The kinetics of lindane were modelled in the male rat with a physiolog
ically-based pharmacokinetic (PB-PK) model. The model was parameterize
d by using reference physiological parameter values and partition coef
ficients that were reported earlier in the literature. First order bio
transformation and gastro-intestinal absorption constants for lindane
were obtained by visually fitting the model to literature data on lind
ane disposition in vivo after a single oral dose. The model was valida
ted by simulating the disposition of lindane in vivo after single intr
aperitoneal and chronic oral dosage and comparing simulated with exper
imental results. It was concluded that the present model can adequatel
y simulate most of the reported data on lindane kinetics. (C) 1997 Els
evier Science Ireland Ltd.