Tamper resistant pharmaceutical formulations
Disclosed in certain embodiments is a solid oral dosage form comprising a heat-labile gelling agent; a thermal stabilizer; and a drug susceptible to abuse.
1. A solid oral dosage form comprising
a heat-labile gelling agent;
a thermal stabilizer comprising an anionic polymer in a neutral pH aqueous solution; and
a drug susceptible to abuse,
wherein the solid oral dosage form releases at least about 85% of the drug susceptible to abuse within 45 minutes as measured by in-vitro dissolution in a USP Apparatus 2 (paddle) at 50 rpm in 500 ml SGF at 37° C.
2. The solid oral dosage form of claim 1 , wherein the polysaccharide is a microbial polysaccharide.
3. The solid oral dosage form of claim 2 , wherein the microbial polysaccharide is xanthan gum.
4. The solid oral dosage form of claim 1 , further comprising a pH-modifying agent.
5. The solid oral dosage form of claim 4 , wherein the pH-modifying agent provides a pH of between about 5.5 and 8.5 to a viscous solution obtained when the dosage form is crushed and mixed with 5 mL of distilled water.
6. The solid oral dosage form of claim 1 , further comprising a disintegrant.
7. The solid oral dosage form of claim 1 , further comprising a filler.
8. The solid oral dosage form of claim 7 , wherein the filler is selected from the group consisting of lactose, dextrose, mannitol, microcrystalline cellulose and a mixture thereof.
9. The solid oral dosage form of claim 1 , comprising the heat-labile gelling agent in an amount from 0.25% to about 75% (w/w) of the dosage form.
10. The solid oral dosage form of claim 1 , comprising the thermal stabilizer in an amount from about 0.25% to about 90% (w/w) of the dosage form.
11. The solid oral dosage form of claim 1 , further comprising an aversive agent.
12. The solid oral dosage form of claim 11 , wherein the aversive agent is a surfactant, capsaicin or a capsaicin analog.
13. The solid oral dosage form of claim 1 , wherein the drug is an opioid agonist.
14. The solid oral dosage form of claim 13 , wherein the opioid agonist is selected from the group consisting of codeine, morphine, oxycodone, oxymorphone, hydrocodone, hydromorphone, pharmaceutically acceptable salts thereof, and mixtures thereof.