Determination of marker residue of Olaquindox in fish tissue by ultra performance liquid chromatography-tandem mass spectrometry

被引:30
|
作者
Zhang, Xiaojun [1 ,2 ]
Zheng, Bin [3 ]
Zhang, Hong [1 ]
Chen, Xuechang [2 ]
Mei, Guangming [2 ]
机构
[1] Zhejiang Gongshang Univ, Sch Food Sci & Biotechnol, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Marine Fisheries Res Inst, Fishery Environm & Aquat Prod Qual Supervising &, Zhoushan, Peoples R China
[3] Zhejiang Marine Dev Res Inst, Zhoushan, Peoples R China
关键词
Fish; Marker residue; Olaquindox; Ultra performance liquid-chromatography-tandem mass pectrometry; QUINOXALINE-2-CARBOXYLIC ACID; PORCINE LIVER; METHYL-3-QUINOXALINE-2-CARBOXYLIC ACID; CARBADOX; CONFIRMATION; ELECTROSPRAY; METABOLITES;
D O I
10.1002/jssc.201000722
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Methyl-3-quinoxaline-2-carboxylic acid (MQCA) is the last major remaining detectable metabolite of Olaquindox in animal tissue. A rapid, sensitive and specific ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method was developed for the detection and quantification of MQCA in fish tissue using deuterated quinoxaline-2-carboxylic acid (d(4)-QCA) as internal standard. Various parameters affecting sample preparation, LC separation and MS/MS detection were investigated, and the optimal conditions concerned were determined. Fish tissue samples were subject to hydrochloric acid hydrolysis followed by Oasis MAX solid-phase extraction clean-up; analysis was performed using UPLC coupled to electrospray MS/MS. The chromatographic separation was achieved in less than 5 min. The limit of detection and the limit of quantification were 0.1 and 0.25 ng/g, respectively. The average recoveries of MQCA, spiked at levels of 0.25-50.0 ng/g, were from 92.7 to 104.3%. The relative standard deviation values were < 6%. The validated method was successfully applied to analyze 60 batch samples collected from the local market.
引用
收藏
页码:469 / 474
页数:6
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