Theoretical and computational basis for drug bioavailability determinations using pharmacological data. II. Drug input ⇄ response relationships
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/BF01063124.pdf
Reference30 articles.
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3. V. F. Smolen. Determination of time course onin vivo pharmacological effects fromin vitro drug release testing.J. Pharm. Sci. 60:878–882 (1971).
4. V. F. Smolen and R. J. Erb. The predictive conversion ofin vitro drug dissolution data intoin vivo drug response vs. time profiles exemplified for plasma levels of warfarin.J. Pharm. Sci (in review).
5. V. F. Smolen, P. B. Kuehn, and E. J. Williams. Idealized approach to the optimal design, development and evaluation of drug delivery systems. 11. Optimization of drug bioavailability inputs andin vitro drug bioavailability testing.Drug. Dev. Comm. 1:231–259 (1974/1975).
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