Quantitative analysis of erythromycin, its major metabolite and clarithromycin in chicken tissues and eggs via QuEChERS extraction coupled with ultrahigh-performance liquid chromatography-tandem mass spectrometry

被引:1
|
作者
Wang, Bo [1 ,2 ]
Zhu, Yali [3 ,4 ]
Liu, Shuyu [3 ,4 ]
Zhang, Han [5 ]
Guan, Tianzhu [1 ,2 ]
Xu, Xuechao [1 ,2 ]
Zheng, Xiangfeng [1 ,2 ]
Yang, Zhenquan [1 ,2 ]
Zhang, Tao [3 ,4 ]
Zhang, Genxi [3 ,4 ]
Xie, Kaizhou [3 ,4 ]
机构
[1] Yangzhou Univ, Coll Food Sci & Engn, Yangzhou 225127, Peoples R China
[2] Yangzhou Univ, Yangzhou Engn Res Ctr Food Intelligent Packaging &, Yangzhou 225127, Peoples R China
[3] Yangzhou Univ, Coll Anim Sci & Technol, Yangzhou 225009, Peoples R China
[4] Yangzhou Univ, Joint Int Res Lab Agr & Agriprod Safety, Yangzhou 225009, Peoples R China
[5] Jiangsu Agrianim Husb Vocat Coll, Sch Anim Sci & Technol, Taizhou 225300, Peoples R China
来源
FOOD CHEMISTRY-X | 2024年 / 22卷
基金
中国国家自然科学基金;
关键词
Erythromycin and its major metabolite; Clarithromycin; UHPLC-ESI-MS/MS; QuEChERS; Chicken tissues and eggs; MACROLIDE ANTIBIOTICS; RESIDUES; FOOD; MILK; MEAT;
D O I
10.1016/j.fochx.2024.101468
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A simple, rapid and novel method involving ultrahigh-performance liquid chromatography-electrospray ionization tandem triple quadrupole mass spectrometry (UHPLC-ESI-MS/MS) was developed to simultaneously detect erythromycin, its major metabolite and clarithromycin in chicken tissues (muscle, liver and kidney) and eggs (whole egg, albumen and yolk). Samples were extracted using acetonitrile-water (80:20, v/v), and a Cleanert MAS-Q cartridge was used to perform quick, easy, cheap, effective, rugged, and safe (QuEChERS) purification. The average recoveries were 87.78-104.22 %, and the corresponding intraday and interday relative standard deviations were less than 7.10 %. The decision limits and detection capabilities of the chicken tissues and eggs were 2.15-105.21 mu g/kg and 2.26-110.42 mu g/kg, respectively. For chicken tissues and eggs, the limits of detection and limits of quantification were 0.5 mu g/kg and 2.0 mu g/kg, respectively. The proposed method was successfully employed to analyse real samples, demonstrating its applicability.
引用
收藏
页数:8
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