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Untargeted analysis of contaminants in river water samples: Comparison between two different sorbents for solid-phase extraction followed by liquid chromatography-high-resolution mass spectrometry determination
被引:6
作者:
Montone, Carmela Maria
[1
]
Moneta, Benedetta Giannelli
[1
]
Aita, Sara Elsa
[1
]
Aulenta, Federico
[2
]
Cavaliere, Chiara
[1
]
Cerrato, Andrea
[1
]
Fazi, Stefano
[2
]
Lagana, Aldo
[1
,3
]
Paolini, Valerio
[4
]
Petracchini, Francesco
[4
]
Piovesana, Susy
[1
]
Capriotti, Anna Laura
[1
]
机构:
[1] Sapienza Univ Rome, Dept Chem, Piazzale Aldo Moro 5, I-00185 Rome, Italy
[2] Natl Res Council CNR, Water Res Inst IRSA, Via Salaria Km 29-300, I-00015 Rome, Italy
[3] Univ Salento, CNR NANOTEC, Campus Ecotekne,Via Monteroni, I-73100 Lecce, Italy
[4] Natl Res Council Italy CNR IIA, Inst Atmospher Pollut Res, Via Salaria Km 29-300, I-00015 Rome, Italy
关键词:
Environmental contaminants;
Liquid chromatography;
High-resolution mass spectrometry;
River water samples;
Solid-phase extraction;
Oasis HLB;
Graphitized carbon black;
ANALYSIS EMERGING CONTAMINANTS;
PHARMACEUTICALS;
MATRICES;
ACIDS;
D O I:
10.1016/j.microc.2021.106979
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
In this work, an untargeted approach based on ultra-high performance liquid chromatography coupled to highresolution tandem mass spectrometry (UHPLC-HRMS/MS) was employed for the analysis of contaminants in surface water samples, possibly deriving from an ineffective removal by wastewater treatment plants or illicit release. First, solid-phase extraction (SPE) conditions for 30 target compounds were optimized for two different sorbents, namely the commercial Oasis HLB and graphitized carbon black (GCB), by Box-Behnken designs of experiments. Upon identification of optimal conditions, the two SPE materials yielded comparable extraction recoveries, ranging between 52 and 110% and 55-100% for Oasis HLB and GCB, respectively. Thereafter, river water samples collected in five locations near Rome (Italy) were extracted using both sorbents and then analyzed by UHPLC-HRMS/MS in both positive and negative electrospray (ESI) ion polarities. The retrieved raw data files were submitted to Compound Discoverer software and compound identification was tentatively assigned by matching their tandem mass spectra with the mzCloud mass spectral library and manual validation, resulting in a total of 241 identified compounds (211 and 40 in positive and negative ESI mode, respectively), mainly belonging to pharmaceuticals.
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页数:8
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