L. Kumar et al., DETERMINATION OF NITROFURAN RESIDUES IN POULTRY MUSCLE TISSUES AND EGGS BY LIQUID-CHROMATOGRAPHY, Journal of AOAC International, 77(3), 1994, pp. 591-595
A liquid chromatographic (LC) method was developed and statistically v
alidated for the determination of nitrofurazone, furazolidone, and fur
altadone residues in poultry and porcine muscle tissues. The antimicro
bial residues were extracted with a mixture of dichloromethane and eth
yl acetate by using ultrasonication followed by solid-phase extraction
cleanup and LC analysis with UV detection. A modification of the meth
od incorporating acetonitrile extraction and solvent partition cleanup
was developed for analysis of poultry eggs. The limits of detection w
ere 1 mug/kg for nitrofurazone and furazolidone and 2 mug/kg for fural
tadone in both muscle tissues and eggs. Average recoveries for spike l
evels of 1, 2, and 5 mug/kg ranged from 84 to 128%, and coefficients o
f variation were between 1.1 and 12.1%. A field trial with these metho
ds was conducted in conjunction with the Western Australian Department
of Agriculture to determine the stability of furaltadone in both poul
try tissue and eggs. Results of this study show that the concentration
of furaltadone in muscle tissue diminished rapidly even when stored a
t -18-degrees-C. Furaltadone was considerably more stable in eggs.