Literature DB >> 8060031

Model parameter estimation and analysis: understanding parametric structure.

H Li1, K Watanabe, D Auslander, R C Spear.   

Abstract

We developed three algorithms to facilitate an analysis of the parameter combinations (PASS points) that fit experimental data to a desired degree of accuracy. The clustering algorithm separates PASS points into clusters (PASS clusters) as a preliminary step for the following geometrical parametric analyses. The PASS region reconstruction algorithm defines the space of a PASS cluster to allow further parametric structural analysis. The feasible parameter space expansion algorithm produces a complete PASS cluster to be used for model predictions to evaluate the effects of variability and uncertainty. These algorithms are demonstrated using two pharmacokinetic models; a single compartment model for procainamide and a three-compartment physiologically based model for benzene. We found a more thorough representation of the parameter space than previously considered. Thus, we obtained model predictions that describe better the variability in population responses. In addition, we also parametrically identified a subpopulation that may have a higher risk for cancer.

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Year:  1994        PMID: 8060031     DOI: 10.1007/bf02368226

Source DB:  PubMed          Journal:  Ann Biomed Eng        ISSN: 0090-6964            Impact factor:   3.934


  11 in total

1.  A design methodology for nonlinear systems containing parameter uncertainty.

Authors:  G E Young; D M Auslander
Journal:  J Dyn Syst Meas Control       Date:  1984-03       Impact factor: 1.372

2.  Structure and parameterization of pharmacokinetic models: their impact on model predictions.

Authors:  T J Woodruff; F Y Bois; D Auslander; R C Spear
Journal:  Risk Anal       Date:  1992-06       Impact factor: 4.000

3.  An analysis of exposure rate effects for benzene using a physiologically based pharmacokinetic model.

Authors:  F Y Bois; D G Paxman
Journal:  Regul Toxicol Pharmacol       Date:  1992-04       Impact factor: 3.271

4.  Complex segregation analysis of primary hepatocellular carcinoma in Chinese families: interaction of inherited susceptibility and hepatitis B viral infection.

Authors:  F M Shen; M K Lee; H M Gong; X Q Cai; M C King
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5.  Modeling benzene pharmacokinetics across three sets of animal data: parametric sensitivity and risk implications.

Authors:  R C Spear; F Y Bois; T Woodruff; D Auslander; J Parker; S Selvin
Journal:  Risk Anal       Date:  1991-12       Impact factor: 4.000

6.  Comparison of three physiologically based pharmacokinetic models of benzene disposition.

Authors:  F Y Bois; T J Woodruff; R C Spear
Journal:  Toxicol Appl Pharmacol       Date:  1991-08       Impact factor: 4.219

7.  Benzene disposition in the rat after exposure by inhalation.

Authors:  D E Rickert; T S Baker; J S Bus; C S Barrow; R D Irons
Journal:  Toxicol Appl Pharmacol       Date:  1979-07       Impact factor: 4.219

8.  Differences in the metabolism and disposition of inhaled [3H]benzene by F344/N rats and B6C3F1 mice.

Authors:  P J Sabourin; W E Bechtold; L S Birnbaum; G Lucier; R F Henderson
Journal:  Toxicol Appl Pharmacol       Date:  1988-06-15       Impact factor: 4.219

9.  Effect of dose on the absorption and excretion of [14C]benzene administered orally or by inhalation in rats and mice.

Authors:  P J Sabourin; B T Chen; G Lucier; L S Birnbaum; E Fisher; R F Henderson
Journal:  Toxicol Appl Pharmacol       Date:  1987-02       Impact factor: 4.219

Review 10.  Genetic studies on lung tumor susceptibility and histogenesis in mice.

Authors:  A M Malkinson
Journal:  Environ Health Perspect       Date:  1991-06       Impact factor: 9.031

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  1 in total

Review 1.  Whole body pharmacokinetic models.

Authors:  Ivan Nestorov
Journal:  Clin Pharmacokinet       Date:  2003       Impact factor: 6.447

  1 in total

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