US2011274726A1PendingUtilityA1
Chitosan foam medical devices and methods
Assignee: PROVIDENCE HEALTH SYS OREGONPriority: Oct 6, 2008Filed: Oct 6, 2009Published: Nov 10, 2011
Est. expiryOct 6, 2028(~2.2 yrs left)· nominal 20-yr term from priority
A61P 31/04A61P 7/04A61P 31/12A61L 15/44A61F 2013/0054A61F 13/15577A61F 2013/0071A61L 15/425A61F 2013/00931B29K 2105/045A61P 17/02A61F 2013/00472A61F 2013/00314A61F 13/00987A61L 2300/408B29K 2995/0037A61F 2013/00106A61F 2013/0091A61L 2300/418B29C 44/005A61F 13/00063A61F 13/00991A61F 2013/00719A61L 2400/04A61L 2430/34A61L 15/28B29L 2031/753A61F 2013/0074A61F 2013/00757B29K 2005/00A61L 2300/404A61L 2300/412A61F 13/01012
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Claims
Abstract
The invention provides a solid foam wound dressing useful for hemorrhage control and wound repair, as well as methods for making such a wound dressing.
Claims
exact text as granted — not AI-modified1 . A method of making a solid foam wound dressing, comprising:
I. introducing gas bubbles into the aqueous solution to form an aqueous foam, wherein the aqueous solution comprises chitosan, at least one protic acid and at least one surface active agent; II. freezing the aqueous foam; and III. dehydrating the aqueous foam to form a solid foam.
2 . The method of claim 1 , wherein said dehydrating the aqueous foam comprises freeze drying the aqueous foam.
3 . The method of claim 1 , further comprising freezing the foam in a reduced pressure environment to expand the gas bubbles in the aqueous foam.
4 . (canceled)
5 . The method of claim 1 , further comprising compressing the solid foam.
6 . (canceled)
7 . (canceled)
8 . The method of claim 1 , wherein the protic acid is a hydrogen donator acid.
9 . (canceled)
10 . The method of claim 1 , wherein the surface-active agent is anionic, cationic, non-ionic, or amphoteric.
11 . (canceled)
12 . (canceled)
13 . The method of claim 1 , wherein the gas is selected from the group consisting of air, nitrogen, helium, hydrogen, argon, and carbon dioxide.
14 . The method of claim 1 , wherein the gas bubbles are introduced by mixing, beating, agitating, aerating, whipping, or injecting the gas into the aqueous solution.
15 . The method of claim 1 , wherein the wound dressing is capable of promoting at least one of hemostasis, wound healing, and adherence to wet tissues.
16 . (canceled)
17 . The method of claim 1 , wherein the wound dressing is antimicrobial and antiviral.
18 . (canceled)
19 . (canceled)
20 . The method of claim 1 , wherein the solid foam comprises at least one of an open-cell structure and a lamella structure.
21 . (canceled)
22 . A solid foam wound dressing comprising chitosan, at least one protic acid and at least one surface active agent wherein said wound dressing has a porous structure that is mechanically flexible and adhesive when in contact with physiological fluids or moisture.
23 . The wound dressing according to claim 22 , wherein the physiological fluid is blood.
24 . The wound dressing of claim 22 , wherein the solid foam wound dressing is a compressed solid foam wound dressing.
25 . (canceled)
26 . The wound dressing of claim 22 , wherein the protic acid is a hydrogen donator acid.
27 . (canceled)
28 . The wound dressing of claim 22 , wherein the surface-active agent is anionic, cationic, non-ionic, or amphoteric.
29 . (canceled)
30 . The wound dressing of claim 22 , wherein the surface-active agent is antimicrobial and antiviral.
31 . The wound dressing of claim 22 , wherein the wound dressing is capable of promoting at least one of hemostasis, wound healing, and adherence to wet tissues.
32 . (canceled)
33 . (canceled)
34 . (canceled)
35 . (canceled)
36 . The wound dressing of claim 22 , wherein the solid porous material comprises at least one of an open-cell structure and a lamella structure.
37 . (canceled)
38 . A method of treating a wound, comprising applying the wound dressing according to claim 22 to the wound.Cited by (0)
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