Department of Analytical Chemistry, Faculty of Chemistry, University College of Science, University of Tehran, P.O. Box 14155-6455, Tehran, Iran.
Department of Applied Chemistry, Faculty of Science, University of Mohaghegh Ardabili, Daneshgah Street, P.B179, 56199-11367 Ardabil, Iran.
Biosens Bioelectron. 2016 Jul 15;81:198-206. doi: 10.1016/j.bios.2016.02.052. Epub 2016 Feb 18.
Molecularly imprinted polymer (MIP) nanoparticles including highly selective recognition sites for fluoxetine were synthesized, utilizing precipitation polymerization. Methacrylic acid and vinyl benzene were used as functional monomers. Ethylene glycol dimethacrylate was used as cross-linker agent. The obtained polymeric nanoparticles were incorporated with carbon paste electrode (CPE) in order to construct a fluoxetine selective sensor. The response of the MIP-CP electrode to fluoxetine was remarkably higher than the electrode, modified with the non-imprinted polymer, indicating the excellent efficiency of the MIP sites for target molecule recognition. It was found that the addition of a little amount of graphene, synthesized via modified hummer's method, to the MIP-CP resulted in considerable enhancement in the sensitivity of the electrode to fluoxetine. Also, the style of electrode components mixing, before carbon paste preparation, was demonstrated to be influential factor in the electrode response. Some parameters, affecting sensor response, were optimized and then a calibration curve was plotted. A dynamic linear range of 6×10(-9)-1.0×10(-7)molL(-1) was obtained. The detection limit of the sensor was calculated equal to 2.8×10(-9)molL(-1) (3Sb/m). This sensor was used successfully for fluoxetine determination in the spiked plasma samples as well as fluoxetine capsules.
分子印迹聚合物(MIP)纳米粒子包括用于氟西汀的高度选择性识别位点,是利用沉淀聚合合成的。甲基丙烯酸和苯乙烯被用作功能单体。乙二醇二甲基丙烯酸酯被用作交联剂。所得的聚合纳米粒子与碳糊电极(CPE)结合,以构建对氟西汀具有选择性的传感器。MIP-CP 电极对氟西汀的响应明显高于用非印迹聚合物修饰的电极,这表明 MIP 位点对目标分子识别的效率很高。结果发现,向 MIP-CP 中添加少量通过改良的 Hummer 法合成的石墨烯,可大大提高电极对氟西汀的灵敏度。此外,在制备碳糊之前,电极组件混合的方式被证明是影响电极响应的因素之一。优化了一些影响传感器响应的参数,然后绘制了校准曲线。获得了 6×10(-9)-1.0×10(-7)molL(-1)的动态线性范围。传感器的检测限计算为 2.8×10(-9)molL(-1)(3Sb/m)。该传感器成功地用于加标血浆样品和氟西汀胶囊中氟西汀的测定。