Showing 3 results for Molecular Imprinted Polymer
Volume 9, Issue 2 (6-2019)
Abstract
Introduction: Along with the extensive production and use of various pesticides for controlling pests and enhancing the production of agricultural crops, there is a growing concern about the adverse effects of these toxic materials on human health. Therefore, the development of sensitive, selective, and accurate methods for continuous assessment of pesticides concentration in occupational and environmental fields and comparing them with national and international standards is of great importance. This study was aimed at synthesis and application of molecularly imprinted polymer as a selective sorbent for residue determination of two pyrethroid isomers in biological samples.
Material and Methods: The MIP particles were prepared by a non-covalent approach using permethrin as a template, chloroform as progen solvent, methacrylic acid as functional monomer and ethyleneglycol dimethacrylate as cross-linker, at 55 °C for 18 hours in an oil bath. Field emission scanning electron microscopy was used to investigate the morphology and size of polymer particles. Afterward, the critical parameters, which could affect the recognition properties of synthesized MIP, were investigated and optimized under the selected operational ranges for the highest adsorption and recycling yield in solid-phase extraction of permethrin in biological samples
Results: using precipitation polymerization technique, uniform and spherical particles with the nano-ranged diameter (less than 21.2 nanometers) were obtained. Under the optimized condition, the designed molecularly imprinted solid-phase extraction (MISPE) technique exhibited great potential for the extraction of pesticide isomers in the real sample. More than 93 % of the recovery obtained from spiked urine samples. The linear calibration curve was obtained from 20-120 μg.L-1 (R2=0.99) and the detection limit was less than 6 ppb for both isomers. The presence of interferences had no effect on the selectivity of the method up to 100-fold.
Conclusion: employing the molecular imprinted solid-phase extraction method along with the high-performance liquid chromatography technique resulted in a selective and sensitive approach, suitable for quantitative monitoring of the desired pesticide in complex biological samples.
Omid Reza Heravizadeh, Monireh Khadem, Ramin Nabizadeh, Seyed Jamaleddin Shahtaheri,
Volume 9, Issue 3 (9-2019)
Abstract
Introduction: Along with the extensive production and use of various pesticides for controlling pests and enhancing the production of agricultural crops, there is a growing concern about the adverse effects of these toxic materials on human health. Therefore, the development of sensitive, selective, and accurate methods for continuous assessment of pesticides concentration in occupational and environmental fields and comparing them with national and international standards is of great importance. This study was aimed at synthesis and application of molecularly imprinted polymer as a selective sorbent for residue determination of two pyrethroid isomers in biological samples.
Material and Methods: The MIP particles were prepared by a non-covalent approach using permethrin as a template, chloroform as progen solvent, methacrylic acid as functional monomer and ethyleneglycol dimethacrylate as cross-linker, at 55 °C for 18 hours in an oil bath. Field emission scanning electron microscopy was used to investigate the morphology and size of polymer particles. Afterward, the critical parameters, which could affect the recognition properties of synthesized MIP, were investigated and optimized under the selected operational ranges for the highest adsorption and recycling yield in solid-phase extraction of permethrin in biological samples
Results: using precipitation polymerization technique, uniform and spherical particles with the nano-ranged diameter (less than 21.2 nanometers) were obtained. Under the optimized condition, the designed molecularly imprinted solid-phase extraction (MISPE) technique exhibited great potential for the extraction of pesticide isomers in the real sample. More than 93 % of the recovery obtained from spiked urine samples. The linear calibration curve was obtained from 20-120 μg.L-1 (R2=0.99) and the detection limit was less than 6 ppb for both isomers. The presence of interferences had no effect on the selectivity of the method up to 100-fold.
Conclusion: employing the molecular imprinted solid-phase extraction method along with the high-performance liquid chromatography technique resulted in a selective and sensitive approach, suitable for quantitative monitoring of the desired pesticide in complex biological samples.
Seyedeh Maryam Taheri, Monireh Khadem, Fariborz Omidi, Alirea Sedighi, , Seyed Jamaleddin Shahtaheri,
Volume 11, Issue 1 (3-2021)
Abstract
Introduction: Pesticides are among the broadest chemical compounds used in the world and are also considered as the most dangerous compounds for living organisms. Although pesticides have significant impact on improving agricultural and food products, the processes of their production, formulation, storage, transportation, and marketing as well as the extensive use of these materials lead to occupational exposure, environmental pollution, and the presence of their residues in foodstuffs. Bentazon as a herbicide is considered as one of the most common pesticides used in agriculture and horticulture. Its effects on human health are widespread and of concern. Occupational and environmental exposure assessment of this compound is, therefore, considered necessary by conducting accurate and valid methods. The purpose of the present study was to synthesize a molecular imprinted polymer (MIP) as a specific adsorbent in the preparation process of bentazon for its selective analysis in biological matrices.
Material and Methods: For synthesis, a precipitation polymerization method was used. This method has been used to prepare particle size distribution and shape appropriately. By applying the aforementioned method, nano particle size is obtained within the sub-micron and nano range. So, crushing and sieving of the sorbent is not necessary. The MIP was synthesized with 1: 4: 30 ratio of template molecule (bentazone): functional monomer (methacrylic acid): cross-linking monomer (ethylene glycol di methacrylate), respectively. Due to particle size and high porosity, the sorption and recovery of template compound was performed faster and with higher efficiency. Some variables affecting the efficiency of MIP for sorption and desorption of analyte were investigated and optimized. They included pH of solution, MIP amount (mg), and sonication time (min) in the sorption step and volume of eluent (ml), sonication time (s), and acid percentage in the desorption step.
Results: The optimum levels of factors for the proposed method were pH of solution: 2، sonication time for sorption 7.3 min, polymer amount of 30.814 mg, acid percentage 1.1, and sonication time for desorption 165 s. According to the obtained results, the interfering factors in the matrix have no significant effect on the determination of analyte. The limit of detection (LOD) and relative standard deviation (RSD) of the optimized method were 0.79.ppb and 2.8931 %, respectively.
Conclusion: The results of this study indicated that the proposed method can be used to extract the bentazon herbicide from complex matrices such as urine samples with high efficiency and selectivity.
