Low swelling starches as tablet disintegrants

Claim 2

A disintegrant for compressed tablets, consisting essentially of a free-flowing, crosslinked and pregelatinized, low swelling starch powder having a moisture content of about 12% by weight or less and derived from a cold-water-insoluble, granular starch base; said starch powder characterized by all of the following: (a) its uniformly swollen, virtually non-birefringent granules, (b) by a cold water swelling value above about 3 and below about 25 ml., and (c) by an acid viscosity breakdown of about 400 B.U. or less; said acid viscosity breakdown determined by heating an aqueous dispersion containing 9% of said starch powder and 1% glacial acetic acid, both by weight and based on anhydrous starch, at from ambient temperature to 95° C., holding at 95° C. until a peak viscosity is reached, but for no more than 1 hr. if no peak viscosity is reached, holding for an additional 10 min. at 95° C. after said peak viscosity is reached, and recording a final viscosity at 95° C. plus 10 min., with the difference between said peak viscosity and said final viscosity being said acid viscosity breakdown and with said acid viscosity breakdown considered as zero when no peak viscosity is reached; said measurement being carried out in a Brabender Visco/Amylo/Graph having a 700 cm.-gm. sensitivity cartridge; said starch powder effectively disintegrating said tablet when placed in a fluid.

Claim 3

The disintegrant of claim 1, wherein said starch base is corn starch, waxy corn starch, potato starch, or tapioca starch and said starch powder has the moisture content of about 6-10% by weight or less and the cold water swelling value of about 4-18 ml.

Claim 4

The disintegrant of claim 2, wherein said starch base is corn starch and said starch powder has a cold water swelling value of about 4 to 12 ml.

Claim 5

The disintegrant of claim 3, wherein said starch powder is characterized by an acid viscosity breakdown of 150 B.U. or less and a swelling vaue of 10 ml. or less.

Claim 6

The method for preparing the disintegrant of claim 1, which comprises the steps of: (a) crosslinking and pregelatinizing a cold-water-insoluble, granular starch base in the presence of water; (b) drying said crosslinked and pregelatinized starch, if necessary, to said moisture content of about 12% by weight or less; and (c) finely pulverizing said crosslinked and pregelatinized starch to said low swelling starch powder having a particle size suitable for tabletting.

Claim 7

The method of claim 5, wherein said crosslinking is carried out with phosphorous oxychloride or sodium trimetaphosphate and wherein said pregelatinization and drying are carried out by drum drying an aqueous slurry of said crosslinked starch.

Claim 8

The method of claim 5, wherein said starch base is simultaneously crosslinked, pregelatinized, and drum dried.

Claim 9

A non-friable, hard compressed tablet comprising a tabletting mixture of an active ingredient, a binder, and a disintegrant, characterized in that said disintegrant consists essentially of a free-flowing, crosslinked and pregelatinized, low swelling starch powder having a moisture content of about 12% by weight or less and derived from a cold-water-insoluble, granular starch base; said starch powder characterized by all of the following: (a) its uniformly swollen virtually non-birefringent granules, (b) a cold water swelling value above about 3 and below about 25 ml., and (c) an acid viscosity breakdown of about 400 B.U. or less; said acid viscosity breakdown determined by heating an aqueous dispersion containing 9% of said modified starch powder and 1% glacial acetic acid, both by weight and based on anhydrous starch, at from ambient temperature to 95° C., holding at 95° C. until a peak viscosity is reached, but for no more than 1 hr. if no peak viscosity is reached, holding for an additional 10 min. at 95° C. when said peak viscosity is reached, and recording a final viscosity at 95° C. plus 10 min., with the difference between said peak viscosity and said final viscosity being said acid viscosity breakdown and with said acid viscosity breakdown considered as zero when no peak viscosity is reached; said measurement being carried out in a Brabender/Visco/Amylo/Graph having a 700 cm.-gm. sensitivity cartridge.

