Development of a rapid method for the determination of antibiotic residues in honey using UPLC-ESI-MS/MS

被引:36
|
作者
Kivrak, Ibrahim [1 ,2 ]
Kivrak, Seyda [3 ]
Harmandar, Mansur [4 ]
机构
[1] Mugla Sitki Kocman Univ, Mugla Vocat Sch, Dept Chem & Chem Treatment Technol, Mugla, Turkey
[2] Mugla Sitki Kocman Univ, Res Lab Ctr, Food Anal Lab, Kotekli, Mugla, Turkey
[3] Mugla Sitki Kocman Univ, Dept Nutr & Dietet, Fac Hlth Sci, Kotekli, Mugla, Turkey
[4] Mugla Sitki Kocman Univ, Fac Sci, Dept Chem, Kotekli, Mugla, Turkey
来源
FOOD SCIENCE AND TECHNOLOGY | 2016年 / 36卷 / 01期
关键词
antibiotics; fast method; honey; UPLC-ESI-MS/MS; chloramphenicol; PERFORMANCE LIQUID-CHROMATOGRAPHY; MULTICLASS DETERMINATION; SULFONAMIDE RESIDUES; EXTRACTION; MS; LC; TETRACYCLINES; PESTICIDES;
D O I
10.1590/1678-457X.0037
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
An accurate, reliable and fast multianalyte/multiclass ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed and validated for the simultaneous analysis of 23 pharmaceuticals, belonging to different classes amphenicols, sulfonamides, tetracyclines, in honey samples. The method developed consists of ultrasonic extraction followed by UPLC-ESI-MS/MS with electrospray ionization in both positive mode and negative mode. The influence of the extraction solvents and mobile phase composition on the sensitivity of the method, and the optimum conditions for sample weight and extraction temperature in terms of analyte recovery were extensively studied. The identification of antibiotics is fulfilled by simultaneous use of chromatographic separation using an Acquity BEH C-18 (100 mm x 2.1 mm, 1.7 mu m) analytical column with a gradient elution of mobile phases and tandem mass spectrometry with an electrospray ionization. Finally, the method developed was applied to the determination of target analytes in honey samples obtained from the local markets and several beekeepers in Mugla, Turkey. Ultrasonic-extraction of pharmaceuticals from honey samples is a well-established technique by UPLC-ESI-MS/MS, the uniqueness of this study lies in the simultaneous determination of a remarkable number of compounds belonging to 23 drug at the sub-nanogram per kilogram level.
引用
收藏
页码:90 / 96
页数:7
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