Using population physiologically based pharmacokinetic modeling to determine optimal sampling times and to interpret biological exposure markers: The example of occupational exposure to styrene-Reference-Cited by-同舟云学术

Using population physiologically based pharmacokinetic modeling to determine optimal sampling times and to interpret biological exposure markers: The example of occupational exposure to styrene

Published:2012-09 Issue:2 Volume:213 Page:299-304
ISSN:0378-4274
Container-title:Toxicology Letters
language:en
Short-container-title:Toxicology Letters

Author:

Verner Marc-André,McDougall Robin,Johanson Gunnar

Publisher

Elsevier BV

Subject

Toxicology,General Medicine

Reference22 articles.

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2. Serum hepatic biochemical activity in two populations of workers exposed to styrene;Brodkin;Occupational and Environmental Medicine,2001

3. Exposure to toluene: uptake, distribution and elimination in man;Carlsson;Scandinavian Journal of Work, Environment and Health,1982

4. A physiologic pharmacokinetic model for styrene and styrene-7,8-oxide in mouse, rat and man;Csanady;Archives of Toxicology,1994

5. Human styrene exposure: V. Development of a model for biological monitoring;Droz;International Archives of Occupational and Environmental Health,1983

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