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Ascorbic acid induced enhancement of room temperature phosphorescence of sodium tripolyphosphate-capped Mn-doped ZnS quantum dots: Mechanism and bioprobe applications

机译:抗坏血酸诱导的三聚磷酸钠掺杂的锰掺杂的ZnS量子点的室温磷光增强:机理和生物探针应用

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摘要

Although quantum dot (QD)-based room temperature phosphorescence (RTP) probes are promising for practical applications in complex matrixes such as environmental, food and biological samples, current QD-based-RTP probes are not only quite limited but also exclusively based on the RTP quenching mechanism. Here we report an ascorbic acid (AA) induced phosphorescence enhancement of sodium tripolyphosphate-capped Mn-doped ZnS QDs, and its application for turn-on RTP detection. The chelating ability allows AA to extract the Mn and Zn from the surface of the QDs and to generate more holes which are subsequently trapped by Mn~(2+), while the reducing property permits AA to reduce Mn ~(3+) to Mn~(2+) in the excited state, thereby enhancing the excitation and orange emission of the QDs. The enhanced RTP intensity of the QDs increases linearly with the concentration of AA in the range of 0.050.8μM. Thus, a QD-based RTP probe for AA is developed. The proposed QD-based turn-on RTP probe avoids tedious sample pretreatment, and offers good sensitivity and selectivity for AA in the presence of the main relevant metal ions and other molecules in biological fluids. The limit of detection (3s) of the developed method is 9nM AA, and the relative standard deviation is 4.8% for 11 replicate detections of 0.1μM AA. The developed method is successfully applied to the analysis of real samples of human urine and plasma for AA with quantitative recoveries from 96 to 105%.
机译:尽管基于量子点(QD)的室温磷光(RTP)探针在诸如环境,食品和生物样品等复杂基质中的实际应用前景广阔,但当前基于QD的RTP探针不仅受到局限,而且还基于RTP淬火机制。在这里,我们报告了抗坏血酸(AA)诱导的三聚磷酸钠封端的Mn掺杂的ZnS QDs的磷光增强,及其在开启RTP检测中的应用。螯合能力使AA从QD的表面提取Mn和Zn并产生更多的空穴,这些空穴随后被Mn〜(2+)捕获,而还原性能使AA将Mn〜(3+)还原为Mn。 〜(2+)处于激发态,从而增强了量子点的激发和橙色发射。 QA的增强的RTP强度随着AA浓度在0.050.8μM范围内线性增加。因此,开发了用于AA的基于QD的RTP探针。所提出的基于QD的开启式RTP探针避免了繁琐的样品预处理,并且在生物流体中存在主要相关金属离子和其他分子的情况下,对AA具有良好的灵敏度和选择性。所开发方法的检出限(3s)为9nM AA,对于0.1μAAA的11次重复检测,相对标准偏差为4.8%。所开发的方法已成功地用于分析人体尿液和血浆中的AA样品,定量回收率为96%至105%。

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