4.6 Article

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

期刊

JOURNAL OF CHROMATOGRAPHY A
卷 1414, 期 -, 页码 41-50

出版社

ELSEVIER
DOI: 10.1016/j.chroma.2015.08.039

关键词

Magnetic solid-phase extraction; Polydopamine; Carbon; Estrogens; High-performance liquid chromatography coupled with ultraviolet/fluorescence detection

资金

  1. National University of Singapore
  2. King Fahd University of Petroleum & Minerals, Saudi Arabia [R-143-000-617-597]
  3. National Research Foundation through the Environment & Water Industry Programme Office, Singapore

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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.

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