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通过鱼精蛋白修饰的金纳米簇的聚集诱导荧光猝灭和基于 9-羟基菲的敏化作用测定 1-羟基芘。

Assay of 1-hydroxypyrene via aggregation-induced quenching of the fluorescence of protamine-modified gold nanoclusters and 9-hydroxyphenanthrene-based sensitization.

机构信息

College of Public Health, University of South China, Hengyang, 421001, People's Republic of China.

出版信息

Mikrochim Acta. 2019 Oct 16;186(11):700. doi: 10.1007/s00604-019-3810-1.

Abstract

This work describes a method for the determination of 1-hydroxypyrene (OH-Py) via aggregation-induced quenching of the emission of protamine-coated gold nanoclusters using 9-hydroxyphenanthrene (OH-Phe) as a sensitizer to boost the emission efficiency of nanoprobe. Under optimum conditions, the drop in fluorescence intensity at excitation/emission wavelengths of 300/596 nm is proportional to the concentrations of OH-Py in the range from 1.0 to 65 nM. The relative standard deviations are 4.2, 2.4 and 1.9% (for n = 11) at concentration levels of 8.0, 32 and 48 nM of OH-Py, respectively. The detection limit is 0.3 nM which is much lower than that of some previously reported methods. The recoveries from urine samples spiked with OH-Py ranged between 94.4 and 98.8%. Graphical abstract 1-Hydroxypyrene (OH-Py) can trigger the aggregation of protamine-gold nanoclusters (PRT-AuNCs), resulting in the emission quenching of PRT-AuNCs. 9-Hydroxyphenanthrene (OH-Phe) can boost the emission efficiency of nanoprobe. Thereby, a highly sensitive assay of OH-Py was established.

摘要

本文描述了一种通过 9-羟基菲(OH-Phe)作为增敏剂来增强纳米探针的发射效率,从而利用凝聚诱导金纳米团簇的发射猝灭来测定 1-羟基芘(OH-Py)的方法。在最佳条件下,激发/发射波长为 300/596nm 时荧光强度的下降与 OH-Py 在 1.0 至 65nM 的浓度范围内成正比。在浓度分别为 8.0、32 和 48nM 的 OH-Py 时,相对标准偏差分别为 4.2%、2.4%和 1.9%(n=11)。检测限为 0.3nM,远低于一些已报道的方法。尿液样品中加入 OH-Py 的回收率在 94.4%至 98.8%之间。

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