Simultaneous analysis of multiclass antibiotic residues in complex environmental matrices by liquid chromatography with tandem quadrupole mass spectrometry

被引:30
|
作者
Rashid, Azhar [1 ,2 ]
Mazhar, Sohaib H. [3 ]
Zeng, Qiaoting [1 ]
Kiki, Claude [1 ,4 ]
Yu, Chang-Ping [1 ,5 ]
Sun, Qian [1 ]
机构
[1] Chinese Acad Sci, Inst Urban Environm, CAS Key Lab Urban Pollutant Convers, Xiamen 361021, Peoples R China
[2] Nucl Inst Food & Agr PAEC, Peshawar 25000, Pakistan
[3] Fujian Agr & Forestry Univ, Coll Resources & Environm, Inst Environm Microbiol, Fuzhou, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100043, Peoples R China
[5] Natl Taiwan Univ, Grad Inst Environm Engn, Taipei 106, Taiwan
基金
中国国家自然科学基金;
关键词
Sediments; Antibiotics; Extraction; Cleanup; Complex solid matrices; Liquid chromatography tandem mass spectrometry; SOLID-PHASE EXTRACTION; PERSONAL CARE PRODUCTS; VETERINARY ANTIBIOTICS; MODIFIED QUECHERS; BROILER MANURE; SEWAGE-SLUDGE; SOIL; PHARMACEUTICALS; SEDIMENTS; CITY;
D O I
10.1016/j.jchromb.2020.122103
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simultaneous extraction and cleanup method was optimized and validated for the determination of 40 antibiotics from cephalosporin, fluoroquinolone, lincosamide, macrolide, nitroimidazole, quinolone, sulfonamide and tetracycline groups in sediments by liquid chromatography with tandem quadrupole mass spectrometry (LC-MS/MS). The method involved hydration of freeze-dried sediment sample (2.0 g) with 2.5 ml of 0.1 M Na-EDTA Mcllvaine buffer and extraction with 5 ml of MeOH and MeCN (1:3 v/v) followed by dispersive solid phase extraction by using 100 mg mix of C18 and PSA (1:2 w/w) and 50 mg MgSO4 prior to LC-MS/MS analysis. The method was validated for 10, 20, 50 and 100 mu g/kg spiking levels by using blank sediment sample obtained from a drinking water reservoir according to the guidelines of European Commission Decision (2002) 2002/657/EC. The method produced clean extracts with generally low matrix effect during LC-MS/MS analysis. The mean recoveries ranged between 24-162%, 48-151%, 51-159%, and 50-149% for 10, 20, 50 and 100 mu g/kg spiking levels, respectively, with acceptable precision. The analytical method was sensitive enough to achieve 0.01-34.3 mu g/kg and 0.03-115 mu g/kg limits of detection and quantitation, respectively. The scope of the method was demonstrated by analyzing complex solid environmental matrices (chicken manure, swine manure, poultry feed and soil) spiked at 10, 20, 50 and 100 mu g/kg levels. The method was also applied for the antibiotic analysis in samples with incurred residues. Different matrices in the order of the magnitude as sediments < poultry feed < swine manure < soil < chicken manure were detected with the residues of fluoroquinolone, macrolide, sulfonamide and tetracycline antibiotics.
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页数:15
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