L-lysine-structure-directed MIL-88A and its application in electrochemical sensing of cholylglycine via molecular imprinting technique

被引:10
作者
Chen, Haicheng [1 ]
Luo, Kang [1 ]
Zhou, Qing [1 ]
Yan, Zhihong [1 ]
Li, Kang [1 ]
机构
[1] Guangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R China
基金
中国国家自然科学基金;
关键词
Structural directing agent; L-lysine; MIL-88A; Electrochemical sensor; Molecular imprinting technology; Cholylglycine; METAL-ORGANIC-FRAMEWORKS; GLYCOCHOLIC ACID; PHOTOCATALYSIS; DEGRADATION; ENZYME; SENSOR;
D O I
10.1016/j.microc.2020.105249
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, we develop a novel strategy to synthesize MIL-88A (an iron-based metal-organic framework) by adding L-lysine as structural directing agent under ambient conditions, and L-lysine could be thoroughly removed after the reaction finished. It was discovered that L-lysine could effectively regulate the size of MIL-88A. The prepared MIL-88A particles, combining with XC-72 (one kind of carbon black) and molecularly imprinted polymer (MIP) films, were applied to fabricate a sensitive electrochemical sensor for the detection of cholylglycine (CG, a biomarker of hepatocellular carcinoma). The surface morphologies of modified electrodes were characterized by scanning electron microscope (SEM). Furthermore, X-ray diffraction (XRD), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR), N-2 adsorption-desorption were used to further characterize the prepared MIL-88A particles. A 5 mM [Fe(CN)(6)](3-)(/4)(-) (containing 0.1 M KCl) solution was used as a redox probe, and differential pulse voltammetry (DPV) was applied to quantitatively detect CG. The linear response range of CG was 1 x 10(-11) to 5 x 10(-8) M with a detection limit of 3.4 x 10(-12) M (S/N = 3). The MIP sensor was successfully applied to detect CG in human serum with satisfactory results.
引用
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页数:8
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