Inhaled chemical toxicants can damage the lungs during two phases: (1) the
first-pass phase, in which toxicants are initially absorbed through the air
/blood barrier, or (2) the circulation-transport phase, in which toxicants
are transported back through the lungs with the circulating blood. While re
spiratory-tract dosimetry for inhaled toxicants is relatively easy to evalu
ate for the circulation-transport phase, it is more problematic for the fir
st-pass phase and can involve higher local concentrations of toxicants. Thi
s article describes a respiratory-tract dosimetry model that simulates both
the rate of absorption and the local concentration of low-volatile organic
toxicants in the airway mucosa. The model simulates the non-steady-state d
iffusion of organic solutes from the air interface through the epithelium a
nd into the capillary bed below. Cellular tissues are described as a hetero
geneous, two-phase medium, with a minor lipid phase dispersed in a major aq
ueous phase. Results show that the lipid-phase/ aqueous-phase partition coe
fficient, PCL/A, is a critical factor in determining the rate of absorption
of solutes in the airway mucosa. For a PCL/A in the range 1 to 100, absorp
tion is limited by blood flow and occurs with typical half-times from about
1 to 10 min. As PCL/A increases above 100, absorption is gradually limited
by the rate of diffusion through the air/blood barrier, and absorption hal
f-times increase to hours. Over the same range, the concentration gradient
in the mucosa changes from almost uniform to more nonuniform, and the site-
of-entry epithelium becomes more selectively exposed. As a result, with inc
reasing PCL/A, protoxicants of lower reactivities can still be activated in
significant quantities in the airway epithelium and thus act as site-of-en
try toxicants. The presented results are important for understanding exposu
re/ target-dose relationships of chemical carcinogens and for conducting re
liable risk assessments.