Abstract

BackgroundHumans are routinely and concurrently exposed to multiple toxic chemicals, including various metals and organics, often at levels that can cause adverse and potentially synergistic effects. However, toxicokinetic modeling studies of exposures to these chemicals are typically performed on a single chemical basis. Furthermore, the attributes of available models for individual chemicals are commonly estimated specifically for the compound studied. As a result, the available models usually have parameters and even structures that are not consistent or compatible across the range of chemicals of concern. This fact precludes the systematic consideration of synergistic effects, and may also lead to inconsistencies in calculations of co-occurring exposures and corresponding risks. There is a need, therefore, for a consistent modeling framework that would allow the systematic study of cumulative risks from complex mixtures of contaminants.MethodsA Generalized Toxicokinetic Modeling system for Mixtures (GTMM) was developed and evaluated with case studies. The GTMM is physiologically-based and uses a consistent, chemical-independent physiological description for integrating widely varying toxicokinetic models. It is modular and can be directly "mapped" to individual toxicokinetic models, while maintaining physiological consistency across different chemicals. Interaction effects of complex mixtures can be directly incorporated into the GTMM.ConclusionsThe application of GTMM to different individual metals and metal compounds showed that it explains available observational data as well as replicates the results from models that have been optimized for individual chemicals. The GTMM also made it feasible to model toxicokinetics of complex, interacting mixtures of multiple metals and nonmetals in humans, based on available literature information. The GTMM provides a central component in the development of a "source-to-dose-to-effect" framework for modeling population health risks from environmental contaminants. As new data become available on interactions of multiple chemicals, the GTMM can be iteratively parameterized to improve mechanistic understanding of human health risks from exposures to complex mixtures of chemicals.

Highlights

  • Humans are routinely and concurrently exposed to multiple toxic chemicals, including various metals and organics, often at levels that can cause adverse and potentially synergistic effects

  • Predictions of biomarkers by the Generalized Toxicokinetic Modeling system for Mixtures (GTMM) were compared with the estimates from the corresponding single-metal Physiologically based toxicokinetic (PBTK) models, using the same input data as the original literature evaluation studies of these models

  • For the case studies involving individual metals, the major physiological parameters for the GTMM were set to the values used in these original modeling case studies, so as to ensure direct comparison

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Summary

Introduction

Humans are routinely and concurrently exposed to multiple toxic chemicals, including various metals and organics, often at levels that can cause adverse and potentially synergistic effects. The available models usually have parameters and even structures that are not consistent or compatible across the range of chemicals of concern This fact precludes the systematic consideration of synergistic effects, and may lead to inconsistencies in calculations of co-occurring exposures and corresponding risks. PBTK models employ mass balances on compartments within a human or animal body, for the purpose of estimating the time-course profiles of toxicant concentrations in tissues and fluids. These models are useful for understanding therapeutic outcomes from internal tissue exposures to pharmaceuticals [2].

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