State Key Laboratory of Environment Health (Incubation), Key Laboratory of Environment and Health, Ministry of Education, Key Laboratory of Environment and Health (Wuhan), Ministry of Environmental Protection, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, #13 Hangkong Road, Wuhan, 430030, China.
Department of Forensic Medicine, Huazhong University of Science and Technology, #13 Hangkong Road, Wuhan, 430030, China.
Mikrochim Acta. 2022 Aug 8;189(9):324. doi: 10.1007/s00604-022-05405-3.
An electromembrane microextraction (EME)-assisted fluorescent molecularly imprinted polymer (MIP) sensing method is presented for detecting the total cathinone drugs in urine samples. In this detection system, the clean-up ability of EME eliminated the matrix effects on both target binding with MIPs and the luminescence of the fluorophore in the sensor. Moreover, by optimizing the extraction conditions of EME, different cathinone drugs with a same concentration show a same response on the single aggregation induced emission (AIE) based MIP (AIE-MIP) sensor (λ = 360 nm, λ = 467 nm). The recoveries were 57.9% for cathinone (CAT) and 78.2% for methcathinone (MCAT). The EME-assisted "light-up" AIE-MIP sensing method displayed excellent performance with a linear range of 2.0-12.0 μmol L and a linear determination coefficient (R) of 0.99. The limit of detection (LOD) value for EME-assisted "light-up" AIE-MIP sensing method was 0.3 μmol L. The relative standard deviation (RSD) values for the detection were found to be within the range 2.0-12.0%. To the best of our knowledge, this is the first time that determination of total illicit drugs with a single fluorescent MIP sensor was achieved and also the first utilization of sample preparation to tune the sensing signal of the sensor to be reported. We believe that this versatile combination of fluorescent MIP sensor and sample preparation can be used as a common protocol for sensing the total amount of a group of analytes in various fields.
一种基于电膜微萃取(EME)辅助的荧光分子印迹聚合物(MIP)传感方法被提出,用于检测尿液样品中的总卡他碱类药物。在这个检测系统中,EME 的净化能力消除了基质效应对目标与 MIP 结合以及传感器中荧光团发光的影响。此外,通过优化 EME 的萃取条件,不同浓度的卡他碱类药物在基于单一聚集诱导发射(AIE)的 MIP(AIE-MIP)传感器上表现出相同的响应(λ=360nm,λ=467nm)。卡他碱(CAT)和甲卡西酮(MCAT)的回收率分别为 57.9%和 78.2%。EME 辅助的“点亮”AIE-MIP 传感方法具有出色的性能,线性范围为 2.0-12.0μmol L,线性决定系数(R)为 0.99。EME 辅助的“点亮”AIE-MIP 传感方法的检测限(LOD)值为 0.3μmol L。检测的相对标准偏差(RSD)值在 2.0-12.0%范围内。据我们所知,这是首次使用单一荧光 MIP 传感器来测定总非法药物,也是首次利用样品制备来调节传感器的传感信号。我们相信,这种荧光 MIP 传感器和样品制备的多功能组合可以用作在各个领域中检测一组分析物总量的通用协议。