Two-compartment dispersion model for analysis of organ perfusion system of drugs by fast inverse laplace transform (FILT)-Reference-Cited by-同舟云学术

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Two-compartment dispersion model for analysis of organ perfusion system of drugs by fast inverse laplace transform (FILT)

Published:1989-04 Issue:2 Volume:17 Page:179-202
ISSN:0090-466X
Container-title:Journal of Pharmacokinetics and Biopharmaceutics
language:en
Short-container-title:Journal of Pharmacokinetics and Biopharmaceutics

Author:

Yano Yoshitaka,Yamaoka Kiyoshi,Aoyama Yoshihiro,Tanaka Hisashi

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics

Link

http://link.springer.com/content/pdf/10.1007/BF01059027.pdf

Reference23 articles.

1. K. S. Pang and M. Rowland. Hepatic clearance of drugs: 1. Theoretical considerations of a “well-stirred” model and a “parallel tube” model. Influence of hepatic blood flow, plasma and blood cell binding, and the hepatocellular enzymatic activity on hepatic drug clearance.J. Pharmacokin. Biopharm. 5:625–653 (1977).

2. G. R. Wilkinson and D. G. Shand. Commentary. A physiological approach to hepatic drug clearance.Clin. Pharmacol. Ther. 18:377–390 (1975).

3. M. Rowland, L. Z. Benet, and G. G. Graham. Clearance concepts in pharmacokinetics.J. Pharmacokin. Biopharm. 1:123–136 (1977).

4. L. Bass, S. Keiding, K. Winkler, and N. Tygstrup. Enzymatic elimination of substrates flowing through the intact liver.J. Theor. Biol. 61:393–409 (1976).

5. R. W. Brauer, G. F. Leong, P. F. McElory, Jr., and R. J. Holloway. Circulatory pathways in the rat liver as revealed by32P chromic phosphate colloid uptake in the isolated perfused liver preparation.Am. J. Physiol. 184:593–598 (1956).

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