A model for absorption of low-volatile toxicants by the airway mucosa

Citation
P. Gerde et Br. Scott, A model for absorption of low-volatile toxicants by the airway mucosa, INHAL TOXIC, 13(10), 2001, pp. 903-929
Citations number
52
Categorie Soggetti
Pharmacology & Toxicology
Journal title
INHALATION TOXICOLOGY
ISSN journal
08958378 → ACNP
Volume
13
Issue
10
Year of publication
2001
Pages
903 - 929
Database
ISI
SICI code
0895-8378(200110)13:10<903:AMFAOL>2.0.ZU;2-U
Abstract
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.