Generic and rapid determination of veterinary drug residues and other contaminants in raw milk by ultra performance liquid chromatography-tandem mass spectrometry

被引:76
作者
Zhan, Jia [1 ,2 ]
Yu, Xue-jun [2 ]
Zhong, Ying-ying [2 ]
Zhang, Zai-ting [2 ]
Cui, Xiao-mei [2 ]
Peng, Jin-feng [2 ]
Feng, Rui [2 ]
Liu, Xiao-tao [3 ]
Zhu, Yan [1 ]
机构
[1] Zhejiang Univ, Dept Chem, Hangzhou 310028, Zhejiang, Peoples R China
[2] Ningbo Entry Exit Inspect & Quarantine Bur PR Chi, Ningbo 315012, Zhejiang, Peoples R China
[3] Ningbo Dairy Grp Co Ltd, Ningbo 315012, Zhejiang, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2012年 / 906卷
关键词
Generic; Multi-class; Veterinary drug; Contaminant; Ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS); Raw milk; SAMPLE PREPARATION; MULTICLASS METHOD; LC-MS/MS; QUANTIFICATION; ANTIBIOTICS; VALIDATION; PESTICIDES; MYCOTOXINS; EXTRACTION; FEED;
D O I
10.1016/j.jchromb.2012.08.018
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A generic, rapid and simple analytical method able to identify 255 veterinary drug residues and other contaminants in raw milk had been developed. The method was based on two-step simple precipitation and ultra performance liquid chromatography coupled with electrospray ionization and tandem mass spectrometry (UPLC-ESI-MS/MS) operating both in positive and negative multiple reaction mode (MRM). For most of the target analytes, the optimized pretreatment processes led to no significant interference on analysis from complicated sample matrix. For quantification, matrix-fortified calibration curves were performed to compensate for the matrix effect and loss in sample preparation. Competent linearity was found for over 90% of target compounds with linear regression coefficients (R) higher than 0.99. Detection limits ranged from 0.05 to 10 mu g/kg. Average recoveries spiked into raw milk were in the range from 63% to 141% with associated RSD values from 1% to 29% under the selected conditions. The method had been validated for its extraction sensitivity, linearity, recoveries and precision. The results clearly demonstrated the feasibility of the approach proposed. Application of this method, which improved efficiency and coverage of residues, would imply a drastic reduction of both effort and time in routine monitoring programs. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:48 / 57
页数:10
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