Gastric retained gabapentin dosage form
View Patent ↗A method of treatment for epilepsy and other disease states is described, which comprises the delivery of gabapentin in a gastric retained dosage form.
1. A method for administering a therapeutically effective amount of gabapentin to a subject, comprising administering a dosage form comprising gabapentin or a pharmaceutically acceptable salt thereof, wherein the dosage form comprises
(a) at least one component that expands on contact with water, a gas-generating agent, and the gabapentin and
(b) at least one hydrophilic membrane which encases the at least one component; and
wherein upon ingestion of the dosage form bioavailability of gabapentin released over 5-12 hours is at least about 80% of that provided by an immediate release dosage form comprising an equal amount of gabapentin as measured by the area under the plasma concentration-time, AUC inf .
2. The method of claim 1 , wherein the gas-generating agent releases carbon dioxide or nitrogen.
3. The method of claim 1 , wherein the at least one component comprises a swellable polymer.
4. The method of claim 1 , wherein the at least one hydrophilic membrane is in the form of a microporous membrane.
5. The method of claim 1 , wherein the at least one hydrophilic membrane is in the form of a sachet.
6. The method of claim 1 , wherein the dosage form further comprises a covering which encases the hydrophilic membrane.
7. The method of claim 1 , wherein the dosage form is administered once-daily or twice-daily.
8. The method of claim 1 , wherein the dosage form comprises between about 100 mg and 4800 mg gabapentin.
9. The method of claim 1 , wherein the dosage form comprises about 300 mg or about 600 mg gabapentin.
10. A method for treating a disorder, comprising administering a dosage form comprising gabapentin or a pharmaceutically acceptable salt thereof, wherein the dosage form comprises
(a) at least one component that expands on contact with water, a gas-generating agent, and the gabapentin; and
(b) at least one hydrophilic membrane which encases the at least one component;
wherein upon ingestion of the dosage form bioavailability of gabapentin released over 5-12 hours is at least about 80% of that provided by an immediate release dosage form comprising an equal amount of gabapentin as measured by the area under the plasma concentration-time curve, AUC inf .
11. The method of claim 10 , wherein the disorder is a neuropathic pain, epilepsy, a movement disorder, or a psychiatric disorder.
12. A method for administering a therapeutically effective amount of gabapentin to a subject, comprising administering a dosage form comprising gabapentin or a pharmaceutically acceptable salt thereof, wherein the dosage form comprises:
(a) a drug layer comprising gabapentin and
(b) a buoyant layer.
13. The method of claim 12 , wherein the buoyant layer is a swelling layer.
14. A dosage form, comprising
gabapentin or a pharmaceutically acceptable salt thereof, wherein the dosage form comprises
(a) at least one component that expands on contact with water, a gas-generating agent, and the gabapentin; and
(b) at least one hydrophilic membrane which encases the at least one component; and
wherein upon ingestion of the dosage form bioavailability of gabapentin released over 5-12 hours is at least about 80% of that provided by an immediate release dosage form comprising an equal amount of gabapentin as measured by the area under the plasma concentration-time curve, AUC inf .
15. The dosage form of claim 14 , further comprising a second therapeutic agent selected from the group consisting of a hydantoin, an iminostilbene, a valproate, a phenyltriazine, a barbiturate, a dexoybarbiturate, a benzodiazepine, a carbamate, an anticonvulsant other than gabapentin, a tricyclic antidepressant, levadopa, carbidopa, an opioid, lithium, carbamazepine, valproate, trifluoperazine, clonazepam, risperidone, lorazepam, venlafaxine, clozapine, olanzapine, a benzodiazepine, a neuroleptic, a serotonin reuptake inhibitor, buproprion, nefadone, venlaxatine, nefadone, diazepam, oxazepam, a dopaminergic agent, clonazepam, a triptine and ergotamine.
16. The method of claim 10 , wherein the gas-generating agent releases carbon dioxide or nitrogen.
17. The method of claim 14 , wherein the gas-generating agent releases carbon dioxide or nitrogen.