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US4372968A Expired / Lapsed US ⏱️ 0.0 years remaining

Granules of sodium ascorbate and the production thereof

Assignee: Takeda Pharmaceutical Co Ltd
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Filing: 1980-10-29
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Granted: 1983-02-08
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Expires: 2000-10-29
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Abstract

Abstract Granules of higher potency of sodium L-ascorbate obtainable by spray-coating sodium L-ascorbate powder in a fluidized-bed granulator with a binder are excellent in terms of color stability and flowability. Tablets obtainable by compressing the granules have a satisfactory mechanical strength.

Inventors

  • 👤 Nobuyuki Kitamori
  • 👤 Keizi Hemmi
  • 👤 Masaya Maeno

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-03 23:12
CPC Classifications
A; A61; A61K; A61K31/00; A61K31/33; A61K31/335; A61K31/365; A61K31/375; A61K9/00; A61K9/14; A61K9/16; A61K9/1682; A61K9/1688; A61K9/20; A61K9/2095

Claims Analysis

Total Claims: 26
Claim 1
Independent Claim 146 words
Sodium L-ascorbate granules consisting substantially of sodium L-ascorbate and a binder, wherein the content of sodium L-ascorbate is from about 98.5 to 99.5 weight percent, on dry basis, of the granule and not less than about 80 weight percent of the granule having a particle size of 177 to 840μ which are produced by spraying sodium L-ascorbate powder having a particle size of not more than 250μ and not less than about 80 weight percent of said powder having a particle size of not more than 149μ, while allowing it to fluidize in a fluidized-bed granulator, with a solution containing a binder in an amount corresponding to about 0.5 to 1.5 weight percent of the total weight of finished product on a dry basis, and while maintaining the water content of the composition during the granulating process below about 7 weight percent throughout the entire process.
Claim 2
Dependent Claim 146 words
Sodium L-ascorbate granules consisting substantially of sodium L-ascorbate and a binder, wherein the content of sodium L-ascorbate is from about 98.5 to 99.5 weight percent, on dry basis, of the granule and not less than about 80 weight percent of the granule having a particle size of 177 to 840μ which are produced by spraying sodium L-ascorbate powder having a particle size of not more than 250μ and not less than about 80 weight percent of said powder having a particle size of not more than 149μ, while allowing it to fluidize in a fluidized-bed granulator, with a solution containing a binder in an amount corresponding to about 0.5 to 1.5 weight percent of the total weight of finished product on a dry basis, and while maintaining the water content of the composition during the granulating process below about 7 weight percent throughout the entire process.
Claim 3
Dependent Claim 21 words
Granules as claimed in claim 1, wherein the binder is a pregelatinized starch, a water-soluble cellulose or a water-soluble high-molecular compound.
Claim 4
Dependent Claim 13 words
Granules as claimed in claim 2, wherein the pregelatinized starch is pregelatinized cornstarch.
Claim 5
Dependent Claim 12 words
Granules as claimed in claim 2, wherein the water-soluble cellulose is hydroxypropylcellulose.
Claim 6
Dependent Claim 14 words
Granules as claimed in claim 2, wherein the water-soluble high-molecular compound is polyvinyl alcohol.
Claim 7
Independent Claim 104 words
A method for producing sodium L-ascorbate granules, which comprises spraying sodium L-ascorbate powder having a particle size of not more than 250μ and not less than about 80 weight percent of said powder having a particle size of not more than 149μ, while allowing it to fluidize in a fluidized-bed granulator, with a solution containing a binder in an amount corresponding to about 0.5 to 1.5 weight percent of the total weight of finished product on a dry basis, and granulating the mixture while maintaining the water content of the composition during the granulating process below about 7 weight percent throughout the entire process.
Claim 8
Independent Claim 104 words
A method for producing sodium L-ascorbate granules, which comprises spraying sodium L-ascorbate powder having a particle size of not more than 250μ and not less than about 80 weight percent of said powder having a particle size of not more than 149μ, while allowing it to fluidize in a fluidized-bed granulator, with a solution containing a binder in an amount corresponding to about 0.5 to 1.5 weight percent of the total weight of finished product on a dry basis, and granulating the mixture while maintaining the water content of the composition during the granulating process below about 7 weight percent throughout the entire process.
Claim 9
Dependent Claim 21 words
A method according to claim 6, wherein the binder is a pregelatinized starch, a water-soluble cellulose or a water-soluble high-molecular compound.
Claim 10
Dependent Claim 13 words
A method according to claim 7, wherein the pregelatinized starch is pregelatinized cornstarch.
Claim 11
Dependent Claim 12 words
A method according to claim 7, wherein the water-soluble cellulose is hydroxypropylcellulose.
Claim 12
Dependent Claim 14 words
A method according to claim 7, wherein the water-soluble high-molecular compound is polyvinyl alcohol.
Claim 13
Dependent Claim 155 words
