M. Horie et al., SIMULTANEOUS DETERMINATION OF BENOFLOXACIN, DANOFLOXACIN, ENROFLOXACIN AND OFLOXACIN IN CHICKEN TISSUES BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY, Journal of chromatography B. Biomedical applications, 653(1), 1994, pp. 69-76
Citations number
22
Categorie Soggetti
Chemistry Analytical
Journal title
Journal of chromatography B. Biomedical applications
A simple, rapid and reliable high-performance liquid chromatographic (
HPLC) method for the simultaneous determination of residual fluoroquin
olones (benofloxacin, danofloxacin, enrofloxacin and ofloxacin) in chi
cken has been developed. The drugs were extracted with 0.2% metaphosph
oric acid-acetonitrile (7:3, v/v), followed by a Bond Elut C18 clean-u
p procedure. The HPLC separation was carried out on a Wakosil II 5C18-
HG column (150 x 4.6 mm I.D.) with 0.05 M phosphate buffer (pH 2.4)-ac
etonitrile (80:20, v/v) containing 2.5 mM 1-heptanesulfonic acid as th
e mobile phase. A fluorescence detector was used at an excitation wave
length of 295 nm and an emission wavelength of 455 nm. The calibration
graphs were linear from 0.1 to 10 ng for danofloxacin and from 1 to 1
00 ng for benofloxacin, enrofloxacin and ofloxacin. The recoveries of
the drugs from tissues fortified at a level of 0.2 mug/g were 81.1-89.
6%, and the detection limits were 0.01 mug/g for ofloxacin, danofloxac
in and enrofloxacin and 0.02 mug/g for benofloxacin. The time needed p
er sample was less than 60 min.