Determination of halofuginone and amprolium in chicken muscle and egg by liquid chromatography

Citation
Y. Yamamoto et F. Kondo, Determination of halofuginone and amprolium in chicken muscle and egg by liquid chromatography, J AOAC INT, 84(1), 2001, pp. 43-46
Citations number
9
Categorie Soggetti
Agricultural Chemistry
Journal title
JOURNAL OF AOAC INTERNATIONAL
ISSN journal
10603271 → ACNP
Volume
84
Issue
1
Year of publication
2001
Pages
43 - 46
Database
ISI
SICI code
1060-3271(200101/02)84:1<43:DOHAAI>2.0.ZU;2-2
Abstract
A liquid chromatographic (LC) method was developed for simultaneous measure ment of halofuginone (HFN) and amprolium (APL) in chicken muscle and egg. H FN and APL were extracted from chicken muscle and egg with acetonitrile, In chicken egg, they were partially purified by solid-phase extraction (SPE) to separate them from impurities, The LC separation was performed on a 4.5 mm id x 250 mm TSK-gel ODS-80TM column using acetonitrile-McIlvaine buffer, pH 3.4, containing 0.01M sodium lauryl sulfate (42 + 58) as the mobile pha se, Ultraviolet detection of HFN and APL was performed at wavelengths of 24 2 and 255 nm, respectively, Recoveries of HFN and APL from chicken muscle s piked at 0.5 mug/g were 74.8 +/- 17.7 and 94.2 +/- 5.0%, respectively (mean a standard deviation [SD], n= 10), In chicken muscle, the lower limit of d etermination for both APL and HFN was 0.03 mug/g. Recoveries of HFN and APL from chicken egg spiked at 0.5 mug/g by a cleanup procedure using SPE were 54.6 +/- 3.4 and 85.0 +/- 2.4%, respectively (mean +/- SD, n = 5), In chic ken egg, the lower limit of determination for both APL and HFN was 0.04 mug /g.