USRE43582EExpiredUtility

Semi-moist delivery system

67
Individually held — no corporate assignee on recordPriority: Sep 24, 1998Filed: Apr 29, 2009Granted: Aug 14, 2012
Est. expirySep 24, 2018(expired)· nominal 20-yr term from priority
Inventors:Edwin H. Christensen
A61K 9/0056
67
PatentIndex Score
0
Cited by
30
References
36
Claims

Abstract

The subject invention is a carrier or product formed of a matrix having starch, sugar, fat, polyhydric alcohol and water in suitable ratios such that there exists a water activity of 0.6-0.75. The water activity of the product matrix may be adjusted up or down so that the availability of water in the finished product is not detrimental to the included active ingredient, be it pharmaceutical, nutraceutical, or a vitamin mineral complex.

Claims

exact text as granted — not AI-modified
1. A composition for the oral administration of an additive selected from the group consisting of pharmaceutical, nutritional supplements, vitamins and minerals, and mixtures thereof mammals in a discrete dosage form, said discrete dosage from comprising:
 said additive,   an extrudate comprising a matrix having about 10 to about 50% wt starch,   a sweetener consisting essentially of sucrose, corn syrup and sorbitol, said sucrose being in an amount of at least 10%, and   at least about 5% wt water,   said composition having A w  of about 0.60 to about 0.75, and a soft and chewy texture, and said A w  being adjusted to permit an appropriate amount of free water in the presence of the additive.   
     
     
       2. The carrier of  claim 1  wherein the water content is about 10%. 
     
     
       3. The carrier of  claim 1  wherein the polyhydric alcohol content is about 40%. 
     
     
       4. The carrier of  claim 1  wherein the starch content is about 32%. 
     
     
       5. The carrier of  claim 1  wherein said carrier has a pregelatinized starch content of about 15%. 
     
     
       6. The carrier of  claim 1  where the A w  is 0.65 and the additive is aspirin. 
     
     
       7. The carrier of  claim 1  wherein the polyhydric alcohol is sorbitol. 
     
     
       8. The carrier of  claim 1  wherein the sugar content is about 15%. 
     
     
       9. A method of making a carrier and additive mixture for use in an oral administration of a therapeutically effective amount of the additive in a discrete dosage form, comprising the steps of:
 a) forming a matrix and additive admixture by mixing, in a one-step procedure additive,   about 10 to about 50% wt starch,   0 to about 40% wt fat or oil,   a sweetener consisting of sucrose, corn syrup and sorbitol, said sucrose being in an amount of at least 10%,   and water,   and mixing;   
       adjusting the relative amounts of polyhydric alcohol and water to control the A w  of said admixture to adjust the level of moisture in the carrier to be a level not inimical to the additive and extruding said admixture to form an extrudate. 
     
     
       10. The method of  claim 9  including adjusting the water content to about 10%. 
     
     
       11. The method of  claim 9  including adjusting the polyhydric alcohol content to about 40%. 
     
     
       12. The method of  claim 9  including adjusting the starch content to about 32%. 
     
     
       13. The method of  claim 9  including adjusting the sugar content to about 15%. 
     
     
       14. The method of  claim 9  further including adding pregelatinized starch to about 15% of the total carrier. 
     
     
       15. The method of  claim 9  including the step of mixing in a pharmaceutical. 
     
     
       16. The method of  claim 9  including the step of mixing in a nutraceutical. 
     
     
       17. The method of  claim 9  including the step of mixing in a vitamin and mineral mix. 
     
     
       18. The method of  claim 9  including the step of adding sorbitol. 
     
     
       19. The method of  claim 9  including the step of controlling the A w  to be at about 0.60 to about 0.75. 
     
     
       20. The method of  claim 9  including the step of adding aspirin as the active ingredient and controlling the A w  of said carrier to about 0.65. 
     
     
       21. The carrier of  claim 2 , wherein the additive constitutes from about 0.1% to about 5.0% of the resulting mixture. 
     
     
       22. The method of  claim 9 , further including adding about 0.1% to about 5.0% additive. 
     
     
       23. A composition for the oral administration of a pharmaceutical additive to mammals in a discrete dosage form, said discrete dosage form comprising:
 an extrudate having a matrix, and comprising:
 10-50% starch, 
 0-40% fat or oil, 
 a sweetener consisting essentially of sucrose, corn syrup and sorbitol, said sucrose being in an amount of least 10%, 
 at least about 5% water, 
   
       said composition having an A w  of about 0.60 to about 0.75, and a soft and chewy texture, and said A w  being adjusted to permit an appropriate amount of free water in the presence of the additive. 
     
     
       24. A method of making a carrier and additive mixture for use in an oral administration of a therapeutically effective amount of the additive in a discrete dosage form, comprising the steps of:
 a) forming an additive admixture by mixing, in a one-step procedure:
 additive, 
 about 10 to about 50% wt starch, 
 0 to about 40% wt fat or oil, 
 a polyhydric alcohol, 
 a sweetener consisting of sucrose, said sucrose being in the amount of at least 10% 
 and water, 
 adjusting the relative amounts of polyhydric alcohol sweetener and water to control the A w  of said admixture to adjust the level of moisture in the carrier to be at a level not inimical to the additive and extruding said admixture to form an extrudate. 
   
     
     
       25. The method of claim 24 including adjusting the water content to about 10%. 
     
     
       26. The method of claim 24 including adjusting the polyhydric alcohol content to about 40%. 
     
     
       27. The method of claim 24 including adjusting the starch content to about 32%. 
     
     
       28. The method of claim 24 including adjusting the sweetener content to about 15%. 
     
     
       29. The method of claim 24 further including adding pregelatinized starch to about 15% of the total carrier. 
     
     
       30. The method of claim 24 including the step of mixing in a pharmaceutical. 
     
     
       31. The method of claim 24 including the step of mixing in a nutraceutical. 
     
     
       32. The method of claim 24 including the step of mixing in a vitamin and mineral mix. 
     
     
       33. The method of claim 24 including the step of controlling the A w  to be at about 0.60 to about 0.75. 
     
     
       34. The method of claim 24 including the step of adding aspirin as the active ingredient and controlling A w  of said carrier to about 0.65. 
     
     
       35. The method of claim 24, further including adding about 0.1% to about 5.0% additive. 
     
     
       36. An extrudate for the oral administration of an additive to mammals in a discrete dosage form, said discrete dosage comprising an extruded composition having
 4.5-22.5% starch,   0-40% fat or oil,   polyhydric alcohol,   a sweetener consisting of sucrose, corn syrup and sorbitol, said sucrose being in the amount of at least 10%,   water, and
 said extrudate having an A w  of about 0.60 to about 0.75, and a soft and chewy texture, and said A w  being adjusted to permit an appropriate amount of free water in the presence of the additive.

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