DRUG FORMULATIONS

• US 20120202838A1
• Filed: 11/04/2011
• Published: 08/09/2012
• Est. Priority Date: 11/04/2010
• Status: Abandoned Application

• Current Assignee: Abbvie Incorporated
• Original Assignee: Abbott GmbH & Company KG (Abbott Laboratories), Abbott Laboratories
• Inventors: Ghosh, Soumojeet, Lefebvre, Didier, Breitenbach, Joerg, Wiesner, Bryan
• Application Number:
  US13/289,982
• Publication Number:
  US 20120202838A1
• Time in Patent Office: Days
• US Class Current: 514/282
• CPC Class Codes: A61K 9/146 with organic macromolecular compounds
• CPC Class Codes: A61K 9/2054 Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
• CPC Class Codes: A61K 9/2077 Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets
• CPC Class Codes: A61P 25/04 Centrally acting analgesics, e.g. opioids

Abstract

In one embodiment, the present invention relates to abuse-deterrent drug formulations comprise a plurality of discrete domains uniformly dispersed in a pharmaceutically acceptable matrix, wherein said domains have high fracture toughness and comprise at least one polymer and at least one abuse-relevant drug. In another embodiment, the present invention relates to a formulation comprising a plurality of discrete mechanically reinforcing particles uniformly dispersed in a pharmaceutically acceptable matrix, wherein said matrix has high fracture toughness and comprises at least one polymer and at least one active agent, at least one abuse-relevant drug or a combination of at least one active agent and at least one abuse-relevant drug.

Claims

1. A formulation comprising a plurality of discrete mechanically reinforcing particles uniformly dispersed in a pharmaceutically acceptable matrix, wherein said matrix has high fracture toughness and comprises at least one polymer and at least one active agent, at least one abuse-relevant drug or a combination of at least one active agent and at least one abuse-relevant drug.

2. The formulation of claim 1, wherein the polymer has a maximum mechanical energy dissipation at a temperature of about 50°

C. or below.

3. The formulation of claim 1, wherein the polymer is semi-crystalline.

4. The formulation of claim 1, wherein the polymer is a semi-crystalline polymer having a maximum mechanical energy dissipation a temperature of about 50°

C. or below.

5. The formulation of claim 1, wherein said mechanically reinforcing particles are composed of a filler or a fiber, or of a combination of a filler and a fiber.

6. The formulation of claim 5, wherein the filler is dicalcium phosphate.

7. The method of claim 5, wherein the fiber comprises a cellulosic excipient.

8. The formulation of claim 1, wherein the polymer comprises at least one poly(ethylene oxide).

9. The formulation of claim 8, wherein the poly(ethylene oxide) has a molecular weight of about 100,000 to about 10,000,000 Daltons.

10. The formulation of claim 1, wherein said matrix additionally comprise a plasticizer.

11. The formulation of claim 1, wherein said matrix additionally comprises an anti-oxidant to protective the active agent or abuse-relevant drug.

12. The formulation of claim 10, wherein said plasticizer is a poly(ethylene oxide) having a molecular weight less than about 900,000 Daltons.

13. The formulation of claim 1, wherein the weight ratio of said active agent, abuse-relevant drug or combination of active agent and abuse-relevant drug and the polymer is from about 50:

50 to about 0.1 to 99.9.

14. The formulation of claim 1, wherein the abuse-relevant drug is an opioid.

15. The formulation of claim 14, 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, etonitazene, fentanyl, heroin, hydrocodone, hydromorphone, hydroxypethidine, isomethadone, ketobemidone, levallorphan, levophenacylmorphan, levorphanol, lofentanil, meperidine, meptazinol, metazocine, methadone, metopon, morphine, myrophine, nalbulphine, narceine, nicomorphine, norpipanone, opium, oxycodone, oxymorphone, papvretum, paladone, pentazocine, phenadoxone, phenazocine, phenomorphan, phenoperidine, piminodine, propiram, propoxyphene, sufentanil, tapenadol, tilidine, and tramadol, and salts, esters, prodrugs and mixtures thereof.

16. The formulation of claim 14, wherein the opiod is hydrocodone.

20. The formulation of claim 10, wherein the plasticizer is poloxamer.

21. The formulation of claim 1, wherein the formulation can be shaped without addition of heat.

17. A method of preparing a formulation, said method comprises the steps of:

a) manufacturing particles which comprise a fracture toughness-imparting polymer and at least one active agent, at least one abuse-relevant drug or a combination of at least one active agent and at least one abuse-relevant drug, and

b) embedding a plurality of said particles in a pharmaceutically acceptable matrix in a unit dosage form.

18. The method of claim 17, wherein said particles comprise a filler or a fiber.

19. The method of claim 18, wherein the filler is dicalcium phosphate.