This paper reports data indicating that, in the rat, sodium monofluoro
phosphate (MFP, CAS 10163-15-2) is absorbed without hydrolysis through
the stomach. This phenomenon and the fact that MFP binds to plasma gl
obulins produce a prompt increase in protein-bound MFP concentration,
significantly greater than the increase in plasma ultrafilterable fluo
ride. Intestinal absorption of MFP was investigated with the isolated
duodenal loop in situ. The drug was hydrolyzed to fluoride at the inte
stinal lumen with a rate of approx. 3 times greater than that for fluo
ride absorption. After filling the duodenal loop with a MFP solution,
ultrafiltrable fluoride accounts for the increase in plasma fluoride c
oncentration, with no evidence of protein-bound MFP. This report also
includes analytical techniques for the measurement of MFP in test solu
tions and and plasma.