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Saadi Samadi

Saadi Samadi

Academic rank: Associate Professor
ORCID:
Education: PhD.
ScopusId: 36017420200
HIndex:
Faculty: Faculty of Science
Address: Department of Chemistry, Faculty of Science, University of Kurdistan, Zip Code 66177-15175, Sanandaj, Iran.
Phone: 4264

Research

Title
Coupling of Molecular Imprinted Polymer Nanoparticles by High Performance Liquid Chromatography as an Efficient Technique for Sensitive and Selective Trace Determination of 4-Chloro-2-Methylphenoxy Acetic Acid in Complex Matrices
Type
JournalPaper
Keywords
Molecular imprinted polymer nanoparticles, 4-chloro-2-methylphenoxy acetic acid, Selective, preconcentration, Urine and water samples.
Year
2014
Journal iranian journal of public health
DOI
Researchers Fariborz Omidi ، Mohammad Behbahani ، Saadi Samadi ، Alireza Sedighi ، Seyed Jamaleddin Shahtaheri

Abstract

Abstract Background: 4-chloro-2-methylphenoxy acetic acid (MCPA) is one of the most important pesticides which is extensively used to control weeds in arable farmland. Exposure to this compound occurs in general population and persons who occupationally handle it. The aim of this present work was the preparation of MCPA imprinting polymer and its application as a selective sample preparation technique for trace determination of MCPA in biological and environmental samples. Methods: In this study, MCPA imprinting polymer was obtained by precipitation polymerization using methacrylic acid (the functional monomer), ethylene glycol dimethacrylate (the cross-linker), 2,2′-azobisisobutyronitrile (the initiator) and MCPA (the template molecule) in acetonitrile solution. The MIP-NPs were characterized by thermogravimetric analysis and scanning electron microscopy. The optimization process was carried out applying batch method. After optimization of the parameters, affecting the adsorption and desorption of analyte, urine and different water samples were used to determine MCPA. Results: Imprinted MCPA molecules were removed from the polymeric structure using acetic acid in methanol (20:80 v/v %) as the eluting solvent. Both sorption and desorption process occur within 10 min. The maximum sorbent capacity of the molecular imprinted polymer is 87.4 mg g-1. The relative standard deviation and limit of detection for water samples by introduced selective solid phase extraction were 4.8% and 0.9 μg L-1, and these data for urine samples were 4.5% and 1.60 μg L-1, respectively. Conclusion: The developed method was successfully applied to determine MCPA in urine and different water samples.