Molecular imprinting-based triple-emission ratiometric fluorescence sensor with aggregation-induced emission effect for visual detection of doxycycline

强力霉素 检出限 荧光 分子印迹 分子印迹聚合物 量子点 荧光团 化学 材料科学 光电子学 光学 色谱法 选择性 物理 生物化学 抗生素 催化作用
作者
Jiaqi Miao,Jialuo Yu,Xinming Zhao,Xinru Chen,Congzheng Zhu,Xin Cao,Yan Huang,Bowei Li,Yixuan Wu,Lingxin Chen,Xiaoyan Wang
出处
期刊:Journal of Hazardous Materials [Elsevier BV]
卷期号:470: 134218-134218 被引量:65
标识
DOI:10.1016/j.jhazmat.2024.134218
摘要

The development of high-performance sensors for doxycycline (DOX) detection is necessary because its residue accumulation will cause serious harm to human health and the environment. Here, a novel tri-emission ratiometric fluorescence sensor was proposed by using "post-mixing" strategy of different emissions fluorescence molecularly imprinted polymers with salicylamide as dummy template (DMIPs). BSA was chosen as assistant functional monomer, and also acted as sensitizers for the aggregation-induced emission (AIE) effect of DOX. The blue-emitting carbon dots and the red-emitting CdTe quantum dots were separately introduced into DMIPs as the response signals. Upon DOX recognition within 2 min, blue and red fluorescence of the tri-emission DMIPs sensor were quenched while green fluorescence of DOX was enhanced, resulting in a wide range of color variations observed over bluish violet-rosered-light pink-orange-yellow-green with a detection limit of 0.061 μM. The sensor possessed highly selective recognition and was successfully applied to detect DOX in complicated real samples. Moreover, with the fluorescent color collection and data processing, the smartphone-assisted visual detection of the sensors showed satisfied sensitivity with low detection limit. This work provides great potential applications for rapid and visual detection of antibiotics in complex substrates.
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