IP Library Granted Patent US 11,213,489
Granted Patent B2
US 11,213,489 · App. 17/027,088 · Granted Jan 4, 2022

Tamper resistant dosage forms

Inventors: William H. McKenna (Yonkers, NY); Richard O. Mannion (Furlong, PA); Edward P. O'Donnell (Basking Ridge, NJ); Haiyong H. Huang (Princeton, NJ)
Assignees: PURDUE PHARMA L.P.; PURDUE PHARMACEUTICALS L.P.
A61K9/28A61J3/005A61J3/06A61J3/10A61K9/0002A61K9/0053A61K9/1641A61K9/209A61K9/2013A61K9/2018A61K9/2027A61K9/2031A61K9/2054A61K9/2077A61K9/2095A61K9/284A61K9/2853A61K9/2866A61K9/2893A61K31/485A61K45/06A61K47/10A61K47/34B29B7/02B29B7/88B29C35/045B29C35/16B29C37/0025B29C43/003B29C43/02B29C43/52B29C71/00B29C71/009A61K9/2072B29C2035/046B29C2035/1658B29K2071/02B29K2105/0035B29K2105/251B29K2995/0088B29L2031/753
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Quick Facts
Patent No.
US 11,213,489
App. No.
17/027,088
Granted
Jan 4, 2022
Kind
B2
Abstract

The present invention relates to pharmaceutical dosage forms, for example to a tamper resistant dosage form including an opioid analgesic, and processes of manufacture, uses, and methods of treatment thereof.

Claims (38)

1. A process of preparing a solid oral extended release pharmaceutical dosage form, comprising the steps of:

(a) combining (1) at least one polyethylene oxide (PEO) having, based on rheological measurements, an approximate molecular weight of at least 800,000, and (2) at least one opioid analgesic, to form a composition;

(b) shaping the composition to form an extended release matrix formulation;

(c) subsequently heating said extended release matrix formulation by subjecting the extended release matrix formulation to an elevated temperature that is at least the softening temperature of said PEO for a time period of at least about 1 minute; and

(d) cooling the heated extended release matrix formulation.

2. The process of claim 1 , wherein said time period is at least about 15 minutes.

3. The process of claim 1 , wherein said elevated temperature is at least about 55° C.

4. The process of claim 1 , wherein said elevated temperature is at least about 62° C.

5. The process of claim 1 , wherein the total PEO content of the shaped composition is at least about 30% (by weight) of the shaped composition.

6. The process of claim 1 , wherein the total PEO content of the shaped composition is at least about 50% (by weight) of the shaped composition.

7. The process of claim 1 , wherein the extended release matrix is shaped by direct compression to form a tablet.

8. The process of claim 1 , wherein said cooling is at a temperature below 50° C.

9. The process of claim 1 , wherein said time period is at least about 5 minutes and said elevated temperature is at least about 55° C.

10. The process of claim 1 , wherein the extended release matrix is shaped to form a tablet; the heating step takes place in a coating pan; said time period is at least about 5 minutes; and said elevated temperature corresponds to the exhaust temperature of the coating pan and is at least about 60° C.

11. The process of claim 10 , wherein the opioid analgesic is oxycodone or a pharmaceutically acceptable salt thereof.

12. The process of claim 10 , wherein the opioid analgesic is hydrocodone or a pharmaceutically acceptable salt thereof.

13. The process of claim 1 , wherein the total PEO content of the shaped composition is at least about 15% (by weight) of the shaped composition.

14. The process of claim 13 , wherein said time period is at least about 5 minutes and said elevated temperature is at least about 55° C.

15. The process of claim 14 , wherein said PEO has, based on rheological measurements, an approximate molecular weight of at least 1,000,000.

16. The process of claim 14 , wherein said PEO has, based on rheological measurements, an approximate molecular weight of at least 4,000,000.

17. The process of claim 14 , wherein said elevated temperature is at least about 60° C.

18. The process of claim 14 , wherein said elevated temperature is at least about 68° C.

19. The process of claim 14 , wherein said opioid analgesic is oxycodone or a pharmaceutically acceptable salt thereof.

20. The process of claim 14 , wherein said active agent is hydrocodone or a pharmaceutically acceptable salt thereof.

21. A process of preparing a solid oral extended release pharmaceutical dosage form, comprising the steps of:

(a) combining (1) at least one polyethylene oxide (PEO) having, based on rheological measurements, an approximate molecular weight of at least 800,000, and (2) at least one opioid analgesic, to form a composition, wherein the total PEO content of the composition is at least about 15% (by weight) of the composition;

(b) shaping the composition to form a plurality of extended release tablets;

(c) subsequently subjecting the tablets to an elevated temperature of at least about 55° C. for a time period of at least about 15 minutes; and

(d) cooling the tablets at a temperature below 50° C.

22. The process of claim 21 , wherein the total PEO content of the composition is at least about 20% (by weight) of the composition.

23. The process of claim 21 , wherein the total PEO content of the composition is at least about 50% (by weight) of the composition.

24. The process of claim 21 , wherein said elevated temperature is at least about 62° C.

25. The process of claim 21 , wherein said opioid analgesic is oxycodone or a pharmaceutically acceptable salt thereof.

26. The process of claim 21 , wherein said opioid analgesic is hydrocodone or a pharmaceutically acceptable salt thereof.

27. The process of claim 21 , wherein said PEO has, based on rheological measurements, an approximate molecular weight of at least 1,000,000.

28. The process of claim 21 , wherein said PEO has, based on rheological measurements, an approximate molecular weight of at least 4,000,000.

29. The process of claim 21 , wherein the dosage form further comprises at least one of a cellulosic additive, magnesium stearate, talc, silica, fumed silica, colloidal silica dioxide, calcium stearate, carnauba wax, stearic acid, stearyl alcohol, mineral oil, paraffin, glycerin, propylene glycol, polyethylene glycol, lactose, povidone, triacetin, and copolymers comprising methyl methacrylate.

30. The process of claim 29 , wherein the cellulosic additive is microcrystalline or hydroxypropylated.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 6, 2026
From: PURDUE PHARMA L.P.
To: KNOA PHARMA LLC
Reel/Frame 075516/0676 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 20, 2021
From: MCKENNA, WILLIAM H.; MANNION, RICHARD O.; O'DONNELL, EDWARD P.; HUANG, HAIYONG H.
To: PURDUE PHARMA L.P.
Reel/Frame 056297/0474 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 20, 2021
From: PURDUE PHARMA L.P.
To: PURDUE PHARMA L.P; PURDUE PHARMACEUTICALS L.P.
Reel/Frame 056298/0571 →
Continuity (12)
Continuation 16931803 · Jul 17, 2020
Continuation 16697855 · Nov 27, 2019
Continuation 16386963 · Apr 17, 2019
Continuation 15885074 · Jan 31, 2018
Continuation 15597885 · May 17, 2017
Continuation 15263932 · Sep 13, 2016
Continuation 14729593 · Jun 3, 2015
Continuation 14515924 · Oct 16, 2014
Continuation 13803132 · Mar 14, 2013
Division 11844872 · Aug 24, 2007
Provisional Application 60840244 · Aug 25, 2006
Related Publication 20210000747A1 · Jan 7, 2021