Chen Panpan, Xu Xin, Ji Jiangrong, Wu Jiafeng, Lu Tian, Xia Yuhong, Wang Liping, Fan Junting, Jin Yang, Zhang Liying, Du Shuhu
School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, 211166, China.
School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, 211166, China.
Anal Chim Acta. 2020 Nov 22;1138:99-107. doi: 10.1016/j.aca.2020.09.011. Epub 2020 Sep 8.
The fluorescence-based assay of iodide ion (I) has been extensively studied by the use of different sensing probes and techniques, but it remains a tricky task to eliminate the interference of chloride ion (Cl) for the analysis of low-level I in complex genuine samples. Herein, we develop a redox pretreatment strategy for specific separating I from human urine. Simultaneously, a novel ratiometric fluorescent probe is constructed by a simple mixing of dimer DNA silver nanoclusters (dDNA-AgNCs) and carbon dots (CDs) with the ratio of 5:1 in fluorescent intensity, and used for visual assay of I. After addition of I, the fluorescence of orange dDNA-AgNCs can be quenched by I as the result of I-induced oxidative etching and aggregation of dDNA-AgNCs, while blue CDs as the stable internal standard are unresponsive to I. With the increase of I, the fluorescence intensity ratio (I/I) of binary-color probe gradually decreased, which leads to color variation from salmon pink to lighter salmon pink to lilac to light steel blue to final deep sky blue (under a UV lamp) with a sensitive detection limit of 19.8 nM. The assay for I can also be convenient to implement for visual monitoring of I by observing color change of test paper printed with the ratiometric probe, responding to 50 nM that is about 1 order of magnitude lower than the median urinary I concentration defined by the World Health Organization (WHO) for school-age children. The sensitive test paper can provide an advanced platform for colorimetric and visual monitoring of I in human urine.
基于荧光的碘离子(I⁻)检测方法已通过使用不同的传感探针和技术进行了广泛研究,但在复杂的真实样品中分析低水平的I⁻时,消除氯离子(Cl⁻)的干扰仍然是一项棘手的任务。在此,我们开发了一种氧化还原预处理策略,用于从人尿中特异性分离I⁻。同时,通过将二聚体DNA银纳米簇(dDNA-AgNCs)和碳点(CDs)以荧光强度比为5:1简单混合构建了一种新型比率荧光探针,并用于I⁻的可视化检测。加入I⁻后,橙色的dDNA-AgNCs的荧光会因I⁻诱导的dDNA-AgNCs的氧化蚀刻和聚集而被淬灭,而蓝色的CDs作为稳定的内标对I⁻无响应。随着I⁻的增加,双色探针的荧光强度比(I₅₂₅/I₄₆₅)逐渐降低,导致颜色从鲑鱼粉变为浅鲑鱼粉再变为丁香紫再变为浅钢蓝最后变为深天蓝(在紫外灯下),检测限低至19.8 nM。通过观察印有比率探针的试纸颜色变化,I⁻检测也可方便地用于I⁻的可视化监测,对50 nM的I⁻有响应,这比世界卫生组织(WHO)为学龄儿童定义的尿I⁻中位数浓度低约1个数量级。这种灵敏的试纸可为人体尿液中I⁻的比色和可视化监测提供一个先进的平台。