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铝(III)离子诱导的单磷酸腺苷封端的双金属纳米簇的聚集诱导发光增强及其在半胱氨酸荧光测定中的应用。

Aggregation-induced emission enhancement of adenosine monophosphate-capped bimetallic nanoclusters by aluminum(III) ions, and its application to the fluorometric determination of cysteine.

机构信息

State Key Laboratory of Supramolecular Structure and Materials, Institute of Theoretical Chemistry, Jilin University, No. 2699 Qianjin Street, Changchun, 130012, China.

Department of Hepatic-Biliary-Pancreatic Medicine, First Hospital, Jilin University, Changchun, 130021, China.

出版信息

Mikrochim Acta. 2019 Dec 12;187(1):41. doi: 10.1007/s00604-019-3901-z.

Abstract

The fluorescence of adenosine monophosphate-capped bimetallic gold and silver nanoclusters (type AuAgNC@AMP) is strongly enhanced and blue shifted in the presence of Al(III). As confirmed by transmission electron microscopy, the AuAgNC nanodots are converted to larger assembled spheres of type AuAgNC-Al(III). The fluorescence enhancement is attributed to aggregation-induced emission enhancement (AIEE). The fluorescence of the AuAgNC-Al(III) assembly (with excitation and emission maxima at 340 and 540 nm) is quenched by cysteine (Cys). The effect was applied to the fluorometric determination of Cys. The assay works in the 1.0 to 16.0 μM Cys concentration range and has a 50 nM limit of detection. The method was successfully applied to analyze Cys-spiked mineral waters and serum. The quenching mechanism is explored in depth. It is attributed to the partial replacement of AMP by Cys at the surface of the AuAgNC and alteration of the assembly structure from large spherical particles to a strip shape. Graphical abstractSchematic representation of the fluorescence enhancement of bimetallic nanoclusters capped with adenosine monophosphate by using Al(III), and its application in selective and sensitive determination of cysteine via ligand replacement and reassembly.

摘要

在三价铝(Al(III))存在的情况下,腺苷单磷酸封端的双金属金和银纳米团簇(AuAgNC@AMP)的荧光得到强烈增强并蓝移。透射电子显微镜证实,AuAgNC 纳米点转化为更大的 AuAgNC-Al(III)组装球体。荧光增强归因于聚集诱导的发射增强(AIEE)。AuAgNC-Al(III) 组装体(激发和发射最大值分别为 340nm 和 540nm)的荧光被半胱氨酸(Cys)猝灭。该效应被应用于半胱氨酸的荧光测定。该测定法在 1.0 至 16.0 μM Cys 浓度范围内有效,检测限为 50 nM。该方法成功应用于分析含 Cys 的矿泉水和血清。深入探讨了猝灭机制。它归因于在 AuAgNC 表面由 Cys 部分取代 AMP,以及组装结构从大球形颗粒改变为带状。

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