Device for the controlled release of drugs with Donnan-like modulation by charged insoluble resins

• US 4,814,183 A
• Filed: 08/31/1987
• Issued: 03/21/1989
• Est. Priority Date: 08/31/1987
• Status: Expired due to Term

• Current Assignee: Merck & Co., Inc.
• Original Assignee: Merck & Co., Inc.
• Inventors: Zentner, Gaylen M.
• Primary Examiner(s): Dixon, Jr., William R.
• Assistant Examiner(s): Griffis, Andrew
• Application Number:
  US07/091,571
• Time in Patent Office: 568 Days
• Field of Search: 424/486, 424/487, 424/485, 424/488, 424/443, 424/444
• US Class Current: 424/485
• CPC Class Codes: A61K 9/0004 Osmotic delivery systems; Sustained release driven by osmosis, thermal energy or gas

Abstract

The instant invention is directed to a drug delivery device for the controlled release of beneficial agents and drugs into an environment of use comprising:

(A) a core composition comprising

(a) a water insoluble, non-diffusible charged resin entity, and

(b) a diffusible, water soluble ionizable therapeutically active ingredient carrying the same charge as said resin entity; and

(B) a substantially imperforate water-insoluble wall surrounding said core composition, prepared from a semipermeable material substantially impermeable to the core composition and permeable to the passage of an external fluid in the environment of use, with said wall having a hole(s) for release of the therapeutic agent through the water insoluble wall.

Claims

1. A drug-delivery device for the controlled release of therapeutically active ingredient into an environment of use which comprises:

(A) a core composition comprising

(a) a water insoluble, non-diffusible charged resin entity, and

(b) a diffusible water soluble ionizable therapeutically active ingredient carrying the same charge as said resin entity; and

(B) a substantially imperforate water insoluble wall surrounding said core composition and prepared from a semipermeable material substantially impermeable to core composition and permeable to the passage of an external fluid in the environment of use, with said wall having a means for release of the therapeutic agent through the water insoluble wall.

2. A drug-delivery device according to claim 1, wherein the resin entity is a cationic resin selected from the group consisting of polystyrene, epoxy-amine, phenolic or condensate polymeric backbones containing an active group of quaternary ammonium, secondary amine, tertiary amine in an aromatic matrix or tertiary amine in an aliphatic matrix.

3. A drug-delivery device according to claim 1, wherein the resin entity is an anionic resin with acrylic, methacrylic or phenolic polymeric backbones with phosphonic acid or carboxylic acid active groups.

4. A drug-delivery device according to claim 1, wherein the resin entity is an anionic resin with polystyrene or phenolic polymeric backbones containing an active group of sulfonic acid.

5. A drug-delivery device according to claim 1, wherein the resin entity is a cellulose polymer selected from the group consisting of diethylamino-ethyl cellulose, carboxymethyl cellulose, guanidoethyl cellulose, sulfoethyl cellulose, and sulfopropyl cellulose.

6. A drug-delivery device according to claim 1, wherein the resin entity is a cross-linked vinyl pyridine polymer.

7. A drug-delivery device according to claim 1, wherein the therapeutically active ingredient is soluble in an external fluid and exhibits an osmotic pressure gradient across the wall against the external fluid.

8. A drug-delivery device according to claim 1, wherein the therapeutically active ingredient has limited solubility in the external fluid and is mixed with an osmotically effective solute that is soluble in the fluid, which exhibit an osmotic pressure gradient across the wall against the external fluid.

9. A drug-delivery device according to claim 1, further comprising:

(C) 0 to 50 parts per 100 parts of wall material, of plasticizer and flux regulating additives and

(D) 0 to 40 parts per 100 parts of wall material, of surfactant additive.

10. A drug-delivery device according to claim 1, wherein said water insoluble wall is 1 to 1,000 microns thick.

11. A drug-delivery device according to claim 10 wherein said wall is 20 to 500 microns thick.

12. A drug-delivery device according to claim 1, wherein at least 0.05 ng of active agent are used.

13. A drug-delivery device according to claim 12, wherein at least 1 microgram of active agent is used.

14. A drug-delivery device according to claim 1, wherein said semipermeable material is selected from the group consisting of cellulose esters, acylated polysaccharides, polyurethane, polymers of acrylic and methacrylic acid and esters thereof, poly (ortho ester)s, polyacetals and mixtures thereof.

15. A drug-delivery device according to claim 14, wherein said semipermeable material is selected from the group consisting of cellulose esters and acylated polysaccharides.

16. A drug-delivery device according to claim 15, wherein said semipermeable material is selected from the group consisting of polyurethanes and polymers of acrylic and methacrylic acid and esters thereof.

17. A drug-delivery device according to claim 15, wherein said semipermeable material is selected from the group consisting of poly(ortho esters)s and polyacetals.

18. A drug-delivery device according to claim 1, further comprising a water insoluble, permeable, non-rate controlling microporous wall.

19. A drug-delivery device according to claim 18, wherein the microporous wall is separated from the semipermeable wall by a layer of fluid soluble material.

20. A drug-delivery device according to claim 18, wherein the microporous wall is in direct contact with the semipermeable wall.