Controlled and sustained delivery of nucleic acid-based therapeutic agents

• US 20050163844A1
• Filed: 01/26/2005
• Published: 07/28/2005
• Est. Priority Date: 01/26/2004
• Status: Abandoned Application

• Current Assignee: Control Delivery Systems Inc. (EyePoint Pharmaceuticals, Inc.)
• Original Assignee: Control Delivery Systems Inc. (EyePoint Pharmaceuticals, Inc.)
• Inventors: Ashton, Paul
• Application Number:
  US11/043,884
• Publication Number:
  US 20050163844A1
• Time in Patent Office: Days
• US Class Current: 424/468
• CPC Class Codes: A61K 48/00 Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
• CPC Class Codes: A61K 9/0024 Solid, semi-solid or solidifying implants, which are implanted or injected in body tissue compositions for intravenous administration, normal injectable solutions or dispersions for, e.g. subcutaneous administration A61K9/0019; brain implants A61K9/0085; (coated) prostheses, catheters or stents A61L
• CPC Class Codes: A61K 9/0051 Ocular inserts, ocular implants
• CPC Class Codes: C12N 15/88 using microencapsulation, e.g. using amphiphile liposome vesicle

Abstract

The invention provides insertable drug delivery devices for the controlled and sustained release of nucleic acid-based therapeutic agents, including antisense agents, siRNAs, ribozymes, and aptamers.

Claims

1. A controlled- and sustained-release drug delivery device comprising

(a) an inner drug core comprising an amount of a nucleic acid-based therapeutic agent, and

(b) a first polymer coating partially covering said core,

wherein said polymer coating is impermeable to said therapeutic agent.

2. The drug delivery device of claim 1, further comprising a second polymer coating covering at least the portion of said core not covered by said first polymer layer, wherein the second polymer coating is permeable to the therapeutic agent.

3. The drug delivery device of claim 2, wherein the second polymer layer is positioned between the core and the first polymer layer.

4. The drug delivery device of claim 2, wherein the first polymer layer is positioned between the core and the second polymer layer.

15. The device according to claim 1, wherein the first polymer coating comprises polyimide, silicone, poly(lactic acid), poly(lactic-co-glycolic acid), or poly(caprolactone).

16. The device according to claim 1, wherein the second polymer coating comprises cross-linked polyvinyl alcohol, poly(lactic acid), poly(lactic-co-glycolic acid), or poly(caprolactone).

17. The device according to claim 1, wherein the second polymer coating further comprises polyethylene glycol.

18. The device according to claim 16, wherein the second polymer coating further comprises polyethylene glycol.

19. A device according to claim 1, wherein the nucleic acid-based therapeutic agent is an aptamer.

20. A device according to claim 1, wherein the nucleic acid-based therapeutic agent is a ribozyme.

21. A device according to claim 1, wherein the nucleic acid-based therapeutic agent is an antisense agent.

22. A device according to claim 1, wherein the nucleic acid-based therapeutic agent is a small inhibitory RNA.

23. A device according to claim 19, wherein the nucleic acid-based therapeutic agent is pegaptanib.

24. A device according to claim 20, wherein the nucleic acid-based therapeutic agent is Angiozyme™

.

25. A device according to claim 21, wherein the nucleic acid-based therapeutic agent is selected from fomivirsen, alicaforsen, oblimersen, Affinitac™

, and Oncomyc-NG™

.

5. A controlled and sustained release drug delivery device comprising

(a) an inner drug core comprising an amount of a nucleic acid-based therapeutic agent,

(b) an inner tube impermeable to the passage of said agent, said inner tube having first and second ends and covering at least a portion of said inner drug core, said inner tube being dimensionally stable,

(c) an impermeable member positioned at said inner tube first end, said impermeable member preventing passage of said agent out of said drug core through said inner tube first end, and

(d) a permeable member positioned at said inner tube second end, said permeable member allowing diffusion of said agent from said drug core through said inner tube second end.

