Abuse resistant forms of extended release morphine, method of use and method of making
An abuse resistant oral pharmaceutical composition, comprising: a barrier layer, comprising a first polymer; a diffusion layer, comprising a second polymer, substantially covering the barrier layer, wherein the diffusion layer is bonded to the barrier layer and comprises a drug that is substantially homogeneously distributed within the second polymer and diffuses from the diffusion layer within the gastrointestinal (GI) tract; and optionally an expansion layer comprising an expandable polymer, wherein the expansion layer is substantially covered by the barrier layer. Methods of making the same and methods of using the same are also provided.
1. An oral, extended release pharmaceutical composition in the form of a layered tablet configured to deter abuse, wherein the layered tablet comprises:
an expansion layer comprising an expandable polymer that forms a gel when exposed to a liquid comprising water and/or alcohol, wherein the expandable polymer is selected from the group consisting of methylcellulose, sodium carboxymethylcellulose, methylhydroxyethylcellulose, hydroxypropylmethyl cellulose, alginic acid, tragacanth, and combinations thereof,
a barrier layer substantially covering the expansion layer, wherein the barrier layer comprises a first polymer selected from the group consisting of: acrylic or methacrylic polymers or copolymers thereof, and mixtures thereof, wherein when the pharmaceutical composition is administered in intact form, the first polymer of the barrier layer is substantially undissolved in the gastrointestinal (GI) tract, and
an outer diffusion layer covering the barrier layer, the diffusion layer comprising a drug comprising morphine or a pharmaceutically acceptable salt thereof in a pharmaceutically effective amount and a second polymer selected from the group consisting of: acrylic or methacrylic polymers or copolymers thereof, and mixtures thereof, wherein the drug is substantially homogeneously distributed within the second polymer and the drug diffuses from the diffusion layer within the GI tract,
wherein the first polymer and second polymer each comprise the same polymer,
wherein the second polymer is present in an amount sufficient to release at least 50% of the amount of drug after 8 hours after administration in intact form,
wherein the diffusion layer is bonded to the barrier layer by curing the layers together,
wherein the pharmaceutical composition does not comprise a drug that is not an opioid agonist or a central nervous system stimulant,
wherein the diffusion layer is the only drug-containing layer in the pharmaceutical composition, and
wherein when the pharmaceutical composition is contacted with ethyl alcohol in intact form, the rate of drug released from the composition at 4 hours is lower than the rate of drug released when the intact pharmaceutical composition is not contacted with ethyl alcohol.
2. The pharmaceutical composition of claim 1 , wherein the composition comprises morphine or a pharmaceutically acceptable salt thereof in an amount of about 15 mg to about 800 mg.
3. The pharmaceutical composition of claim 1 , wherein the expansion layer comprises an expandable polymer present in the range of 5 to 90% by weight based on the total weight of the pharmaceutical composition.
4. The pharmaceutical composition of claim 1 , wherein when the pharmaceutical composition is crushed and particles of the pharmaceutical composition containing the expansion layer are formed and exposed to a liquid, the expandable polymer of the expansion layer absorbs at least a portion of the liquid.
5. The pharmaceutical composition of claim 1 , wherein when the pharmaceutical composition is contacted with ethyl alcohol, the rate of drug released from the composition at 4 hours is less than 40% of the rate of drug released when the pharmaceutical composition is not contacted with ethyl alcohol.
6. The pharmaceutical composition of claim 1 , wherein when the pharmaceutical composition is contacted with ethyl alcohol, the rate of drug released from the composition at 4 hours is less than 30% of the rate of drug released when the pharmaceutical composition is not contacted with ethyl alcohol.
7. The pharmaceutical composition of claim 1 , wherein when the pharmaceutical composition is contacted with ethyl alcohol, the rate of drug released from the composition at 4 hours is less than 20% of the rate of drug released when the pharmaceutical composition is not contacted with ethyl alcohol.
