Theoretical and computational basis for drug bioavailability determinations using pharmacological data. I. General considerations and procedures
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics
Link
http://link.springer.com/content/pdf/10.1007/BF01063123.pdf
Reference29 articles.
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2. V. F. Smolen, P. B. Kuehn, and E. J. Williams. Idealized approach to the optimal design, development, and evaluation of drug delivery systems II: Drug bioavailability inputs andin-vitro drug release testing.Drug. Dev. Comm. 1:231–258 (1974/1975).
3. V. F. Smolen, R. D. Barile, and T. G. Theophanous. The relationship between dose, effect, time, and biophasic drug levels.J. Pharm. Sci. 61:467–470 (1972).
4. V. F. Smolen. Determination of time course ofin-vivo pharmacological effects fromin-vitro drug-release testing.J. Pharm. Sci. 60:878–882 (1971).
5. V. F. Smolen and W. A. Weigland. Optimally predictivein-vitro drug dissolution testing forin-vivo bioavailability.J. Pharm. Sci. (in press).
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