Determination of Seven Lincosamides and Macrolides Residues in Honeys by High Performance Liquid Chromatography-Tandem Mass Spectrometry with ZnO QuEChERS
|更新时间:2023-04-18
|
Determination of Seven Lincosamides and Macrolides Residues in Honeys by High Performance Liquid Chromatography-Tandem Mass Spectrometry with ZnO QuEChERS
杨明, 伊鋆, 陈丹, 王梦颖, 许晴, 田甜, 管卓龙, 侯靖, 周原, 刘坤, 王冬梅, 胡筱静, 卢跃鹏, 江小明, 涂凤琴. Determination of Seven Lincosamides and Macrolides Residues in Honeys by High Performance Liquid Chromatography-Tandem Mass Spectrometry with ZnO QuEChERS[J]. 2020, 39(8): 974-979.
DOI:
杨明, 伊鋆, 陈丹, 王梦颖, 许晴, 田甜, 管卓龙, 侯靖, 周原, 刘坤, 王冬梅, 胡筱静, 卢跃鹏, 江小明, 涂凤琴. Determination of Seven Lincosamides and Macrolides Residues in Honeys by High Performance Liquid Chromatography-Tandem Mass Spectrometry with ZnO QuEChERS[J]. 2020, 39(8): 974-979.DOI: doi:10.3969/j.issn.1004-4957.2020.08.005.
Determination of Seven Lincosamides and Macrolides Residues in Honeys by High Performance Liquid Chromatography-Tandem Mass Spectrometry with ZnO QuEChERS
A rapid analytical method for the simultaneous determination of 7 lincosamides and macrolides residues in honeys was developed by high performance liquid chromatography-tandem mass spectrometry(HPLC-MS/MS).The samples were dissolved with phosphate buffer(pH 8.0)
then extracted with 1% ammonia acetonitrile and salted out with anhydrous sodium sulfate.The extract was cleaned up with 80 mg ZnO and 20 mg PSA.The target compounds were separated on a Waters XBridge C18(150 mm×2.1 mm,5 μm) column with 0.1% formic acid solution and acetonitrile as mobile phases
then determined with electrospray ionization source in positive ion mode under multiple reaction monitoring(MRM) acquisition mode
and quantified by external standard method using matrix matched standard solution.Results showed that the 7 target compounds showed good linearity in their respective mass concentration ranges with correlation coefficients(r) not less than 0.999 3.The limits of detection of the method were in the range of 0.21-0.35 μg/kg
while the limits of quantitation were 0.69-1.16 μg/kg.At three spiked levels of 5.0
10.0 and 20.0 μg/kg
the average recoveries for 7 target compounds were in the range of 75.5%-99.0% with relative standard deviations of 0.78%-5.9%.The method could be applied to the rapid determination of 7 lincosamides and macrolides residues in honeys with the advantages of simplicity
Determination of Acrylamide in Honey Samples by Modified QuEChERS/Ultra High Performance Liquid Chromatography-Tandem Mass Spectrometry
Determination of 11 Phenoxy Acid Herbicides in Infant Cereal Food by High Performance Liquid Chromatography-Tandem Mass Spectrometry
Determination of 61 Hormone Residues in Soil by QuEChERS/High Performance Liquid Chromatography-Tandem Mass Spectrometry
Determination of 11 Doping Agents in Soft Capsule-type Chinese Patent Medicines by QuEChERS/Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry
Comparison of Performance and Applicability Analysis of μ-FTIR and Py-GC-MS for the Detection of Microplastics in Airborne Dust
Related Author
ZHANG Lin-yun
JI Wen-liang
SHEN Fei
WANG Xin-nan
ZHONG Cheng
ZHU Feng
王可
曹倩玉
Related Institution
Jiangsu Provincial Center for Disease Prevention and Control
Waters Corporation
石家庄市疾病预防控制中心理化检验所
辽宁省分析科学研究院
School of Investigation,People's Public Security University of China