Topical diclofenac sodium compositions
The invention relates to beneficial topical pharmaceutical compositions comprising diclofenac sodium in high amounts, and methods for their use. Said compositions represent emulsion-gels as well as gels with unique properties such as high skin penetration, no irritation, high stability, complete dissolution of the active and effective pain relief. The invention also provides methods for treating pain or inflammation in a mammalian subject in need thereof, including acute and chronic pain or inflammation; and kits therefor.
1. A topical pharmaceutical composition in the form of a gel or emulsion gel which comprises:
(a) 2% of diclofenac sodium salt,
(b) at least about 55% of water,
(c) from about 10 to about 15% of isopropyl alcohol,
(d) from about 10 to about 15% of 1,2-propanediol,
(e) from about 2 to about 3% of at least one gelling agent selected from the group consisting of carbomers,
(f) from 0 to about 10% of a lipid forming an oil phase,
(g) from 0 to about 5% of at least one non-ionic surfactant, and
(h) a basic agent to adjust the pH of the total composition to 6-9,
wherein (c) and (d) together comprise from about 20% to about 25% of the composition, and the viscosity of the composition is from about 5,000 to about 10,000 cPs at 25° C.,
all percentages being by weight (w/w) based on the total composition.
2. A topical pharmaceutical composition according to claim 1 in the form of an emulsion gel, comprising:
(f) from about 2 to about 8% (w/w) of at least one lipid forming the oil phase of the emulsion gel; and
(g) from about 1 to about 5% (w/w) of at least one non-ionic surfactant.
3. A topical pharmaceutical composition according to claim 2 wherein (f) comprises mineral oil and cocoyl caprylocaprate and (g) is selected from the group consisting of esters of fatty acids with monohydroxy or polyhydroxy compounds, polyoxyethylated surfactants and mixtures thereof.
4. A topical pharmaceutical composition according to claim 1 in the form of a gel, which is free of (f).
5. A topical pharmaceutical composition according to claim 4 , which is free of (f) and (g).
6. A topical pharmaceutical composition according to claim 1 , in the form of an emulsion gel, which comprises:
(a) 2% (w/w) of diclofenac sodium salt,
(b) at least about 60% of water,
(c) from about 10 to about 15% of isopropyl alcohol,
(d) from about 10 to about 15% of 1,2-propanediol,
(e) from about 2 to about 3% of at least one gelling agent selected from the group consisting of carbomers, and
(f) from about 3 to about 7% of at least one liquid lipid forming the oily phase of the emulsion-gel,
(g) from about 1 to about 3% of at least one non-ionic surfactant, and
(h) a basic agent to adjust the pH of the total composition to 7-9,
wherein (c) and (d) together comprise from about 20% to about 25% of the composition, and the viscosity of the composition is from about 5,000 to about 10,000 cPs at 25° C.,
all percentages being by weight (w/w) based on the total composition.
7. A topical pharmaceutical composition according to claim 6 wherein (f) comprises mineral oil and cocoyl caprylocaprate and (g) is selected from the group consisting of esters of fatty acids with monohydroxy or polyhydroxy compounds, polyoxyethylated surfactants and mixtures thereof.
8. A topical pharmaceutical composition according to claim 6 wherein (g) comprises polyoxyl 20 cetostearyl ether.
9. A topical pharmaceutical composition according to claim 1 , said composition having a high skin permeation, (B) said composition showing a very low systemic absorption only, (C) said composition showing essentially no irritation on human skin after administration as demonstrated by a mean erythema score of less than 2.5 on a scale of 0-4, and (D) said composition being chemically and physically stable when stored at 25° C. and a relative humidity of 60% for 12 months, in that (i) the emulsion-gel structure of the composition is maintained without breaking of the emulsion, and (ii) the original color of the composition does not visibly change over a period of at least 12 months when stored at 25° C. and at a relative humidity of 60%, and (E) said composition further keeping the diclofenac sodium salt fully dissolved, which means that even upon microscopic examination at 100× magnification no crystals of diclofenac sodium salt can be observed therein.
10. A method for treating pain or inflammation in a mammalian subject comprising topically administering a therapeutically effective amount of a composition according to claim 1 to a mammalian subject in need thereof.
11. A method according to claim 10 for treating acute pain or inflammation.
12. A method according to claim 10 for treating chronic pain or inflammation.
13. A method for treating a mammalian subject in need thereof to provide temporary relief from mild-to-moderate aches and pains of muscles and joints associated with conditions selected from one or more of arthritis, strains, sprains, bruises and backache, by administering to the subject a therapeutically effective amount of a composition according to claim 1 .
14. A kit for administering a composition for the treatment of pain or inflammation comprising
(a) a composition according to claim 1
(b) instructions for topically administering the composition, and optionally
(c) a pre-calibrated dosing device.
