Topical compositions comprising polyunsaturated fatty acids
The present disclosure provides topical compositions comprising a polyunsaturated fatty acid (PUFA) derivative of formula (I): or a salt thereof.
1. A method of treating dermatitis in a subject in need thereof, the method comprising administering a therapeutically effective amount of a composition comprising 5-HETrE, 8-HETrE or 15-HETrE, or an ester or pharmaceutically acceptable salt thereof, to skin of the subject.
2. The method of claim 1 , wherein the composition comprises about 0.01 wt % to about 50 wt % 15-HETrE.
3. The method of claim 1 , wherein the composition comprises about 0.01 wt % to about 50 wt % 5-HETrE.
4. The method of claim 1 , wherein the composition comprises about 0.01 wt % to about 50 wt % 8-HETrE.
5. The method of claim 1 , wherein the composition comprises about 0.01 wt % to about 25 wt % 15-HETrE.
6. The method of claim 1 , wherein the composition comprises about 1 mg to about 1000 mg of 15-HETrE.
7. The method of claim 1 , wherein the composition is administered topically to the skin of the mammal.
8. The method of claim 1 , wherein the composition further comprises a pharmaceutically acceptable diluent or carrier.
9. The method of claim 1 , wherein the composition is co-administered with a corticosteroid selected from the group consisting of clobetasol diproprionate, betamethasone diproprionate, halbetasol proprionate, diflorasone diacetate, fluocinonide, halcinonide, amcinonide, desoximetasone, triamcinolone acetonide, mometasone furoate, fluticasone proprionate, fluocinolone acetonide, hydrocortisone valerate, hydrocortisone butyrate, triamcinalone acetonide, desonide, prednicarbate, prednisolone, methylprednisolone, dexamethasone, naflocort, deflazacort, halopredone acetate, budesonide, beclomethasone dipropionate, hydrocortisone, clocortolone pivalate, methylprednisolone aceponate, dexamethasone palmitoate, tipredane, hydrocortisone aceponate, alclometasone dipropionate, halometasone, methylprednisolone suleptanate, rimexolone, prednisolone farnesylate, ciclesonide, deprodone propionateloteprednol etabonate, betamethasone butyrate propionate, flunisolide, prednisone, dexamethasone sodium phosphate, triamcinolone, betamethasone 17-valerate, betamethasone, betamethasone dipropionate, hydrocortisone acetate, hydrocortisone sodium succinate, prednisolone sodium phosphate, hydrocortisone probutate, and combinations thereof.
10. The method of claim 9 , wherein the corticosteroid is co-administered in an amount sufficient to provide 50% or less of the recommended daily dosage of said corticosteroid in said mammal.
11. The method of claim 10 , wherein the corticosteroid is hydrocortisone.
12. The method of claim 1 , wherein the composition is co-administered with a further therapeutic agent selected from the group consisting of immunomodulators, antibiotics, immunosuppressants, and anti-itch drugs.
13. A method of treating psoriasis in a subject in need thereof, the method comprising administering a therapeutically effective amount of a composition comprising 5-HETrE, 8-HETrE or 15-HETrE, or an ester or pharmaceutically acceptable salt thereof, to skin of the subject.
14. The method of claim 13 , wherein the composition comprises about 0.01 wt % to about 50 wt % 15-HETrE.
15. The method of claim 13 , wherein the composition comprises about 1 mg to about 1000 mg of 15-HETrE.
16. The method of claim 13 , wherein the composition is co-administered with a corticosteroid selected from the group consisting of clobetasol diproprionate, betamethasone diproprionate, halbetasol proprionate, diflorasone diacetate, fluocinonide, halcinonide, amcinonide, desoximetasone, triamcinolone acetonide, mometasone furoate, fluticasone proprionate, fluocinolone acetonide, hydrocortisone valerate, hydrocortisone butyrate, triamcinalone acetonide, desonide, prednicarbate, prednisolone, methylprednisolone, dexamethasone, naflocort, deflazacort, halopredone acetate, budesonide, beclomethasone dipropionate, hydrocortisone, clocortolone pivalate, methylprednisolone aceponate, dexamethasone palmitoate, tipredane, hydrocortisone aceponate, alclometasone dipropionate, halometasone, methylprednisolone suleptanate, rimexolone, prednisolone farnesylate, ciclesonide, deprodone propionateloteprednol etabonate, betamethasone butyrate propionate, flunisolide, prednisone, dexamethasone sodium phosphate, triamcinolone, betamethasone 17- valerate, betamethasone, betamethasone dipropionate, hydrocortisone acetate, hydrocortisone sodium succinate, prednisolone sodium phosphate, hydrocortisone probutate, and combinations thereof.
17. A method of treating pruritus in a subject in need thereof, the method comprising topically administering a therapeutically effective amount of a composition comprising 5-HETrE or 8-HETrE, or an ester or pharmaceutically acceptable salt thereof, to skin of the subject.
18. The method of claim 17 , wherein the composition comprises about 0.01 wt % to about 50 wt % DGLA.
19. The method of claim 17 , wherein the composition is co-administered with a corticosteroid selected from the group consisting of clobetasol diproprionate, betamethasone diproprionate, halbetasol proprionate, diflorasone diacetate, fluocinonide, halcinonide, amcinonide, desoximetasone, triamcinolone acetonide, mometasone furoate, fluticasone proprionate, fluocinolone acetonide, hydrocortisone valerate, hydrocortisone butyrate, triamcinalone acetonide, desonide, prednicarbate, prednisolone, methylprednisolone, dexamethasone, naflocort, deflazacort, halopredone acetate, budesonide, beclomethasone dipropionate, hydrocortisone, clocortolone pivalate, methylprednisolone aceponate, dexamethasone palmitoate, tipredane, hydrocortisone aceponate, alclometasone dipropionate, halometasone, methylprednisolone suleptanate, rimexolone, prednisolone farnesylate, ciclesonide, deprodone propionateloteprednol etabonate, betamethasone butyrate propionate, flunisolide, prednisone, dexamethasone sodium phosphate, triamcinolone, betamethasone 17- valerate, betamethasone, betamethasone dipropionate, hydrocortisone acetate, hydrocortisone sodium succinate, prednisolone sodium phosphate, hydrocortisone probutate, and combinations thereof.
20. The method of claim 17 , wherein the composition is co-administered with a further therapeutic agent selected from the group consisting of immunomodulators, antibiotics, immunosuppressants, and anti-itch drugs.