4.6 Article

Core-shell magnetic molecularly imprinted polymers used rhodamine B hydroxyproline derivate as template combined with in situ derivatization for the specific measurement of L-hydroxyproline

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1532, Issue -, Pages 30-39

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2017.11.053

Keywords

L-Hydroxyproline; In situ derivatization; Magnetic molecularly imprinted polymer; Specific extraction; Dairy products

Funding

  1. National Natural Science Foundation of China [21775088, 81603286, 21405094, 81303179]
  2. Natural Science Foundation of Qinghai Province of China [2016-ZJ-955]
  3. Open Projects Program of the Key Laboratory of Tibetan Medicine Research of Chinese Academy of Sciences
  4. Open Funds of Key Laboratory of TCM Quality Control Technology of Shandong Academy of Sciences
  5. Experimental Research Project of Qufu Normal University [sj201402]
  6. Foundation of Qufu Normal University [BSQD2012019, BSQD2012023]

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In this work, a novel core-shell magnetic molecularly imprinted polymers (MMIPs) for the measurement of L-Hydroxyproline (Hyp) in dairy products was prepared. The derivative of Hyp using N-hydroxysuccinimidyl rhodamine B ester (RBS) as derivatization reagent was employed as template to prepare RBS-Hyp-MMIPs (Fe3O4@MIPs for RBS-Hyp). A new analytical procedure of in situ derivatization with MMIPs (ISD-MMIPs) has been developed for the specific extraction and determination of Hyp in dairy products by ultra high performance liquid chromatography tandem mass spectrometry. The RBS-Hyp-MMIPs was characterized by fourier transform infrared spectrometer and transmission electron microscopy, and evaluated by adsorption experiments. The adsorption process followed Langumuir adsorption isotherm with maximum adsorption capacity of RBS-Hyp on RBS-Hyp-MMIPs at 96 mg/g. In addition, RBS-Hyp-MMIPs showed a short equilibrium time (15.0 min), rapid magnetic separation (5 s) and high stability (retained 95.3% after six cycles). Under the optimized conditions, good linearity was observed with the limits of detection (S/N > 3) and limits of quantification (S/N >10) at 0.1 and 0.5 ng/mL, respectively. On account of the specific extraction performance of RBS-Hyp-MMIPs, not any interference peak from real sample matrix was observed in the chromatograms of milk powder, liquid milk and milk drink. The proposed procedure was successfully applied for selective determination of Hyp from dairy products with satisfactory validation results, which is of great significance to food safety. (C) 2017 Elsevier B.V. All rights reserved.

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