Use of debranched starch in extrusion-spheronization pharmaceutical pellets
View Patent ↗This patent pertains to the use of debranched starch in the preparation of pharmaceutical pellets by extrusion spheronization. Such excipients are useful in any dry dosage form, including tablets and capsules, for either immediate or sustained release.
1. A process comprising the steps of:
a) mixing at least one crystalline debranched high amylose starch and water to form a moistened plastically deformable mass, wherein the mass comprises greater than 50%, by weight on a dry basis, of the starch;
b) extruding the mass to obtain an extrudate;
c) spheronizing of the extrudate to obtain a plurality of substantially spherical pellets; and
d) drying of the pellets;
wherein the starch has an amylose content of at least 70% by weight.
2. The process of claim 1 , wherein at least one excipient is mixed in with the starch and water of step (a).
3. The process of claim 1 , wherein at least one active agent is mixed in with the starch and water of step (a).
4. The process of claim 1 , further comprising depositing at least one active agent on the surface of the pellets.
5. The process of claim 1 , further comprising coating at least one active agent and/or functional ingredient on the surface of the pellets.
6. The process of claim 5 , wherein the functional ingredient provides a function to the pellets selected from the group consisting of controlled release, taste masking, improved shelf-life, and identification.
7. The process of claim 1 , wherein the starch is debranched using pullulanase or isoamylase.
8. The process of claim 1 , wherein the starch is a corn starch.
9. The process of claim 2 , wherein the starch is present in an amount of 10-100% by weight of the plastically deformable mass on a dry basis.
10. The process of claim 2 , wherein the excipient is a binder present in an amount of up to 15% by weight of the plastically deformable mass on a dry weight basis.
11. The process of claim 10 , wherein the binder is selected from the group consisting of hydroxypropyl methylcellulose, drum dried waxy corn starch, hydroxypropyl cellulose and polyvinylpyrrolidone.
12. The process of claim 11 , wherein the binder is selected from the group consisting of hydroxypropyl methyl cellulose and drum dried waxy corn starch.
13. The process of claim 2 , wherein the at least one excipient is a plasticizer in an amount of up to 30% by weight plastically deformable mass on a dry basis.
14. The process of claim 13 , wherein the plasticizer is a polyol.
15. The process of claim 14 , wherein the polyol is sorbitol.
16. The process of claim 1 , wherein the water is in an amount of from 20 to 55% based on the wet weight of the plastically deformable mass.
17. The process of claim 1 , further comprising re-extruding the extrudate.
18. The process of claim 1 , wherein greater than 80% of the pellets have a diameter of from about 0.70 to 1.40 mm.
19. The process of claim 3 wherein the active agent is selected from the group consisting of pharmaceuticals, nutritional supplements, detergents, dyes, pesticides, agricultural chemicals, enzymes, and foods.
20. The process of claim 3 , wherein the active agent is a pharmaceutical.
21. The process of claim 4 , wherein the active agent is selected from the group consisting of pharmaceuticals, nutritional supplements, detergents, dyes, pesticides, agricultural chemicals, enzymes, and foods.
22. The process of claim 5 , wherein the active agent is selected from the group consisting of pharmaceuticals, nutritional supplements, detergents, dyes, pesticides, agricultural chemicals, enzymes, and foods.
23. The process of claim 4 , wherein the active agent is a pharmaceutical.
24. The process of claim 5 , wherein the active agent is a pharmaceutical.