4.7 Article

A microflow chemiluminescence system for determination of chloramphenicol in honey with preconcentration using a molecularly imprinted polymer

Journal

TALANTA
Volume 82, Issue 2, Pages 560-566

Publisher

ELSEVIER
DOI: 10.1016/j.talanta.2010.05.007

Keywords

Chloramphenicol; Molecularly imprinted polymer (MIP); Chemiluminscence; Microfluidics; MicroFIA

Funding

  1. Thailand Research Fund (TRF) [PHD/0223/2548 Code 5.G.CM/48/A.1]
  2. Department of Pharmaceutical Sciences, Faculty of Pharmacy, Chiang Mai University
  3. Center for Innovation in Chemistry: Postgraduate Education and Research Program in Chemistry (PERCH-CIC)
  4. Chemistry Department, Faculty of Science, Chiang Mai University
  5. Commission on Higher Education

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A novel chemiluminescence (CL) microfluidic system incorporating a molecularly imprinted polymer (MIP) preconcentration step was used for the determination of chloramphenicol in honey samples. The MIP was prepared by using chloramphenicol as the template, diethylaminoethyl methacrylate (DAM) as the function monomer, ethylene glycol dimethacrylate (EGDMA) as the cross-linking monomer, 2, 2'-dimethoxy-2-phenylacetophenone (DMPA) as the free radical initiator and toluene and dodecanol as the solvent. The MIP was pre-loaded into a 10 mm long, 2 mm wide and 1501,,m deep channel in a planar glass microfluidic device. When the sample containing chloramphenicol was introduced into the microfluidic device it was first preconcentrated on the MIP then detected by an enhancement effect on the chemiluminescence reaction of tris(2, 2'-bipyridyl) ruthenium(II) with cerium(IV) sulphate in sulphuric acid. A micro-syringe pump was used to pump the reagents. The CL intensity was linear in relationship to the chloramphenicol concentrations from 1.55 x 10(-4) to 3.09 x 10(-3) mu mol L-1 (r(2) = 0.9915) and the detection limit (3 sigma) and the quantitation limit (10 sigma)were found to be 7.46 x 10(-6) and 2.48 x 10(-5) mu mol L-1, respectively. This method offered a high selectivity and sensitivity for quantitative analysis of chloramphenicol in the honey samples. (C) 2010 Elsevier B.V. All rights reserved.

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