Tablet excipient
View Patent ↗This invention relates to a composition comprising physically modified, partially pregelatinized starch, which is useful as a multi-functional excipient for solid dosage forms, a method of making such composition, and solid dosage forms prepared using the composition. Such composition is characterized by a predominance of particles having both birefringent and non-birefringent portions, a sedimentation volume of between 1.5 and 9 ml/g, and a cold water solubility of between 1 and 8%. This free-flowing starch may have an average particle size greater than 30 μm, and a moisture content of between 5 and 12% by weight. The 500 mg placebo tablet prepared from such composition at 13 kN using a manual tablet press equipped with a 1.11 cm ( 7/16″) standard concave punches has a crushing strength of at least 160 Newtons, and a disintegration time of no more than 10 minutes.
1. A solid dosage form comprising an extruded partially pregelatinized starch characterized by:
a) a plurality of particles, a majority consisting of a non-birefringent portion and a birefringent portion;
b) a sedimentation volume of between 1.5 and 9 ml/g;
c) a cold water solubility of between 1 and 8%; and
d) an average particle size between 40 and 150 microns;
e) wherein, when the starch is used to prepare a placebo starch tablet consisting of the starch, the placebo starch tablet is characterized by at least the following:
i) a crushing strength of at least 160 N; and
ii) a disintegration time of no more than 10 minutes.
2. The solid dosage form of claim 1 , wherein the sedimentation volume is between 3 and 6 ml/g.
3. The solid dosage form of claim 1 , wherein the cold water solubility is between 2 and 5%.
4. The solid dosage form of claim 1 , wherein the average particle size is between 60 and 100 pm.
5. The solid dosage form of claim 1 , wherein the starch has a moisture content of from 5 to 12% by weight.
6. The solid dosage form of claim 1 , wherein the starch has a moisture content of between 8 and 10%.
7. The solid dosage form of claim 1 , wherein the starch has a mean time for avalanche of no more than 10 seconds.
8. The solid dosage form of claim 1 , wherein the starch has a mean time for avalanche of no more than 7 seconds.
9. The solid dosage form of claim 1 , wherein the starch is further characterized by a particle strength of about 2 pm/min.
10. The solid dosage form of claim 1 , wherein the dosage form is selected from the group consisting of tablets, caplets, powders and dry dosage capsules.
11. The solid dosage form of claim 10 , wherein the dosage form is a tablet.
12. The tablet of claim 11 , wherein the tablet has a moisture content of at least 7%.
13. The tablet of claim 12 , wherein the tablet has a crushing strength of at least 180 Newtons.
14. The tablet of claim 12 , wherein the tablet has a crushing strength of at least 200 Newtons.
15. The tablet of claim 12 , wherein the tablet has a disintegration time of no more than 8 minutes.
16. The tablet of claim 12 , wherein the tablet has a disintegration time of no more than 5 minutes.