Methods of treating wounds using cathepsin K inhibitors
Diabetic wounds have elevated levels of cathepsin K, a protease enzyme, which degrades proteins, such as collagen, causing delayed wound healing. By targeting cathepsin K, diabetic wound healing is ameliorated. Methods and devices for treatment include intradermal injection of odanacatib at or adjacent a wound. Methods and devices for treatment include topical application of pharmacological inhibitors of cathepsin K, for example, in the form of gel, powder, or bandage. Other methods and systems include localized genetic knock out of the cathepsin K gene by topical application of a small interfering RNA (siRNA) or antisense oligonucleotide to aid in wound healing.
1. A method for treating a skin wound comprising:
administering to the skin wound a therapeutic composition comprising an agent that degrades or inhibits cathepsin K;
wherein the agent comprises at least one of odanacatib, cathepsin K inhibitor II, or an siRNA that has a sequence that is complementary to a nucleic acid sequence encoding cathepsin K; and,
wherein the agent is intradermally administered in dosages ranging from 0.3 ng to 3000 ng per mm 2 wound.
2. The method of claim 1 , wherein the agent is intradermally administered in dosages ranging from 30 ng to 300 ng per mm 2 wound.
3. The method of claim 1 , wherein the agent is intradermally administered in dosages ranging from 10 ng to 250 ng per mm 2 wound at a dosing frequency ranging from three times per day to once every three days.
4. The method of claim 1 , wherein the agent is administered in a time-dependent regime, with an initial small dose, a subsequent large dose, and one or more following small doses, wherein the large dose provides the agent in a range of 1.5 to 100 times greater than provided in the small dose.
5. The method of claim 1 , wherein the agent is initially administered 2 to 10 days after initial wounding.
6. The method of claim 1 , wherein the agent comprises odanacatib.
7. The method of claim 1 , wherein the agent is intradermally administered at prescribed intervals of 0, 3, 7, 14 and 21 days after initial wounding.
8. The method of claim 1 , wherein the therapeutic composition is first administered at least 3 days after initial wounding.
9. The method of claim 1 , wherein the skin wound is on a lower limb of a diabetic subject.
10. The method of claim 1 , wherein the skin wound is a chronic wound.
11. A topical formulation for treating a cutaneous wound comprising:
a therapeutic composition comprising becaplermin and at least one of: odanacatib, cathepsin K inhibitor II, or an siRNA that has a sequence that is complementary to a nucleic acid sequence encoding cathepsin K; and
a carrier, wherein:
the carrier is provided as one of: a gel, an ointment, a paste, a lotion, a cream, a liquid, a spray, a foam, or a powder,
the topical formulation is a mixture, suspension, solution, or emulsion, of the therapeutic composition with the carrier, and
the topical formulation is configured to be applied to a skin surface without using physical penetration.
12. The topical formulation of claim 11 , wherein the therapeutic composition is provided in a medical compress, a medicated sponge, a surgical patch, a dry adhesive coating, an aerosol, a dry aerosol, a pump spray, a film, a hemostatic fleece, a hemostatic pad, a gauze, a salve, a semi-gel, a gel, a foam, a paste, a suspension, an ointment, an emulsion, a moldable form, a surgical dressing, a wound packing, or a swab.
13. The topical formulation of claim 11 , wherein the therapeutic composition comprises odanacatib.
14. The topical formulation of claim 11 , wherein the topical formulation further comprises one or more of: an anti-inflammatory agent, an immunosuppressive agent, an immunomodulatory agent, an anti-microbial agent, an anti-viral agent, a matrix metalloproteinase (MMP), fibrinogen, thrombin, factor XIII, hydrocolloid, collagen, cellulose, chitosan, zeolite, or calcium.
15. The topical formulation of claim 11 , wherein the therapeutic composition is provided in a wound dressing comprising:
a contact layer,
an intermediate layer comprising a porous support structure, and
an outer layer,
wherein the therapeutic composition is incorporated into at least one of the contact layer or the intermediate layer.
16. A method for treating a skin wound comprising:
administering to the skin wound a therapeutic composition comprising an agent that degrades or inhibits cathepsin K;
wherein the agent comprises at least one of: odanacatib, cathepsin K inhibitor II, or an siRNA that has a sequence that is complementary to a nucleic acid sequence encoding cathepsin K; and,
wherein the agent is administered in a time-dependent regime, with an initial small dose, a subsequent large dose, and one or more following small doses, wherein the large dose provides the agent in a range of 1.5 to 100 times greater than provided in the small dose.
17. The method of claim 16 , wherein the agent comprises odanacatib.
18. The method of claim 16 , wherein the therapeutic composition is administered topically to the skin wound.
19. The method of claim 16 , wherein the therapeutic composition comprises an agarose matrix-based media.
20. The method of claim 16 , wherein the therapeutic composition is provided in at least one of: a medical compress, a medicated sponge, a surgical patch, a dry adhesive coating, an aerosol, a dry aerosol, a pump spray, a film, a hemostatic fleece, a hemostatic pad, a gauze, a salve, a semi-gel, a gel, a foam, a paste, a suspension, an ointment, an emulsion, a moldable form, a surgical dressing, a wound packing, or a swab.
21. The method of claim 16 , wherein the therapeutic composition further comprises becaplermin.
22. The method of claim 16 , wherein the therapeutic composition further comprises at least one of: an anti-inflammatory agent, an immunosuppressive agent, an immunomodulatory agent, an anti-microbial agent, an anti-viral agent, fibrinogen, thrombin, factor XIII, hydrocolloid, collagen, cellulose, chitosan, zeolite, calcium, or a matrix metalloproteinase (MMP).
23. The method of claim 16 , wherein administering the therapeutic composition to the skin wound comprises: applying the therapeutic composition to a wound-adjacent skin surface, wherein the wound-adjacent skin surface is a region within 10 mm of a break in the epidermis.
24. The method of claim 16 , wherein the therapeutic composition is first administered at least 3 days after initial wounding.
25. The method of claim 16 , wherein the agent is initially administered 2 to 7 days after initial wounding.
26. The method of claim 16 , wherein the skin wound is on a lower limb of a diabetic subject.
27. The method of claim 16 , wherein the skin wound is a chronic wound.
28. A method for treating a skin wound comprising:
administering to the skin wound a therapeutic composition comprising an agent that degrades or inhibits cathepsin K;
wherein the agent comprises at least one of odanacatib, cathepsin K inhibitor II, or an siRNA that has a sequence that is complementary to a nucleic acid sequence encoding cathepsin K; and,
wherein the agent is intradermally administered at prescribed intervals of 2 to 7 days after initial wounding.
29. The method of claim 28 , wherein the agent comprises odanacatib.
30. A method for treating a skin wound in a diabetic subject, comprising:
topically administering to the skin wound a topical formulation comprising:
an agent that degrades or inhibits cathepsin K, wherein the agent comprises odanacatib; and
a carrier provided as one of: a gel, an ointment, a paste, a lotion, a cream, a liquid, a spray, a foam, or a powder; wherein:
the topical formulation is a mixture, suspension, solution, or emulsion, of the agent with the carrier.
31. The method of claim 30 , wherein the carrier comprises a liquid.
32. The method of claim 30 , wherein the topical formulation further comprises becaplermin.
33. The method of claim 30 , wherein the carrier comprises a gel.
34. The method of claim 30 , wherein the skin wound comprises a skin injury that extends through the epidermis into the dermis.