US2014154235A1PendingUtilityA1

Wound debridement compositions containing seaprose and methods of wound treatment using same

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Assignee: SHI LEIPriority: May 12, 2011Filed: May 11, 2012Published: Jun 5, 2014
Est. expiryMay 12, 2031(~4.8 yrs left)· nominal 20-yr term from priority
A61P 43/00A61K 9/0019A61K 9/06A61K 47/38C12Y 304/21063A61K 47/44A61K 9/0014A61K 38/482A61K 47/10A61K 47/06A61P 17/02
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Claims

Abstract

Wound debridement compositions containing the proteolytic enzyme Seaprose and use of such compositions in wound treatment for the enzymatic debridement of wounds.

Claims

exact text as granted — not AI-modified
1 . A method of debriding a wound that includes necrotic tissue comprising applying to the wound a composition comprising Seaprose, wherein application of the composition debrides necrotic tissue in the wound. 
     
     
         2 . The method of  claim 1 , wherein the necrotic tissue is an eschar. 
     
     
         3 . The method of  claim 1 , wherein the composition is topically applied to the wound. 
     
     
         4 . The method of  claim 1 , wherein the composition further comprises a pharmaceutically acceptable topical carrier. 
     
     
         5 . The method of  claim 1 , wherein the wound is a chronic wound. 
     
     
         6 . The method of  claim 5 , wherein the chronic wound is a diabetic foot ulcer, a venous leg ulcer, an arterial leg ulcer, a decubitus ulcer, a stasis ulcer, a dermal ulcer, a burn, or a pressure ulcer. 
     
     
         7 . The method of  claim 1 , wherein the composition includes 0.1 to 2% by weight of Seaprose. 
     
     
         8 . The method of  claim 7 , wherein the composition includes 0.5 to 1% by weight of Seaprose. 
     
     
         9 . The method of  claim 1 , wherein the Seaprose is isolated or purified Seaprose. 
     
     
         10 . The method of  claim 1 , wherein the composition is formulated as a gel, cream, or ointment. 
     
     
         11 . The method of  claim 1 , wherein the composition further comprises glycerin polyacrylate clatharate, glycerin, hydroxyethylcellulose, an emulsifying wax, or petrolatum, or any combination thereof. 
     
     
         12 . The method of  claim 1 , wherein the composition is injected into the wound. 
     
     
         13 . The method of  claim 12 , wherein the composition further comprises a pharmaceutically acceptable injectible carrier. 
     
     
         14 - 24 . (canceled) 
     
     
         25 . A topical composition for the debridement of wounds comprising a wound debridement effective amount of Seaprose and a pharmaceutically acceptable topical carrier. 
     
     
         26 . The topical composition of  claim 25 , wherein the composition includes 0.1 to 2% by weight of Seaprose. 
     
     
         27 . The topical composition of  claim 26 , wherein the composition includes 0.5 to 1% by weight of Seaprose. 
     
     
         28 . The topical composition of  claim 25 , wherein the Seaprose is isolated or purified Seaprose. 
     
     
         29 . The topical composition of  claim 25 , wherein the composition is formulated as a gel, cream, or ointment. 
     
     
         30 . The topical composition of  claim 25 , wherein the composition is an ointment comprising petrolatum. 
     
     
         31 . The topical composition of  claim 25 , wherein the composition is a gel comprising glycerin polyacrylate clatharate. 
     
     
         32 . The topical composition of  claim 25 , wherein the composition is a gel comprising hydroxyethylcellulose. 
     
     
         33 . The topical composition of  claim 25 , wherein the composition is a cream comprising glycerin and an emulsifying wax.

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