Sensitive detection of ketamine with an electrochemical sensor based on UV-induced polymerized molecularly imprinted membranes at graphene and MOFs modified electrode

被引:67
作者
Fu, Kaixin [1 ]
Zhang, Ruilin [2 ]
He, Jingcheng [1 ]
Bai, Huiping [1 ]
Zhang, Genlin [1 ]
机构
[1] Yunnan Univ, Yunnan Key Lab Micro Nano Mat & Technol, Sch Mat Sci & Technol, Kunming 650091, Yunnan, Peoples R China
[2] Kunming Med Univ, Inst Forens Med, Kunming 650050, Yunnan, Peoples R China
关键词
Ketamine; Molecularly imprinted sensor; MOFs@G nanocomposite; UV-Induced; Screen printed electrode; METAL-ORGANIC FRAMEWORKS; NORKETAMINE; PLASMA; URINE; HAIR; IMMUNOSENSOR; EXTRACTION; CHEMISTRY;
D O I
10.1016/j.bios.2019.111636
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Ketamine is one of the most widely abused drugs in the world and poses a serious threat to human health and social stability; therefore, the ability to accurately monitor the substance in real-time is necessary. However, several problems still exists towards this goal, such as the generally low concentration of the target molecules disturbed in the complex samples that undergo analysis during criminal investigations. In this work, the sensitive and selective detection of ketamine was accomplished by molecularly imprinted electrochemical sensor. The molecularly imprinted membrane as a biomimetic recognition element was fabricated by the UV-induced polymerization of methacrylic acid (MAA) and ethylene glycol dimethacrylate (EGDMA) on a metal-organic framework/graphene nanocomposite (MOFs@G) modified screen-printed electrode. The screen printed electrode (SPE) provided good adhesion for the formation of the imprinted membranes and increased the stability of the sensor. The morphology and performance of the imprinted films were characterized in detail by scanning electron microscopy (SEM), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and differential pulse voltammetry (DPV). The experimental results demonstrated that the imprinted sensor had excellent sensitivity, selectivity, and long-term stability. It offered a low detection limit (4.0 x 10(-11) mol L-1) and had a dynamic range from 1.0 x 10(-10) mol L-1 to 4.0 x 10(-5) mol L-1. Furthermore, the established method was successfully applied for the determination of ketamine in urine and saliva samples.
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页数:7
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