# US 2014/0154235 A1 · Wound debridement compositions containing seaprose and methods of wound treatment using same

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- Number: US 2014/0154235 A1
- Document ID: US20140154235A1
- Status: Published application
- Kind: A1
- Application number: 14/116,728
- Filed: 2012-05-11
- Published: 2014-06-05
- Earliest claimed: 2011-05-12
- Assignees: Smith & Nephew Orthopaedics AG
- Inventors: Lei Shi; Aleksa Jovanovic; Dennis Carson
- Web page: https://patentgrep.com/patent/US20140154235A1

## CPC

- A61K 38/482: {Serine endopeptidases (3.4.21)}
- A61K 9/0014: {Skin, i.e. galenical aspects of topical compositions (non-active ingredients are additionally classified in A61K47/00; A61K9/0009, A61K9/0021, A61K9/7015, A61K9/7023 take precedence; cosmetic preparations A61K8/00, A61Q; preparations for wound dressings or bandages A61L26/00)}
- A61K 9/0019: {Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner (non-active ingredients are additionally classified in A61K47/00)}
- A61K 9/06: Ointments; Bases therefor; {Other semi-solid forms, e.g. creams, sticks, gels (composition of ointments, creams or gels A61K47/00)}
- A61K 47/06: Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K 47/10: Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
- A61K 47/38: Cellulose; Derivatives thereof
- A61K 47/44: Oils, fats or waxes according to two or more groups of A61K47/02-A61K47/42; Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin (synthetic glycerides, e.g. medium-chain triglycerides, A61K47/14)
- A61P 17/02: for treating wounds, ulcers, burns, scars, keloids, or the like
- A61P 43/00: Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
- C12Y 304/21063: Oryzin (3.4.21.63)
- A61K: PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES (devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms A61J3/00; chemical aspects of, or use of materials for deodorisation of air, for disinfection or sterilisation, or for bandages, dressings, absorbent pads or surgical articles A61L; soap compositions C11D)
- A61P: SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- C12Y: ENZYMES

## Abstract

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

## Claims

### Claim 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.

### Claim 2 (depends on 1)

The method of claim 1, wherein the necrotic tissue is an eschar.

### Claim 3 (depends on 1)

The method of claim 1, wherein the composition is topically applied to the wound.

### Claim 4 (depends on 1)

The method of claim 1, wherein the composition further comprises a pharmaceutically acceptable topical carrier.

### Claim 5 (depends on 1)

The method of claim 1, wherein the wound is a chronic wound.

### Claim 6 (depends on 5)

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.

### Claim 7 (depends on 1)

The method of claim 1, wherein the composition includes 0.1 to 2% by weight of Seaprose.

### Claim 8 (depends on 7)

The method of claim 7, wherein the composition includes 0.5 to 1% by weight of Seaprose.

### Claim 9 (depends on 1)

The method of claim 1, wherein the Seaprose is isolated or purified Seaprose.

### Claim 10 (depends on 1)

The method of claim 1, wherein the composition is formulated as a gel, cream, or ointment.

### Claim 11 (depends on 1)

The method of claim 1, wherein the composition further comprises glycerin polyacrylate clatharate, glycerin, hydroxyethylcellulose, an emulsifying wax, or petrolatum, or any combination thereof.

### Claim 12 (depends on 1)

The method of claim 1, wherein the composition is injected into the wound.

### Claim 13 (depends on 12)

The method of claim 12, wherein the composition further comprises a pharmaceutically acceptable injectible carrier.

### Claim at position 14

14-24. (canceled)

### Claim 25

A topical composition for the debridement of wounds comprising a wound debridement effective amount of Seaprose and a pharmaceutically acceptable topical carrier.

### Claim 26 (depends on 25)

The topical composition of claim 25, wherein the composition includes 0.1 to 2% by weight of Seaprose.

### Claim 27 (depends on 26)

The topical composition of claim 26, wherein the composition includes 0.5 to 1% by weight of Seaprose.

### Claim 28 (depends on 25)

The topical composition of claim 25, wherein the Seaprose is isolated or purified Seaprose.

### Claim 29 (depends on 25)

The topical composition of claim 25, wherein the composition is formulated as a gel, cream, or ointment.

### Claim 30 (depends on 25)

The topical composition of claim 25, wherein the composition is an ointment comprising petrolatum.

### Claim 31 (depends on 25)

The topical composition of claim 25, wherein the composition is a gel comprising glycerin polyacrylate clatharate.

### Claim 32 (depends on 25)

The topical composition of claim 25, wherein the composition is a gel comprising hydroxyethylcellulose.

### Claim 33 (depends on 25)

The topical composition of claim 25, wherein the composition is a cream comprising glycerin and an emulsifying wax.