8. The pharmaceutical composition of claim 1 , wherein the first polymer and the second polymer each independently comprise an acrylic copolymer.
9. The pharmaceutical composition of claim 1 , wherein the expansion polymer comprises hydroxypropylmethylcellulose.
10. The pharmaceutical composition of claim 1 , wherein the expansion polymer is selected from the group consisting of: methylcellulose, sodium carboxymethylcellulose, methylhydroxyethylcellulose, and hydroxypropylmethylcellulose.
11. An oral, extended release pharmaceutical composition in the form of a layered tablet configured to deter abuse, wherein the layered tablet comprises:
an expansion layer comprising an expandable polymer that forms a gel when exposed to a liquid comprising water and/or alcohol, wherein the expandable polymer is selected from the group consisting of methylcellulose, sodium carboxymethylcellulose, methylhydroxyethylcellulose, hydroxypropylmethyl cellulose, alginic acid, tragacanth, and combinations thereof,
a barrier layer substantially covering the expansion layer, wherein the barrier layer comprises a first polymer comprising a copolymer of ethyl acrylate and methyl methacrylate, wherein when the pharmaceutical composition is administered in intact form, the first polymer of the barrier layer is substantially undissolved in the gastrointestinal (GI) tract; and
an outer diffusion layer covering the barrier layer, the diffusion layer comprising a drug comprising morphine or a pharmaceutically acceptable salt thereof in a pharmaceutically effective amount and a second polymer comprising a copolymer of ethyl acrylate and methyl methacrylate, wherein the drug is substantially homogeneously distributed within the second polymer and the drug diffuses from the diffusion layer within the GI tract,
wherein the second polymer is present in an amount sufficient to release at least 50% of the amount of drug after 8 hours after administration in intact form,
wherein the diffusion layer is bonded to the barrier layer by curing the layers together,
wherein the pharmaceutical composition does not comprise a drug that is not an opioid agonist or a central nervous system stimulant,
wherein the diffusion layer is the only drug-containing layer in the pharmaceutical composition,
wherein when the pharmaceutical composition is contacted with ethyl alcohol in intact form, the rate of drug released from the composition at 4 hours is lower than the rate of drug released when the intact pharmaceutical composition is not contacted with ethyl alcohol.
12. The pharmaceutical composition of claim 11 , wherein the composition comprises morphine or a pharmaceutically acceptable salt thereof in an amount of about 15 mg to about 800 mg.
13. The pharmaceutical composition of claim 11 , wherein the expansion layer comprises an expandable polymer present in the range of 5 to 90% by weight based on the total weight of the pharmaceutical composition.
14. The pharmaceutical composition of claim 11 , wherein when the pharmaceutical composition is crushed and particles of the pharmaceutical composition containing the expansion layer are formed and exposed to a liquid, the expandable polymer of the expansion layer absorbs at least a portion of the liquid.
15. The pharmaceutical composition of claim 11 , wherein when the pharmaceutical composition is contacted with ethyl alcohol, the rate of drug released from the composition at 4 hours is less than 40% of the rate of drug released when the pharmaceutical composition is not contacted with ethyl alcohol.
16. The pharmaceutical composition of claim 11 , wherein when the pharmaceutical composition is contacted with ethyl alcohol, the rate of drug released from the composition at 4 hours is less than 30% of the rate of drug released when the pharmaceutical composition is not contacted with ethyl alcohol.
17. The pharmaceutical composition of claim 11 , wherein when the pharmaceutical composition is contacted with ethyl alcohol, the rate of drug released from the composition at 4 hours is less than 20% of the rate of drug released when the pharmaceutical composition is not contacted with ethyl alcohol.
18. The pharmaceutical composition of claim 11 , wherein the expansion polymer comprises hydroxypropylmethylcellulose.
19. The pharmaceutical composition of claim 11 , wherein the expansion polymer is selected from the group consisting of: methylcellulose, sodium carboxymethylcellulose, methylhydroxyethylcellulose, and hydroxypropylmethylcellulose.