李 丹,吴翠玲,张聪聪,张玉洁,沈 昕,朱馨乐,李 倩,王鹤佳.亲水作用色谱柱-高效液相色谱法测定鸡蛋中氨丙啉的残留量[J].食品安全质量检测学报,2019,10(17):5648-5652
亲水作用色谱柱-高效液相色谱法测定鸡蛋中氨丙啉的残留量
Determination of amprolium residues in egg by hydrop interaction liquid chromatography column-high performance liquid chromatography
投稿时间:2019-06-12  修订日期:2019-07-24
DOI:
中文关键词:  亲水作用色谱柱-高效液相色谱法  氨丙啉  残留  鸡蛋
英文关键词:hydrop interaction liquid chromatography column-high performance liquid chromatography  amprolium  residues  egg
基金项目:2018年农业农村部农业行业标准制修订项目(2018-58)
作者单位
李 丹 中国兽医药品监察所, 国家兽药残留基准实验室 
吴翠玲 安捷伦科技(中国)有限公司 
张聪聪 安捷伦科技(中国)有限公司 
张玉洁 中国兽医药品监察所, 国家兽药残留基准实验室 
沈 昕 中国兽医药品监察所, 国家兽药残留基准实验室 
朱馨乐 中国兽医药品监察所, 国家兽药残留基准实验室 
李 倩 中国兽医药品监察所, 国家兽药残留基准实验室 
王鹤佳 中国兽医药品监察所, 国家兽药残留基准实验室 
AuthorInstitution
LI Dan Reference Laboratory for the Test of Veterinary Drug Residues, China Institute of Veterinary Drug Control 
WU Cui-Ling Agilent Technologies (China) Co., Ltd 
ZHANG Cong-Cong Agilent Technologies (China) Co., Ltd 
ZHANG Yu-Jie Reference Laboratory for the Test of Veterinary Drug Residues, China Institute of Veterinary Drug Control 
SHEN Xin Reference Laboratory for the Test of Veterinary Drug Residues, China Institute of Veterinary Drug Control 
ZHU Xin-Le Reference Laboratory for the Test of Veterinary Drug Residues, China Institute of Veterinary Drug Control 
LI Qian Reference Laboratory for the Test of Veterinary Drug Residues, China Institute of Veterinary Drug Control 
WANG He-Jia Reference Laboratory for the Test of Veterinary Drug Residues, China Institute of Veterinary Drug Control 
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中文摘要:
      目的 建立亲水作用色谱柱-高效液相色谱法检测鸡蛋中氨丙啉残留的分析方法。方法 样品加入10 mL 5%三氯乙酸水溶液进行提取, 离心后取一半上清液过HLB柱净化。色谱柱为Poroshell 120 HILIC-Z (100 mm ×3.0 mm, 2.7 μm), 流动相为5 mmol/L乙酸铵-0.1%甲酸水溶液和乙腈, 等度洗脱, 5 mmol/L乙酸铵-0.1%甲酸水溶液:乙腈=20:80(V:V), 流速为0.4 mL/min, 进样量为20 μL, 检测波长267 nm。 结果 氨丙啉在0.35~10.0 μg/mL呈良好的线性关系, r大于0.999。方法的最低定量限为250 μg/kg。氨丙啉在250~2000 μg/kg的浓度添加水平上, 其回收率在85.0%~96.7%, 批内、批间的相对标准偏差小于6%。结论 该方法具有简便快捷、灵敏度高等特点, 适用于鸡蛋中氨丙啉的残留检测。
英文摘要:
      Objective To establish a method for determination of amprolium in egg by hydrop interaction liquid chromatography column- high performance liquid chromatography (HILIC-HPLC). Methods Amprolium was extracted with 10 mL 5% trichloroacetic acid, and the half of supernatant was purified with HLB column. The chromatography column was poroshell 120 HILIC-Z (100 mm×3.0 mm, 2.7 μm). The mobile phase was acetonitrile and 5 mmol/L ammonium acetate -0.1% formic acid water with equivalent elution, the flow rate was 0.4 mL/min, injection volume was 20 μL and detection wavelengths was 267 nm. Results Amprolium had good linear relationships in the range of 0.35?10.0 μg/mL (r2>0.999), and the limit of quantification of amprolium was 250 μg/kg. The average recoveries at 250?2000 μg/kg were 85.0%?96.7%. In day-between days batch variation coefficients were both less than 6%. Conclusion This method is simple, rapid, sensitive and accurate, which can be applied for the determination of amprolium in egg.
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