A portable and antibody-free sandwich assay for determination of chloramphenicol in food based on a personal glucose meter

被引:27
|
作者
Chen, Si [1 ]
Gan, Ning [2 ]
Zhang, Huairong [2 ]
Hu, Futao [1 ]
Li, Tianhua [2 ]
Cui, Huan [2 ]
Cao, Yuting [2 ]
Jiang, Qianli [3 ]
机构
[1] Ningbo Univ, Fac Marine Sci, Ningbo 315211, Zhejiang, Peoples R China
[2] Ningbo Univ, State Key Lab Base Novel Funct Mat & Preparat Sci, Fac Mat Sci & Chem Engn, Ningbo 315211, Zhejiang, Peoples R China
[3] Southern Med Univ, Dept Hematol, Nanfang Hosp, Guangzhou 510515, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Chloramphenicol; Antibody-free; Sandwich-type assay; Molecularly imprinted; beta-Cyclodextrin; Personal glucose meter; MOLECULARLY IMPRINTED POLYMER; QUARTZ-CRYSTAL MICROBALANCE; ELECTROCHEMICAL IMMUNOASSAY; QUANTITATIVE DETECTION; SIGNAL AMPLIFICATION; MILK; NITROPHENOL; EXTRACTION; SEPARATION; READOUT;
D O I
10.1007/s00216-015-8478-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A portable and antibody-free sandwich assay was fabricated for determination of chloramphenicol (CAP) in animal-derived food by a personal glucose meter (PGM). The sandwich-type strategy was developed on the basis of magnetic molecularly imprinted probe (m-MIP) nanoparticles and a beta-cyclodextrin/invertase-functionalized signal tag. Firstly, the m-MIPs were fabricated using polydopamine molecularly imprinted film modified Fe3O4 nanoparticles with 2, 2-dichloroacetamide as a template that could capture the 2,2-dichloroacetamide segment of CAP. Secondly, beta-cyclodextrin/invertase polymer bioconjungate was synthesized as a signal tag that could recognize the nitrobenzene segment of CAP through host-guest interaction. The dual-specificity recognition model relies on the formation of a sandwich between m-MIPs, different segments of CAP, and the beta-cyclodextrin-functionalized signal tag. The sandwich-type complex formed was then subjected to detection with a PGM. The complexes can hydrolyze sucrose to glucose, which can be used for detection with a PGM through invertase. According to our experiment, the concentration of CAP was proportional to the amount of glucose formed, which could quantitatively assess the CAP with a dynamic range of 0.5-50 ng mL(-1) and a detection limit of 0.16 ng mL(-1) (signal-to-noise ratio of 3). The detection time of the assay was about 1 h, which was obviously shorter than that of competitive ELISA. More importantly, we have successfully applied this on-site assay for CAP screening in animal-derived food.
引用
收藏
页码:2499 / 2507
页数:9
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