Pitfalls and valid approaches to pharmacokinetic analysis of mean concentration data following intravenous administration David M. CocchettoWilliam A. WarginJames W. Crow OriginalPaper 01 December 1980 Pages: 539 - 552
Evaluation of methods for estimating population pharmacokinetic parameters. I. Michaelis-menten model: Routine clinical pharmacokinetic data Lewis B. SheinerStuart L. Beal OriginalPaper 01 December 1980 Pages: 553 - 571
The effect of infusion time on the time course of drug concentration in blood Kenneth RaymondDenis J. Morgan OriginalPaper 01 December 1980 Pages: 573 - 582
In vitro binding of14C-labeled acidic compounds to serum albumin and their tissue distribution in the rat S. C. FangF. T. Lindstrom OriginalPaper 01 December 1980 Pages: 583 - 597
Controlled release of tetracycline—III: A physiological pharmacokinetic model of the pregnant rat Lawrence S. OlanoffJames M. Anderson OriginalPaper 01 December 1980 Pages: 599 - 620
Concentration profile for the dissolution of drug tablets undergoing simultaneous degradation H. -S. George ChenSai Y. ChangJoseph F. Gross OriginalPaper 01 December 1980 Pages: 621 - 631
Identifiable pharmacokinetic models: The role of extra inputs and measurements Keith R. GodfreyR. Peter JonesReginald F. Brown OriginalPaper 01 December 1980 Pages: 633 - 648