Lisinopril formulations
Provided herein are stable lisinopril oral liquid formulations. Also provided herein are methods of using lisinopril oral liquid formulations for the treatment of certain diseases including hypertension, heart failure and acute myocardial infarction.
1. A method of treating hypertension in a subject comprising administering to that subject a therapeutically effective amount of a stable oral liquid formulation, comprising:
(i) lisinopril or a pharmaceutically acceptable salt or solvate thereof;
(ii) a preservative selected from the group consisting of sodium benzoate, benzoic acid, sorbic acid, methylparaben, ethylparaben, propylparaben, butylparaben, and pharmaceutically acceptable salts thereof;
(iii) a liquid vehicle, wherein the liquid vehicle comprises water; and
(iv) optionally a sweetener;
wherein the formulation is stable at about 25±5° C. for at least 6 months.
2. The method of claim 1 , wherein the lisinopril is present in the formulation at about 1 mg/mL, and wherein the lisinopril is lisinopril dihydrate.
3. The method of claim 1 , wherein the pH of the formulation is between about 4 and about 5.2.
4. The method of claim 1 , wherein the lisinopril or a pharmaceutically acceptable salt or solvate thereof functions as a buffer.
5. The method of claim 1 , wherein the formulation is stable at about 25±5° C. for at least 18 months.
6. The method of claim 1 , wherein the formulation comprises a sweetener selected from the group consisting of xylitol, mannitol, sucralose, saccharin, and pharmaceutically acceptable salts thereof.
7. The method of claim 1 , wherein the formulation comprises a sweetener that is xylitol, sucralose, or saccharin, wherein the xylitol is present in the formulation at about 140 mg/ml to about 160 mg/ml, and wherein the sucralose is present in the formulation at about 0.5 mg/ml to about 3 mg/ml.
8. The method of claim 1 , wherein the preservative is present in the formulation at about 0.1 mg/ml to about 2 mg/ml.
9. A method of treating heart failure in a subject comprising administering to that subject a therapeutically effective amount of a stable oral liquid formulation, comprising:
(i) lisinopril or a pharmaceutically acceptable salt or solvate thereof;
(ii) a preservative selected from the group consisting of sodium benzoate, benzoic acid, sorbic acid, methylparaben, ethylparaben, propylparaben, butylparaben, and pharmaceutically acceptable salts thereof;
(iii) a liquid vehicle, wherein the liquid vehicle comprises water; and
(iv) optionally a sweetener;
wherein the formulation is stable at about 25±5° C. for at least 6 months.
10. The method of claim 9 , wherein the subject is not responding adequately to diuretics and digitalis.
11. The method of claim 1 , wherein the hypertension is primary (essential) hypertension or secondary hypertension.
12. The method of claim 1 , wherein the subject has blood pressure values greater than or equal to 140/90 mm Hg.
13. The method of claim 1 , wherein the formulation is further administered in combination with an agent selected from the group consisting of diuretics, beta blockers, alpha blockers, mixed alpha and beta blockers, calcium channel blockers, angiotensin II receptor antagonists, ACE inhibitors, aldosterone antagonists, and alpha-2 agonists.
14. The method of claim 9 , wherein the lisinopril is present in the formulation at about 1 mg/mL, and wherein the lisinopril is lisinopril dihydrate.
15. The method of claim 9 , wherein the pH of the formulation is between about 4 and about 5.2.
16. The method of claim 9 , wherein the lisinopril or a pharmaceutically acceptable salt or solvate thereof functions as a buffer.
17. The method of claim 9 , wherein the formulation is stable at about 25±5° C. for at least 18 months.
18. The method of claim 9 , wherein the formulation comprises a sweetener selected from the group consisting of xylitol, mannitol, sucralose, saccharin, and pharmaceutically acceptable salts thereof.
19. The method of claim 9 , wherein the formulation comprises a sweetener that is xylitol, sucralose, or saccharin, wherein the xylitol is present in the formulation at about 140 mg/ml to about 160 mg/ml, and wherein the sucralose is present in the formulation at about 0.5 mg/ml to about 3 mg/ml.
20. The method of claim 9 , wherein the preservative is present in the formulation at about 0.1 mg/ml to about 2 mg/ml.
21. A method of treating a hemodynamically stable subject within 24 hours of acute myocardial infarction comprising administering to that subject a therapeutically effective amount of a stable oral liquid formulation, comprising:
(i) lisinopril or a pharmaceutically acceptable salt or solvate thereof;
(ii) a preservative selected from the group consisting of sodium benzoate, benzoic acid, sorbic acid, methylparaben, ethylparaben, propylparaben, butylparaben, and pharmaceutically acceptable salts thereof;
(iii) a liquid vehicle, wherein the liquid vehicle comprises water; and
(iv) optionally a sweetener;
wherein the formulation is stable at about 25±5° C. for at least 6 months.
22. The method of claim 21 , wherein the formulation is further administered in combination with an agent selected from the group consisting of beta blockers, aspirin, and thrombolytics.
23. The method of claim 21 , wherein the lisinopril is present in the formulation at about 1 mg/mL, and wherein the lisinopril is lisinopril dihydrate.
24. The method of claim 21 , wherein the pH of the formulation is between about 4 and about 5.2.
25. The method of claim 21 , wherein the lisinopril or a pharmaceutically acceptable salt or solvate thereof functions as a buffer.
26. The method of claim 21 , wherein the formulation is stable at about 25±5° C. for at least 18 months.
27. The method of claim 21 , wherein the formulation comprises a sweetener selected from the group consisting of xylitol, mannitol, sucralose, saccharin, and pharmaceutically acceptable salts thereof.
28. The method of claim 21 , wherein the formulation comprises a sweetener that is xylitol, sucralose, or saccharin, wherein the xylitol is present in the formulation at about 140 mg/ml to about 160 mg/ml, and wherein the sucralose is present in the formulation at about 0.5 mg/ml to about 3 mg/ml.
29. The method of claim 21 , wherein the preservative is present in the formulation at about 0.1 mg/ml to about 2 mg/ml.