Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111, Iran.
Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111, Iran.
Biosens Bioelectron. 2014 Oct 15;60:77-83. doi: 10.1016/j.bios.2014.03.028. Epub 2014 Apr 13.
In the present study, a novel sensitive and selective nanocomposite imprinted electrochemical sensor for the indirect determination of caffeine has been prepared. The imprinted sensor was fabricated on the surface of pencil graphite electrode (PGE) via one-step electropolymerization of the imprinted polymer composed of conductive polymer, sol-gel, gold nanoparticles (AuNPs), and caffeine. Due to such combination like the thin film of molecularly imprinted polymer (MIP) with specific binding sites, the sensor responded quickly to caffeine. AuNPs were introduced for the enhancement of electrical response by facilitating charge transfer processes of Fe(CN)6/Fe(CN)6 which was used as an electrochemical active probe. The fabrication process of the sensor was characterized by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Several important parameters controlling the performance of the sensor were investigated and optimized. The imprinted sensor has the advantages of high porous surface structure, inexpensive, disposable, excellent stability, good reproducibility and repeatability. The linear ranges of the MIP sensor were in the range from 2.0 to 50.0 and 50.0 to 1000.0 nmol L(-1), with the limit of detection (LOD) of 0.9 nmol L(-1) (S/N=3). Furthermore, the proposed method was successfully intended for the determination of caffeine in real samples (urine, plasma, tablet, green tea, energy and soda drink).
在本研究中,制备了一种用于间接测定咖啡因的新型灵敏选择性纳米复合印迹电化学传感器。印迹传感器通过在铅笔石墨电极(PGE)表面上的一步电聚合由导电聚合物、溶胶-凝胶、金纳米粒子(AuNPs)和咖啡因组成的印迹聚合物来制备。由于像具有特定结合位点的分子印迹聚合物(MIP)的薄膜这样的组合,传感器对咖啡因的响应很快。AuNPs 的引入通过促进 Fe(CN)6/Fe(CN)6 的电荷转移过程来提高电响应,Fe(CN)6/Fe(CN)6 被用作电化学活性探针。传感器的制备过程通过循环伏安法(CV)和电化学阻抗谱(EIS)进行了表征。研究并优化了控制传感器性能的几个重要参数。印迹传感器具有高多孔表面结构、廉价、一次性、优异的稳定性、良好的重现性和重复性等优点。MIP 传感器的线性范围在 2.0 至 50.0 和 50.0 至 1000.0 nmol L(-1) 之间,检测限(LOD)为 0.9 nmol L(-1)(S/N=3)。此外,该方法成功地用于测定实际样品(尿、血浆、片剂、绿茶、能量和苏打饮料)中的咖啡因。