Pharmaceutical compositions comprising meloxicam
View Patent ↗Disclosed herein are compositions comprising an NSAID such as meloxicam in combination with a cyclodextrin and/or a carbonate or a bicarbonate. These compositions may be orally administered, for example, to improve the bioavailability or pharmacokinetics of the NSAID for the treatment of conditions such as pain.
1. A method of improving dissolution of meloxicam in the stomach of a mammal, comprising orally administering a solid dosage form comprising both a bicarbonate and meloxicam to the mammal, wherein the dosage form contains 400 mg to 1000 mg of the bicarbonate, and wherein the rate of dissolution of meloxicam for the solid dosage form in simulated gastric fluid is improved as compared with a reference dosage form that: 1) contains the same amount of meloxicam; 2) contains an amount of potassium carbonate that achieves about the same pH as the bicarbonate; and 3) does not contain the bicarbonate.
2. The method of claim 1 , wherein the mammal is a human being.
3. The method of claim 1 , wherein the solid dosage form further comprises a cyclodextrin.
4. The method of claim 3 , wherein the cyclodextrin is a sulfobutyl ether β-cyclodextrin (SBEβCD).
5. The method of claim 1 , wherein the solid dosage form further comprises an acid inhibitor.
6. The method of claim 5 , wherein the acid inhibitor is esomeprazole.
7. The method of claim 1 , wherein the solid dosage form is in a tablet form.
8. The method of claim 1 , wherein the solid dosage form comprises about 1 mg to about 50 mg of meloxicam.
9. The method of claim 8 , wherein the solid dosage form comprises about 15 mg of meloxicam.
10. The method of claim 1 , wherein the bicarbonate is sodium bicarbonate or potassium bicarbonate.
11. The method of claim 10 , wherein the solid dosage form comprises 500 mg to 1000 mg of sodium bicarbonate.
12. The method of claim 11 , wherein the solid dosage form comprises 500 mg of sodium bicarbonate.
13. The method of claim 6 , wherein about 30 mg to about 50 mg of esomeprazole is present in the solid dosage form.
14. The method of claim 1 , wherein, 120 minutes after oral administration of the solid dosage form, the dissolution of meloxicam is at least about 3 times that of the reference dosage form.
15. The method of claim 3 , wherein, 120 minutes after oral administration of the solid dosage form, the dissolution of meloxicam is at least about 5 times that of the reference dosage form.
16. The method of claim 1 , wherein, 15 minutes after oral administration of the solid dosage form, the dissolution of meloxicam is at least 10% more than that of the reference dosage form.
17. The method of claim 3 , wherein, 15 minutes after oral administration of the solid dosage form, the dissolution of meloxicam is at least about 2 times that of the reference dosage form.
18. The method of claim 1 , wherein the solid dosage form is orally administered to the mammal to treat pain.
19. The method of claim 18 , wherein the pain is inflammatory pain.
20. The method of claim 1 , wherein the solid dosage form is orally administered to the mammal to treat osteoarthritis, rheumatoid arthritis, or juvenile rheumatoid arthritis.