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Title of Journal: Journal of Pharmacokinetics and Biopharmaceutics

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Abbravation: Journal of Pharmacokinetics and Biopharmaceutics

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Kluwer Academic Publishers-Plenum Publishers

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10.1016/0301-4215(91)90101-s

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0090-466X

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Relationship between plasma or serum drug concentr

Authors: Donald Perrier Milo Gibaldi
Publish Date: 2015/07/17
Volume: 1, Issue: 1, Pages: 17-22
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Abstract

The average amount of drug in the body at steady state bar Xupon repetitive dosing in a twocompartment open system is related to the average steadystate plasma level bar Cby the apparent volume of distribution at steady state Vssrather than by Vβthe apparent volume of distribution at pseudodistribution equilibrium despite the fact thatbar Cis directly proportional to 1/VβMultiplication ofbar C by ddot V beta results in an overestimate ofbar Xthe magnitude of which depends on the distribution and elimination parameters of the drug The significance and utility of the volume parameters Vβand Vssemployed in multicompartment systems are considered


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  1. Influence of plasma protein binding kinetics on hepatic clearance assessed from a “tube” model and a “well-stirred” model
  2. Quinidine pharmacokinetics in man: Choice of a disposition model and absolute bioavailability studies
  3. Effect of plasma protein and tissue binding on the time course of drug concentration in plasma
  4. A nonlinear mixed-effects pharmacokinetic model comparing two formulations of cyclosporine in stable renal transplant patients
  5. Linear pharmacokinetic models: Geometric construction to determine transfer and elimination rate constants
  6. Modeling of drug response in individual subjects
  7. Prediction of diazepam disposition in the rat and man by a physiologically based pharmacokinetic model
  8. Pharmacokinetics of piroxicam, a new nonsteroidal anti-inflammatory agent, under fasting and postprandial states in man
  9. Pharmacokinetics and bioavailability of intravenous, oral, and rectal nitrazepam in humans
  10. Application of optimal sampling theory to the determination of metacycline pharmacokinetic parameters: Effect of model misspecification
  11. Estimation of drug binding parameters
  12. Pharmacokinetics of teicoplanin in man after intravenous administration
  13. Theoretical considerations in the calculation of bioavailability of drugs exhibiting Michaelis-Menten elimination kinetics
  14. Mathematical model for in vivo pharmacodynamics integrating fluctuation of the response: Application to the prolactin suppressant effect of the dopaminomimetic drug DCN 203–922
  15. Mathematical model for in vivo pharmacodynamics integrating fluctuation of the response: Application to the prolactin suppressant effect of the dopaminomimetic drug DCN 203–922
  16. Simulation for population analysis of Michaelis-Menten elimination kinetics
  17. Pharmacodynamic modeling of the in vitro vasodilating effects of organic mononitrates

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