US2016317355A1PendingUtilityA1
Solid dressing for treating wounded tissue
Est. expiryAug 4, 2026(~0.1 yrs left)· nominal 20-yr term from priority
A61P 7/04A61P 17/02A61L 15/64A61L 2400/04A61F 2013/00106A61L 15/38A61L 15/325A61L 15/32A61L 15/58A61F 2013/0054A61F 13/00991A61L 26/0052A61L 15/44A61F 2013/00536A61L 26/0066A61L 2300/604A61F 2013/0091A61L 26/0042A61F 2013/00472A61F 2013/00174A61L 26/009A61F 13/02A61L 2300/252A61K 38/4833A61L 2300/418A61L 15/28A61F 13/0226A61L 15/26A61F 2013/00931C12Y 304/21005A61K 38/363A61L 2300/606A61F 13/00063A61L 2300/254A61L 15/225A61L 15/18A61L 2300/10A61L 2300/608A61F 13/0246A61F 13/00017A61F 13/00034A61F 13/00012A61F 13/00029A61F 13/01012A61F 13/01017A61F 13/01021A61F 13/01034A61F 13/05A61F 13/01029
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Claims
Abstract
Disclosed are solid dressings for treated wounded tissue in mammalian patients, such as a human, comprising a haemostatic layer consisting essentially of fibrinogen and a fibrinogen activator, wherein the fibrinogen is present in an amount between 3.0 mg/cm 2 of the wound facing surface of the dressing and 13.0 mg/cm 2 of the wound facing surface of the dressing. Also disclosed are methods for treating wounded tissue.
Claims
exact text as granted — not AI-modified1 . A solid dressing for treating wounded tissue in a mammal comprising at least one haemostatic layer consisting essentially of fibrinogen and a solvent consisting of water and a fibrinogen activator wherein said haemostatic layer is substantially homogeneous, wherein said fibrinogen is present in an amount about 13.0 mg/cm 2 of the wound facing surface of said dressing, and wherein the moisture content of said solid dressing is from 6% to 44%.
2 . The solid dressing of claim 1 , further comprising at least one support layer.
3 . The solid dressing of claim 2 , wherein said support layer comprises a backing material.
4 . The solid dressing of claim 2 , wherein said support layer comprises an internal support material.
5 . The solid dressing of claim 2 ; wherein said support layer comprises a resorbable material.
6 . The solid dressing of claim 2 , wherein said support layer comprises a non resorbable material.
7 . (canceled)
8 . The solid dressing of claim 3 , further comprising at least physiologically acceptable adhesive between said haemostatic layer and said backing layer.
9 - 11 . (canceled)
12 . The solid dressing of claim 1 , wherein said haemostatic layer also contains a fibrin crosslinker and/or a source of calcium ions.
13 . The solid dressing of claim 1 , wherein said haemostatic layer also contains one or more of the following: at least one filler, at least one solubilizing agent, at least one foaming agent and at least one release agent.
14 - 21 . (canceled)
22 . The solid dressing of claim 1 , wherein said haemostatic layer is composed of a plurality of particles, each of said particles consisting essentially of fibrinogen and thrombin.
23 . The solid dressing of claim 22 , wherein said haemostatic layer further contains at least one binding agent in an amount effective to improve the adherence of said particles to one another.
24 . (canceled)
25 . The solid dressing of claim 1 , wherein said haemostatic layer is a monolith.
26 . The solid dressing of claim 1 , wherein said haemostatic layer has been lyophilized.
27 - 37 . (canceled)
38 . The solid dressing of claim 1 , wherein said fibrinogen activator is present in an amount between 2.50 Units/mg of fibrinogen component and 0.025 Units/mg of the fibrinogen.
39 . (canceled)
40 . A method of treating wounded tissue in a mammal, comprising placing a solid dressing of claim 1 to said wounded tissue and applying sufficient pressure to said dressing for a sufficient time for enough fibrin to form to reduce the loss of blood and/or other fluid from said wounded tissue.
41 . The solid dressing of claim 1 , wherein said moisture content is at least 28%.Cited by (0)
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