Styrene is a widely used industrial solvent associated with acute neur
otoxicity. To investigate the relationships between exposure, blood co
ncentrations, and the appearance of neurotoxic effects, four healthy m
ales were exposed to styrene concentrations of 5-200 ppm in four diffe
rent exposure-time profiles, A digit recognition test and P300 event-r
elated evoked potential were used to measure neurologic function. A ph
ysiologically based Kinetic (PBK) model generated close predictions of
measured styrene blood concentrations, in the range of 0.01-12 mg/L,
from this and 21 previous studies. Simulated peak brain concentration,
durationxaverage exposure, and peak exposure level were predictive of
toxicity, Central nervous system effects were expected at a blood con
centration near 2.4 mg/L. A standard of 20 ppm was expected to protect
styrene-exposed workers from acute central nervous system toxicity un
der light work conditions.