曲斌,耿士伟,陆桂萍,蒋天梅,邵德佳,陈 蓉,郭良雪.新型QuEChERS方法结合液相色谱串联质谱法快速测定猪肝中-受体激动剂残留[J].食品安全质量检测学报,2015,6(12):4747-4754
新型QuEChERS方法结合液相色谱串联质谱法快速测定猪肝中-受体激动剂残留
Rapid determination of -agonists residuals in pig liver by liquid chromatography- tandem mass spectrometry combined with novel QuEChERS method
投稿时间:2015-11-09  修订日期:2015-12-03
DOI:
中文关键词:  -受体激动剂  残留  QuEChERS  液相色谱串联质谱法
英文关键词:-agonists  residuals  QuEChERS  liquid chromatography-tandem mass spectrometry
基金项目:江苏省自然科学基金青年基金项目(BK20130644)、江苏省第四期“333工程”科研资助项目、国家留学基金委青年骨干教师出国研修项目(CSC201407060048)、中央高校基本科研业务费项目(JKQZ2013006)
作者单位
曲斌 江苏省畜产品质量检验测试中心 
耿士伟 江苏省畜产品质量检验测试中心 
陆桂萍 江苏省畜产品质量检验测试中心 
蒋天梅 江苏省畜产品质量检验测试中心 
邵德佳 江苏省畜产品质量检验测试中心 
陈 蓉 中国药科大学理学院 
郭良雪 安捷伦科技(中国)有限公司 
AuthorInstitution
QU Bin Jiangsu Quality Inspection and Testing Center for Animal Products 
GENG Shi-Wei Jiangsu Quality Inspection and Testing Center for Animal Products 
LU Gui-Ping Jiangsu Quality Inspection and Testing Center for Animal Products 
JIANG Tian-Mei Jiangsu Quality Inspection and Testing Center for Animal Products 
SHAO De-Jia Jiangsu Quality Inspection and Testing Center for Animal Products 
CHEN Rong School of Sciences, China Pharmaceutical University 
GUO Liang-Xue Agilent Technologies (China) Co., Ltd. 
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中文摘要:
      目的 建立一种基于新型QuEChERS材料测定猪肝中?-受体激动剂的方法。方法 猪肝样品经酶解、酸化乙腈提取后, 提取液用增强基质去脂质材料(EMR-lipid)脱脂, 盐析浓缩后经液相色谱质谱联用仪测定, 稳定同位素内标法定量。结果 19种?-受体激动剂在0.5~10.0 ?g/kg范围内线性关系良好, 高、中、低浓度日内、日间精密度小于20%, 回收率在60%~120%之间。结论 本方法简便快速, 适宜于大批量样品的快速筛选和定量分析。
英文摘要:
      Objective To develop a method to determine the ?-agonists residuals in pig liver based on a novel QuEChERS material. Methods The sample of pig liver was enzymatic hydrolysis and extracted by aci-dified acetonitrile. The extraction was cleaned-up by enhanced matrix removal (EMR-lipid) material. After polished and salted out, the analytes were detected by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Stable isotopes were used as internal standard. Results Nineteen ?-agonists were detected at the range between 0.5 ?g/kg and 10.0 ?g/kg with good linearity. The intra- and inter-precision were lower than 20%, and the recoveries were between 60% and 120% with high, medium and low concentrations. Conclusions The method is simple, rapid and effective, and it is suitable for rapid screening and quantitative analysis of large scale samples.
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