SOLID DISPERSING VACCINE COMPOSITION FOR ORAL DELIVERY

• US 20080014260A1
• Filed: 07/17/2007
• Published: 01/17/2008
• Est. Priority Date: 10/27/1997
• Status: Abandoned Application

• Current Assignee: Harry Seager
• Original Assignee: Harry Seager
• Inventors: SEAGER, HARRY
• Application Number:
  US11/778,788
• Publication Number:
  US 20080014260A1
• Time in Patent Office: Days
• US Class Current: 424/458
• CPC Class Codes: A61K 2039/542 oral/gastrointestinal
• CPC Class Codes: A61K 2039/55583 Polysaccharides
• CPC Class Codes: A61K 39/08 Clostridium, e.g. Clostridium tetani
• CPC Class Codes: A61K 9/0056 Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
• CPC Class Codes: A61P 37/04 Immunostimulants

Abstract

The invention disclosed herein relate to an oral vaccine in which the vaccine composition and adjuvant(s) are carried on a solid fast-dispersing dosage form. The vaccines are targeted toward mucosal tissue and the adjuvant serves to ensure sufficient residence time for the vaccine composition on the mucosal tissue to facilitate its absorption thereby. The fast-dispersing oral solid vaccine dosage form of the invention is particularly useful to administer the vaccine to patients that have difficulty swallowing medications. In one embodiment, the invention provides a fast disintegrating oral solid vaccine dosage form comprising: an immunogenic amount of an antigenic preparation, the antigenic preparation comprising a microsphere-antigen complex; an adjuvant, wherein the adjuvant enhances the absorption of the antigen or potentiates the immunogenic response; a mucoadhesive substance; and a low density dosage form matrix.

Claims

1. A fast disintegrating oral solid vaccine dosage form comprising:

an immunogenic amount of an antigenic preparation, said antigenic preparation comprising a microsphere-antigen complex;

an adjuvant, wherein said adjuvant enhances the absorption of the antigen or potentiates the immunogenic response;

a mucoadhesive substance; and

a low density dosage form matrix.

2. The oral vaccine dosage form according to claim 1, wherein the dosage form disintegrates within 60 seconds after being placed in the oral cavity.

3. The oral vaccine dosage form according to claim 2, wherein the dosage form disintegrates within 30 seconds of being placed in the oral cavity.

4. The oral vaccine dosage form according to claim 3, wherein the dosage form disintegrates within 10 seconds of being placed in the oral cavity.

5. The oral vaccine dosage form according to claim 1, wherein said microsphere of said microsphere-antigen complex comprises antigen encapsulated in biodegradable polymeric material.

6. The oral vaccine dosage form according to claim 5, wherein said biodegradable polymeric material is selected from poly(lactic acid), poly (lactide-co-glycide), and combinations thereof.

7. The oral vaccine dosage form according to claim 1, wherein said microsphere of said microsphere-antigenic complex comprises latex.

8. The oral vaccine dosage form according to claim 1, wherein the low density matrix is formed by removal of solvent by lyophilization from a frozen suspension.

9. The oral vaccine dosage form according to claim 1, wherein the low density matrix is formed by removal of solvent from a frozen suspension by contact with a second solvent, in which the matrix forming materials are insoluble.

10. The oral vaccine dosage form according to claim 1, wherein low density matrix is formed by compacting finely divided extruded materials.

11. The oral vaccine dosage form according to claim 1 wherein the low density matrix is formed by loosely compacting particles formed by spray-coating, spray drying, spray-chilling, coaservation or fluid-bed drying.

12. The oral vaccine dosage form according to claim 1, wherein the low density matrix is formed by gelling a suspension and then removing solvent by drying.

13. The oral vaccine dosage form according to claim 1, wherein said microsphere-antigen complex comprises an antigenic preparation is absorbed onto polymeric particles.

14. The oral vaccine dosage form according to claim 1, wherein said mucoadhesive increases the residency of the antigen in contact with the mucosal tissue in the oral cavity, and maintains adhesive properties following the solid dosage form state.

15. The oral vaccine dosage form according to claim 14, wherein the mucoadhesive is a polyacrylic polymer.

16. The oral vaccine dosage form according to claim 14, wherein the mucoadhesive is a cellulose derivative.

17. The oral vaccine dosage form according to claim 14, wherein the mucoadhesive is selected from gelatin, sodium alginate, and pectin.

18. A fast disintegrating oral solid vaccine dosage form comprising:

an immunogenic amount of an antigenic preparation comprising tetanus toxoid (TT), said antigenic preparation comprising a microsphere-antigen complex;

an adjuvant, wherein said adjuvant enhances the absorption of the antigen or potentiates the immunogenic response;

a mucoadhesive substance; and

a low density dosage form matrix.

19. The oral vaccine dosage form according to claim 18, wherein the dosage form disintegrates within 60 seconds after being placed in the oral cavity.

20. The oral vaccine dosage form according to claim 19, wherein the dosage form disintegrates within 30 seconds of being placed in the oral cavity.

21. The oral vaccine dosage form according to claim 20, wherein the dosage form disintegrates within 10 seconds of being placed in the oral cavity.

22. The oral vaccine dosage form according to claim 18, wherein said microsphere of said microsphere-antigen complex comprises antigen encapsulated in biodegradable polymeric material.

23. The oral vaccine dosage form according to claim 22, wherein said biodegradable polymeric material is selected from poly(lactic acid), poly (lactide-co-glycide), and combinations thereof.

24. The oral vaccine dosage form according to claim 18 wherein said microsphere of said microsphere-antigenic complex comprises latex.

25. The oral vaccine dosage form according to claim 18, wherein the low density matrix is formed by removal of solvent by lyophilization from a frozen suspension.

26. The oral vaccine dosage form according to claim 18, wherein the low density matrix is formed by removal of solvent from a frozen suspension by contact with a second solvent, in which the matrix forming materials are insoluble.

27. The oral vaccine dosage form according to claim 18, wherein low density matrix is formed by compacting finely divided extruded materials.

28. The oral vaccine dosage form according to claim 18, wherein the low density matrix is formed by loosely compacting particles formed by spray-coating, spray drying, spray-chilling, coaservation or fluid-bed drying.

29. The oral vaccine dosage form according to claim 18, wherein the low density matrix is formed by gelling a suspension and then removing solvent by drying.

30. The oral vaccine dosage form according to claim 18, wherein said microsphere-antigen complex comprises an antigenic preparation is absorbed onto polymeric particles.

31. The oral vaccine dosage form according to claim 18, wherein said mucoadhesive increases the residency of the antigen in contact with the mucosal tissue in the oral cavity, and maintains adhesive properties following the solid dosage form state.

32. The oral vaccine dosage form according to claim 18, wherein the mucoadhesive is a polyacrylic polymer.

33. The oral vaccine dosage form according to claim 18, wherein the mucoadhesive is a cellulose derivative.

34. The oral vaccine dosage form according to claim 18, wherein the mucoadhesive is selected from gelatin, sodium alginate, and pectin.