wA HPLC method for the determination of lonidamine in serum and testis, sui
table for pharmacological studies in the rat and other mammals, has been de
veloped. Briefly, 0.5 mL of serum or about 0.2 g of testicular tissue were
extracted with ethyl acetate and evaporated to dryness under nitrogen. The
residue was redissolved in methanol and an aliquot was injected onto a C-18
column eluted with a mobile phase consisting of acetonitrile:water (51:49,
v/v), containing 0.1% trifluoroacetic acid. The eluate was monitored at 23
0 nm with a sensitivity of 0.05 AUFS. By this method, the pharmacokinetics
and the serum and testicular levels of the drug up to 120 h after the admin
istration of one single dose (100 mg/kg body weight) of lonidamine to Sprag
ue-Dawley rats have been studied. Results were highly variable, as previous
ly reported, but a very good Linear correlation was found between the serum
and the testicular levels, suggesting that, in the rat, and possibly in th
e human, testicular levels could be estimated based on the serum concentrat
ions. Copyright (C) 2001 John Wiley & Sons, Ltd.