Porcine insulin was labeled with Tc-99m by direct tin reduction. More
than 95% labeling efficiency was obtained on paper chromatography in s
aline and methyl ethyl ketone. The stability of the labeled compound w
as confirmed by paper chromatography at 3 h post-labeling and by human
serum albumin (HSA) challenge. PAGE pattern indicated no change in th
e electrophoretic behavior and the molecular size of insulin after the
labeling procedure. Biodistribution in rats shows that kidney took up
the maximum amount of Tc-99m-insulin; maxima being maintained through
out 24 h post-injection. Liver and intestine were the other organs wit
h significant uptake; the rest localizing little or negligible radioac
tivity. Most of the radioactivity was excreted via the renal pathway i
nto urine. Scintiimages conformed to the biodistribution data. The res
ults of this study present the potential of Tc-99m-labeling of insulin
by a simple method.