Orally administrable compositions and methods of deterring abuse by intranasal administration
Orally administrable pharmaceutical compositions and methods of administration are provided. The pharmaceutical compositions provide abuse deterrent properties.
1. An orally administrable, extended release pharmaceutical composition in a single tablet unit dosage form configured to deter abuse by nasal insufflation, wherein the tablet unit dosage form comprises:
a drug comprising morphine or a salt thereof in an amount of about 60 mg, and
about 500 mg of pharmaceutically acceptable excipients,
wherein the tablet unit dosage form comprises about 400 mg of a mixture of magnesium stearate, microcrystalline cellulose, and mannitol,
wherein when the pharmaceutical composition is intranasally administered in crushed form to a subject, the AUC of the drug achieved after a time period is lower than the AUC of the drug achieved after intranasal administration of a crushed form of an orally bioequivalent composition not containing about 400 mg of a mixture of magnesium stearate, microcrystalline cellulose, and mannitol,
and wherein morphine or a salt thereof is the only active ingredient in the pharmaceutical composition.
2. The pharmaceutical composition of claim 1 , wherein when the pharmaceutical composition is intranasally administered in crushed form to a subject, the AUC of the drug achieved after intranasal administration after a time period is at least 5% lower than the AUC of the drug achieved after intranasal administration of an orally bioequivalent composition in crushed form.
3. The pharmaceutical composition of claim 1 , wherein when the pharmaceutical composition is intranasally administered in crushed form to a subject, the AUC of the drug achieved after intranasal administration after a time period is at least 10% lower than the AUC of the drug achieved after intranasal administration of an orally bioequivalent composition in crushed form.
4. The pharmaceutical composition of claim 1 , wherein when the pharmaceutical composition is intranasally administered in crushed form to a subject, the AUC of the drug achieved after intranasal administration after a time period is at least 15% lower than the AUC of the drug achieved after intranasal administration of an orally bioequivalent composition in crushed form.
5. The pharmaceutical composition of claim 1 , wherein the time period is selected from the group consisting of: 30 minutes, 1 hour, 2 hours, 4 hours, 8 hours, 12 hours, and 24 hours.