期刊
JOURNAL OF SEPARATION SCIENCE
卷 38, 期 21, 页码 3774-3780出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/jssc.201500497
关键词
High internal phase emulsion; Monoliths; Solid-phase extraction; Tetracycline antibiotics
资金
- National Natural Science Foundation of China [21265004, 21465008, 21065003]
- Natural Science Foundation from Guangxi Zhuang Autonomous Region [2014GXNSFAA118063, 2015GXNSFAA139024]
- project of high level innovation team and outstanding scholar in Guangxi colleges and universities
A polymerized high internal phase emulsion monolith was used as a novel sorbent for solid-phase extraction coupled with high-performance liquid chromatography and fluorescence detection for the determination of oxytetracycline, tetracycline, doxycycline, and chlorotetracycline in environmental water samples. The polymerized high internal phase emulsion monolithic column was prepared by the in situ polymerization of the continuous phase of a high internal phase emulsion containing glycidyl methacrylate, styrene, and divinylbenzene in pipette tips, and then functionalized with iminodiacetic acid. The resulting monolith exhibited highly interconnected porosity and large surface areas, making it an excellent candidate as an solid-phase extraction sorbent for the enrichment of trace tetracycline antibiotics. Several factors affecting the extraction performance of polymerized high internal phase emulsion monoliths, including the pH of sample solution, the eluting solvents, the sample loading flow rate and volume, were investigated, respectively. Under the optimized conditions, the mean recoveries of oxytetracycline, tetracycline, doxycycline, and chlorotetracycline spiked in pond and farm wastewater samples ranged from 78.1 to 119.3% with relative standard deviation less than 15%. The detection limits (S/N = 3) of the proposed method were in the range of 51-137 pg/mL. This study demonstrated that the monolithic polymerized high internal phase emulsion would be promising solid-phase extraction sorbents in the extraction and proconcentration of trace analytes from complex samples.
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