Voltammetric lidocaine sensor by using a glassy carbon electrode modified with porous carbon prepared from a MOF, and with a molecularly imprinted polymer

被引:0
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作者
Junjie Zhang
Jiang Liu
Yang Zhang
Feng Yu
Fu Wang
Zhengchun Peng
Yingchun Li
机构
[1] Shihezi University,Key Laboratory of Xinjiang Phytomedicine Resource and Utilization, Ministry of Education
[2] Harbin Institute of Technology,College of Science
[3] Shihezi University,Key Laboratory for Green Processing of Chemical Engineering of Xinjiang Bingtuan, School of Chemistry and Chemical Engineering
[4] Chinese Academy of Sciences,Laboratory of Environmental Science and Technology, The Xinjiang Technical Institute of Physics and Chemistry; Key Laboratory of Functional Materials and Devices for Special Environments
[5] Shenzhen University,College of Optoelectronic Engineering
来源
Microchimica Acta | 2018年 / 185卷
关键词
MOF derived carbon; Electrochemical sensor; Cyclic voltammetry; Trace measurement; Scanning electron microscopy; X-ray photoelectron spectroscopy; Raman spectra; Brunauer-Emmett-Teller; Nanoporous material; Hexacyanoferrate;
D O I
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中图分类号
学科分类号
摘要
The work describes a hybrid electrochemical sensor for highly sensitive detection of the anesthetic lidocaine (LID). Porous carbon (PC) was synthesized from an isoreticular metal-organic framework-8 (IRMOF-8) and drop cast onto a glassy carbon electrode (GCE). A layer of a molecularly imprinted polymer (MIP) layer was then fabricated in situ on the modified GCE by electro-polymerization, with LID acting as the template and resorcinol as the functional monomer. Hexacyanoferrate is used as an electrochemical probe. The electrical signal (typically acquired at 0.335 V vs. SCE) increases linearly in the 0.2 pM to 8 nM LID concentration range, with a remarkable 67 fM detection limit (at an S/N ratio of 3). The sensor is stable and selective. Eventually, rapid and accurate detection of LID in spiked real samples was successfully realized.
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