Literature DB >> 14140001

RATES OF DISSOLUTION OF TOLBUTAMIDE TABLETS.

N BRUDNEY, D J STEWART, B T EUSTACE.   

Abstract

An investigation was made of the pharmaceutical properties and the in vitro dissolution rates of 18 commercially available brands of tolbutamide tablets, all of which met the limits set by the Food and Drug Regulations for tablets sold in Canada.A marked variation in dissolution rates was found, which bore no relation to the official disintegration time. These wide variations in dissolution rate point to a need for (a) a comprehensive study of the in vivo effects of different tolbutamide tablets, and (b) an official test that sets limits for the rate of dissolution of tolbutamide tablets, in addition to the one that places limits on disintegration time.

Entities:  

Keywords:  ABSORPTION; CANADA; CHEMISTRY, PHARMACEUTICAL; EXPERIMENTAL LAB STUDY; GASTROINTESTINAL SYSTEM; LEGISLATION, MEDICAL; TABLETS; TOLBUTAMIDE

Mesh:

Substances:

Year:  1964        PMID: 14140001      PMCID: PMC1922635     

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN: 0008-4409            Impact factor:   8.262


  2 in total

1.  Physicochemical basis of the buffered acetylsalicylic acid controversy.

Authors:  G LEVY; B A HAYES
Journal:  N Engl J Med       Date:  1960-05-26       Impact factor: 91.245

2.  Substitution for Brand-Name Drugs.

Authors:  S Caminetsky
Journal:  Can Med Assoc J       Date:  1963-05-04       Impact factor: 8.262

  2 in total
  1 in total

1.  A COMPARATIVE STUDY OF SOME BRANDS OF TOLBUTAMIDE AVAILABLE IN CANADA. II. PHARMACEUTICAL ASPECTS.

Authors:  F C LU; W B RICE; C W MAINVILLE
Journal:  Can Med Assoc J       Date:  1965-05-29       Impact factor: 8.262

  1 in total

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