IP Library Granted Patent US 8,617,607
Granted Patent B2
US 8,617,607 · App. 12/500,852 · Granted Dec 31, 2013

Sustained release formulations of psychoactive drugs

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Quick Facts
Patent No.
US 8,617,607
App. No.
12/500,852
Granted
Dec 31, 2013
Kind
B2
Abstract

This invention provides biodegradable, sustained-release pharmaceutical compositions of a psychoactive drug formulated with biocompatible, biodegradable tyrosine-derived polyarylates.

Claims (25)

1. A sustained-release formulation comprising a tyrosine-derived polyarylate having at least one p(DT-succinate) group and a psychoactive drug physically admixed, dissolved, dispersed, or embedded within said tyrosine-derived polyarylate, and wherein said tyrosine-derived polyarylate and said psychoactive drug form a homogeneous solid matrix, and wherein said formulation provides a burst-free, sustained release of said psychoactive drug.

2. The formulation according to claim 1 , wherein when measured in vitro under physiological conditions at 37° C., amounts are such that the formulation releases the psychoactive for at least 1 to 5 days.

3. The formulation of claims 2 , wherein the physiological conditions are in phosphate buffered saline (PBS).

4. The formulation according to claim 1 , wherein the psychoactive drug is an atypical psychoactive drug.

5. The formulation according to claim 4 , wherein the atypical psychoactive drug is olanzapine.

6. The formulation according to claim 1 , wherein the formulation is prepared as a microparticle or a microsphere.

7. The formulation according to claim 1 , wherein the tyrosine-derived polyarylate is a poly(DT-DTE succinate) or a poly(DTE succinate), wherein, DT, when present ranges from about 5% to about 50%, from about 5% to about 30%, from about 10% to about 20% of the polyarylate or is about 5%, 10%, 15%, 20%, 25% or 30% of said polyarylate.

8. The formulation according to claim 1 , wherein the formulation comprises an amount of psychoactive drug ranging from about 10% to about 40% by weight.

9. A sustained-release formulation comprising a tyrosine-derived polyarylate and a psychoactive drug physically admixed, dissolved, dispersed, or embedded within said tyrosine-derived polyarylate, and wherein said tyrosine-derived polyarylate and said psychoactive drug form a homogeneous solid matrix, and wherein said formulation is prepared as a solvent-cast film or a solvent-free film.

10. The formulation according to claim 9 , wherein when measured in vitro under physiological conditions at 37° C., amounts are such that the formulation releases the psychoactive for at least 1 to 5 days.

11. The formulation of claim 8 , wherein the physiological conditions are in phosphate buffered saline (PBS).

12. The formulation according to claim 9 , wherein the psychoactive drug is an atypical psychoactive drug.

13. The formulation according to claim 12 , wherein the atypical psychoactive drug is olanzapine.

14. The formulation according to claim 9 , wherein the psychoactive drug is olanzapine.

15. The formulation according to claim 9 , wherein the formulation is prepared as a microparticle or a microsphere.

16. The formulation according to claim 9 , wherein the formulation comprises an amount of psychoactive drug ranging from about 10% to about 40% by weight.

17. A burst-free, sustained-release microsphere or microparticle comprising a tyrosine-derived polyarylate having at least one p(DT-succinate) group and a psychoactive drug.

18. The microsphere or microparticle according to claim 17 , wherein when measured in vitro under physiological conditions at 37° C., amounts are such that the formulation releases the psychoactive for at least 1 to 5 days.

19. The microsphere or microparticle of claims 18 , wherein the physiological conditions are in phosphate buffered saline (PBS).

20. The microsphere or microparticle according to claim 17 , wherein the psychoactive drug is an atypical psychoactive drug.

21. The microsphere or microparticle according to claim 17 , wherein the atypical psychoactive drug is olanzapine.

22. The microsphere or microparticle according to claim 17 , wherein the formulation comprises an amount of psychoactive drug ranging from about 10% to about 40% by weight.

23. The formulation of claim 1 , wherein said tyrosine-derived polyarylate is comprised of a mixture of p(DTE-succinate) and p(DT-succinate) monomers.

24. The formulation of claim 1 , wherein said formulation is prepared as a solvent-cast film or a solvent-free film.

25. The formulation of claim 9 , wherein said said tyrosine-derived polyarylate is comprised of a mixture of p(DTE-succinate) and p(DT-succinate) monomers.

Assignments (4)
MERGER AND CHANGE OF NAME Recorded Feb 10, 2020
From: TYRX, INC.; MEDTRONIC, INC.
To: MEDTRONIC, INC.
Reel/Frame 051770/0976 →
MERGER Recorded Jun 3, 2014
From: TYRX, INC.
To: TYRX, INC.
Reel/Frame 033019/0930 →
CHANGE OF NAME Recorded Nov 22, 2011
From: TYRX PHARMA, INC.
To: TYRX, INC.
Reel/Frame 027311/0694 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 20, 2009
From: MOSES, ARIKHA; BUEVICH, FATIMA; PULAPURA, SATISH
To: TYRX PHARMA, INC.
Reel/Frame 023550/0821 →