Chemiluminescence sensor for sulfonylurea herbicide using molecular imprinted microspheres as recognition element

Luminescence. 2011 Jul-Aug;26(4):271-9. doi: 10.1002/bio.1224. Epub 2010 Jul 13.

Abstract

Uniform molecular imprinting microspheres were prepared using precipitation polymerization with thifensulfuron-methyl (TFM) as template, acrylamide as functional monomer and ethylene glycol dimethacrylate as cross-linker. TFM could be selectively adsorbed on the molecularly imprinted polymers (MIPs) matrix through the hydrogen bonding interaction and the adsorbed TFM could be sensed by its strikingly enhancing effect on the weak chemiluminescence (CL) reaction between luminol and hydrogen peroxide. On this basis, a novel CL sensor for the determination of TFM using MIPs as recognition elements was established. The logarithm of net CL intensity (ΔI) is linearly proportional to the logarithm of TFM concentration (C) in the range from 1.0 × 10(-9) to 5.0 × 10(-5) mol L(-1) with a detection limit of 8.3 × 10(-10) mol L(-1) (3σ). The results demonstrated that the MIP-CL sensor was reversible and reusable and that it could strikingly improve the selectivity and sensitivity of CL analysis. Furthermore, it is suggested that the CL enhancement of luminol-H(2)O(2) by TFM might be ascribed to the enhancement effect of CO(2), which came from TFM hydrolysis in basic medium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adsorption
  • Herbicides / analysis*
  • Luminescent Measurements / instrumentation
  • Luminescent Measurements / methods*
  • Microspheres*
  • Molecular Imprinting*
  • Molecular Structure
  • Particle Size
  • Polymers / chemical synthesis
  • Polymers / chemistry
  • Sulfonylurea Compounds / analysis*
  • Surface Properties
  • Thiophenes / analysis*

Substances

  • Herbicides
  • Polymers
  • Sulfonylurea Compounds
  • Thiophenes
  • thifensulfuron methyl