Estimating the fraction reabsorbed in drugs undergoing enterohepatic circulation
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/BF01065175.pdf
Reference9 articles.
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2. H.-S. G. Chen and J. F. Gross. Pharmacokinetics of drugs subject to enterohepatic circulation.J. Pharm. Sci. 68:792–794 (1979).
3. W. A. Colburn. Pharmacokinetic and biopharmaceutic parameters during enterohepatic circulation of drugs.J. Pharm. Sci. 71:131–133 (1982).
4. B. E. Dahlström and L. K. Paalzow. Pharmacokinetic interpretation of the enterohepatic recirculation and first-pass elimination of morphine in the rat.J. Pharmacokin. Biopharm. 6:505–519 (1978).
5. W. A. Colburn, P. C. Hirom, R. J. Parker, and P. Milburn. A pharmacokinetic model for enterohepatic recirculation in the rat: phenolphthalein, a model drug.Drug. Metab. Dispos. 7:100–102 (1979).
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