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DNA 酶介导的基于磁球负载金纳米粒子和 CdSe/ZnS 量子点的比率荧光法测定 Pb(II)离子。

DNA enzyme mediated ratiometric fluorescence assay for Pb(II) ion using magnetic nanosphere-loaded gold nanoparticles and CdSe/ZnS quantum dots.

机构信息

National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Key Laboratory of Fermentation Engineering (Ministry of Education), College of Bioengineering and Food, Hubei University of Technology, Wuhan, 430068, Hubei, People's Republic of China.

College of Life Science, Yangtze University, Jingzhou, 434023, Hubei, People's Republic of China.

出版信息

Mikrochim Acta. 2020 Apr 15;187(5):273. doi: 10.1007/s00604-020-04230-w.

Abstract

Based on the inner filter effect mechanism of quantum dots, a ratiometric fluorescence nanoprobe was constructed for the determination of Pb(II) ion. Green emitting quantum dots conjugated with DNA substrate (DNA) acted as donors providing green fluorescence, while gold nanoparticles coupled with DNA enzyme (DNA) as acceptors quench the green fluorescence. Meanwhile, FeO nanosphere served as magnetic substrates to facilitate separation process and red fluorescence as an "inner rule" to eliminate the background signal. In the presence of Pb(II) ion, the DNA specifically recognize and capture Pb(II) ion with enhanced catalytic activity, which can cleave DNA and "turn on" the green fluorescence (I), while the red fluorescence (I) remained unchanged. In this way, the ratio of I/I reflects the Pb(II) ion in the system, enabling the quantitative and selective determination of Pb(II) ion over nine different metal ions. Under optimal conditions, the ratiometric fluorescence assay showed good linearity (R = 0.98) within the range 10 to 100 ng mL. The limit of detection (LOD) was calculated to be 1.79 pg mL (S/N = 3, n = 3, ±3.8%). The proposed fluorescence nanoprobe provides better sensitivity and accuracy than non-ratiometric signal evaluation for Pb(II) ion determination. Schematic representation of ratiometric fluorescence nanoprobe for Pb(II) ion detection using green fluorescence of I as "signal switch" and red fluorescence of I as "inner rule." Graphical abstract.

摘要

基于量子点的内滤效应机制,构建了一种比率荧光纳米探针用于测定 Pb(II)离子。绿色发射的量子点与 DNA 底物(DNA)缀合作为供体提供绿色荧光,而金纳米粒子与 DNA 酶(DNA)偶联作为受体猝灭绿色荧光。同时,FeO 纳米球作为磁性基质促进分离过程,红色荧光作为“内标”消除背景信号。在存在 Pb(II)离子的情况下,DNA 特异性识别并捕获具有增强催化活性的 Pb(II)离子,可切割 DNA 并“开启”绿色荧光(I),而红色荧光(I)保持不变。这样,I/I 的比值反映了体系中的 Pb(II)离子,实现了对 9 种不同金属离子的定量和选择性测定 Pb(II)离子。在最佳条件下,比率荧光分析显示出在 10 至 100ng mL 范围内良好的线性关系(R=0.98)。检测限(LOD)计算为 1.79 pg mL(S/N=3,n=3,±3.8%)。与非比率信号评估相比,该荧光纳米探针为 Pb(II)离子测定提供了更好的灵敏度和准确性。

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