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用于锌和锰的双功能量子点中的多重能量转移机制。

Multiplexed energy transfer mechanisms in a dual-function quantum dot for zinc and manganese.

作者信息

Ruedas-Rama Maria Jose, Hall Elizabeth A H

机构信息

Institute of Biotechnology, Department of Chemical Engineering and Biotechnology, University of Cambridge, Tennis Court Road, Cambridge, UKCB2 1QT.

出版信息

Analyst. 2009 Jan;134(1):159-69. doi: 10.1039/b814879a. Epub 2008 Nov 24.

Abstract

Photoexcited quantum dots (QDs) offer a wealth of mechanisms for interactions with the valence band holes or conduction band electrons, influencing electron-hole recombination. The potential to use combinations of these mechanistic pathways to achieve detection of different metal ions with one modified QD system has been tested. Dual-function water-soluble core/shell-modified CdSe/ZnS quantum dot nanoparticles have been created, that exploit two different fluorescence emission pathways for the detection of two heavy metal ions: Zn(2+) and Mn(2+). A QD-zincon system is proposed, which shows a static Perrin-type quenching mechanism, with sphere of action radii 1.1, 1.3 and 1.6 nm respectively, for 500, 540 and 620 nm QD emission. The QD-zincon system was produced using a layer-by-layer approach: mercaptopropionic acid-capped QDs were modified with a positive polyelectrolyte by electrostatic interaction and then a negatively charged chromogenic reagent, zincon, classically used for the determination of metals. QD-zincon is able to coordinate both Zn(2+) and Mn(2+) and, by exploiting two different mechanisms, QD-zincon conjugates can be tailored to respond to Zn(2+) or Mn(2+). Upon coordination of zincon with Mn(2+), a dramatic enhancement of the fluorescence intensity results as the quenching interaction between zincon and QDs is deactivated, thereby 'switching on the fluorescence emission'. The versatility of this system is demonstrated in terms of fluorescent emission wavelength, which could be selected across a wide range, through choice of QDs (examples are shown for lambda(max) = 500, 540 and 620 nm). In contrast, in the case of Zn(2+) detection, the mechanism is based on the radiationless resonance energy transfer (RET) from QDs acting as donor, to the acceptor zincon-Zn(2+), since its absorption spectra offer adequate overlap with the emission spectra of QD(540) and QD(620), producing a useful analytical signal by the RET process. Using these different operating principles, CdSe/ZnS core/shell QD-zincon conjugates showed very good linearity in the range 10-1000 microM and 5-500 microM for Zn(2+) and Mn(2+) nanosensors, respectively, and RSDs about 3% (n = 10). In a study of interferences, the QD-zincon conjugate showed higher selectivity than the corresponding method with zincon in solution. The results from synthetic ionic mixtures suggested very good applicability in the determination of Zn(2+) and Mn(2+) in samples containing other metal ions, with just a small reduction of sensitivity at very high ionic concentration.

摘要

光激发量子点(QDs)提供了丰富的与价带空穴或导带电子相互作用的机制,影响着电子-空穴复合。利用这些机制途径的组合,通过一个修饰的量子点系统实现对不同金属离子的检测,这一潜力已得到验证。已制备出具有双功能的水溶性核/壳修饰的CdSe/ZnS量子点纳米颗粒,其利用两种不同的荧光发射途径来检测两种重金属离子:Zn(2+)和Mn(2+)。提出了一种量子点-锌试剂系统,该系统显示出静态的佩林型猝灭机制,对于500、540和620 nm的量子点发射,其作用球半径分别为1.1、1.3和1.6 nm。量子点-锌试剂系统采用层层组装法制备:巯基丙酸封端的量子点通过静电相互作用用阳离子聚电解质进行修饰,然后再与经典用于金属测定的带负电荷的显色试剂锌试剂结合。量子点-锌试剂能够与Zn(2+)和Mn(2+)都发生配位,并且通过利用两种不同的机制,可以对量子点-锌试剂共轭物进行定制,使其对Zn(2+)或Mn(2+)作出响应。当锌试剂与Mn(2+)配位时,由于锌试剂与量子点之间的猝灭相互作用被消除,荧光强度会显著增强,从而“开启荧光发射”。该系统的多功能性体现在荧光发射波长方面,通过选择量子点(给出了λ(max)=500、540和620 nm的示例),可以在很宽的范围内进行选择。相比之下,在检测Zn(2+)的情况下,其机制基于从作为供体的量子点到受体锌试剂-Zn(2+)的无辐射共振能量转移(RET),因为其吸收光谱与量子点(540)和量子点(620)的发射光谱有足够的重叠,通过RET过程产生有用的分析信号。利用这些不同的工作原理,CdSe/ZnS核/壳量子点-锌试剂共轭物对于Zn(2+)和Mn(2+)纳米传感器分别在10 - 1000 μM和5 - 500 μM范围内显示出非常好的线性,相对标准偏差约为3%(n = 10)。在干扰研究中,量子点-锌试剂共轭物比溶液中相应的锌试剂方法显示出更高的选择性。合成离子混合物的结果表明,该方法在测定含有其他金属离子的样品中的Zn(2+)和Mn(2+)时具有很好的适用性,只是在非常高的离子浓度下灵敏度略有降低。

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