Properties of the recirculation model: Calculation of the amount of drug in the body from blood concentration data, with application to absorption rate calculations
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/BF01068084.pdf
Reference5 articles.
1. D. J. Cutler. A linear recirculation model for drug disposition.J. Pharmacokin. Biopharm. 7:101–116 (1979).
2. D. J. Cutler. Linear systems analysis in pharmacokinetics.J. Pharmacokin. Biopharm. 6:265–281 (1978).
3. W. L. Chiou. Potential pitfalls in the conventional pharmacokinetic studies: effects of the initial mixing of drug in blood and the pulmonary first-pass elimination.J. Pharmacokin. Biopharm. 7:527–536 (1979).
4. J. G. Wagner and E. Nelson. Percent absorbed time plots derived from blood level and/or urinary excretion data.J. Pharm. Sci. 52:610–611 (1963).
5. J. C. K. Loo and S. Riegelman. New method for calculating the intrinsic absorption rate of drugs.J. Pharm. Sci. 57:918–928 (1968).
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