . The method of claim 1 wherein the diverticular disease is diverticulosis or diverticulitis.
3 . The method of claim 1 wherein the fibrosing agent promotes regeneration, fibrosis and regeneration, angiogenesis, fibroblast migration, fibroblast proliferation, deposition of extracellular matrix (ECM), or tissue remodeling, or a combination thereof.
4 . The method of claim 1 wherein the fibrosing agent is a diverticular wall irritant.
5 . The method of claim 4 wherein the diverticular wall irritant is talc, talcum powder, metallic beryllium or oxides thereof, copper, silica, crystalline silicates, quartz dust, calcium phosphate, calcium sulfate, calcium carbonate, hydroxyapatite, synthetic mineral, silver nitrate, or ceramic.
6 . The method of claim 4 wherein the diverticular wall irritant is starch or polymethylmethacrylate.
7 . The method of claim 1 wherein the polymer is or comprises a biodegradable polymer.
8 . The method of claim 1 wherein the polymer is or comprises a non-biodegradable polymer.
9 . The method of claim 1 wherein the polymer is a naturally occurring polymer.
10 . The method of claim 9 wherein the naturally occurring polymer is a protein, polypeptide, carbohydrate, or polysaccharide.
11 . The method of claim 10 wherein the naturally occurring polymer is collagen or a derivative thereof, fibrinogen, thrombin, albumin, gelatin, hyaluronic acid, starch, cellulose, methylcellulose, dextran, sodium alginate, heparin, or chitosan.
12 . The method of claim 1 wherein the polymer is a synthetic polymer.
13 . The method of claim 12 wherein the synthetic polymer is or comprises a polyester, a polyalkylene oxide, or a cyanoacrylate.
14 . The method of claim 1 wherein the composition is in the form of a gel, paste, microsphere, particle, foam, spray or aerosol.
15 . The method of claim 1 wherein the composition is introduced by delivery from an implant.
16 . The method of claim 15 wherein the implant is a thread, fiber, coil, film, mesh, tuft, sponge, rod, tube, slab or sphere.
17 . The method of claim 1 or 15 wherein the composition further comprises a bulking agent, tissue filler, sealant, or haemostatic agent.
18 . The method of claim 1 wherein the composition further comprises a second pharmaceutically active agent.
19 . The method of claim 18 wherein the second pharmaceutically active agent is an anti-inflammatory agent, an agent that inhibits infection, an inflammatory cytokine, or an agent that stimulates cell proliferation.
20 . The method of claim 1 further comprising irrigating the diverticulum with an irrigation solution prior to introducing the fibrosing agent.
21 . The method of claim 20 wherein the irrigation solution comprises an anti-infective agent; an antiseptic agent; or both an anti-infective agent and an antiseptic agent.Cited by (0)
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