Study and comparison of polydopamine and its derived carbon decorated nanoparticles in the magnetic solid-phase extraction of estrogens

被引:45
作者
Huang, Zhenzhen [1 ]
Lee, Hian Kee [1 ,2 ]
机构
[1] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
[2] Natl Univ Singapore, Environm Res Inst, Singapore 117411, Singapore
基金
新加坡国家研究基金会;
关键词
Magnetic solid-phase extraction; Polydopamine; Carbon; Estrogens; High-performance liquid chromatography coupled with ultraviolet/fluorescence detection; POLYCYCLIC AROMATIC-HYDROCARBONS; LIQUID-LIQUID MICROEXTRACTION; MOLECULARLY IMPRINTED POLYMER; COATED FE3O4 NANOPARTICLES; ORTHOGONAL ARRAY DESIGN; ENVIRONMENTAL WATER; MICROWAVE DISSOLUTION; SELECTIVE EXTRACTION; SORPTIVE EXTRACTION; SYNTHETIC ESTROGENS;
D O I
10.1016/j.chroma.2015.08.039
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Surface functionalization enabled by bioinspired polydopamine (FDA) is recognized as a convenient route for fabrication of multifunctional nanoparticles. In the present work, magnetic nanoparticles with polymer (Fe3O4@PDA) and carbon shell (Fe3O4@C) were prepared by self-oxidation of dopamine, and carbonization of the PDA coating. The performance of the two magnetic sorbents in the extraction and determination of four estrogens, estrone (E1), estradiol (E2), estriol (E3) and diethylstilbestrol (DES) from water samples in the form of magnetic solid-phase extraction was investigated. Orthogonal array design was utilized to facilitate the optimization of the proposed sample preparation approach. The highest extraction capabilities of the two sorbents were achieved under different experimental conditions. Fe3O4@PDA was shown to be superior to Fe3O4@C in the enrichment of estrogens, suggesting stronger interactions were established between the FDA coating and the target compounds. The extraction and desorption operations were enabled more conveniently by magnetic separation and the extracts were analyzed by high-performance liquid chromatography coupled with ultraviolet and fluorescence detection. The limits of detection achieved in the proposed method were in the range of 0.072-0.15 ng/mL for El and DES, and 0.0017-0.0062 ng/mL for E2 and E3. Good precision (>0.9995) was obtained with the linearity ranging from 0.2 to 100 ng/mL, and from 0.01 to 5 ng/mL. The method developed was assessed by analysis of the estrogens in tap water, drain water and bottled mineral water samples. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:41 / 50
页数:10
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