Simultaneous determination of kasugamycin and validamycin-A residues in cereals by consecutive solid-phase extraction combined with liquid chromatography-tandem mass spectrometry

被引:5
|
作者
Zhang, Hong [1 ,2 ]
Wang, Chenchen [1 ,2 ]
Li, Huidong [1 ,2 ]
Nie, Yan [1 ,2 ]
Fang, Liping [1 ,2 ]
Chen, Zilei [1 ,2 ]
机构
[1] Shandong Acad Agr Sci, Inst Qual Stand & Testing Technol Agroprod, Jinan 250100, Shandong, Peoples R China
[2] Inst Qual Stand & Testing Technol Agroprod, Shandong Prov Key Lab Testing Technol Food Qual &, Jinan, Shandong, Peoples R China
关键词
Kasugamycin; validamycin-A; residue; cereals; high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS; MS); ANTIBIOTIC FUNGICIDE KASUGAMYCIN; FORMULATED PRODUCTS; STREPTOMYCIN; MILK;
D O I
10.1080/19440049.2017.1411615
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Two polar aminoglycosides, kasugamycin and validamycin-A, were determined in cereals (brown rice, wheat and corn) by high-performance liquid chromatography-tandem mass spectrometry. The analytes were extracted from samples using methanol and water (70:30, v/v) at pH 5.5, purified using both a hydrophilic-hydrophobic-balanced cartridge and a strong cation-exchange cartridge, and then analysed using multiple reaction monitoring in positive electrospray ionisation mode with a special ReproSil 100 C-18 high-performance liquid chromatography column. This newly proposed method yielded good sensitivity and excellent chromatographic performance. The limits of quantification for kasugamycin and validamycin-A were 4.1 mu g/kg and 1.0 mu g/kg, respectively. The recoveries for both compounds at three fortification levels (4, 100 and 500 mu g/kg for kasugamycin; 1, 10 and 100 mu g/kg for validamycin-A) ranged from 75% to 110%, and the relative standard deviations were below 15%.
引用
收藏
页码:487 / 497
页数:11
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