Bioavailability assessment and pharmacologie response: Impact of first-pass loss when both drug and metabolites are active
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/BF01062013.pdf
Reference16 articles.
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2. V. F. Smolen. Theoretical and computational basis for drug bioavailability determinations using pharmacological data. I. General considerations and procedures.J. Pharmacokin. Biopharm. 4:337–353 (1976).
3. Code of (USA) Federal Regulations.Bioavailability and Bioequivalence Requirements, Vol. 21. Part 320.
4. S. Pond and T. N. Tozer. First pass elimination: Basic concepts and clinical consequences.Clin. Pharmacokin. 9:1–25 (1984).
5. B. Ablad, K. O. Borg, G. Johnsson, C-G. Regärdh, and L. Sölvell. Combined pharmacokinetic and pharmacodynamic studies of alprenolol and 4-hydroxy-alprenolol in man.Life Sci. 14:693–700 (1974).
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