15. A topical pharmaceutical composition according to claim 1 in the form of a gel which comprises:
(a) 2% of diclofenac sodium salt,
(b) at least about 55% of water,
(c) from about 10 to about 15% of isopropyl alcohol,
(d) from about 10 to about 15% of 1,2-propanediol,
(e) from about 2 to about 3% of at least one gelling agent selected from the group consisting of carbomers, and
(h) a basic agent to adjust the pH of the total composition to 6-9,
wherein (c) and (d) together comprise from about 20% to about 25% of the composition, and the viscosity of the composition is from about 5,000 to about 10,000 cPs at 25° C.,
said composition being free of (f) and (g),
all percentages being by weight (w/w) based on the total composition.
16. A topical pharmaceutical composition according to claim 1 in the form of a gel or emulsion gel which comprises:
(a) 2% of diclofenac sodium salt,
(b) at least about 55% of water,
(c) about 12.5% of isopropyl alcohol,
(d) about 12.5% of 1,2-propanediol
(e) from about 2 to about 3% of at least one gelling agent selected from the group consisting of carbomers,
(f) from 0 to about 10% of a lipid forming an oil phase,
(g) from 0 to about 5% of at least one non-ionic surfactant, and
(h) a basic agent to adjust the pH of the total composition to 6-9,
wherein the viscosity of the composition is from about 5,000 to about 10,000 cPs at 25° C.,
all percentages being by weight (w/w) based on the total composition.
17. A topical pharmaceutical composition in the form of a gel or emulsion gel which consists essentially of:
(a) 2% of diclofenac sodium salt,
(b) at least about 55% of water,
(c) about 12.5% of isopropyl alcohol,
(d) about 12.5% of 1,2-propanediol
(e) from about 2 to about 3% of at least one gelling agent selected from the group consisting of carbomers,
(f) from 0 to about 10% of a lipid forming an oil phase,
(g) from 0 to about 5% of at least one non-ionic surfactant, and
(h) a basic agent to adjust the pH of the total composition to 6-9,
wherein the viscosity of the composition is from about 5,000 to about 10,000 cPs at 25° C.,
all percentages being by weight (w/w) based on the total composition.
18. A topical pharmaceutical composition according to claim 17 in the form of a gel which is free of (f) and (g).
19. A composition according to claim 1 wherein the gelling agent comprises carbomer homopolymer.
20. A composition according to claim 15 wherein the gelling agent comprises carbomer homopolymer.
21. A composition according to claim 16 wherein the gelling agent comprises carbomer homopolymer.
22. A composition according to claim 17 wherein the gelling agent comprises carbomer homopolymer.
23. A composition according to claim 1 which is free of penetration enhancers selected from saturated or unsaturated C 10 -C 18 fatty alcohols, hyaluronic acid or its salts, and dimethylsulfoxide.
24. A composition according to claim 15 which is free of penetration enhancers selected from saturated or unsaturated C 10 -C 18 fatty alcohols, hyaluronic acid or its salts, and dimethylsulfoxide.
25. A composition according to claim 16 which is free of penetration enhancers selected from saturated or unsaturated C 10 -C 18 fatty alcohols, hyaluronic acid or its salts, and dimethylsulfoxide.
26. A composition according to claim 17 which is free of penetration enhancers selected from saturated or unsaturated C 10 -C 18 fatty alcohols, hyaluronic acid or its salts, and dimethylsulfoxide.
27. A topical pharmaceutical composition in the form of a gel or emulsion gel which consists essentially of:
(a) 2% of diclofenac sodium salt,
(b) at least about 55% of water,
(c) about 12.5% of isopropyl alcohol,
(d) about 12.5% of 1,2-propanediol
(e) from about 2 to about 3% of at least one carbomer homopolymer,
(f) from 0 to about 10% of a lipid forming an oil phase,
(g) from 0 to about 5% of at least one non-ionic surfactant, and
(h) a basic agent to adjust the pH of the total composition to 6-9,
all percentages being by weight (w/w) based on the total composition.
28. A method for treating pain or inflammation in a mammalian subject comprising topically administering a therapeutically effective amount of a composition according to claim 6 to a mammalian subject in need thereof.
29. A method for treating pain or inflammation in a mammalian subject comprising topically administering a therapeutically effective amount of a composition according to claim 16 to a mammalian subject in need thereof.
30. A method for treating pain or inflammation in a mammalian subject comprising topically administering a therapeutically effective amount of a composition according to claim 17 to a mammalian subject in need thereof.
31. A method for treating pain or inflammation in a mammalian subject comprising topically administering a therapeutically effective amount of a composition according to claim 27 to a mammalian subject in need thereof.