Parameter variability and the interpretation of physiologically based pharmacokinetic modeling results

Environ Health Perspect. 1994 Dec;102 Suppl 11(Suppl 11):61-6. doi: 10.1289/ehp.94102s1161.

Abstract

For the past several years we have been working with models of benzene distribution and metabolism, principally in the rat, but more recently in humans. Our biologically related objectives have been primarily to assist our laboratory-based colleagues in their quest for understanding of the mechanisms by which benzene exerts its toxic action. A secondary goal has been to develop or adapt models useful in risk assessment applications. We have also had methodological goals that relate to applications of sensitivity analysis on the one hand, but more fundamentally to the connection between experimental data and model structure and parameterization. This paper presents an overview of our work in these areas.

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Animals
  • Benzene / pharmacokinetics*
  • Benzene / toxicity
  • Humans
  • Male
  • Models, Biological
  • Monte Carlo Method
  • Multivariate Analysis
  • Rats
  • Rats, Inbred F344
  • Reproducibility of Results
  • Risk Assessment
  • Sensitivity and Specificity

Substances

  • Benzene