Biodegradable hydrogel matrices for the controlled release of pharmacologically active agents

• US 4,925,677 A
• Filed: 08/31/1988
• Issued: 05/15/1990
• Est. Priority Date: 08/31/1988
• Status: Expired due to Term

• Current Assignee: Watson Pharmaceuticals, Inc. (Abbvie Incorporated)
• Original Assignee: Theratech, Inc. (Dynatronics Corporation)
• Inventors: Feijen, Jan
• Primary Examiner(s): NOT, DEFINED
• Assistant Examiner(s): NOT, DEFINED
• Application Number:
  US07/238,802
• Time in Patent Office: 622 Days
• Field of Search: 424/488, 424/426, 424/423, 424/484, 424/499
• US Class Current: 424/484
• CPC Class Codes: A61K 9/1652 Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin homeopathic globules A61K9/1623
• CPC Class Codes: A61K 9/1658 Proteins, e.g. albumin, gelatin
• CPC Class Codes: A61K 9/205 Polysaccharides, e.g. alginate, gums; Cyclodextrin
• CPC Class Codes: A61K 9/2063 Proteins, e.g. gelatin

Abstract

A biodegradable hydrogen matrix is provided, useful for the controlled release of pharmacologically active agents. The matrix is formed by cross-linking a proteinaceous component and a polysaccharide or mucopolysaccharide, and then loading a selected drug therein. By varying temperature, ionic strength, and the composition of the hydrogel matrix, one can control degradation kinetics, the degree of uptake of a particular pharmacologically active agent, and the overall timed release profile.

Claims

1. A drug delivery system comprising:

(a) a biodegradable endogenous hydrogel matrix comprising a protein, a polysaccharide, and a cross-linking agent providing network linkage therebetween, wherein the weight ratio of polysaccharide to protein in the matrix is in the range of about 10;

90 to 90;

10; and

(b) an effective amount of a drug contained within the matrix to provide the desired systemic or local effect.

2. The drug delivery system of claim 1, wherein the protein is selected from the group consisting of albumin, casein, fibrinogen, γ

-globulin, hemoglobin, ferritin, elastin and synthetic α

-amino peptides.

3. The drug delivery system of claim 1, wherein the polysaccharide is selected from the group consisting of heparin, heparin fragments, heparan, heparan sulfate, chondroitin sulfate, dextran and mixtures thereof.

4. The drug delivery system of claim 3, wherein the polysaccharide is selected from the group consisting of heparin, heparin fragments, heparan and heparan sulfate.

5. The drug delivery system of claim 2, wherein the protein is albumin.

6. The drug delivery system of claim 1, wherein the ratio of polysaccharide to protein is in the range of about 10:

90 to 60;

40.

7. The drug delivery system of claim 1, wherein the cross-linking agent is an amide bond-forming agent.

8. The drug delivery system of claim 7, wherein the amide bond-forming agent is a carbodiimide.

9. The drug delivery system of claim 8, wherein the carbodiimide is N-(3-dimethylaminopropyl)-N'"'"'-ethylcarbodiimide.

10. The drug delivery system of claim 1, wherein the cross-linking agent contains at least two aldehyde groups.

11. The drug delivery system of claim 10, wherein the cross-linking agent is glutaraldehyde.

12. The drug delivery system of claim 1, wherein the drug contained in the hydrogel matrix is either dissolved or dispersed therein.

13. The drug delivery system of claim 12, wherein the drug is selected from the group consisting of proteins, enzymes, mucopolysaccharides, peptides, hormones, antibodies and cytostatic agents.

14. A method for making a drug delivery system, comprising:

dissolving a protein and a polysaccharide in an aqueous medium wherein the weight ratio of polysaccharide to protein is in the range of 10;

90 to 90;

10;

cross-linking the protein and polysaccharide to provide a cross-linked hydrogel matrix; and

loading an effective amount of a drug in solution or in liquid form into said hydrogel matrix to a predetermined degree wherein the cross-linking is effected by admixture of the protein and polysaccharide components with a cross-linking agent.

15. The method of claim 14, wherein the cross-linking agent is an amide bond-forming agent.

16. The method of claim 15, wherein the amide bond-forming agent is a carbodiimide.

17. The method of claim 16, wherein the carbodiimide is N-(3-dimethylaminopropyl)-N'"'"'-ethylcarbodiimide.

18. The method of claim 14, wherein the cross-linking agent contains at least two aldehyde groups, and wherein cross-linking is followed by reduction with NaCNBH₃.

19. The method of claim 18, wherein the cross-linking agent is glutaraldehyde, followed by reduction with NaCNBH₃.

20. The method of claim 14, wherein the cross-linking is effected by:

(a) initially dissolving the polysaccharide as a quaternary ammonium complex component in an organic reaction medium;

(b) reacting the polysaccharide component with carbonyldiimidazole to give a preactivated polysaccharide compound;

(c) further reacting the preactivated polysaccharide with saccharine, followed by

(d) reacting the activated polysaccharide with a selected protein dissolved in the aqueous medium.

21. The method of claim 14, wherein the protein is selected from the group consisting of albumin, casein, fibrinogen, γ

-globulin, hemoglobin, ferritin and elastin and synthetic α

-amino peptides.

22. The method of claim 21, wherein the protein is albumin.

23. The method of claim 14, wherein the polysaccharide is selected from the group consisting of heparin, heparin fragments, heparan, heparan sulfate, chondroitin sulfate and dextran.

24. The method of claim 14, wherein the ratio of polysaccharide to protein is in the range of about 10;

90 to 60;

40.

25. The method of claim 14, wherein the degree of drug loading is controlled by the ratio of polysaccharide to protein and cross-linker in the hydrogel matrix.

26. The method of claim 14, wherein the degree of drug loading is controlled by temperature.

27. The method of claim 14, wherein the degree of drug loading is controlled by ionic strength.

28. The method of claim 14, wherein the degree of drug loading is controlled by pH.

29. A method of administering a drug to a patient so that release of the drug is controlled, comprising the steps of administering the drug in a biodegradable hydrogel matrix which comprises a protein, a polysaccharide, and a cross-linking agent providing network linkage therebetween, wherein the weight ratio of polysaccharide to protein is in the range of about 10:

90 to 90;

10.

30. The method of claim 29, wherein the administering of the agent in the biodegradable matrix is oral.

31. The method of claim 29, wherein the administering of the agent in the biodegradable matrix is parenteral.