Controlled-release melatonin compositions and related methods
An oral melatonin pharmaceutical dosage form that contains a sustained release dose of melatonin includes melatonin and an acid dispersed in a hydrogel-forming polymer matrix that combine after ingestion to form an acidic hydrogel containing the melatonin. The dosage form is effective to release melatonin therefrom for at least six hours after oral ingestion.
1. A composition comprising:
an oral melatonin pharmaceutical dosage form that contains a sustained release dose of melatonin in an effective amount;
the dosage form including melatonin and an acid dispersed in a hydrogel-forming polymer matrix that combine after ingestion to form an acidic hydrogel containing the melatonin; and
wherein the dosage form is effective to release melatonin therefrom for at least six hours after oral ingestion wherein the amount of acid is sufficient to impart a pH of less than 4.7 to the acidic hydrogel.
2. The composition of claim 1 , wherein the dosage form is effective to release approximately 50% of the melatonin in the dosage form within approximately two hours after oral ingestion.
3. The composition of claim 1 , wherein the dosage form is effective to release substantially all of the melatonin therein within ten hours after oral ingestion.
4. The composition of claim 1 , wherein the amount of the acid is sufficient to impart a pH of 2-4 to the acidic hydrogel.
5. The composition of claim 1 , wherein the dosage form further comprises at least one other active ingredient in addition to the melatonin.
6. The composition of claim 1 , wherein the effective amount includes 5 micrograms to 10 milligrams of melatonin.
7. The composition of claim 1 , wherein the effective amount includes about 2 milligrams of melatonin.
8. The method of claim 1 , wherein the hydrogel-forming polymer matrix includes a cellulosic polymer.
9. The composition of claim 1 , wherein the dosage form is a compressed tablet.
10. The composition of claim 1 , wherein the each of the melatonin, acid, and hydrogel-forming polymer are in granular form.
11. The composition of claim 10 , wherein the dosage form is a compressed tablet.
12. The composition of claim 1 , further comprising at least one member selected from the group ramelteon, agomelatine, and TIK-301.
13. The composition of claim 1 , wherein the dosage form is coated with a seal coating.