Multiclass screening of >200 pharmaceutical and other residues in aquatic foods by ultrahigh-performance liquid chromatography-quadrupole-Orbitrap mass spectrometry

被引:35
作者
Kong, Cong [1 ]
Wang, Yang [1 ,2 ]
Huang, Yuanfei [1 ,2 ]
Yu, Huijuan [3 ]
机构
[1] Chinese Acad Fishery Sci, East China Sea Fisheries Res Inst, Key Lab East China Sea Fishery Resources Exploita, Minist Agr, Shanghai 200090, Peoples R China
[2] Shanghai Ocean Univ, Coll Food Sci & Technol, Shanghai 201306, Peoples R China
[3] Chinese Acad Fishery Sci, East China Sea Fisheries Res Inst, Key Lab Ocean & Polar Fisheries, Minist Agr, Shanghai 200090, Peoples R China
关键词
Veterinary drug; Aquatic food; Screening; Orbitrap; Pesticide; Contaminant residue; VETERINARY DRUG RESIDUES; TIME-OF-FLIGHT; FISH TISSUE; SAMPLE PREPARATION; TRIPLE QUADRUPOLE; PESTICIDES; MILK; VALIDATION; QUECHERS; IDENTIFICATION;
D O I
10.1007/s00216-018-1124-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A quick screening method of more than 200 pharmaceutical and other residues in aquatic foods based on ultrahigh-performance liquid chromatography-quadrupole-Orbitrap mass spectrometry (UHPLC-Q/Orbitrap MS) was established. In this method, after the addition of 200 mu L of 1 M EDTA-Na-2, 2 g of each sample homogenate was extracted successively with 10 mL of acetonitrile and 10 mL of ethyl acetate. The extracts were combined, dried under nitrogen flow, and redissolved in 0.1% formic acid in acetonitrile/water (4:6, v/v) for analysis. The prepared samples were analyzed by UHPLC- Q/Orbitrap MS system in Full MS/ddMS(2) (full-scan data-dependent MS/MS) mode. Compound identification was performed through comparison of the sample data with the database for standard chemicals, including the retention time, precursor ion, product ions, and isotope pattern for all 206 compounds. Five different aquatic food matrices (carp, shrimp, crab, eel, and mussel) spiked with the analytes at 1, 10, and 50 ng/g were evaluated to assess recoveries, precision, matrix effects, stability, and detection limits using the method. UHPLC analyses required 25 min, and 178-200 analytes met identification criteria at 50 ng/g depending on the matrix. Furthermore, practical application of this method for real samples displayed strong screening capability.
引用
收藏
页码:5545 / 5553
页数:9
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