基于合金CdZnSeS/ZnS量子点的发光关闭纳米传感器检测血浆和血液中的阿霉素。

IF 5.3 2区 化学 Q1 CHEMISTRY, ANALYTICAL
Svetlana A Mescheryakova, Daria G Koganova, Daria V Tsyupka, Danila A Kornilov, Pavel S Pidenko, Daniil D Drozd, Olga A Goryacheva, Irina Yu Goryacheva
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引用次数: 0

摘要

研究了基于合金CdZnSeS/ZnS量子点(QDs)的发光关闭纳米传感器检测血浆和血液中阿霉素(Dox)的可行性。仔细研究了Dox存在下的QD发光猝灭。选择最佳检测条件,包括血浆稀释度和QD浓度。计算出的检出限为0.02µg/mL。时间分辨量子点发光猝灭和吸收测量使我们能够确定猝灭过程是通过组合机制发生的。在低还原浓度下,动态猝灭占主导地位,而在2.5 μM以上的还原浓度下,静态猝灭的贡献急剧增加。采用全血Dox检测方法,并与其他血药检测方法进行比较。该方法的结果与紫外可见高效液相色谱法相当。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Doxorubicin detection in plasma and blood using a luminescence turn-off nanosensor based on alloyed CdZnSeS/ZnS quantum dots.

The feasibility of doxorubicin (Dox) detection in plasma and blood using a luminescence turn-off nanosensor based on alloyed CdZnSeS/ZnS quantum dots (QDs) is demonstrated. The QD luminescence quenching in the presence of Dox was carefully examined. Optimal assay conditions were selected, including plasma dilution and QD concentration. The calculated limit of detection value was 0.02 µg/mL. Time-resolved QD luminescence quenching and absorption measurements allowed us to determine that the quenching process occurs via a combined mechanism. At low Dox concentrations, the dynamic quenching is predominant, while at Dox concentrations above 2.5 μM, the contribution of static quenching increases drastically. Dox detection in whole human blood was performed and compared with other methods for the drug detection in blood. The results of the method are comparable with those of the high-performance liquid chromatography with ultraviolet-visible detection.

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来源期刊
Microchimica Acta
Microchimica Acta 化学-分析化学
CiteScore
9.80
自引率
5.30%
发文量
410
审稿时长
2.7 months
期刊介绍: As a peer-reviewed journal for analytical sciences and technologies on the micro- and nanoscale, Microchimica Acta has established itself as a premier forum for truly novel approaches in chemical and biochemical analysis. Coverage includes methods and devices that provide expedient solutions to the most contemporary demands in this area. Examples are point-of-care technologies, wearable (bio)sensors, in-vivo-monitoring, micro/nanomotors and materials based on synthetic biology as well as biomedical imaging and targeting.
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