A liquid chromatographic (LC) method was developed for the quantitatio
n of furazolidone residues in shrimp muscle. The shrimp homogenate (1.
0 g) is extracted with acetonitrile, and the extract is taken to dryne
ss. The residue is dissolved in acetonitrile, and the solution is pass
ed through alumina and C18 cleanup columns. The eluate is taken to dry
ness and reconstituted in a suitable solvent for reversed-phase (C18)
LC with UV detection at 365 nm. Recoveries of furazolidone from shrimp
homogenates spiked from 5 to 80 ng/g ranged from 74.3 to 79.7%, and r
elative standard deviations (RSDs) were 5.0-8.9%. RSDs for incurred fu
razolidone quantitated at 5.9 and 9.2 ng/g were 6.6 and 7.6%, respecti
vely.