Inhalation dosimetry modeling with decamethylcyclopentasiloxane in rats and humans

Abstract

Decamethylcyclopentasiloxane (D5), a volatile cyclic methyl siloxane (VCMS), is used in industrial and consumer products. Inhalation pharmacokinetics of another VCMS, octamethylcyclotetrasiloxane (D4), have been extensively investigated and successfully modeled with a multispecies physiologically based pharmacokinetic (PBPK) model. Here, we develop an inhalation PBPK description for D5, using the D4 model structure as a starting point, with the objective of understanding factors that regulate free blood and tissue concentrations of this highly lipophilic vapor after inhalation in rats and humans. Compared with D4, the more lipophilic D5 required deep compartments in lung, liver, and plasma to account for slow release from tissues after cessation of exposures. Simulations of the kinetics of a stable D5 metabolite, HO-D5, required diffusion-limited uptake in fat, a deep tissue store in lung, and its elimination by fecal excretion and metabolism to linear silanols. The combined D5/ HO-D5 model described blood and tissue concentrations of parent D5 and elimination of total radioactivity in single and repeat exposures in male and female rats at 7 and 160 ppm. In humans, D5 kinetic data are more sparse and the model structure though much simplified, still required free and bound blood D5 to simulate exhaled air and blood time courses from 1 h inhalation exposures at 10 ppm in five human volunteers. This multispecies PBPK model for D5 highlights complications in interpreting kinetic studies where chemical in blood and tissues represents various pools with only a portion free. The ability to simulate free concentrations is essential for dosimetry based risk assessments for these VCMS. © The Author 2008. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved.