Jd. Macneil et al., CHLORTETRACYCLINE, OXYTETRACYCLINE, AND TETRACYCLINE IN EDIBLE ANIMAL-TISSUES, LIQUID-CHROMATOGRAPHIC METHOD - COLLABORATIVE STUDY, Journal of AOAC International, 79(2), 1996, pp. 405-417
Thirteen laboratories analyzed samples of edible animal tissues for te
tracycline residues, The method included extraction of analytes into b
uffer, elution from a C-18 solid-phase extraction (SPE) cartridge, and
reversed-phase liquid chromatographic (LC) analysis, including use of
a confirmation column, An additional laboratory, using an alternative
LC assay based on a different sample cleanup, also analyzed the sampl
es, Results showed the 2 methods are comparable, The LC method for det
ermination of cholortetracycline, oxytetracycline, and tetracycline in
edible animal tissues has been adopted by AOAC INTERNATIONAL, Results
from 13 laboratories indicate that the method under study provides ge
nerally better results at the higher concentrations tested than at con
centrations near the detection limit and that there is less problem wi
th interferences in muscle tissue than in kidney, The method can achie
ve reliable results for analytes and matrixes studied at concentration
s from 0.1 to 0.6 ppm and above, depending on the analyte-matrix combi
nation, with generally better performance to be expected with muscle t
han with kidney, The poorer performance for fortified samples, particu
larly kidney, was attributed to additional homogenization steps requir
ed to prepare these samples, Recovery of analytes from different lots
of solid-phase extraction (SPE) cartridges was an important variable.