A molecularly imprinted polypyrrole electrochemiluminescence sensor based on a novel zinc-based metal-organic framework and chitosan for determination of enrofloxacin

被引:7
|
作者
Bu, Liyin [1 ]
Su, Chang [2 ]
Song, Qingyuan [1 ]
Jiang, Ding [1 ,3 ,4 ]
Shan, Xueling [3 ,4 ]
Wang, Wenchang [5 ]
Chen, Zhidong [1 ]
机构
[1] Changzhou Univ, Sch Petrochem Engn, Changzhou 213164, Jiangsu, Peoples R China
[2] Changzhou Univ, Sch Mat Sci & Engn, Changzhou 213164, Jiangsu, Peoples R China
[3] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Jiangsu, Peoples R China
[4] Changzhou Univ, Adv Catalysis & Green Mfg Collaborat Innovat Ctr, Changzhou 213164, Jiangsu, Peoples R China
[5] Changzhou Univ, Anal & Testing Ctr, NERC Biomass, Changzhou 213164, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
NANOPARTICLES; POLYMER; PRECONCENTRATION;
D O I
10.1039/d3an01236k
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Nowadays, bacterial resistance caused by the abuse of antibiotics has become a worldwide problem. In this work, a quinolone antibiotic, enrofloxacin (ENR), was rapidly monitored by combining a selective molecular imprinting polymer (MIP) with the electrochemiluminescence (ECL) method. Zn-PTC, a novel zinc-based metal-organic framework (MOF) that has a large specific surface area and ultra-high luminous efficiency, was used as the ECL luminophore. Chitosan (CHIT) was used to contact the specific surface area of molecularly imprinted polymer films and further improved the detection sensitivity. Subsequently, the molecularly imprinted polypyrrole was electropolymerized on the surface of the Zn-PTC and CHIT modified glassy carbon electrode (GCE). The specific sites that could target recombining ENR were shaped on the surface of MIP after extracting the ENR templates. The specific concentrations of ENR could be detected according to the difference in ECL intensity (Delta ECL) between the eluting and rebinding of ENR. After optimization, a good linear response of Delta ECL and a logarithm of specific ENR concentrations could be obtained in the range of 1.0 x 10-12-1.0 x 10-4 mol L-1, with a detection limit of 9.3 x 10-13 mol L-1 (S/N = 3). Notably, this study provided a rapid, convenient, and cheap method for the detection of ENR in actual samples. A schematic illustration of the preparation of a Ppy-MIP/CHIT/Zn-PTC/GCE and the sensing strategy for enrofloxacin.
引用
收藏
页码:6087 / 6096
页数:10
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