共 25 条
Determination of multi-class pharmaceuticals in wastewater by liquid chromatography-tandem mass spectrometry (LC-MS-MS)
被引:78
作者:
Babic, Sandra
[1
]
Pavlovic, Dragana Mutavdzic
[1
]
Aperger, Danijela
[1
]
Perisa, Martina
[1
]
Zrncic, Mirta
[1
]
Horvat, Alka J. M.
[1
]
Kastelan-Macan, Marija
[1
]
机构:
[1] Univ Zagreb, Dept Analyt Chem, Fac Chem Engn & Technol, Zagreb 10000, Croatia
关键词:
Pharmaceuticals;
Wastewater;
Liquid chromatography-tandem mass spectrometry;
Solid phase extraction;
SOLID-PHASE EXTRACTION;
SAMPLE PREPARATION;
FATE;
TRIMETHOPRIM;
SULFONAMIDE;
EFFLUENT;
RESIDUES;
SURFACE;
D O I:
10.1007/s00216-010-4004-1
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
An analytical method for multi-class pharmaceuticals determination in wastewater has been developed and validated. Target compounds were: sulfonamides (sulfadiazine, sulfaguanidine, sulfamethazine, sulfamethoxazole), fluoroquinolones (ciprofloxacin, enrofloxacin, norfloxacin), diaminopyrimidine (trimethoprim), anaesthetic (procaine), anthelmintic (praziquantel and febantel), and macrolide (roxithromycin). The method involves pre-concentration and clean-up by solid-phase extraction (SPE) using Strata-X extraction cartridges at pH 4.0. Target analytes were identified and quantitatively determined by liquid chromatography-tandem mass spectrometry using multiple reaction monitoring (MRM). Recoveries were higher than 50% with relative standard deviation (RSD) below 18.3% for three concentrations. Only for sulfaguanidine was low recovery obtained. Matrix effect was evaluated using matrix-matched standards. The method detection limit (MDL) was between 0.5 and 5 ng L-1 in spiked water samples. The precision of the method, calculated as relative standard deviation, ranged from 0.5 to 2.0% and from 1.4 to 8.3 for intra-day and inter-day analysis, respectively. The described analytical method was used for determination of pharmaceuticals in effluent wastewaters from the pharmaceutical industry.
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页码:1185 / 1194
页数:10
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