Liu Shanshan, Chen Yanmei, Ruan Zhijun, Lin Junqi, Kong Wen
Hubei Key Laboratory of Processing and Application of Catalytic Materials, College of Chemistry and Chemical Engineering, Huanggang Normal University, Huanggang, 438000, China.
Hubei Key Laboratory of Processing and Application of Catalytic Materials, College of Chemistry and Chemical Engineering, Huanggang Normal University, Huanggang, 438000, China.
Environ Res. 2022 Apr 15;206:112617. doi: 10.1016/j.envres.2021.112617. Epub 2021 Dec 27.
The abuse of antibiotics has caused serious threat to human health, so it is of great significance to develop a simple and sensitive method for the detection of trace residues of antibiotics in the environment and food. Herein, a novel label-free fluorescent biosensing platform based on the fluorescence change of aptamers-capped zeolitic imidazolate framework-8 (ZIF-8) @ 2,2',2″,2‴-((ethene-1,1,2,2-tetrayltetrakis (benzene-4,1-diyl)) tetrakis (oxy)) tetraacetic acid (TPE) through ATP-assisted competitive coordination reaction was designed for such an end. ZIF-8@TPE/Aptamer (Apt) emits strong fluorescence at 425 nm in HEPES buffer due to the aggregation induced luminescence properties of TPE molecules in confined state. Once kanamycin was added, the conformation of aptamer capped on the surface of ZIF-8@TPE changes because of the specific recognition of kanamycin with aptamer, leading to the collapse of ZIF-8 and release of TPE, accompanied with a dramatic decrease of fluorescence intensity. Under the optimal conditions, a good correlation was obtained between the fluorescence intensity of ZIF-8@TPE/Apt and the concentration of kanamycin ranging from 10 to 10 ng/mL with a detection limit of 7.3 ng/mL. The satisfactory analytical performance of the assay for kanamycin detection suggests good prospect for its application in food safety analysis.
抗生素的滥用已对人类健康造成严重威胁,因此开发一种简单且灵敏的方法来检测环境和食品中的抗生素微量残留具有重要意义。在此,基于适体封端的沸石咪唑酯骨架-8(ZIF-8)@2,2',2″,2‴-((乙烯-1,1,2,2-四亚基四(苯-4,1-二基))四(氧基))四乙酸(TPE)通过ATP辅助的竞争性配位反应的荧光变化,设计了一种新型无标记荧光生物传感平台用于此目的。由于TPE分子在受限状态下的聚集诱导发光特性,ZIF-8@TPE/适体(Apt)在HEPES缓冲液中于425nm处发射强荧光。一旦加入卡那霉素,由于卡那霉素与适体的特异性识别,封端在ZIF-8@TPE表面的适体构象发生变化,导致ZIF-8结构坍塌和TPE释放,同时荧光强度急剧下降。在最佳条件下,ZIF-8@TPE/Apt的荧光强度与卡那霉素浓度在10至10ng/mL范围内具有良好的相关性,检测限为7.3ng/mL。该卡那霉素检测方法令人满意的分析性能表明其在食品安全分析中的应用前景良好。