IP Library Granted Patent US 7,744,924
Granted Patent B2
US 7,744,924 · App. 11/675,831 · Granted Jun 29, 2010

Venlafaxine formulations and methods of preparing the same

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Quick Facts
Patent No.
US 7,744,924
App. No.
11/675,831
Filed
Feb 16, 2007
Granted
Jun 29, 2010
Kind
B2
Art Unit
1618
USPC
424/490
Abstract

A method of forming a multi-particulate dosage form using rotary granulation is described in which polyethylene oxide is employed as s binder in a rotary granulation process. A multi-particulate oral dosage form comprises a plurality of pellets, the pellets comprising a core having disposed thereon a core composition layer. The core composition layer comprises venlafaxine and a binder, wherein the binder comprises a polyethylene oxide. In other embodiments, the binder comprises a 1:2:1 bis (butyl methacrylate-co-(2-dimethylaminoethyl)methacrylate-co-methyl methacrylate.

Claims (18)

1. A multi-particulate oral dosage form, comprising a plurality of pellets, the pellets comprising a core having disposed thereon a core composition layer, the core composition layer comprising an admixture of venlafaxine and a binder, wherein the binder comprises polyethylene oxide, wherein the polyethylene oxide has an average molecular weight of about 100,000 to about 6,000,000, and wherein a ratio of polyethylene oxide to venlafaxine is about 1:30 to about 1:5.

2. The multi-particulate oral dosage form of claim 1 , wherein the binder comprises about 0.2 wt % to about 12 wt % of the total weight of the core and the core composition layer.

3. The multi-particulate oral dosage form of claim 1 , comprising about 10 wt % to about 98 wt % of the core, about 2 wt % to about 85 wt % of the venlafaxine, and about 0.1 wt % to about 20 wt % of the binder, all based on the total weight of the core and the core composition layer.

4. The multi-particulate oral dosage form of claim 3 , comprising about 10 wt % to about 70 wt % of the venlafaxine, based on the total weight of the core and the core composition layer.

5. The multi-particulate oral dosage form of claim 1 , further comprising an additional coating layer, wherein the additional coating layer is a controlled-release coating, a seal coating, or a combination of one or more of the foregoing coatings.

6. The multi-particulate dosage form of claim 1 , wherein the core is an inert sphere.

7. The multi-particulate dosage form of claim 6 , wherein the inert sphere comprises nonpareils, sugar spheroids, microcrystalline cellulose spheres, spheres made of microcrystalline cellulose and one or more sugars, or a combination of one or more of the foregoing cores.

8. The multi-particulate dosage form of claim 1 , wherein the inert sphere is a sugar sphere.

9. The multi-particulate dosage form of claim 1 , wherein the core composition layer further comprises a plasticizer.

10. A multi-particulate oral dosage form, comprising a plurality of pellets, the pellets comprising an inert sphere core having disposed thereon a core composition layer, the core composition layer comprising an admixture of venlafaxine, a plasticizer, and a binder, wherein the binder comprises a 1:2:1 (butyl methacrylate-co-(2-dimethylaminoethyl)methacrylate-co-methyl methacrylate).

11. The multi-particulate oral dosage form of claim 10 , wherein the ratio of binder to venlafaxine in the core composition layer is about 1:30 to about 1:5.

12. The multi-particulate oral dosage form of claim 10 , wherein the binder comprises about 0.2 wt % to about 12 wt % of the total weight of the core and the core composition layer.

13. The multi-particulate oral dosage form of claim 10 , comprising about 10 wt % to about 98 wt % of the core, about 2 wt % to about 85 wt % of the venlafaxine, and about 0.1 wt % to about 20 wt % of the binder, all based on the total weight of the core and the core composition layer.

14. The multi-particulate oral dosage form of claim 13 , comprising about 10 wt % to about 70 wt % of the venlafaxine, based on the total weight of the core and the core composition layer.

15. The multi-particulate oral dosage form of claim 1 , further comprising an additional coating layer, wherein the additional coating layer is a controlled-release coating, a seal coating, or a combination of one or more of the foregoing coatings.

16. The multi-particulate dosage form of claim 10 , wherein the inert sphere is a sugar sphere.

17. A method of making a multi-particulate oral dosage form, of claim 1 comprising mixing venlafaxine, a binder comprising polyethylene oxide, and a dispersing agent to form a coating mixture, and

atomizing the coating mixture in the presence of a plurality of cores in a fluidized bed with a rotor-disk granulator to produce a plurality of pellets, the pellets comprising the core having disposed thereon a core composition layer comprising the venlafaxine and the binder.

Assignments (6)
RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY Recorded Nov 1, 2012
From: DEUTSCHE BANK AG, LONDON BRANCH
To: ACTAVIS GROUP PTC EHF
Reel/Frame 029227/0314 →
RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY Recorded Nov 1, 2012
From: DEUTSCHE BANK AG, LONDON BRANCH
To: ACTAVIS GROUP HF
Reel/Frame 029229/0470 →
RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY Recorded Nov 1, 2012
From: DEUTSCHE BANK AG, LONDON BRANCH
To: ACTAVIS ELIZABETH LLC
Reel/Frame 029229/0894 →
PATENT SECURITY AGREEMENT SUPPLEMENT Recorded Mar 22, 2012
From: ACTAVIS ELIZABETH LLC
To: DEUTSCHE BANK AG, LONDON BRANCH, AS SECURITY AGENT
Reel/Frame 027906/0450 →
PATENT SECURITY AGREEMENT SUPPLEMENT Recorded Dec 10, 2010
From: ACTAVIS GROUP PTC EHF.
To: DEUTSCHE BANK AG, LONDON BRANCH
Reel/Frame 025463/0758 →
PATENT SECURITY AGREEMENT SUPPLEMENT Recorded Dec 10, 2010
From: ACTAVIS GROUP HF.
To: DEUTSCHE BANK AG, LONDON BRANCH
Reel/Frame 025468/0833 →