The site-dependent small-intestinal absorption pattern of griseofulvin
was investigated in man. Griseofulvin was chosen as a model substance
having extremely low water solubility and moderate lipid solubility.
A conventional steady-state perfusion technique (triple-lumen tubing s
ystem with a 20 cm test segment) was applied. Dissolved griseofulvin (
10.0 mg L(-1)) was perfused (10 mL min(-1)) during 160 min into differ
ent parts of the small intestine with the middle of the test segment b
etween 85 cm and 270 cm beyond the teeth. Each of the ten healthy volu
nteers was examined twice with the test segment localized in different
regions to allow for intraindividual comparisons. Mean drug absorptio
n rates calculated from intestinal aspirate concentrations were simila
r in the two intestinal parts (proximal, 15.0 +/- 5.9 mu g (20 cm min)
(-1); distal, 16.2 +/- 4.3 mu g (20 cm min)(-1); mean +/- SD). Absorpt
ion rate was strongly correlated to the amount of griseofulvin offered
to the test segment per unit time. Extrapolating these findings it fo
llows that an amount of griseofulvin, once dissolved, would be absorbe
d completely (> 99%) along 100 cm of the small intestine. A significan
t, positive correlation between the rate of transmucosal fluid transpo
rt and the absorption rate of griseofulvin was observed in the distal
parts investigated.