Spironolactone aqueous formulations
Disclosed herein is a pharmaceutical composition, comprising: (a) spironolactone; (b) a xanthan gum; (c) an anti-foaming agent; (d) a preservative; (f) a dispersing agent; (g) a sweetening agent; (h) a flavoring agent; (i) optionally a buffer to maintain the pH of the pharmaceutical composition within a range described herein; and (j) a sufficient amount of a water vehicle.
1. A pharmaceutical composition, comprising:
(a) 0.50% w/v of spironolactone;
(b) from 0.18% w/v to 0.36% w/v of a xanthan gum;
(c) an anti-foaming agent comprised of 0.20% w/v of a simethicone emulsion;
(d) a preservative comprised of from 0.025% w/v to 0.050% w/v of sorbic acid and from 0.10% w/v to 0.20% w/v of potassium sorbate;
(e) a dispersing agent comprised of from 2.0% w/v to 2.2% w/v glycerin;
(f) a sweetening agent comprises 0.14% w/v sodium saccharin and from 0.03% w/v to 0.04% w/v ammonium glycyrrhizinate;
(g) a flavoring agent in an amount that ranges from 0.1% w/v to 0.5% w/v;
(h) a buffer to maintain the pH of the pharmaceutical composition from 4.5 to 5.5;
wherein the buffer is comprised of from 0.17% w/v to 0.24% w/v citric acid and from 0.36% w/v to 0.48% w/v of a citrate salt; and
(i) a sufficient amount of a water vehicle.
2. The pharmaceutical composition of claim 1 , wherein the viscosity of the composition ranges from 100 cP to 300 cP.
3. The pharmaceutical composition of claim 1 , wherein
the anti-foaming agent (c) is comprised of 0.20% w/v of a simethicone emulsion;
the preservative (d) is comprised of 0.050% w/v of sorbic acid and 0.20% w/v of potassium sorbate;
the dispersing agent (e) is comprised of 2.1% w/v to 2.2% w/v glycerin; and
wherein the pharmaceutical composition comprises the buffer comprised of 0.20% w/v citric acid and 0.43% w/v sodium citrate.
4. The pharmaceutical composition of claim 3 , wherein xanthan gum is present in an amount of 0.25% w/v.
5. The pharmaceutical composition of claim 4 , wherein the viscosity of the composition ranges from 130 cP to 170 cP.
6. The pharmaceutical composition of claim 4 , wherein the pH of the pharmaceutical composition ranges from 4.8 to 5.2.
7. An enclosed, amber polyethylene terephthalate (PETE) bottle comprising the composition of claim 4 .
8. The PETE bottle of claim 7 , wherein the volume of said bottle is 4 oz. or 16 oz.
9. A process for preparing the pharmaceutical composition of claim 1 , which comprises:
(1) mixing the xanthan gum, anti-foaming agent, preservative, a portion of the sweetening agent, and, the buffer, in water in a first container;
(2) mixing the spironolactone, the dispersing agent, and the remaining portion of the sweetening agent in a second container;
(3) transferring the contents of the second container to the first container followed by mixing the contents of the first container;
(4) adding the flavoring agent to the contents of the first container from step (3);
(5) adding water to the first container of step (3) and mixing the contents of the first container;
and
(6) dispensing the contents of the first container from step (5) into an amber polyethylene terephthalate bottle.
10. A pharmaceutical product prepared by the process as claimed in claim 9 .
11. A method for the treatment of hypertension in a subject in need thereof, which comprises administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 1 .
12. The method of claim 11 , wherein the composition is administered orally or by a nasogastric tube.
13. A method for the treatment of severe heart failure in a subject in need thereof, which comprises administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 1 ;
wherein the composition is administered orally or by a nasogastric tube.
14. A pharmaceutical composition comprising: (a) 0.50% w/v spironolactone; (b) 0.25% w/v of a xanthan gum; (c) 0.20% w/v of a simethicone emulsion; (d) a preservative comprised of 0.050% w/v of sorbic acid and 0.20% w/v of potassium sorbate; (e) from 2.1% w/v to 2.2% w/v glycerin; (f) a sweetening agent containing 0.14% w/v sodium saccharin and from 0.03% w/v to 0.04% w/v ammonium glycyrrhizinate; (g) 0.30% w/v of a fruit flavoring agent; (h) a buffer comprised of 0.20% w/v citric acid and 0.43% w/v sodium citrate; and (i) a sufficient amount of a water vehicle.
15. The pharmaceutical composition of claim 14 , said composition having a pH of from 4.5 to 5.5.
16. The pharmaceutical composition of claim 14 , said composition having a pH of from 4.8 to 5.2.
17. The pharmaceutical composition of claim 14 , said composition having a viscosity that ranges from 100 cP to 300 cP.
18. The pharmaceutical composition of claim 14 , said composition having a viscosity that ranges from 130 cP to 170 cP.
19. An enclosed, amber polyethylene terephthalate (PETE) bottle having a volume of 4 oz or 16 oz comprising the composition of claim 14 .
20. A method for the treatment of hypertension in a subject in need thereof, which comprises administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 14 .
21. The method of claim 14 , wherein the composition is administered orally or by a nasogastric tube.
22. A method for the treatment of severe heart failure in a subject in need thereof, which comprises administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 14 ;
wherein the composition is administered orally or by a nasogastric tube.
23. A method for the treatment of a patient suffering from a skin disorder, which comprises administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 14 , wherein said skin disorder is selected from the group consisting of acne, hirsutism, androgenic alopecia, rosacea, and combinations thereof.
24. The pharmaceutical composition of claim 1 , wherein the spironolactone content is 100±10% of labeled content when stored under 40° C. and not more than 25% relative humidity for 6-months.
25. The pharmaceutical composition of claim 14 , wherein the spironolactone content is 100±10% labeled content when stored under 40° C. and not more than 25 % relative humidity for 6-months.
26. The pharmaceutical composition of claim 1 , wherein the spironolactone content is 100±10% of labeled content when stored under 25° C. and 40% relative humidity for 24-months.
27. The pharmaceutical composition of claim 14 , wherein the spironolactone content is 100±10% of labeled content when stored under 25° C. and 40% relative humidity for 24-months.