Dosage form with sustained release melatonin pellets
A composition comprises a therapeutically effective oral pharmaceutical dosage form. The dosage form includes an aqueous carrier material having an acidic pH and a plurality of individual pellets having a first dose of melatonin therein. The individual pellets comprises (i) a solid core; (ii) an active coating over the solid core, the active coating including melatonin and a hydrophilic binder; and (iii) an enteric coating over the active coating. A dissolution pH of the enteric coating is higher than the acidic pH of the aqueous carrier material.
1 . A composition comprising a therapeutically effective oral pharmaceutical dosage form comprising:
(a) an aqueous carrier material having an acidic pH; and
(b) a plurality of individual pellets having a first dose of melatonin therein, the individual pellets comprising (i) a solid core; (ii) an active coating over the solid core, the active coating including melatonin and a hydrophilic binder; and (iii) an enteric coating over the active coating, a dissolution pH of the enteric coating being higher than the acidic pH of the aqueous carrier material,
the individual pellets further comprising a separation coating over the active coating, a subcoat between over the separation coating, and enteric coating over the subcoat,
wherein the subcoat includes a hydrogel-forming polymer and an acid, the acid imparting a pH of 0.1 to 4.4 to the hydrogel-forming polymer, and
the separation coating separates the acid from the melatonin, wherein the dosage form is a beverage or gummy.
2 . The composition of claim 1 , wherein the melatonin is a powder having a median melatonin particle size of 5 μm to 40 μm.
3 . The composition of claim 1 , wherein the aqueous carrier material includes a second dose of melatonin therein and dosage form releases the second dose of melatonin into the subject's oral cavity and stomach.
4 . The composition of claim 1 , wherein the dosage form is a beverage.
5 . The composition of claim 1 , wherein the dosage form is a gummy and the aqueous carrier material is a gummy gelling agent.
6 . The composition of claim 1 , wherein the aqueous carrier material is hydroxypropyl methylcellulose, the solid core is a microcrystalline cellulose bead having a diameter of 0.1 to 2 mm, the hydrophilic binder includes hydroxypropyl methylcellulose, the melatonin is a powder having a median melatonin particle size of 5 μm to 40 μm lodged in the hydrophilic binder, the separation coating includes hydroxypropyl methylcellulose, the hydrogel-forming polymer includes hydroxypropyl methylcellulose, the acid includes citric acid, and the separation coating includes hydroxypropyl methylcellulose.
7 . A method comprising administering a therapeutically effective amount of an oral pharmaceutical dosage form to a patient in need thereof, the dosage form comprising:
(a) an aqueous carrier material having an acidic pH; and
(b) a plurality of individual pellets having a first dose of melatonin therein, the individual pellets comprising (i) a solid core; (ii) an active coating over the solid core, the active coating including melatonin and a hydrophilic binder; and (iii) an enteric coating over the active coating, a dissolution pH of the enteric coating being higher than the acidic pH of the aqueous carrier material,
the individual pellets further comprising a separation coating over the active coating, a subcoat between over the separation coating, and enteric coating over the subcoat,
wherein the subcoat includes a hydrogel-forming polymer and an acid, the acid imparting a pH of 0.1 to 4.4 to the hydrogel-forming polymer, and
the separation coating separates the acid from the melatonin, wherein the dosage form is a beverage or gummy.
8 . The method of claim 7 , wherein the melatonin is a powder having a median melatonin particle size of 5 μm to 40 μm.
9 . The method of claim 7 , wherein the aqueous carrier material includes a second dose of melatonin therein and dosage form releases the second dose of melatonin into the subject's oral cavity and stomach.
10 . The method of claim 7 , wherein the dosage form is a beverage and.
11 . The method of claim 7 , wherein the dosage form is a gummy and the aqueous carrier material is a gummy gelling agent.
12 . The method of claim 7 , wherein the aqueous carrier material is hydroxypropyl methylcellulose, the solid core is a microcrystalline cellulose bead having a diameter of 0.1 to 2 mm, the hydrophilic binder includes hydroxypropyl methylcellulose, the melatonin is a powder having a median melatonin particle size of 5 μm to 40 μm lodged in the hydrophilic binder, the separation coating includes hydroxypropyl methylcellulose, the hydrogel-forming polymer includes hydroxypropyl methylcellulose, the acid includes citric acid, and the separation coating includes hydroxypropyl methylcellulose.
13 . The method of claim 7 , wherein the dosage form is therapeutically effective for assisting the patient to sleep.
14 . A method comprising:
combining an aqueous carrier material with a plurality of individual pellets to form a therapeutically effective oral pharmaceutical dosage form;
the aqueous carrier material having an acidic pH; and
the a plurality of individual pellets having a first dose of melatonin therein, the individual pellets comprising (i) a solid core; (ii) an active coating over the solid core, the active coating including melatonin and a hydrophilic binder; and (iii) an enteric coating over the active coating, a dissolution pH of the enteric coating being higher than the acidic pH of the aqueous carrier material,
the individual pellets further comprising a separation coating over the active coating, a subcoat between over the separation coating, and enteric coating over the subcoat,
wherein the subcoat includes a hydrogel-forming polymer and an acid, the acid imparting a pH of 0.1 to 4.4 to the hydrogel-forming polymer, and
the separation coating separates the acid from the melatonin, wherein the dosage form is a beverage or gummy.
15 . The method of claim 14 , wherein the melatonin is a powder having a median melatonin particle size of 5 μm to 40 μm.
16 . The method of claim 14 , wherein the aqueous carrier material includes a second dose of melatonin therein and dosage form releases the second dose of melatonin into the subject's oral cavity and stomach.
17 . The method of claim 14 , wherein the dosage form is a gummy and the aqueous carrier material is a gummy gelling agent.