Orally disintegrable tablets

US 20020142034A1
Filed: 10/30/2001
Published: 10/03/2002
Est. Priority Date: 05/18/1998
Status: Active Grant

First Claim

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1. An orally disintegrable tablet which comprises (i) fine granules having an average particle diameter of 400 μ

m or less, which fine granules comprise a composition coated by an enteric coating layer, said composition having 10 weight % or more of an acid-labile physiologically active substance and (ii) an additive.

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Abstract

An orally disintegrable tablet, of the present invention, which comprises (i) fine granules having an average particle diameter of 400 μm or less, which fine granules comprise a composition coated by an enteric coating layer, said composition having 10 weight % or more of an acid-labile physiologically active substance and (ii) an additive, has superior disintegrability or dissolution in the oral cavity so that it can be used for treatment or prevention of various diseases, as an orally disintegrable tablet capable of being administered to the aged or children and easily administered without water. Also, because the tablet of the present invention contains fine granules having the average particle diameter such that it will not impart roughness in mouth, it can be administered easily without discomfort at the administration.

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49 Claims

1. An orally disintegrable tablet which comprises (i) fine granules having an average particle diameter of 400 μ
- m or less, which fine granules comprise a composition coated by an enteric coating layer, said composition having 10 weight % or more of an acid-labile physiologically active substance and (ii) an additive.
- View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31)
- - 2. An orally disintegrable tablet of claim 1, wherein the average particle diameter of the fine granules is 300 to 400 μ
    - m.
  - 3. An orally disintegrable tablet of claim 1, wherein the fine granules further comprise a basic inorganic salt.
  - 4. An orally disintegrable tablet of claim 1, wherein the additive comprises a water-soluble sugar alcohol.
  - 5. An orally disintegrable tablet of claim 1, wherein the composition coated by an enteric coating layer is further coated by a coating layer which comprises a water-soluble sugar alcohol.
  - 6. An orally disintegrable tablet of claim 4, wherein the additive comprises (i) crystalline cellulose and/or (ii) low-substituted hydroxypropyl cellulose.
  - 7. An orally disintegrable tablet of claim 1, wherein the particle diameter of the fine granules is practically 425 μ
    - m or less.
  - 8. An orally disintegrable tablet of claim 1, wherein the particle diameter of the fine granules is practically 400 μ
    - m or less.
  - 9. An orally disintegrable tablet of claim 1, wherein the acid-labile physiologically active substance is a benzimidazole compound or a salt thereof.
  - 10. An orally disintegrable tablet of claim 9, wherein the benzimidazole compound is lansoprazole.
  - 11. An orally disintegrable tablet of claim 3, wherein the basic inorganic salt is a salt of magnesium and/or a salt of calcium.
  - 12. An orally disintegrable tablet of claim 1, wherein the composition comprises a core being coated by a benzimidazole compound and a basic inorganic salt, said core comprising crystalline cellulose and lactose.
  - 13. An orally disintegrable tablet of claim 12, wherein the core comprises 50 weight % or more of lactose.
  - 14. An orally disintegrable tablet of claim 12, wherein the core comprises 40 to 50 weight % of crystalline cellulose and 50 to 60 weight % of lactose.
  - 15. An orally disintegrable tablet of claim 1, wherein the composition comprises 20 weight % or more of an acid-labile physiologically active substance.
  - 16. An orally disintegrable tablet of claim 1, wherein the composition comprises 20 to 50 weight % of an acid-labile physiologically active substance.
  - 17. An orally disintegrable tablet of claim 1, wherein the fine granules are produced by fluidized-bed granulation method.
  - 18. An orally disintegrable tablet of claim 1, wherein the enteric coating layer comprises an aqueous enteric polymer agent.
  - 19. An orally disintegrable tablet of claim 18, wherein the aqueous enteric polymer agent is a methacrylate copolymer.
  - 20. An orally disintegrable tablet of claim 18, wherein the enteric coating layer further comprises a sustained-release agent.
  - 21. An orally disintegrable tablet of claim 20, wherein the sustained-release agent is a methacrylate copolymer.
  - 22. An orally disintegrable tablet of claim 20, wherein the sustained-release agent is in an amount of 5 to 15 weight % relative to 100 weight % of the aqueous enteric polymer agent.
  - 23. An orally disintegrable tablet of claim 4, wherein the water-soluble sugar alcohol is erythritol.
  - 24. An orally disintegrable tablet of claim 4, wherein the water-soluble sugar alcohol is mannitol.
  - 25. An orally disintegrable tablet of claim 5, wherein the water-soluble sugar alcohol is in an amount of 5 to 97 weight % relative to 100 weight % of the orally disintegrable tablet apart from the fine granules.
  - 26. An orally disintegrable tablet of claim 4, wherein the crystalline cellulose is in an amount of 3 to 50 weight % relative to 100 weight % of the tablet apart from the fine granule.
  - 27. An orally disintegrable tablet of claim 6, wherein the content of hydroxypropoxyl group in the low-substituted hydroxypropyl cellulose is 7.0 to 9.9 weight %.
  - 28. An orally disintegrable tablet of claim 6, wherein the content of hydroxypropoxyl group in the low-substituted hydroxypropyl cellulose is 5.0 to 7.0 weight %.
  - 29. An orally disintegrable tablet of claim 1, which further comprises crospovidone.
  - 30. An orally disintegrable tablet of claim 1, wherein the oral disintegration time is one minute or less.
  - 31. An orally disintegrable tablet of claim 1, which comprises no lubricant inside the tablet.

