Issue 101, 2016, Issue in Progress

Determination of triazine herbicides from honey samples based on hydrophilic molecularly imprinted resins followed by high performance liquid chromatography-tandem mass spectrometry

Abstract

A facile, novel and efficient approach to extract six triazine herbicides from honey samples based on hydrophilic molecularly imprinted resins (MIRs) was described. The MIRs were prepared in a one-pot polycondensation with resorcinol and melamine as the double functional monomers, formaldehyde as a crosslinking agent, and ametryn as the template. The obtained MIRs have a uniform spherical morphology and excellent dispersibility in water due to them having a large number of hydrophilic groups. The MIRs were successfully used as a solid-phase extraction material to rapidly extract and clean up to six triazines in honey samples followed by high performance liquid chromatography-tandem mass spectrometry detection. Under optimal conditions, the method showed higher recoveries and a shorter extraction time. The detection limits of the six triazines are in the range of 0.02–0.15 ng g−1. The recoveries of the six triazines are in the range of 83 ± 4% to 97 ± 4% at the spiked level of 5 ng g−1. The proposed method is simple and quick and has the potential to detect triazine herbicides in other aqueous samples.

Graphical abstract: Determination of triazine herbicides from honey samples based on hydrophilic molecularly imprinted resins followed by high performance liquid chromatography-tandem mass spectrometry

Article information

Article type
Paper
Submitted
17 Aug 2016
Accepted
07 Oct 2016
First published
07 Oct 2016

RSC Adv., 2016,6, 98663-98673

Determination of triazine herbicides from honey samples based on hydrophilic molecularly imprinted resins followed by high performance liquid chromatography-tandem mass spectrometry

T. Zhou, J. Hou, D. Yuan, H. Li, P. Zhang, Y. Li, H. Ding, Y. Chen and L. Ding, RSC Adv., 2016, 6, 98663 DOI: 10.1039/C6RA20698K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements