Literature DB >> 10716057

Consequence of equal absorption, distribution and/or elimination rate constants.

Y Plusquellec1, F Courbon, S Nogarede.   

Abstract

When fitting experimental data to an open one- or two-compartment model, with first order kinetics, it may happen that no optimized value is obtained for model parameters. Several authors pointed out that this case is especially encountered when absorption and elimination coefficients approach each other in a one-compartment model or when absorption and exponential elimination or distribution rate constants are equal in a two-compartment model. We analyze these situations of equal coefficients here. Firstly, dealing with a one-compartment model, we get the concentration in the central compartment after a single oral dose and after successive various doses at various times (first order kinetics). Secondly, dealing with a two-compartment model, also for single or successive various doses, the concentration is expressed when absorption and exponential elimination or distribution rate constants are equal. In all cases, the areas under concentration curves and the mean residence time of the drug are calculated even when cancellation of one exponential term occurs. Furthermore, the concentration at steady-state is taken into account.

Mesh:

Year:  1999        PMID: 10716057     DOI: 10.1007/BF03190021

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.441


  9 in total

1.  Evaluation of methods for estimating the rate constant of a one-compartment absorption model when absorption and elimination rate constants are equal.

Authors:  J F Hoke; W R Ravis
Journal:  J Pharm Sci       Date:  1992-04       Impact factor: 3.534

2.  Analytical study of open four compartment pharmacokinetic models: concentrations, area under curves, mean residence times.

Authors:  Y Plusquellec; G Houin
Journal:  J Biomed Eng       Date:  1990-07

3.  Unique pharmacokinetic characteristics of the one-compartment first-order absorption model with equal absorption and elimination rate constants.

Authors:  J G Zhi
Journal:  J Pharm Sci       Date:  1990-07       Impact factor: 3.534

4.  Analytical study of three-compartment pharmacokinetic models: concentration, area under curves, mean residence time.

Authors:  Y Plusquellec
Journal:  J Biomed Eng       Date:  1989-07

5.  Pharmacokinetic model equations for the one- and two-compartment models with first-order processes in which the absorption and exponential elimination or distribution rate constants are equal.

Authors:  H P Wijnand
Journal:  J Pharmacokinet Biopharm       Date:  1988-02

6.  Noncompartmental analysis for a one-compartment model with equal absorption and elimination rate constants.

Authors:  H Ko; J F Caputo; W J Adams
Journal:  Pharm Res       Date:  1989-08       Impact factor: 4.200

7.  Anomalous parameter estimates in the one-compartment model with first-order absorption.

Authors:  R D Purves
Journal:  J Pharm Pharmacol       Date:  1993-10       Impact factor: 3.765

8.  Simplified methods for the evaluation of the parameters of the time course of plasma concentration in the one-compartment body model with first-order invasion and first-order drug elimination including methods for ascertaining when such rate constants are equal.

Authors:  E R Garrett
Journal:  J Pharmacokinet Biopharm       Date:  1993-12

9.  A simple method for determining whether absorption and elimination rate constants are equal in the one-compartment open model with first-order processes.

Authors:  M Bialer
Journal:  J Pharmacokinet Biopharm       Date:  1980-02
  9 in total

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