Oral delivery of peptide pharmaceutical compositions
View Patent ↗Bioavailability of peptide active agents to be administered orally is enhanced by a pharmaceutical composition providing targeted release of the peptide to the intestine by combining the composition with an absorption enhancer. Bioavailability is further significantly increased by administering the composition in an acid-resistant protective vehicle which transports components of the invention through the stomach. The composition may optionally further include a sufficient amount of a pH-lowering agent to lower local intestinal pH. All components are released together into the intestine with the peptide.
1. A single solid dosage capsule comprising:
a peptide comprising a 2,6-dimethyltyrosine (Dmt) residue or a prodrug thereof;
at least one pharmaceutically acceptable pH-lowering agent having a pKa no higher than 4.2 and comprising a carboxylic acid, wherein the at least one pH-lowering agent is one of acetylsalicylic acid, ascorbic acid, citric acid, fumaric acid, glucuronic acid, glyceric acid, glycocholic acid, glyoxylic acid, isocitric acid, lactic acid, maleic acid, oxaloacetic acid, oxalosuccinic acid, pyruvic acid, succinic acid, tartaric acid, or combinations thereof, wherein the weight ratio of the at least one pH lowering agent to the peptide exceeds 40:1; and
at least one absorption enhancer.
2. The solid dosage capsule of claim 1 wherein the peptide further comprises an arginine residue, a phenylalanine residue, and a lysine residue.
3. The solid dosage capsule of claim 1 wherein the pH-lowering agent is citric acid.
4. The solid dosage capsule of claim 1 wherein the at least one absorption enhancer comprises an acylcarnitine.
5. The solid dosage capsule of claim 4 wherein the acylcarnitine is lauroyl carnitine.
6. The solid dosage capsule of claim 1 further comprising an enteric coating.
7. The solid dosage capsule of claim 6 wherein the enteric coating is present at a weight which is no more than 20% of the weight of the remainder of the solid dosage capsule excluding the enteric coating.
8. The solid dosage capsule of claim 6 further comprising a water-soluble barrier separating the at least one pH-lowering agent from the enteric coating.
9. The solid dosage capsule of claim 1 wherein the at least one pH-lowering agent is present in the single dosage form in a quantity which, if added to 10 milliliters of 0.1M aqueous sodium bicarbonate solution, would be sufficient to lower the pH of the solution to no higher than 3.5.
10. The solid dosage capsule of claim 1 comprising a therapeutically-effective amount of the peptide comprising the 2,6-dimethyltyrosine (Dmt) residue or prodrug thereof to achieve analgesia.
11. A method for relieving pain comprising administering to a subject in need thereof a therapeutically-effective amount of the solid dosage capsule of claim 1 .
12. A single solid dosage capsule comprising:
a deltorphin analog or a prodrug thereof comprising a dimethylphenylalanine residue;
at least one pharmaceutically acceptable pH-lowering agent having a pKa no higher than 4.2 and comprising a carboxylic acid, wherein the at least one pH-lowering agent is one of acetylsalicylic acid, ascorbic acid, citric acid, fumaric acid, glucuronic acid, glyceric acid, glycocholic acid, glyoxylic acid, isocitric acid, lactic acid, maleic acid, oxaloacetic acid, oxalosuccinic acid, pyruvic acid, succinic acid, tartaric acid, or combinations thereof, wherein the weight ratio of the at least one pH lowering agent to the peptide exceeds 40:1; and
at least one absorption enhancer.
13. The solid dosage capsule of claim 12 wherein the deltorphin analog is Tyrosine-D-alanine-Xaa-Glutamic Acid-Valine-Valine-Glycine-NH 2 , wherein Xaa is L- or D-dimethylphenylalanine.
14. The solid dosage capsule of claim 12 wherein the pH-lowering agent is citric acid.
15. The solid dosage capsule of claim 12 wherein the at least one absorption enhancer comprises lauroyl carnitine.
16. The solid dosage capsule of claim 12 further comprising an enteric coating.
17. The solid dosage capsule of claim 16 wherein the enteric coating is present at a weight which is no more than 20% of the weight of the remainder of the solid dosage capsule excluding the enteric coating.
18. The solid dosage capsule of claim 12 wherein the pH-lowering agent is present in the single dosage form in a quantity which, if added to 10 milliliters of 0.1M aqueous sodium bicarbonate solution, would be sufficient to lower the pH of the solution to no higher than 3.5.
19. The solid dosage capsule of claim 12 comprising a therapeutically-effective amount of the deltorphin analog or prodrug thereof comprising the dimethylphenylalanine residue to achieve analgesia.
20. A method for relieving pain comprising administering to a subject in need thereof a therapeutically-effective amount of the solid dosage capsule of claim 12 .
21. The solid dosage capsule of claim 1 wherein the at least one pH-lowering agent is present in the single dosage form in a quantity which, if added to 10 milliliters of 0.1M aqueous sodium bicarbonate solution, would be sufficient to lower the pH of the solution to no higher than 5.5.
22. The solid dosage capsule of claim 1 wherein the at least one pH-lowering agent is present in the single dosage form in a quantity which, if added to 10 milliliters of 0.1M aqueous sodium bicarbonate solution, would be sufficient to lower the pH of the solution to no higher than 4.7.
23. The solid dosage capsule of claim 1 wherein the weight ratio of the at least one pH lowering agent to the peptide exceeds 400:1.
24. The solid dosage capsule of claim 1 comprising at least 300 mg of the at least one pH-lowering agent.
25. The solid dosage capsule of claim 1 wherein the at least one pH-lowering agent is one of fumaric acid, maleic acid, oxaloacetic acid, oxalosuccinic acid, pyruvic acid, tartaric acid, or combinations thereof and has a pKa no higher than 3.0.