Abstract
Two new preparations of spironolactone tablets containing 25 and 100 mg of spironolactone have been characterized by their disintegration time, tablet spironolactone content, dissolution profile and bioavailability in comparison with two known spironolactone preparations as reference material. The preparations were found to possess almost identical characteristics, assuring a proper clinical use of the new tablet preparations. For spironolactone, a positive outcome of thein vitro dissolution test coincides with an excellent bioavailability.
Similar content being viewed by others
References
Abshagen, U., D. Platt andH.-J. Horn (1981)Klin. Wochenschr. 59, 909–910.
Clarke, J.M., L.E. Ramsay, J.R. Shelton, M.J. Tidd, S. Murray andR.F. Palmer (1977)J. Pharm. Sci. 66, 1429–1432.
Cumming, D.C., J.C. Yang, R.W. Rebar andS.C. Yen (1982)JAMA 247, 1295–1298.
Gochman, N., andC.L. Gantt (1962)J. Pharmacol. Exp. Ther. 135, 313–316.
Karim, A. (1978)Drug Metab. Rev. 8, 151–188.
Karim, A., J. Zagarella, T.C. Hutsell, A. Chao andB.J. Baltes (1976)Clin. Pharmacol. Ther. 19, 170–176.
Melander, A. (1983) In:Handbook of Clinical Pharmacokinetics (Gibaldi, M., andL. Prescott, Eds.). Adis Press, New York, Section 1, 39–54.
Poole, J.W. (1969)Drug Inf. Bull. 3, 8–16.
Sadée, W., andG.C.M. Beelen (1980)Drug Level Monitoring. John Wiley & Sons, New York, 423–426.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Nijkerk, A.J., Vermeer, J.M., Imanse, M. et al. The bioavailability of two new preparations of spironolactone tablets. Pharmaceutisch Weekblad Scientific Edition 5, 210–212 (1983). https://doi.org/10.1007/BF02332945
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF02332945