Simultaneous determination of thirty non-steroidal anti-inflammatory drug residues in swine muscle by ultra-high-performance liquid chromatography with tandem mass spectrometry

被引:56
作者
Hu, Ting [2 ]
Peng, Tao [1 ]
Li, Xiao-Juan [1 ]
Chen, Dong-Dong [1 ]
Dai, Han-Hui [1 ]
Deng, Xiao-Jun [3 ]
Yue, Zhen-Feng [4 ]
Wang, Guo-Min [5 ]
Shen, Jian-Zhong [2 ]
Xia, Xi [2 ]
Ding, Shuang-Yang [2 ]
Zhou, Yue-Ning [6 ]
Zhu, Ai-Ling [2 ]
Jiang, Hai-Yang [2 ]
机构
[1] Chinese Acad Inspect & Quarantine, Beijing 100123, Peoples R China
[2] China Agr Univ, Coll Vet Med, Beijing 100193, Peoples R China
[3] Shanghai Entry Exit Inspect & Quarantine Bur, Shanghai 200135, Peoples R China
[4] Shenzhen Entry Exit Inspect & Quarantine Bur, Shenzhen 518045, Peoples R China
[5] Chongqing Entry Exit Inspect & Quarantine Bur, Chongqing 400020, Peoples R China
[6] Shanxi Univ, Coll Chem & Chem Engn, Taiyuan 030006, Peoples R China
关键词
Ultra-high-performance liquid chromatography; Tandem mass spectrometry; Non-steroidal anti-inflammatory drugs; Multi-residue analysis; Swine muscle; HUMAN PLASMA; BOVINE-MILK; HUMAN URINE; FLUNIXIN; HPLC; PHENYLBUTAZONE; CONFIRMATION; NABUMETONE; EXTRACTION; ACID;
D O I
10.1016/j.chroma.2011.11.009
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An ultra-high-performance liquid chromatography with tandem mass spectrometric detection (UHPLC-MS/MS) method was established for the simultaneous determination of residues of thirty non-steroidal anti-inflammatory drugs (NSAIDs) in swine muscle. The samples were extracted with acetonitrile and phosphoric acid. The extracts were defatted with n-hexane, and then purified by HLB solid-phase extraction cartridge. Analysis was carried out on UHPLC-ESI-MS/MS working with multiple reaction monitoring mode with polarity switching. Limits of detection were between 0.4 mu g/kg and 2.0 mu g/kg, and limits of quantification were between 1.0 mu g/kg and 5.0 mu g/kg. The recoveries of NSAIDs were between 61.7% and 125.7% at spiked levels of 1.0-500 mu g/kg. The repeatability was less than 8% and the within-laboratory reproducibility was not more than 12.3%. The method was reliable, convenient and sensitive. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:104 / 113
页数:10
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