Therapeutic compositions and methods

• US 5,484,609 A
• Filed: 01/21/1994
• Issued: 01/16/1996
• Est. Priority Date: 07/24/1991
• Status: Expired due to Fees

• Current Assignee: Enzacor Properties Limited
• Original Assignee: Enzacor Properties Limited
• Inventors: Ko, Thomas S. Y.
• Primary Examiner(s): GRIFFIN, RONALD
• Application Number:
  US08/185,061
• Time in Patent Office: 725 Days
• Field of Search: 424/470, 424/474, 424/78.01, 424/490, 424/491, 424/597, 514/964, 514/965, 514/867, 514/885, 514/2
• US Class Current: 424/470
• CPC Class Codes: A61K 9/0095 Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches A61K9/0007 takes precedence; eatable gels or foams A61K9/0056; oral mucosa adhesive forms A61K9/006
• CPC Class Codes: A61K 9/06 Ointments; Bases therefor; Other semi-solid forms, e.g. creams, sticks, gels composition of ointments, creams or gels A61K47/00
• CPC Class Codes: A61K 9/1611 Inorganic compounds
• CPC Class Codes: A61K 9/5042 Cellulose; Cellulose derivatives, e.g. phthalate or acetate succinate esters of hydroxypropyl methylcellulose
• CPC Class Codes: A61P 1/12 Antidiarrhoeals
• CPC Class Codes: A61P 31/04 Antibacterial agents
• CPC Class Codes: Y02A 50/30 Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Abstract

Compositions comprising (i) granules comprising a biologically active material in association with a weak base and partially coated with a delayed release material soluble in intestinal juice, (ii) an acidifying agent having a pH between 1.5 to 6, and (iii) a gel forming agent are described. There is also described a composition comprising an acidic gel having a pH between 1.5 to 6 and containing microgranules comprising a biologically active material in association with a weak base and partially coated with a delayed release material soluble in intestinal juice. The compositions may be used in the treatment of diseases associated with intestinal pathogens in animals. Where the biologically active material is a protease, receptor/adhesion sites in the intestines for pathogens may be proteolysed so as to prevent pathogen binding to intestinal surfaces.

Claims

1. A composition comprising:

(i) granules comprising a biologically active material in association with a week base, the granules being partially coated with a delayed release material substantially impermeable at pH below about 6.0 and soluble in intestinal joice;

(ii) an acidifying agent having a pH between about 1.5 to about 6 when in solution; and

(iii) a gel forming agent.

2. The composition according to claim 1, wherein the biologically active material is a protein and is selected from the growth consisting of enzymes, growth factors and hormones.

3. The composition according to claim 2, wherein the protein is an enzyme selected from the group consisting of bromelin, papain, ficin, chymotrypsin, trypsin, ribonuclease, carboxypeptidate A, carboxypeptidate B, and subtilisin.

4. The composition according to claim 1, wherein the biological material is a non-proteinaceous biological material.

5. The composition according to claim 4, wherein the non-proteinaceous biological material is selected from the group consisting of vitamins, co-factors, metal ions and antibiotics.

6. The composition according to claim 1, wherein the gel forming agent forms a gel when mixed with a solvent.

7. The composition according to claim 1, wherein from 10 to 90% of the surface area of the granules is coated with the delayed release material.

8. The composition according to claim 1, wherein the acidifying agent is in particulate form.

9. The composition according to claim 1, wherein an acidic gel containing microgranules forms on the addition of an aqueous solution to the composition.

10. The composition according to claim 1, further comprising an antibiotic.

18. A method for the delivery of a biologically active substance to the upper small intestinal tract of an animal, the method comprising:

reacting the composition of claim 1 with a solvent to form a gel; and

orally administering the gel to the animal.

19. A method for the delivery of a biologically active substance to the upper small intestinal tract of an animal, the method comprising orally administering to the animal a composition according to claim 10.

20. A method for the treatment of intestinal pathogens and diseases associated with intestinal pathogen infection in an animal, the method comprising:

reacting the composition of claim 1, wherein said biologically active material is a protease, with a solvent to form a gel; and

orally administering the gel to the animal.

22. A method according to claim 20 wherein said protease is bromelin.

23. The method according to claim 20, wherein said intestinal pathogen is selected from the group consisting of bacteria, viruses, and parasites.

24. The method according to claim 23, wherein said intestinal pathogen is selected from the group consisting of enterotoxigenic Escherichia coli, Shigella, Yersinia, Pleisiomonas, Vibrios, Aeromonas, Campylobacter, rotavirus, Cryptosporidia and Coccidosis.

25. The method according to claim 20 wherein said composition further comprises an antibiotic.

26. The method according to claim 20, wherein the administering comprises administering an antibiotic.

27. The method according to claim 20, wherein said animal is a monogastrate or immature ruminant.

28. The method according to claim 20, wherein said animal is selected from the group consisting of humans, pigs, calves, horses, fish and crustacea.

33. A method for the non-specific stimulation of the immune system of an animal, comprising:

reacting the composition of claim 1, wherein said biologically active material is a protease, with a solvent to form a gel; and

orally administering the gel to the animal.

34. A method for the non-specific stimulation of the immune system of an animal, comprising:

orally administering to the animal a composition according to claim 10 wherein said biologically active material is a protease.

35. The method according to claim 33, wherein said protease is bromelin.

36. The method according to claim 33, wherein the animal is selected from the group consisting of humans, pigs, calf, horses, fish, and crustacea.

37. A method of using a composition according to claim 1, wherein the biologically active material is a protease, the method comprising preparing a medicament for treatment of intestinal pathogens or diarrhoea in animals.

38. The method of claim 37, wherein the protease is bromelin.

11. A composition comprising:

an acidic gel having a pH between about 1.5 to about 6; and

microgranules comprising a biologically active material in association with a weak base, the microgranules being partially coated with a delayed release material substantially impermeable at pH below about 6.0 and soluble in intestinal juice.

12. The composition according to claim 11, wherein the biologically active material is a protein and is selected from the growth consisting of enzymes, growth factor, and hormones.

13. The composition according to claim 12, wherein the protein is an enzyme selected from the group consisting of bromelin, papain, ficin, chymotrypsin, trypsin, ribonuclease, carboxypeptidate A, carboxypeptidate B, and subtilisin.

14. The composition according to claim 11, wherein the biological material is a non-proteinaceous biological material.

15. The composition according to claim 14, wherein the non-proteinaceous biological material is selected from the group consisting of vitamins, co-factors, metal ions and antibiotics.

16. The composition according to claim 11, wherein from about 10 to about 90% of the surface area of the microgranules is coated with the delayed release material.

17. The composition according to claim 11, further comprising an antibiotic.

21. A method for the treatment of intestinal pathogens and diseases associated with intestinal pathogen infection in an animal the method comprising orally administering the animal a therapeutically effective mount of a composition according to claim 11, wherein said biologically active material is a protease.

31. The method according to claim 21, wherein said gel comprises an antibiotic.

29. A method for the treatment of diarrhoea in an animal comprising administering to the animal an acidic gel having a pH between about 1.5 to about 6, said gel containing microgranules comprising a proteolytic enzyme in association with a weak base, the microgranules being partially coated with a delayed release material soluble in intestinal juice but substantially impermeable at a pH below about 6.0.

30. The method according to claim 29, wherein said proteolytic enzyme is bromelin.

32. A method according to claim 29, wherein the administering comprises administering an antibiotic.