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一种基于银纳米簇和 MoSe 纳米片相互调节的新型无标记双模式适体传感器,用于可靠检测氨苄西林。

A novel label-free dual-mode aptasensor based on the mutual regulation of silver nanoclusters and MoSe nanosheets for reliable detection of ampicillin.

机构信息

Center for Global Health, School of Public Health, Nanjing Medical University, 101 Longmian Avenue, Nanjing, 211166, PR China.

Key Lab of Modern Toxicology of Ministry of Education, School of Public Health, Nanjing Medical University, 101 Longmian Avenue, Nanjing, Jiangsu, 211166, China.

出版信息

Anal Chim Acta. 2023 Apr 22;1251:340997. doi: 10.1016/j.aca.2023.340997. Epub 2023 Feb 23.

DOI:10.1016/j.aca.2023.340997
PMID:36925307
Abstract

Current methods for the rapid detection of trace antibiotics in the environment remains problems of low accuracy and false negative or false positive, making the development of fast, and accurate, and reliable methods for antibiotic testing a major challenge that needs to be addressed. Herein, we developed a novel label-free colorimetric and fluorescent dual-mode aptasensor assembled by the strong interaction of layered MoSe nanosheets (MoSe NSs) with ampicillin (AMP) aptamer functionalized silver nanoclusters (Apt-AgNCs) that specifically bind AMP to allow the sensitive and selective detection of AMP. Apt-AgNCs could be adsorbed on the surface of MoSe NSs via van der Waals force to form a nanocomposite, Apt-AgNCs/MoSe NSs. Interestingly, Apt-AgNCs/MoSe NSs act together to construct dual mode aptasensor through modulation of the intrinsic peroxidase activity of MoSe NSs and the fluorescence of Apt-AgNCs. In the presence of AMP, Apt-AgNCs could specifically bind AMP, triggering desorption from the MoSe NSs surface, leading to a decrease in the peroxidase activity of the system with the recovery in Apt-AgNCs fluorescence. The dual-signal aptasensor exhibited good linear colorimetric and fluorescence responses in the AMP concentration ranges of 0.115-2.00 μM and 6-100 nM, respectively. Furthermore, the aptasensor was successfully measured AMP levels in commercially-bought milk and lake water with satisfactory results. Unlike single-signal aptasensors, the constructed dual-signal aptasensor could not only improve the detection precision, but also reduce the false positive or false negative results. These promising results suggest that the dual-readout strategy as demonstrated is general mode for the detection of other antibiotics or compounds using various aptamers functionalized AgNCs in concert with MoSe NSs.

摘要

目前,环境中痕量抗生素的快速检测方法仍然存在准确性低、假阴性或假阳性的问题,因此开发快速、准确、可靠的抗生素检测方法是一个亟待解决的主要挑战。在这里,我们开发了一种新型的无标记比色和荧光双模适体传感器,由层状 MoSe 纳米片(MoSe NSs)与氨苄西林(AMP)适体功能化的银纳米簇(Apt-AgNCs)的强相互作用组装而成,该适体传感器特异性结合 AMP 以实现对 AMP 的灵敏和选择性检测。Apt-AgNCs 可以通过范德华力吸附在 MoSe NSs 的表面上形成纳米复合材料,即 Apt-AgNCs/MoSe NSs。有趣的是,Apt-AgNCs/MoSe NSs 通过调节 MoSe NSs 的固有过氧化物酶活性和 Apt-AgNCs 的荧光来协同作用构建双模适体传感器。在 AMP 的存在下,Apt-AgNCs 可以特异性地结合 AMP,触发从 MoSe NSs 表面解吸,导致系统过氧化物酶活性降低,同时恢复 Apt-AgNCs 的荧光。该双模适体传感器在 AMP 浓度范围为 0.115-2.00 μM 和 6-100 nM 时分别表现出良好的比色和荧光响应线性。此外,该适体传感器成功地测量了市售牛奶和湖水样品中的 AMP 水平,结果令人满意。与单信号适体传感器不同,所构建的双模适体传感器不仅可以提高检测精度,还可以减少假阳性或假阴性结果。这些有前景的结果表明,所展示的双读数策略是使用各种与 MoSe NSs 协同作用的功能化 AgNCs 适体检测其他抗生素或化合物的通用模式。

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