Literature DB >> 9044167

Volumes of distribution and mean residence time of drugs with linear tissue distribution and binding and nonlinear protein binding.

H Cheng1, W R Gillespie.   

Abstract

Based on a generalized model, equations for calculating the mean residence time in the body at single dose (MRT) and at steady state (MRTss), apparent steady-state volume of distribution (Vss), and steady-state volume of distribution (Vss) are derived for a drug exhibiting nonlinear protein binding. Interrelationships between Vss and Vss as well as between MRT and MRTss are also discussed and illustrated with simulated data. In addition, a method for estimating the central volume of distribution of the bound drug and the sum of the central volume of distribution of the unbound drug and the area under the first moment curve of distribution function for drugs with nonlinear protein binding is proposed and illustrated with both simulated and published data.

Mesh:

Year:  1996        PMID: 9044167     DOI: 10.1007/bf02353519

Source DB:  PubMed          Journal:  J Pharmacokinet Biopharm        ISSN: 0090-466X


  24 in total

1.  Simple model to explain effects of plasma protein binding and tissue binding on calculated volumes of distribution, apparent elimination rate constants and clearances.

Authors:  J G Wagner
Journal:  Eur J Clin Pharmacol       Date:  1976       Impact factor: 2.953

2.  Mean residence time concepts for pharmacokinetic systems with nonlinear drug elimination described by the Michaelis-Menten equation.

Authors:  H Y Cheng; W J Jusko
Journal:  Pharm Res       Date:  1988-03       Impact factor: 4.200

Review 3.  Factors affecting drug metabolism.

Authors:  J R Gillette
Journal:  Ann N Y Acad Sci       Date:  1971-07-06       Impact factor: 5.691

4.  Numerical solution of nonlinear pharmacokinetic equations: effects of plasma protein binding on drug distribution and elimination.

Authors:  J J Coffey; F J Bullock; P T Schoenemann
Journal:  J Pharm Sci       Date:  1971-11       Impact factor: 3.534

5.  Effect of saturable binding on the pharmacokinetics of drugs: a simulation.

Authors:  S Oie; T W Guentert; T N Tozer
Journal:  J Pharm Pharmacol       Date:  1980-07       Impact factor: 3.765

6.  Distribution volume related to body weight and protein binding.

Authors:  W J Jusko; S T Chiang
Journal:  J Pharm Sci       Date:  1982-04       Impact factor: 3.534

7.  Theorems and implications of a model-independent elimination/distribution function decomposition of linear and some nonlinear drug dispositions. II. Clearance concepts applied to the evaluation of distribution kinetics.

Authors:  W R Gillespie; P Veng-Pedersen
Journal:  J Pharmacokinet Biopharm       Date:  1985-08

8.  Pharmacokinetic models regarding protein binding of drugs.

Authors:  E Krüger-Thiemer; W Diller; P Bünger
Journal:  Antimicrob Agents Chemother (Bethesda)       Date:  1965

9.  Kinetics of elimination of drugs possessing high affinity for the plasma proteins.

Authors:  B K Martin
Journal:  Nature       Date:  1965-08-28       Impact factor: 49.962

10.  Dose-dependent protein binding and disposition of prednisolone in rabbits.

Authors:  M L Rocci; W J Jusko
Journal:  J Pharm Sci       Date:  1981-11       Impact factor: 3.534

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  2 in total

1.  A new stochastic approach to multi-compartment pharmacokinetic models: probability of traveling route and distribution of residence time in linear and nonlinear systems.

Authors:  Liang Zhao; Na Li; Harry Yang
Journal:  J Pharmacokinet Pharmacodyn       Date:  2010-12-17       Impact factor: 2.745

2.  In vitro-in vivo studies of the quantitative effect of calcium, multivitamins and milk on single dose ciprofloxacin bioavailability.

Authors:  Baishakhi Dey; Prakash Katakam; Fathi H Assaleh; Babu Rao Chandu; Shanta Kumari Adiki; Analava Mitra
Journal:  J Pharm Anal       Date:  2015-03-10
  2 in total

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