We have developed and applied a new measurement methodology to investi
gate dermal absorption of chloroform while bathing. Ten subjects bathe
d in chlorinated water while breathing pure air through a face mask. T
heir exhaled breath was delivered to a glow discharge source/ion trap
mass spectrometer for continuous real-time measurement of chloroform i
n the breath. This new method provides abundant data compared to previ
ous discrete time-integrated breath sampling methods. The method is pa
rticularly well suited to studying dermal exposure because the full fa
ce mask eliminates exposure to contaminated air. Seven of the 10 subje
cts bathed in water at two or three different temperatures between 30
degrees C and 40 degrees C. Subjects at the highest temperatures exhal
ed about 30 times more chloroform than the same subjects at the lowest
temperatures. This probably results from a decline in blood Bow to th
e skin at the lower temperatures as the body seeks to conserve heat fo
rcing the chloroform to diffuse over a much greater path length before
encountering the blood. These results suggest that pharmacokinetic mo
dels need to employ temperature-dependent parameters. Two existing mod
els predict quite different times of about 12 min and 29 min for chlor
oform flux through the stratum corneum to reach equilibrium. At 40 deg
rees C, the time for the flux to reach a near steady-state value is 6-
9 min. Although uptake and decay processes involve several body compar
tments, the complicating effect of the stratum corneum lag time made i
t difficult to fit multiexponential curves to the data; however, a sin
gle-compartment model gave a satisfactory fit.