| Literature DB >> 14140001 |
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