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高效液相色谱-串联质谱法检测鸡肉中9种化学合成类抗球虫药多残留
引用本文:施祖灏,张小燕,卜士金,陈大伟,蒲俊华,高玉时,唐修君.高效液相色谱-串联质谱法检测鸡肉中9种化学合成类抗球虫药多残留[J].色谱,2012,30(9):883-888.
作者姓名:施祖灏  张小燕  卜士金  陈大伟  蒲俊华  高玉时  唐修君
作者单位:1. 中国农业科学院家禽研究所 农业部家禽品质监督检验测试中心(扬州), 江苏 扬州 225125; 2. 扬州大学兽医学院, 江苏 扬州 225009
基金项目:国家科技支撑计划项目(2012BAD39B04-3);江苏省自然科学基金项目(BK2010299);扬州市社会发展项目(2008040)
摘    要:建立了鸡肉中氯羟吡啶、二硝托胺、4,4′-二硝基均二苯脲(尼卡巴嗪代谢物)、磺胺氯吡嗪、磺胺喹口恶啉、地克珠利、妥曲珠利、妥曲珠利砜和妥曲珠利亚砜9种化学合成类抗球虫药多残留的高效液相色谱-串联质谱分析方法。样品采用2%乙酸酸化的乙腈/二甲亚砜(4:1, v/v)提取,150 mg二甲基十八碳硅烷粉(octadecylsilyl, ODS)、100 mg石墨化炭黑(graphitized carbon black, GCB)和100 mg弗罗里硅土(Florisil)吸附剂分散固相萃取净化,经Hypersil GOLD C18色谱柱(150 mm×4.6 mm, 5 μm)分离,电喷雾串联四极杆质谱多反应离子监测方式测定。9种分析物在20~150 μg/kg范围内线性关系良好,相关系数均大于0.995。样品基质中9种分析物在20、50和150 μg/kg加标水平下,平均回收率为81.5%~103.6%,相对标准偏差为4.5%~14.5%。该方法稳定、可靠,可满足鸡肉中化学合成类抗球虫药多残留的检测与确证。

关 键 词:高效液相色谱-串联质谱  化学合成抗球虫药  多残留  鸡肉
收稿时间:2012-05-14

Simultaneous extraction and determination of nine chemically synthetic anticoccidial drug multi-residues in chicken meat using high performance liquid chromatographytandem mass spectrometry
SHI Zuhao,ZHANG Xiaoyan,BU Shijin,CHEN Dawei,PU Junhua,GAO Yushi,TANG Xiujun.Simultaneous extraction and determination of nine chemically synthetic anticoccidial drug multi-residues in chicken meat using high performance liquid chromatographytandem mass spectrometry[J].Chinese Journal of Chromatography,2012,30(9):883-888.
Authors:SHI Zuhao  ZHANG Xiaoyan  BU Shijin  CHEN Dawei  PU Junhua  GAO Yushi  TANG Xiujun
Institution:1. Poultry Institute, Chinese Academy of Agricultural Sciences/Supervision, Inspection and Testing Center of Poultry Quality, Ministry of Agriculture (Yangzhou), Yangzhou 225125, China; 2. College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China
Abstract:A high performance liquid chromatography-tandem mass spectrometric (HPLC-MS/MS) method was developed for the simultaneous extraction and determination of multi-residues of nine chemically synthetic anticoccidial drugs in chicken meat. Toltrazuril-D3 was used as the internal standard. The sample was extracted by 15 mL acetonitrile/dimethyl sulfoxide (4:1, v/v, containing 2% acetic acid), cleaned-up by a QuEChERS (quick, easy, cheap, effective, rugged and safe) clean-up tube with 150 mg octadecylsilyl (ODS), 100 mg Florisil and 100 mg graphitized carbon black (GCB). After the concentration, the extract was analyzed by HPLC-MS/MS. The results showed that good linearity in the range of 20~150 μg/L for each target compound. The recoveries were between 81.5% and 103.6% with the relative standard deviations lower than 15%. The method is simple, rapid, and suitable to detect the chemically synthetic anticoccidial drug residues with high throughput.
Keywords:high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS)  chemically synthetic anticoccidial drugs  multi-residues  chicken meat
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