Foamable formulation
View Patent ↗The present invention provides DMSO-containing foamable formulations, methods for preparation, and methods of treatment. The formulations can provide good permeability and bioavailability at the target site. Preferably, the formulations are useful for treating osteoarthritis. In one embodiment, the invention provides a foamable formulation for topical use, said formulation comprising DMSO, polyalkylene glycol alkyl ether, an active agent, a monohydric lower alcohol, a diol, and water. Preferably, the active agent is a non-steroidal anti-inflammatory drug, such as diclofenac sodium or ibuprofen.
1. A foamable formulation, said formulation comprising:
(i) dimethyl sulfoxide (DMSO); wherein DMSO is present in an amount ranging from about 12-80% w/w;
(ii) a pharmaceutically active agent; wherein the active agent is selected from the group consisting of an anti-inflammatory steroid, a non-stereoidal anti-inflammatory drug, and a local anesthetic; and
(iii) a polyalkylene glycol alkyl ether;
wherein the formulation is foamable by manual aeration; and wherein the formulation comprises from 0 to 1% or from 30 to 45% w/w propellant.
2. The foamable formulation of claim 1 , said formulation further comprising a monohydric lower alcohol.
3. The foamable formulation of claim 1 , wherein said formulation comprises from 0 to 1% propellant.
4. The foamable formulation of claim 1 , wherein said formulation comprises 15-80% w/w DMSO.
5. The foamable formulation of claim 1 , wherein said active agent is a non-steroidal anti-inflammatory drug.
6. The foamable formulation of claim 5 , wherein said non-steroidal anti-inflammatory drug is ibuprofen or a diclofenac salt.
7. The foamable formulation of claim 6 , wherein said non-steroidal anti-inflammatory drug is ibuprofen;
wherein the ibuprofen is present at 3-8% w/w; DMSO is present at 14-30% w/w; and the polyalkylene glycol alkyl ether is present at up to 3% w/w;
wherein the formulation further comprises (iv) a diol and (v) water;
wherein the formulation optionally further comprises a monohydric lower alcohol;
wherein the diol is present at 5-9% w/w; the monohydric lower alcohol is present at 0-17% w/w; and the water is present at a concentration of q.s.
8. The foamable formulation of claim 6 , wherein said diclofenac salt is diclofenac sodium.
9. The foamable formulation of claim 8 , wherein diclofenac sodium is present at 1-10% w/w, DMSO is present at 20-60% w/w, and the polyalkylene glycol alkyl ether is present at up to 10% w/w;
wherein the formulation further comprises (iv) a monohydric alcohol, (v) propylene glycol, and (vi) water; and
wherein the monohydric alcohol is present at 1-50% w/w, propylene glycol is present at 1-15% w/w, and the water is present at a concentration of q.s.
10. The foamable formulation of claim 6 , wherein the polyalkylene glycol alkyl ether is present at up to 5% w/w.
11. The foamable formulation of claim 10 , further comprising 1-15% w/w glycerol.
12. The foamable formulation of claim 10 , wherein said polyalkylene glycol alkyl ether is a polyethylene glycol alkyl ether.
13. The foamable formulation of claim 10 , wherein said formulation further comprises a steroid.
14. The foamable formulation of claim 13 , wherein said steroid is cholesterol; and wherein said formulation comprises at most 0.5% w/w of said steroid.
15. The foamable formulation of claim 13 , wherein said formulation further comprises a surfactant.
16. The foamable formulation of claim 15 , wherein said surfactant is a salt of an aryl sulfonate, alkyl sulfonate, aryl sulfate, or alkyl sulfate.
17. The foamable formulation of claim 16 , wherein said salt is sodium dodecyl benzene sulfonate, sodium laureth sulfate, or sodium lauryl sulfate.
18. The foamable formulation of claim 13 , wherein the formulation further comprises sodium carbonate.
19. A foam comprising the foamable formulation of claim 1 .
20. The foam of claim 19 , further comprising air.
21. The foam of claim 19 , wherein the foam is a quick-breaking foam.
22. A method for treating a subject suffering from pain, said method comprising the topical administration to an afflicted area of said subject a therapeutically effective amount of the foamable formulation of claim 1 , thereby treating the subject's pain.
23. The method of claim 22 , wherein said pain is associated with osteoarthritis.
24. The method of claim 23 , wherein said topical administration provides a reduction of pain over 12 weeks.
25. The method of claim 23 , wherein said formulation is applied one, two, three, or four times daily.
26. The foamable formulation of claim 1 , wherein said formulation comprises 12-48% w/w DMSO.
27. The foamable formulation of claim 26 , wherein said formulation comprises 14-30% w/w DMSO.
28. The foamable formulation of claim 1 , wherein said polyalkylene glycol alkyl ether is present at up to 2% w/w.
29. The foamable formulation of claim 4 , wherein said formulation comprises 25-80% w/w DMSO.
30. A method for manually foaming the foamable formulation of claim 1 , the method comprising the steps of:
(i) providing a dispenser comprising a reservoir operably linked in fluid communication with a release assembly;
(ii) filling the reservoir with the foamable formulation; and
(iii) actuating the release assembly to manually aerate the foamable formulation, thereby releasing a foam from the release assembly.