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Fully-automated SPE coupled to UHPLC-MS/MS method for multiresidue analysis of 26 trace antibiotics in environmental waters: SPE optimization and method validation

文献类型： 外文期刊

作者： Zheng, Ming 1 ; Tang, Suwen 1 ; Bao, Yangyang 2 ; Daniels, Kevin D. 3 ; How, Zuo Tong 4 ; El-Din, Mohamed Gamal 4 ; Wa 1 ;

作者机构： 1.Shanghai Univ, Sch Environm & Chem Engn, Key Lab Organ Compound Pollut Control Engn, Shanghai 200444, Peoples R China

2.Pudong New Area Environm Monitoring Stn, 51 Lingshan Rd Pudong New Area, Shanghai, Peoples R China

3.Hazen & Sawyer, 1400 E Southern Ave, Tempe, AZ 85282 USA

4.Univ Alberta, Dept Civil & Environm Engn, Edmonton, AB T6G 1H9, Canada

5.Chinese Acad Fishery Sci, Fishery Machinery & Instrument Res Inst, Shanghai, Peoples R China

关键词： SPE optimization; UHPLC-MS; MS; Environmental water samples; Sulfonamide; quinolone, and macrolide antibiotics; Validation

期刊名称：ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH （ 影响因子：4.223； 五年影响因子：4.306 ）

ISSN： 0944-1344

年卷期：

页码：

收录情况： SCI

摘要： Achieving simultaneous determination of antibiotic multiresidues in environmental waters by solid phase extraction (SPE) coupled with ultra-high-performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS) with detection limits <= ng L-1 is still a huge challenge. Moreover, the offline SPE procedure was performed manually, costly, and time-consuming, while the online SPE required precision pretreatment instruments that require highly-skilled personnel. In this paper, a fully automated SPE coupled with UHPLC-MS/MS method was developed for analysis of antibiotics (sulfonamides, quinolones, and macrolides) in water matrices. Sample preparation optimization included SPE materials and configuration (HLB disks), sample volume (500-1000 mL), and pH (pH = 3) with a flow rate at 2 similar to 5 mL min(-1), and an elution procedure with 2 x 6 mL methanol, and 2 x 6 mL acetone. Meanwhile, the parameters for UHPLC-MS/S detection of analytes were optimized, including LC retention time, and MS parameters. The instrumental limits of detection (LOD) and quantification (LOQ) of analytes ranged from 0.01-0.72 mu g L-1 and 0.05-2.39 mu g L-1, respectively, with satisfactory linear calibration (R-2 > 0.995) and precision (< 9.9%). Recoveries in spike samples ranged between 77.5-104.9% in pure water, 59.4-97.8% in surface water (SW), and 58.2-108.6% in wastewater effluent (WWE) with relative standard deviations <= 12.8%. The matrix effects observed for most analytes were suppression (0-28.1%) except for five analytes having presented enhancement (0-14.6 %) in SW or WWE. This method can basically meet the needs of trace antibiotic residues detection in waters, with examples of concentrations of detected antibiotics being lower than LOQ (LLQ) -94.47 ng L-1 in WWEs and LLQ-15.47 ng L-1 in SW in the lower reaches of the Yangtze River Basin.

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