Room-temperature stable dronabinol formulations
View Patent ↗A room temperature stable cannabinoid formulation is disclosed. In preferred embodiments, the cannabinoid formulation is dronabinol in an oil-based carrier contained within a hard gelatin capsule.
1. A cannabinoid dosage form consisting essentially of:
synthetic dronabinol in an amount of 0.05 to 20 mg per dose and L-ascorbic acid-6-palmitate in an amount of 0.01% to 1% by weight, both dispersed in sesame oil; and
a gelatin capsule encapsulating said synthetic dronabinol, said L-ascorbic acid-6-palmitate, and said sesame oil, said dosage form being stable at room temperature for at least one year.
2. The dosage form of claim 1 , which contains not less than 90% of the initial dronabinol content upon exposure of the formulation to storage conditions selected from the group consisting of (i) elevated temperature and humidity conditions of 40° C./75% relative humidity (RH) for 6 months; (ii) room temperature (25° C.) for two years; and (iii) any combination thereof.
3. The dosage form of claim 1 , wherein the dronabinol does not contain more than 5% dronabinol degradants in the dosage form, the degradants selected from the group consisting of no more than 2% delta-8 tetrahydrocannabinol (D8THC), no more than 2% cannabinol (CBN), no more than 0.2% cannabidiol (CBD), and any combination thereof.
4. The dosage form of claim 1 , which contains an effective amount of one or more organic bases to promote stability of the cannabinoid against unacceptable degradation.
5. The dosage form of claim 4 , which comprises from 0.001% to 5% organic base, by weight.
6. The dosage form of claim 4 , which comprises from 0.005% to 2% organic base, by weight.
7. The dosage form of claim 4 , wherein said organic base is selected from the group consisting of ethanolamine, methanolamine, meglumine, and any combination of the foregoing.
8. The dosage form of claim 1 , wherein said gelatin capsule is soft or hard.
9. The dosage form of claim 1 , which further comprises one or more additional therapeutically active agents.
10. The dosage form of claim 9 , wherein said additional therapeutically active agent is selected from a narcotic analgesic, a non-narcotic analgesic, an anti-emetic, a steroid, and mixtures of any of the foregoing.
11. The dosage form of claim 1 which contains dronabinol as the active ingredient, the dosage form containing ingredients at a level selected from the following during its claimed shelf-life as follows: (i) not less than 90% of the initial dronabinol content; (ii) not greater than 2% cannabinol; (iii) not greater than 2% cannabidiol; (iv) not greater than 2% delta-8-THC; and (v) any combination of the foregoing.
12. The dosage form of claim 1 , further comprising a pharmaceutical excipient selected from the group consisting of solubilizers; stabilizers; surfactants; emulsifiers, absorption enhancers, and mixtures thereof.
13. The dosage form of claim 1 , wherein the gelatin capsule is a capsule having a coating on its surface selected from the group consisting of an enteric coating, a seal coating, or both.
14. The dosage form of claim 13 , wherein the gelatin capsule is selected from the group consisting of a starch capsule; a cellulosic capsule; a hydrocolloid film-forming composition comprising a mixture of iota carrageenan, a bulking agent and kappa carrageenan; and a gelatin capsule.
15. A cannabinoid dosage form consisting essentially of:
synthetic dronabinol in an amount of 0.05 mg to 20 mg per unit dose and L-ascorbic acid-6-palmitate in an amount of 0.001% to 1% by weight, both dispersed in sesame oil; and
a gelatin capsule encapsulating said dronabinol, said L-ascorbic acid-6-palmitate, and said sesame oil, said dosage form contains at least about 90% w/w of the synthetic dronabinol in undegraded form after storage at room temperature for at least one year.