Opioid formulations having reduced potential for abuse
The invention provides opioid formulations having reduced potential for abuse, and having reduced potential for illegal sale and distribution. The opioid formulations of the invention comprise at least one opioid and a sustained release delivery system.
1 . A method for relieving pain comprising administering to a patient in need thereof a reduced abuse potential solid dosage formulation comprising an opioid mixed with a granulated sustained release delivery system,
wherein the granulated sustained release delivery system comprises at least one heteropolysaccharide gum, at least one homopolysaccharide gum, and at least one pharmaceutical diluent.
2 . The method of claim 1 , wherein the reduced abuse potential solid dosage formulation forms a gel matrix with muco-adhesive properties when crushed or powdered upon contact with a fluid.
3 . The method of claim 1 , wherein the reduced abuse potential solid dosage formulation forms a viscous solution when crushed or powdered upon contact with a fluid.
4 . The method of claim 1 , wherein the granulated sustained release delivery system further comprises at least one hydrophobic polymer.
5 . The method of claim 1 , wherein the granulated sustained release delivery system further comprises at least one cationic cross-linking compound selected from monovalent cations, multivalent cations, and salts.
6 . The method of claim 5 , wherein the cationic cross-linking agent is selected from the group consisting of: alkali metal sulfate, alkali metal chloride, alkali metal borate, alkali metal bromide, alkali metal citrate, alkali metal acetate, alkali metal lactate, alkaline earth metal sulfate, alkaline earth metal chloride, alkaline earth metal borate, alkaline earth metal bromide, alkaline earth metal citrate, alkaline earth metal acetate, alkaline earth metal lactate and a mixture thereof.
7 . The method of claim 5 , wherein the cationic cross-linking agent is selected from the group consisting of: calcium sulfate, sodium chloride, potassium sulfate, sodium carbonate, lithium chloride, tripotassium phosphate, sodium borate, potassium bromide, potassium fluoride, sodium bicarbonate, calcium chloride, magnesium chloride, sodium citrate, sodium acetate, calcium lactate, magnesium sulfate, sodium fluoride and a mixture thereof.
8 . The method of claim 1 , wherein the reduced abuse potential solid dosage formulation further comprises an outer coating, wherein the outer coating comprises at least one hydrophobic polymer.
9 . The method of claim 1 , wherein the reduced abuse potential solid dosage formulation further comprises an outer coating, wherein the outer coating comprises at least one plasticizer.
10 . The method of claim 1 , wherein the opioid is a mu-agonist or a mixed mu-agonist/antagonist.
11 . The method of claim 1 , wherein the opioid is selected from the group consisting of alfentanil, allylprodine, alphaprodine, anileridine, benzylmorphine, bezitramide, buprenorphine, butorphanol, clonitazene, codeine, cyclazocine, desomorphine, dextromoramide, dezocine, diampromide, dihydrocodeine, dihydromorphine, dimenoxadol, dimepheptanol, dimethylthiambutene, dioxaphetyl butyrate, dipipanone, eptazocine, ethoheptazine, ethylmethylthiambutene, ethylmorphine, etonitazine, fentanyl, heroin, hydrocodone, hydromorphone, hydroxypethidine, isomethadone, ketobemidone, levallorphan, levorphanol, levophenacylmorphan, lofentanil, meperidine, meptazinol, metazocine, methadone, metopon, morphine, myrophine, nalbuphine, narceine, nicomorphine, norlevorphanol, normethadone, nalorphine, normophine, norpipanone, opium, oxycodone, oxymorphone, 6-hydroxyoxymorphone, papaveretum, pentazocine, phenadoxone, phenomorphan, phenazocine, phenoperidine, piminodine, piritramide, propheptazine, promedol, properidine, propiram, propoxyphene, sufentanil, tramadol, tilidine, a stereoisomer thereof, a metabolite thereof, a salt thereof, an ether thereof, an ester thereof and a derivative thereof.
12 . The method of claim 1 , wherein the solid dosage formulation is a tablet.
