Multi-residue analysis of veterinary drugs, pesticides and mycotoxins in dairy products by liquid chromatography-tandem mass spectrometry using low-temperature cleanup and solid phase extraction

被引:47
作者
Xie, Jie [1 ]
Peng, Tao [2 ]
Zhu, Ailing [1 ]
He, Jianli [3 ]
Chang, Qiaoying [2 ]
Hu, Xueyan [2 ]
Chen, Hui [2 ]
Fan, Chunlin [2 ]
Jiang, Wenxiao [4 ,5 ]
Chen, Min [1 ]
Li, Jiancheng [1 ]
Ding, Shuangyang [1 ]
Jiang, Haiyang [1 ]
机构
[1] China Agr Univ, Dept Vet Pharmacol & Toxicol, Coll Vet Med, Beijing 100193, Peoples R China
[2] Chinese Acad Inspect & Quarantine, Beijing 100176, Peoples R China
[3] Tianjin Agr Univ, Coll Anim Sci & Vet Med, Tianjin 300384, Peoples R China
[4] Shenzhen Univ, Engn Lab Synthet Biol, Shenzhen 518060, Peoples R China
[5] Shenzhen Univ, Key Lab Biomed Engn, Sch Med, Shenzhen 518060, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2015年 / 1002卷
关键词
Veterinary drugs; Pesticides; Mycotoxins; LC-MS/MS; Low-temperature cleanup; Dairy products; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; FREEZING-LIPID FILTRATION; RAPID-DETERMINATION; SOLVENT-EXTRACTION; BOVINE MUSCLE; MILK SAMPLES; CONTAMINANTS; TISSUES; FISH; PURIFICATION;
D O I
10.1016/j.jchromb.2015.08.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A multi-class multi-residue analysis method for determination of veterinary drugs, pesticides and mycotoxins in dairy products by liquid chromatography-tandem mass spectrometry (LC-MS/MS) has been established. These 17 classes, a total of 40 kinds of target compounds were chosen because their administration to food-producing animals is banned or regulated in China and may be potentially abused or misused. Samples were extracted with acetonitrile-ethyl acetate-acetic acid (49.5 + 49.5 + 1, v/v/v). Most of lipids in the extract were removed by low-temperature cleanup, prior to solid phase extraction on HLB cartridges. The quantification and confirmation of the 40 analytes were performed by LC-MS/MS with electro-spray ionization (ESI) interface in multiple reaction monitoring (MRM) mode. The limits of detection (LODs) and limits of quantification (LOQs) were 0.006-0.3 mu g/kg and 0.02-1.0 mu g/kg, respectively. The spiked recoveries in milk, yogurt, milk powder and cheese samples were from 67.3% to 106.9%. The repeatability and the within-laboratory reproducibility were less than 12.7% and 13.9%. Applying this method, our results revealed the presences of chloramphenicol, cimeterol, and flunixin at the concentration of 0.027-0.452 mu g/kg in some samples. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:19 / 29
页数:11
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