Rapid determination of 134 pesticides in tea through multi-functional filter cleanup followed by UPLC-QTOF-MS

被引:22
|
作者
Meng, Xiaodi [1 ]
Song, Wei [1 ]
Xiao, Yu [1 ]
Zheng, Ping [1 ]
Cui, Chuanjian [1 ]
Gao, Wanjun [1 ]
Hou, Ruyan [1 ]
机构
[1] Anhui Key Lab Anal & Detect Food Safety, State Key Lab Tea Plant Biol & Utilizat Hefei Cus, Hefei 230022, Peoples R China
关键词
Pesticide; Tea; UPLC-QTOF-MS; QuEChERS; Multi-residue analysis; MULTIWALLED CARBON NANOTUBES; SAMPLE PREPARATION METHODS; SOLID-PHASE EXTRACTION; MULTI-RESIDUE ANALYSIS; LIQUID-CHROMATOGRAPHY; MASS-SPECTROMETRY; NEONICOTINOID INSECTICIDES; MULTIRESIDUE METHOD; QUECHERS; COMBINATION;
D O I
10.1016/j.foodchem.2021.130846
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Ensuring the safety of tea requires effective methods for the simultaneous analysis of pesticide residues in the product. A sensitive and reliable method to scan for 134 pesticide residues in tea was developed that employs a novel Multi-Functional Filter (MFF) based on d-SPE extraction and ultra-high-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry. The adsorption material was developed by porous polyvinylpolypyrrolidone (PVPP) for the removal of polyphenols. Acetonitrile extraction was passed through a syringe and then detected by UPLC-Q-TOF-MS. Method validation revealed satisfactory linearity with correlation coefficients higher than 0.985 for all pesticides. All limits of quantification were below 10 mu g/kg. The matrix effects of 133 of the pesticides were nearly negligible (<20%), except for Sebutylazine (=22%). The recoveries at two spiked levels (50, 100 mu g/kg) were 66.83-118.33%, and the Relative standard deviation (RSD) was lower than 20%, indicating accuracy and precision of the new method.
引用
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页数:12
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