13 . A method for relieving pain comprising administering to a patient in need thereof a reduced abuse potential solid dosage formulation comprising an opioid mixed with a granulated sustained release delivery system,
wherein the granulated sustained release delivery system comprises at least one heteropolysaccharide gum, at least one homopolysaccharide gum, at least one pharmaceutical diluent, and at least one cationic cross-linking agent selected from the group consisting of: calcium sulfate, sodium chloride, potassium sulfate, sodium carbonate, lithium chloride, tripotassium phosphate, sodium borate, potassium bromide, potassium fluoride, sodium bicarbonate, calcium chloride, magnesium chloride, sodium citrate, sodium acetate, calcium lactate, magnesium sulfate, sodium fluoride and a mixture thereof.
14 . The method of claim 13 , wherein the at least one heteropolysaccharide gum is xanthan gum.
15 . The method of claim 14 , wherein the at least one homopolysaccharide gum is locust bean gum or guar gum.
16 . The method of claim 15 , wherein the at least one cationic cross-linking agent is calcium sulfate.
17 . The method of claim 16 , wherein the solid dosage formulation is a tablet.
18 . A method for relieving pain comprising administering to a patient in need thereof a reduced abuse potential solid dosage formulation comprising oxymorphone mixed with a granulated sustained release delivery system,
wherein the granulated sustained release delivery system comprises at least one heteropolysaccharide gum, at least one homopolysaccharide gum, and at least one pharmaceutical diluent.
19 . The method of claim 18 , wherein the reduced abuse potential solid dosage formulation forms a gel matrix with muco-adhesive properties when crushed or powdered upon contact with a fluid.
20 . The method of claim 18 , wherein the reduced abuse potential solid dosage formulation forms a viscous solution when crushed or powdered upon contact with a fluid.
21 . The method of claim 18 , wherein the granulated sustained release delivery system further comprises at least one hydrophobic polymer.
22 . The method of claim 18 , wherein the granulated sustained release delivery system further comprises at least one cationic cross-linking compound selected from monovalent cations, multivalent cations, and salts.
23 . The method of claim 22 , wherein the cationic cross-linking agent is selected from the group consisting of: alkali metal sulfate, alkali metal chloride, alkali metal borate, alkali metal bromide, alkali metal citrate, alkali metal acetate, alkali metal lactate, alkaline earth metal sulfate, alkaline earth metal chloride, alkaline earth metal borate, alkaline earth metal bromide, alkaline earth metal citrate, alkaline earth metal acetate, alkaline earth metal lactate and a mixture thereof.
24 . The method of claim 22 , wherein the cationic cross-linking agent is selected from the group consisting of: calcium sulfate, sodium chloride, potassium sulfate, sodium carbonate, lithium chloride, tripotassium phosphate, sodium borate, potassium bromide, potassium fluoride, sodium bicarbonate, calcium chloride, magnesium chloride, sodium citrate, sodium acetate, calcium lactate, magnesium sulfate, sodium fluoride and a mixture thereof.
25 . The method of claim 18 , wherein the reduced abuse potential solid dosage formulation further comprises an outer coating, wherein the outer coating comprises at least one hydrophobic polymer.
26 . The method of claim 18 , wherein the reduced abuse potential solid dosage formulation further comprises an outer coating, wherein the outer coating comprises at least one plasticizer.
27 . The method of claim 18 , wherein the solid dosage formulation is a tablet.
28 . A method for relieving pain comprising administering to a patient in need thereof a reduced abuse potential solid dosage formulation comprising oxymorphone mixed with a granulated sustained release delivery system,
wherein the granulated sustained release delivery system comprises at least one heteropolysaccharide gum, at least one homopolysaccharide gum, at least one pharmaceutical diluent, and at least one cationic cross-linking agent selected from the group consisting of: calcium sulfate, sodium chloride, potassium sulfate, sodium carbonate, lithium chloride, tripotassium phosphate, sodium borate, potassium bromide, potassium fluoride, sodium bicarbonate, calcium chloride, magnesium chloride, sodium citrate, sodium acetate, calcium lactate, magnesium sulfate, sodium fluoride and a mixture thereof.
29 . The method of claim 28 , wherein the at least one heteropolysaccharide gum is xanthan gum.
30 . The method of claim 29 , wherein the at least one homopolysaccharide gum is locust bean gum or guar gum.
31 . The method of claim 30 , wherein the at least one cationic cross-linking agent is calcium sulfate.
32 . The method of claim 31 , wherein the solid dosage formulation is a tablet.