4.6 Article

Design of an imprinted clean-up method for mycophenolic acid in maize

期刊

JOURNAL OF CHROMATOGRAPHY A
卷 1218, 期 8, 页码 1122-1130

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2010.12.085

关键词

Molecularly imprinted polymer; Mycophenolic acid; Maize; Solid-phase extraction; Molecular recognition

资金

  1. BOF of Ghent University [01J08409]

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In the present work, the development of imprinted polymers selective towards mycophenolic acid and their application in food analysis are reported for the first time. To synthesize the molecularly imprinted polymer (MIP) 4-vinylpyridine and ethyleneglycol dimethacrylate were applied as functional monomer and cross-linker, respectively. Besides the toxin itself, the implementation of structural analogues as templates was evaluated. A molecularly imprinted solid-phase extraction (MISPE) procedure was designed for the selective clean-up of maize extracts. Binding experiments and Scatchard analysis indicated the presence of specific binding sites in the imprinted polymers. The imprinting effect varied along with the selected template. The dissociation constant (K(D)) of the higher affinity binding sites ranged from 0.8 mu mol/l to 15.6 mu mol/l, while the K(D) of the lower affinity binding sites was in the range of 138.5-519.3 mu mol/l. The performance of the MIPs throughout the clean-up of spiked maize sample extracts was evaluated and compared with the results obtained when applying a non-imprinted polymer. Depending on the polymers and the spiked concentration, recoveries after MISPE and non-imprinted solid-phase extraction varied respectively from 49% to 84% and from 28% to 31%. The imprinted polymers were superior regarding matrix effect, limit of detection (LOD) and limit of quantification (LOQ). LOD ranged from 0.17 mu g/kg to 0.25 mu g/kg and LOQ varied from 0.57 mu g/kg to 0.82 mu g/kg. Analysis of 15 maize samples by liquid chromatography tandem mass spectrometry revealed that the MIPs could be excellent sorbents for clean-up of contaminated food samples. (C) 2011 Elsevier B.V. All rights reserved.

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