4.7 Article

Preparation of magnetic molecularly imprinted polymer for rapid determination of bisphenol A in environmental water and milk samples

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 395, Issue 4, Pages 1125-1133

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-009-3020-5

Keywords

Magnetic molecularly imprinted polymer; Solid-phase extraction; Magnetic separation; High-performance liquid chromatography; Bisphenol A

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A magnetic molecularly imprinted polymer (M-MIP) of bisphenol A (BPA) was prepared by miniemulsion polymerization. The morphological and magnetic characteristics of the M-MIP were characterized by Fourier-transform infrared spectroscopy, transmission electron microscopy, and vibrating sample magnetometry. The adsorption capacities of the M-MIP and the nonimprinted polymer were investigated using static adsorption tests, and were found to be 390 and 270 mg g(-1), respectively. Competitive recognition studies of the M-MIP were performed with BPA and the structurally similar compound DES, and the M-MIP displayed high selectivity for BPA. A method based on molecularly imprinted solid-phase extraction assisted by magnetic separation was developed to extract BPA from environmental water and milk samples. Various parameters such as the mass of sorbent, the pH of the sample, the extraction time, and desorption conditions were optimized. Under selected conditions, extraction was completed in 15 min. High-performance liquid chromatography with UV detection was employed to determine BPA after the extraction. For water samples, the developed method exhibited a limit of detection (LOD) of 14 ng L-1, a relative standard deviation of 2.7% (intraday), and spiked recoveries ranging from 89% to 106%. For milk samples, the LOD was 0.16 A mu g L-1, recoveries ranged from 95% to 101%, and BPA was found in four samples at levels of 0.45-0.94 A mu g L-1. The proposed method not only provides a rapid and reliable analysis but it also overcomes problems with conventional solid-phase extraction (SPE), such as the packing of the SPE column and the time-consuming nature of the process of loading large-volume samples.

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