32. Fine granules having an average particle diameter of 400 μ
- m or less, which comprise a composition coated by an enteric coating layer, said composition having (i) 25 weight % or more of an acid-labile physiologically active substance and (ii) a basic inorganic salt.
- View Dependent Claims (33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49)
- - 33. Fine granules of claim 32, wherein the average particle diameter of the fine granules is 300 to 400 μ
    - m.
  - 34. Fine granules of claim 32, wherein the particle diameter of the fine granules is practically 425 μ
    - m or less.
  - 35. Fine granules of claim 32, wherein the particle diameter of the fine granules is practically 400 μ
    - m or less.
  - 36. Fine granules of claim 32, wherein the acid-labile physiologically active substance is a benzimidazole compound or a salt thereof.
  - 37. Fine granules of claim 36, wherein the benzimidazole compound is lansoprazole.
  - 38. Fine granules of claim 32, wherein the basic inorganic salt is a salt of magnesium and/or a salt of calcium.
  - 39. Fine granules of claim 32, wherein the composition comprises a core being coated by a benzimidazole compound and a basic inorganic salt, said core comprising crystalline cellulose and lactose.
  - 40. Fine granules of claim 39, wherein the core comprises 50 weight % or more of lactose.
  - 41. Fine granules of claim 32, wherein the composition comprises 25 to 40 weight % of an acid-labile physiologically active substance.
  - 42. Fine granules of claim 32, which are produced by fluidized-bed granulation method.
  - 43. Fine granules of claim 32, wherein the enteric coating layer comprises an aqueous enteric polymer agent.
  - 44. Fine granules of claim 43, wherein the aqueous enteric polymer agent is a methacrylate copolymer.
  - 45. Fine granules of claim 43, wherein the enteric coating layer further comprise a sustained-release agent.
  - 46. Fine granules of claim 45, wherein the sustained-release agent is a methacrylate copolymer.
  - 47. Fine granules of claim 45, wherein the sustained-release agent is in an amount of 5 to 15 weight % relative to 100 weight % of the aqueous enteric polymer agent.
  - 48. Fine granules of claim 32, wherein the enteric coating layer is in an amount of 50 to 70 weight % relative to 100 weight % of the fine granules.
  - 49. A tablet, granule, fine granule, capsule, effervescent or suspension preparation which comprises the fine granules of claim 32.

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Current Assignee
Takeda Pharmaceutical Company Limited
Original Assignee
Takeda Pharmaceutical Company Limited
Inventors
Tabata, Tetsuro, Morimoto, Shuji, Shimizu, Toshihiro

Granted Patent

US 7,431,942 B2
Time in Patent Office

Days
Field of Search
US Class Current

424/470
CPC Class Codes

A61K 31/4439   containing a five-membered ...

A61K 9/0056   Mouth soluble or dispersibl...

A61K 9/1611   Inorganic compounds

A61K 9/1652   Polysaccharides, e.g. algin...

A61K 9/2081   with microcapsules or coate...

A61K 9/28   Dragees; Coated pills or ta...

A61K 9/5026   obtained by reactions only ...

A61K 9/5042   Cellulose; Cellulose deriva...

A61K 9/5073   having two or more differen...

A61P 1/04   for ulcers, gastritis or re...

A61P 43/00   Drugs for specific purposes...

Orally disintegrable tablets

First Claim

1 Assignment

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Abstract

Citations

49 Claims

Specification

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Orally disintegrable tablets

First Claim

1 Assignment

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Subscription Required

0 Petitions

Subscription Required

Accused Products

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Abstract

Citations

49 Claims

Specification

Subscription Required

Solutions

Use Cases

Quick Links