4.6 Article

Synthesis and application of a T-2 toxin imprinted polymer

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1217, Issue 17, Pages 2879-2886

Publisher

ELSEVIER
DOI: 10.1016/j.chroma.2010.02.068

Keywords

Molecularly imprinted polymer; T-2 toxin; Solid-phase extraction; Mycotoxins; Molecular recognition; Food

Funding

  1. Federal Public Service of Health, Food Chain Safety and Environment [RF 6178]

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The synthesis of a T-2 toxin imprinted polymer and its application in food analysis are reported for the first time. A molecularly imprinted polymer (MIP) for the selective recognition of T-2 toxin (T-2) was synthesized by bulk polymerization. Methacrylamide and ethyleneglycol dimethacrylate were applied as functional monomer and cross-linker, respectively. Molecularly imprinted solid-phase extraction (MISPE) procedures were optimized for further application in the analysis of T-2. Scatchard plot analysis revealed that two classes of imprinted binding sites were formed in the imprinted polymer. The dissociation constant (K-D) of the higher affinity binding sites was 7.0 mu mol/l, while the K-D of the lower affinity binding sites was 54.7 mu mol/l. The performance of the MW throughout the clean-up of spiked maize, barley and oat sample extracts was compared with the results obtained when using non-imprinted polymer, OASIS HLB (R) and immunoaffinity columns (IAC). Depending on the food matrix and the spiked concentration, recoveries after MISPE and non-imprinted solid-phase extraction varied respectively from 60% to 73% and from 21% to 57%. Recoveries obtained after clean-up using OASIS HLB (R) and IAC were in the range of 74-104% and 60-85%, respectively. Although highest recoveries were obtained with OASIS HLB (R) sorbents, the designed MIP and the IAC were superior regarding selectivity, cross-reactivity, matrix effect, limits of detection (LOD) and limits of quantification (LOQ). Depending on the matrix, LOD after MISPE ranged from 0.4 mu g/kg to 0.6 mu g/kg and LOQ from 1.4 mu g/kg to 1.9 mu g/kg. LOD and LOQ after OASIS HLB (R) clean-up varied from 0.9 mu g/kg to 3.5 mu g/kg and from 3.1 mu g/kg to 11.7 mu g/kg, respectively. The LOD and LOQ values obtained with IAC were in the range of 0.3-2.3 mu g/kg and 1.0-7.7 mu g/kg, respectively. Analysis of 39 naturally contaminated samples (maize, barley and oat) by liquid chromatography tandem mass spectrometry revealed that the MIP could be an excellent alternative for clean-up of contaminated food samples. (C) 2010 Elsevier B.V. All rights reserved.

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