Claim 10

A non-friable, hard compressed tablet comprising a tabletting mixture of an active ingredient, a binder, and a disintegrant, characterized in that said disintegrant consists essentially of a free-flowing, crosslinked and pregelatinized, low swelling starch powder having a moisture content of about 12% by weight or less and derived from a cold-water-insoluble, granular starch base; said starch powder characterized by all of the following: (a) its uniformly swollen virtually non-birefringent granules, (b) a cold water swelling value above about 3 and below about 25 ml., and (c) an acid viscosity breakdown of about 400 B.U. or less; said acid viscosity breakdown determined by heating an aqueous dispersion containing 9% of said modified starch powder and 1% glacial acetic acid, both by weight and based on anhydrous starch, at from ambient temperature to 95° C., holding at 95° C. until a peak viscosity is reached, but for no more than 1 hr. if no peak viscosity is reached, holding for an additional 10 min. at 95° C. when said peak viscosity is reached, and recording a final viscosity at 95° C. plus 10 min., with the difference between said peak viscosity and said final viscosity being said acid viscosity breakdown and with said acid viscosity breakdown considered as zero when no peak viscosity is reached; said measurement being carried out in a Brabender/Visco/Amylo/Graph having a 700 cm.-gm. sensitivity cartridge.

Claim 11

The table of claim 8, wherein said starch powder is derived from corn starch, waxy corn starch, potato starch, or tapioca starch crosslinked by treatment with phosphorus oxychloride or sodium trimetaphosphate and drum dried, said starch powder having the moisture content of about 6-10% by weight or less, the swelling value of 10 ml. or less, and the breakdown of 150 B.U. or less.

Claim 12

The tablet of claim 8, wherein said disintegrant is present in an amount of 10% by weight or less, based on the total weight of said tabletting mixture.

Claim 13

In a method for preparing compressed tablets, the step which comprises adding, as a disintegrant to a tabletting mixture at any time prior to compression thereof, a free-flowing, crosslinked and pregelatinized, low swelling starch powder having a moisture content of about 12% by weight or less and derived from a cold water insoluble, granular starch base; said starch powder characterized by all of the following: (a) its uniformly swollen, virtually non-birefringent granules; (b) a cold water swelling value of above about 3 and below about 25 ml., and (c) an acid viscosity breakdown of 400 B.U. or less; said acid viscosity breakdown determined by heating an aqueous dispersion containing 9% of said modified starch powder and 1% glacial acetic acid, both by weight and based on anhydrous starch, at from ambient temperature to 95° C., holding at 95° C. until a peak viscosity is reached, but for no more than 1 hr. if no peak viscosity is reached, holding for an additional 10 min. at 95° C. after said peak viscosity is reached, and recording a final viscosity at 95° plus 10 min., with the difference between said peak viscosity and said final viscosity being said acid viscosity breakdown and with said acid viscosity breakdown considered as zero when no peak viscosity is reached; said measurement being carried out in a Brabender Visco/Amylo/Graph having a 700 cm.-gm. sensitivity cartridge.

Claim 14

In a method for preparing compressed tablets, the step which comprises adding, as a disintegrant to a tabletting mixture at any time prior to compression thereof, a free-flowing, crosslinked and pregelatinized, low swelling starch powder having a moisture content of about 12% by weight or less and derived from a cold water insoluble, granular starch base; said starch powder characterized by all of the following: (a) its uniformly swollen, virtually non-birefringent granules; (b) a cold water swelling value of above about 3 and below about 25 ml., and (c) an acid viscosity breakdown of 400 B.U. or less; said acid viscosity breakdown determined by heating an aqueous dispersion containing 9% of said modified starch powder and 1% glacial acetic acid, both by weight and based on anhydrous starch, at from ambient temperature to 95° C., holding at 95° C. until a peak viscosity is reached, but for no more than 1 hr. if no peak viscosity is reached, holding for an additional 10 min. at 95° C. after said peak viscosity is reached, and recording a final viscosity at 95° plus 10 min., with the difference between said peak viscosity and said final viscosity being said acid viscosity breakdown and with said acid viscosity breakdown considered as zero when no peak viscosity is reached; said measurement being carried out in a Brabender Visco/Amylo/Graph having a 700 cm.-gm. sensitivity cartridge.

Claim 15

The method of claim 11, wherein said starch powder is added in an amount of 10% by weight or less, based on the total weight of said tabletting mixture.