A Smartphone-Integrated Molecularly Imprinted Fluorescence Sensor for Visual Detection of Chlortetracycline Based on N,P-Codoped Carbon Dots Decorated Iron-Based Metal–Organic Frameworks

检出限 荧光 分子印迹聚合物 化学 金属有机骨架 选择性 材料科学 分析化学(期刊) 色谱法 吸附 有机化学 物理 量子力学 催化作用
作者
Jinni Zhang,Yan Liu,Xueyan Cui,Yichuan Cao,Yan Li,Guozhen Fang,Shuo Wang
出处
期刊:Journal of Agricultural and Food Chemistry [American Chemical Society]
卷期号:71 (43): 16303-16309 被引量:30
标识
DOI:10.1021/acs.jafc.3c05406
摘要

The residue of chlortetracycline is potentially hazardous to human health; it is meaningful to exploit a portable, rapid, sensitive, and selective method for detection of chlortetracycline (CTC). In this study, a novel fluorescence bionic sensing probe (NH2-MIL-53&N,P-CDs@MIP) was successfully prepared based on the nitrogen and phosphorus codoped carbon dots decorated iron-based metal-organic frameworks combining with molecular imprinted polymer for the detection of CTC. A fluorescence intensity-responsive "on-off" detection of CTC on account of the inner-filter effect (IFE) was achieved by NH2-MIL-53&N,P-CDs@MIP. Under the optimal conditions, the fluorescence quenching degree of NH2-MIL-53&N,P-CDs@MIP presented a good linear relationship with the CTC concentration in the range 0.06-30 μg mL-1 and the limit of detection (LOD) was 0.019 μg mL-1. The fluorescent probe was applied to detect CTC in milk samples, and experimental results showed a good recovery rate (88.73%-96.28%). Additionally, a smartphone-integrated fluorescence sensing device based on NH2-MIL-53&N,P-CDs@MIP was exploited to replace the expensive and bulky fluorescence spectrophotometer for quantitative determination of CTC with the LOD of 0.033 μg mL-1. The sensing system showed high selectivity, strong stability, high specificity, and portability, which provide a great strategy for the quantitative detection of antibiotic residue.
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