6. A controlled and sustained release drug delivery device comprising

(e) an inner drug core comprising an amount of a nucleic acid-based therapeutic agent,

(f) an inner tube impermeable to the passage of said agent, said inner tube having first and second ends and covering at least a portion of said inner drug core, said inner tube being dimensionally stable, and

(g) permeable members positioned at said inner tube first and second ends, said permeable members allowing diffusion of said agent from said drug core through said inner tube first and second ends.

7. A controlled- and sustained-release drug delivery device comprising

(a) a drug core comprising an amount of a nucleic acid-based therapeutic agent,

(b) a first polymer coating permeable to the passage of said agent, and

(c) a second polymer coating impermeable to the passage of said agent,

wherein the second polymer coating covers a portion of the surface area of the drug core and/or the first polymer coating.

8. A controlled- and sustained-release drug delivery device comprising

(a) a drug core comprising an amount of a nucleic acid-based therapeutic agent, and

(b) a first polymer coating and a second polymer coating permeable to the passage of said agent,

wherein the two polymer coatings are bioerodable and erode at different rates.

9. A controlled- and sustained-release drug delivery device comprising

(a) a drug core comprising an amount of a nucleic acid-based therapeutic agent,

(b) a first polymer coating permeable to the passage of said agent covering at least a portion of the drug core,

(c) a second polymer coating impermeable to the passage of said agent covering at least a portion of the drug core or the first polymer coating, and

(d) a third polymer coating permeable to the passage of said agent covering the drug core and the second polymer coating,

wherein a dose of said agent is released for at least 7 days.

10. A controlled- and sustained-release drug delivery device comprising

(a) a drug core comprising an amount of a nucleic acid-based therapeutic agent,

(b) a first polymer coating permeable to the passage of said agent covering at least a portion of the drug core,

(c) a second polymer coating impermeable to the passage of said agent covering at least a portion of the drug core or the first polymer coating, and

(d) a third polymer coating permeable to the passage of said agent covering the drug core and the second polymer coating,

wherein release of said agent maintains a desired concentration of said agent for at least 7 days.

11. A controlled- and sustained-release drug delivery device comprising

(a) a drug core comprising an amount of a nucleic acid-based therapeutic agent, and

(b) a non-erodable polymer coating, the polymer coating being permeable to the passage of said agent covering the drug core and essentially non-release rate limiting,

wherein a dose of said agent is released for at least 7 days.

12. A controlled- and sustained-release drug delivery device comprising

(a) a drug core comprising an amount of a nucleic acid-based therapeutic agent, and

(b) a non-erodable polymer coating, the polymer coating being permeable to the passage of said agent covering the drug core and being essentially non-release rate limiting,

wherein release of said agent maintains a desired concentration of said agent for at least 7 days.

13. A controlled- and sustained-release drug delivery device comprising

(a) a drug core comprising an amount of a nucleic acid-based therapeutic agent,

(b) a first polymer coating permeable to the passage of said agent covering at least a portion of the drug core,

(c) a second polymer coating impermeable to the passage of said agent covering at least 50% of the drug core and/or the first polymer coating, said second polymer coating comprising an impermeable film and at least one impermeable disc, and

(d) a third polymer coating permeable to the passage of said agent covering the drug core, the uncoated portion of the first polymer coating, and the second polymer coating,

wherein a dose of said agent is released for at least 7 days.

14. A controlled- and sustained-release drug delivery device comprising

(a) a drug core comprising an amount of a nucleic acid-based therapeutic agent,

(b) a first polymer coating permeable to the passage of said agent covering at least a portion of the drug core,

(c) a second polymer coating impermeable to the passage of said agent covering at least 50% of the drug core and/or the first polymer coating, said second polymer coating comprising an impermeable film and at least one impermeable disc, and

(d) a third polymer coating permeable to the passage of said agent covering the drug core, the uncoated portion of the first polymer coating, and the second polymer coating,

wherein release of said agent maintains a desired concentration of said agent for at least 7 days.