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US4101651A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for preparing preparations for oral administration

Assignee: Meiji Seika Kaisha Ltd
•
Filing: 1976-02-03
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Granted: 1978-07-18
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Expires: 1996-02-03
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Abstract

Abstract A process for preparing preparations for oral administration which do not have a bitter taste which comprises either dissolving a bitter taste-masking substance at a high concentration in a solvent to be used for dissolving or suspending a bitter active ingredient and adding the active ingredient to the resulting solution followed by kneading, or kneading a solution or suspension in which a bitter active ingredient has been dissolved or suspended with the bitter taste-masking substance, adding silicic acid anhydride to the resulting kneaded substance to form a powder and granulating the powder using a solution of the bitter taste-masking substance in a fluidized bed granulator.

Inventors

  • 👤 Toshiyuki Kobayashi
  • 👤 Akio Okada
  • 👤 Takeshi Mayama
  • 👤 Akira Okada

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 13:50
CPC Classifications
A; A61; A61K; A61K9/00; A61K9/14; A61K9/16; A61K9/1605; A61K9/1629; A61K9/1652; A61K9/1611; A61K9/1635; A61P; A61P31/00; A61P31/04

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 159 words
A process for preparing granular preparations for oral administration having no bitter taste which comprises dissolving a pharmaceutically acceptable water insoluble ethyl cellulose as a bitter taste-masking substance having a molecular weight higher than about 2,000 in high concentration in a volatile solvent to be used for dissolving or suspending midecamycin as a bitter pharmaceutical ingredient, adding the midecamycin to the resulting solution followed by kneading, adding silicic acid anhydride to the resulting kneaded substance to form a powder and granulating said powder using a solution of the ethyl cellulose in a fluidized bed granulator, said volatile solvent not exerting a degrading effect upon said ethyl cellulose or upon said midecamycin, the amount of said ethyl cellulose to be dissolved in said solvent being about 0.5 to about three times the amount of said midecamycin and the amount of said ethyl cellulose used for said granulation being about 1/10 to about 1/5 the amount thereof used for said dissolving.
Claim 2
Dependent Claim 159 words
A process for preparing granular preparations for oral administration having no bitter taste which comprises dissolving a pharmaceutically acceptable water insoluble ethyl cellulose as a bitter taste-masking substance having a molecular weight higher than about 2,000 in high concentration in a volatile solvent to be used for dissolving or suspending midecamycin as a bitter pharmaceutical ingredient, adding the midecamycin to the resulting solution followed by kneading, adding silicic acid anhydride to the resulting kneaded substance to form a powder and granulating said powder using a solution of the ethyl cellulose in a fluidized bed granulator, said volatile solvent not exerting a degrading effect upon said ethyl cellulose or upon said midecamycin, the amount of said ethyl cellulose to be dissolved in said solvent being about 0.5 to about three times the amount of said midecamycin and the amount of said ethyl cellulose used for said granulation being about 1/10 to about 1/5 the amount thereof used for said dissolving.
Claim 3
Dependent Claim 158 words
A process for preparing granular preparations for oral administration having no bitter taste which comprises dissolving or suspending midecamycin as a bitter pharmaceutical ingredient in high concentration in a volatile solvent for dissolving a pharmaceutically acceptable, water insoluble ethyl cellulose as a bitter taste-masking substance having a molecular weight higher than about 2,000, adding the ethyl cellulose to the resulting solution or suspension followed by kneading, adding silicic acid anhydride to the resulting kneaded substance to form a powder and granulating said powder using a solution of said ethyl cellulose in a fluidized bed granulator, said volatile solvent not exerting a degrading effect upon said ethyl cellulose or upon said midecamycin, the amount of said ethyl cellulose added to said solution or said suspension being about 0.5 to about three times the amount of said midecamycin and the amount of said ethyl cellulose used for said granulation being about 1/10 to 1/5 the amount used for said addition.
Claim 4
Dependent Claim 158 words
A process for preparing granular preparations for oral administration having no bitter taste which comprises dissolving or suspending midecamycin as a bitter pharmaceutical ingredient in high concentration in a volatile solvent for dissolving a pharmaceutically acceptable, water insoluble ethyl cellulose as a bitter taste-masking substance having a molecular weight higher than about 2,000, adding the ethyl cellulose to the resulting solution or suspension followed by kneading, adding silicic acid anhydride to the resulting kneaded substance to form a powder and granulating said powder using a solution of said ethyl cellulose in a fluidized bed granulator, said volatile solvent not exerting a degrading effect upon said ethyl cellulose or upon said midecamycin, the amount of said ethyl cellulose added to said solution or said suspension being about 0.5 to about three times the amount of said midecamycin and the amount of said ethyl cellulose used for said granulation being about 1/10 to 1/5 the amount used for said addition.
Claim 5
Dependent Claim 28 words
The process according to claim 1, wherein the amount of said ethyl cellulose is dissolved in an amount of 0.5 to 2 times the amount of the midecamycin.
Claim 6
Dependent Claim 30 words
The process according to claim 2, wherein said ethyl cellulose is added to said solution or suspension in an amount of 0.5 to 2.0 times the amount of said midecamycin.

References Cited (Backward Citations)

GB908282A Cited
US3242049A Cited
US3247065A Cited
GB1033684A Cited
US3906086A Cited
US3859228A Cited
US3891570A Cited
US3879511A Cited
US3860733A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-07-17 1982-01-16 1982-07-18 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-07-17 1986-01-16 1986-07-18 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-07-17 1990-01-16 1990-07-18 $7700.00 Window Closed / Lapsed

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