Tablets containing sodium L-ascorbate obtained by compressing into tablets granules consisting substantially of sodium L-ascorbate and a binder, the granules comprising sodium L-ascorbate within the range of about 98.5 to 99.5 weight percent on a dry basis of the granule and not less than about 80 weight percent of the granule having a particle size of 177 to 840μ and being produced by spraying sodium L-ascorbate powder having a particle size of not more than 250μ and not less than about 80 weight percent of said powder having a particle size of not more than 149μ, while allowing it to fluidize in a fluidized-bed granulator, with a solution containing a binder in an amount corresponding to about 0.5 to 1.5 weight percent of the total weight of finished product on a dry basis, and while maintaining the water content of the composition during the granulating process below about 7 weight percent throughout the entire process.
Claim 14
Dependent Claim 155 words
Tablets containing sodium L-ascorbate obtained by compressing into tablets granules consisting substantially of sodium L-ascorbate and a binder, the granules comprising sodium L-ascorbate within the range of about 98.5 to 99.5 weight percent on a dry basis of the granule and not less than about 80 weight percent of the granule having a particle size of 177 to 840μ and being produced by spraying sodium L-ascorbate powder having a particle size of not more than 250μ and not less than about 80 weight percent of said powder having a particle size of not more than 149μ, while allowing it to fluidize in a fluidized-bed granulator, with a solution containing a binder in an amount corresponding to about 0.5 to 1.5 weight percent of the total weight of finished product on a dry basis, and while maintaining the water content of the composition during the granulating process below about 7 weight percent throughout the entire process.
Claim 15
Dependent Claim 23 words
Tablets containing sodium L-ascorbate as claimed in claim 11, wherein said tablets are obtained by compression in the presence of L-ascorbic acid granules.
Claim 16
Dependent Claim 21 words
A tablet according to claim 11, wherein the binder is a pregelatinized starch, a water-soluble cellulose, or a water-soluble high-molecular compound.
Claim 17
Dependent Claim 13 words
A tablet according to claim 13, wherein the pregelatinized starch is pregelatinized cornstarch.
Claim 18
Dependent Claim 12 words
A tablet according to claim 13, wherein the water-soluble cellulose is hydroxypropylcellulose.
Claim 19
Dependent Claim 14 words
A tablet according to claim 13, wherein the water-soluble high-molecular compound is polyvinyl alcohol.
Claim 20
Independent Claim 153 words
A method for producing tablets containing sodium L-ascorbate by compressing granules consisting substantially of sodium L-ascorbate and a binder, the granules comprising sodium L-ascorbate within the range of about 98.5 to 99.5 weight percent on a dry basis and not less than about 80 weight percent of the granule having a particle size of 177 to 840∞ and being produced by spraying sodium L-ascorbate powder having a particle size of not more than 250μ and not less than about 80 weight percent of said powder having a particle size of not more than 149μ, while allowing it to fluidize in a fluidized-bed granulator, with a solution containing a binder in an amount corresponds to about 0.5 to 1.5 weight percent of the total weight of finished product on a dry basis, and while maintaining the water content of the composition during the granulating process below about 7 weight percent throughout the entire process.
Claim 21
Independent Claim 153 words
A method for producing tablets containing sodium L-ascorbate by compressing granules consisting substantially of sodium L-ascorbate and a binder, the granules comprising sodium L-ascorbate within the range of about 98.5 to 99.5 weight percent on a dry basis and not less than about 80 weight percent of the granule having a particle size of 177 to 840∞ and being produced by spraying sodium L-ascorbate powder having a particle size of not more than 250μ and not less than about 80 weight percent of said powder having a particle size of not more than 149μ, while allowing it to fluidize in a fluidized-bed granulator, with a solution containing a binder in an amount corresponds to about 0.5 to 1.5 weight percent of the total weight of finished product on a dry basis, and while maintaining the water content of the composition during the granulating process below about 7 weight percent throughout the entire process.
Claim 22
Dependent Claim 19 words
A method as claimed in claim 17, wherein the compression is conducted in the presence of L-ascorbic acid granules.
Claim 23
Dependent Claim 21 words
A method according to claim 17, wherein the binder is a pregelatinized starch, a water-soluble cellulose or a water-soluble high-molecular compound.
Claim 24
Dependent Claim 13 words
A method according to claim 19, wherein the pregelatinized starch is pregelatinized cornstarch.
Claim 25
Dependent Claim 12 words
A method according to claim 19, wherein the water-soluble cellulose is hydroxypropylcellulose.
Claim 26
Dependent Claim 14 words
A method according to claim 19, wherein the water-soluble high-molecular compound is polyvinyl alcohol.

References Cited (Backward Citations)

US3493659A Cited
US4036948A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1986-02-07 1986-08-09 1987-02-08 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1990-02-07 1990-08-09 1991-02-08 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1994-02-07 1994-08-09 1995-02-08 $7700.00 Window Closed / Lapsed

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