Literature DB >> 8314616

Effect of various exposure scenarios on the biological monitoring of organic solvents in alveolar air. I. Toluene and m-xylene.

S Laparé1, R Tardif, J Brodeur.   

Abstract

The present study was undertaken to investigate the influence of different exposure scenarios on the elimination of toluene and m-xylene in alveolar air and other biological fluids in human volunteers. The study was also aimed at establishing the effectiveness of physiologically based toxicokinetic models in predicting the value of biological monitoring data after exposure to toluene and m-xylene. Two adult male and two adult female white volunteers were exposed by inhalation, in a dynamic, controlled-environment exposure chamber, to various concentrations of toluene (21-66 ppm) or m-xylene (25-50 ppm) in order to establish the influence of exposure concentration, duration of exposure, variation of concentration within day, and work load on respective biological exposure indices. The concentrations of unchanged solvents in end-exhaled air and in blood as well as the urinary excretion of hippuric acid and m-methyl-hippuric acid were determined. The results show that doubling the exposure concentration for both solvents led to a proportional increase in the concentrations of unchanged solvents in alveolar air and blood at the end of a 7-h exposure period. Cumulative urinary excretion of the respective metabolites exhibited a nearly proportional increase. Adjustment of exposure concentration to account for a prolongation of the duration of exposure resulted in essentially identical cumulative urinary excretion of the metabolites. Induced within-day variations in the exposure concentration led to corresponding but not proportional changes in alveolar concentration for both solvents, depending on whether or not sampling preceded or followed peak exposure to solvent. At the end of repeated 10-min periods of physical exercise at 50 W, alveolar air concentrations of both solvents were increased by 40%. Experimental data collected during the present study were adequately simulated by physiologically based toxicokinetic modeling. These results suggest that alveolar air solvent concentration is a reliable index of exposure to both toluene and m-xylene under various experimental exposure scenarios. For clinical situations likely to be encountered in the workplace, physiologically based toxicokinetic modeling appears to be a useful tool both for developing strategies of biological monitoring of exposure to volatile organic solvents and for predicting alveolar air concentrations under a given set of exposure conditions.

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Year:  1993        PMID: 8314616     DOI: 10.1007/bf00517703

Source DB:  PubMed          Journal:  Int Arch Occup Environ Health        ISSN: 0340-0131            Impact factor:   3.015


  34 in total

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Authors:  V Fiserova-Bergerova
Journal:  Ann Occup Hyg       Date:  1990-12

2.  Precision and sensitivity of pharmacokinetic models for cancer risk assessment: tetrachloroethylene in mice, rats, and humans.

Authors:  F Y Bois; L Zeise; T N Tozer
Journal:  Toxicol Appl Pharmacol       Date:  1990-02       Impact factor: 4.219

3.  The influence of assay variability on pharmacokinetic parameter estimation.

Authors:  D A Graves; C S Locke; K T Muir; R P Miller
Journal:  J Pharmacokinet Biopharm       Date:  1989-10

4.  Variability in biological monitoring of solvent exposure. I. Development of a population physiological model.

Authors:  P O Droz; M M Wu; W G Cumberland; M Berode
Journal:  Br J Ind Med       Date:  1989-07

5.  Variability in biological monitoring of organic solvent exposure. II. Application of a population physiological model.

Authors:  P O Droz; M M Wu; W G Cumberland
Journal:  Br J Ind Med       Date:  1989-08

6.  Control of industrial exposure to tetrachloroethylene by measuring alveolar concentrations: theoretical approach using a mathematical model.

Authors:  E Guberan; J Fernandez
Journal:  Br J Ind Med       Date:  1974-04

7.  Predictable "individual differences" in uptake and excretion of gases and lipid soluble vapours simulation study.

Authors:  V Fiserova-Bergerova; J Vlach; J C Cassady
Journal:  Br J Ind Med       Date:  1980-02

Review 8.  The effect of environmental factors on the pharmacokinetic behaviour of organic solvent vapours.

Authors:  A Sato
Journal:  Ann Occup Hyg       Date:  1991-10

9.  Kinetics of methyl ethyl ketone in man: absorption, distribution and elimination in inhalation exposure.

Authors:  J Liira; V Riihimäki; P Pfäffli
Journal:  Int Arch Occup Environ Health       Date:  1988       Impact factor: 3.015

Review 10.  Effects of biosolubility on pulmonary uptake and disposition of gases and vapors of lipophilic chemicals.

Authors:  V Fiserova-Bergerova; M Tichy; F J Di Carlo
Journal:  Drug Metab Rev       Date:  1984       Impact factor: 4.518

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  5 in total

1.  Determination of low level exposure to volatile aromatic hydrocarbons and genotoxic effects in workers at a styrene plant.

Authors:  O Holz; G Scherer; S Brodtmeier; F Koops; K Warncke; T Krause; A Austen; J Angerer; A R Tricker; F Adlkofer
Journal:  Occup Environ Med       Date:  1995-06       Impact factor: 4.402

2.  Effect of various exposure scenarios on the biological monitoring of organic solvents in alveolar air. II. 1,1,1-Trichloroethane and trichloroethylene.

Authors:  S Laparé; R Tardif; J Brodeur
Journal:  Int Arch Occup Environ Health       Date:  1995       Impact factor: 3.015

3.  Comparison of unchanged n-hexane in alveolar air and 2,5-hexanedione in urine for the biological monitoring of n-hexane exposure in human volunteers.

Authors:  G Hamelin; G Truchon; R Tardif
Journal:  Int Arch Occup Environ Health       Date:  2004-03-13       Impact factor: 3.015

Review 4.  Physiological modeling of toxicokinetic interactions: implications for mixture risk assessment.

Authors:  S Haddad; K Krishnan
Journal:  Environ Health Perspect       Date:  1998-12       Impact factor: 9.031

5.  The application of global sensitivity analysis in the development of a physiologically based pharmacokinetic model for m-xylene and ethanol co-exposure in humans.

Authors:  George D Loizou; Kevin McNally; Kate Jones; John Cocker
Journal:  Front Pharmacol       Date:  2015-06-30       Impact factor: 5.810

  5 in total

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