Literature DB >> 2635739

An integrated approach to pharmacokinetic analysis for linear mammillary systems in which input and exit may occur in/from any compartment.

E Nakashima1, L Z Benet.   

Abstract

The general treatment of linear mammillary models employing input and disposition functions and Laplace transforms is expanded to solve concentration-time equations AUC and AUMC in any compartment without restricting sites of input or output. In this integrated approach to noncompartmental pharmacokinetic analysis, the values of AUC and AUMC can be calculated from Laplace transforms with some very simplified treatments. Tables of input functions, disposition functions, Laplace transforms, and derivatives of the Laplace transforms are presented. The relationships between the integrated parameters and various mammillary model parameters are presented using several examples.

Mesh:

Year:  1989        PMID: 2635739     DOI: 10.1007/bf01062124

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


  13 in total

1.  Determination of mean input time, mean residence time, and steady-state volume of distribution with multiple drug inputs.

Authors:  N Watari; L Z Benet
Journal:  J Pharmacokinet Biopharm       Date:  1989-10

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

3.  General method for assessing bioavailability of drugs undergoing reversible metabolism in a linear system.

Authors:  S S Hwang; W F Bayne
Journal:  J Pharm Sci       Date:  1986-08       Impact factor: 3.534

4.  General treatment of linear mammillary models with elimination from any compartment as used in pharmacokinetics.

Authors:  L Z Benet
Journal:  J Pharm Sci       Date:  1972-04       Impact factor: 3.534

5.  Use of general partial fraction theorem for obtaining inverse laplace transforms in pharmacokinetic analysis.

Authors:  L Z Benet; J S Turi
Journal:  J Pharm Sci       Date:  1971-10       Impact factor: 3.534

6.  General treatment of mean residence time, clearance, and volume parameters in linear mammillary models with elimination from any compartment.

Authors:  E Nakashima; L Z Benet
Journal:  J Pharmacokinet Biopharm       Date:  1988-10

7.  Mean residence time for drugs subject to reversible metabolism.

Authors:  L Aarons
Journal:  J Pharm Pharmacol       Date:  1987-07       Impact factor: 3.765

8.  Mean residence time in the body versus mean residence time in the central compartment.

Authors:  L Z Benet
Journal:  J Pharmacokinet Biopharm       Date:  1985-10

9.  Comments on mean residence time determination.

Authors:  E M Landaw; D Katz
Journal:  J Pharmacokinet Biopharm       Date:  1985-10

10.  Statistical moments in pharmacokinetics.

Authors:  K Yamaoka; T Nakagawa; T Uno
Journal:  J Pharmacokinet Biopharm       Date:  1978-12
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  4 in total

1.  Determination of mean input time, mean residence time, and steady-state volume of distribution with multiple drug inputs.

Authors:  N Watari; L Z Benet
Journal:  J Pharmacokinet Biopharm       Date:  1989-10

2.  Similar effect of oxidation deficiency (debrisoquine polymorphism) and quinidine on the apparent volume of distribution of (+/-)-metoprolol.

Authors:  T D Leemann; K P Devi; P Dayer
Journal:  Eur J Clin Pharmacol       Date:  1993       Impact factor: 2.953

3.  GPU-accelerated compartmental modeling analysis of DCE-MRI data from glioblastoma patients treated with bevacizumab.

Authors:  Yu-Han H Hsu; Ziyin Huang; Gregory Z Ferl; Chee M Ng
Journal:  PLoS One       Date:  2015-03-18       Impact factor: 3.240

Review 4.  Human serum albumin homeostasis: a new look at the roles of synthesis, catabolism, renal and gastrointestinal excretion, and the clinical value of serum albumin measurements.

Authors:  David G Levitt; Michael D Levitt
Journal:  Int J Gen Med       Date:  2016-07-15
  4 in total

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