Efficient HPLC method for the determination of nicarbazin, as dinitrocarbanilide in broiler liver

被引:14
作者
Capurro, E
Danaher, M [1 ]
Anastasio, A
Cortesi, ML
O'Keeffe, M
机构
[1] TEAGASC, Natl Food Ctr, Dublin 15, Ireland
[2] Univ Naples Federico II, Fac Vet Med, Inst Inspect Food Anim Origin, Naples, Italy
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2005年 / 822卷 / 1-2期
关键词
dinitrocarbanilide; nicarbazin; broiler liver; C18SPE; HPLC-UV;
D O I
10.1016/j.jchromb.2005.05.033
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simple, fast and reliable HPLC-UV method has been developed for the determination of dinitrocarbanilide residues in broiler liver. Liver samples (2 g) were extracted with two portions of acetonitrile (10 and 5 ml), defatted with hexane and evaporated to dryness under nitrogen. Extracts were reconstituted in acetonitrile-water (70/30, v/v, 500 mu l), loaded onto C Is solid phase (SPE) cartridges and eluted with acetonitrile-water (70/30, v/v, 2.5 ml) into clean test-tubes. Extracts were evaporated to dryness and reconstituted in acetonitrile-water (80/20, v/v, 500 mu l). An aliquot of the extract was assayed by high performance liquid chromatography (HPLC) with UV detection at 350 nm. The method was validated according to EU guidelines using liver tissues fortified at levels of 100, 200 and 300 mu g/kg, with dinitrocarbanilide. The decision limit (CC alpha) and the detection capability (CC beta) were calculated from the within laboratory repeatability data to be 228 and 266 mu gkg, respectively. The mean recovery was typically > 70% and the limits of quantitation was 12.5 mu g/kg (based on the lowest standard on the calibration curve). (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:154 / 159
页数:6
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