US2003206944A1PendingUtilityA1
Wound dressings with elastase-sequestering
Priority: Feb 29, 2000Filed: May 29, 2003Published: Nov 6, 2003
Est. expiryFeb 29, 2020(expired)· nominal 20-yr term from priority
A61L 2300/434A61L 15/44A61L 15/28Y10T442/2525
48
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Claims
Abstract
The invention provides wound dressings and methods of their use, especially for the treatment of chronic, non-healing wounds. The wound dressings are composed of a support matrix, such as cotton cellulose, and an active agent associated with the support matrix. The active agent may be a protease inhibitor or a protease sequestrant, in particular an inhibitor or sequestrant of a neutrophil-derived cationic protease such as elastase.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A method for sequestering elastase at a wound site comprising the step of contacting said wound site with a wound dressing selected from the group consisting of carboxymethylcellulose, dialdehyde gauze, sulfonated gauze, and phosphorylated gauze.
2 . The method of claim 1 wherein said wound dressing is carboxymethylcellulose.
3 . The method of claim 1 wherein said wound dressing is dialdehyde gauze.
4 . The method of claim 1 wherein said wound dressing is sulfonated gauze.
5 . The method of claim 1 wherein said wound dressing is phosphorylated gauze.
6 . A wound dressing for treating a wound, comprising
a support matrix, and an active agent associated with said support matrix, wherein said active agent is selected from the group consisting of an inhibitor of a neutrophil-derived protease and a protease sequestrant.
7 . The wound dressing of claim 6 wherein said support matrix is selected from the group consisting of cellulose and carboxymethylcellulose.
8 . The wound dressing of claim 6 wherein said neutrophil-derived protease is elastase.
9 . The wound dressing of claim 6 wherein said inhibitor is selected from the group consisting of Val—Pro—Val, Val—Pro—Val-O Methylester, Ala—Ala—Pro—Val-chloromehylketone, Ala—Ala—Pro—Val-pentafluoroethylketone, propyl-3-ketone, glucose-6-citrate, and levulinate.
10 . The wound dressing of claim 6 wherein said protease sequestrant is selected from the group consisting of aldehyde, sulfate and phosphate.
11 . The wound dressing of claim 6 wherein said active agent is associated with said support matrix by a means selected from the group consisting of covalent bonding, non-covalent bonding and ionic bonding.
12 . A method for enhancing would healing, comprising,
contacting said wound with the wound dressing of claim 6 .
13 . The method of claim 12 wherein said wound is chronic.Join the waitlist — get patent alerts
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