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基于高效稳定的 CH3NH3PbI3 量子点敏化 ZnO 纳米片作为光收集器的 miR-155 的超灵敏光电流型适体传感。

Ultrasensitive photoelectrochemical aptasensing of miR-155 using efficient and stable CH3NH3PbI3 quantum dots sensitized ZnO nanosheets as light harvester.

机构信息

Key Laboratory of Chemical Sensing & Analysis in Universities of Shandong, Key Laboratory of Fluorine Chemistry and Chemical Materials of Shandong Province, University of Jinan, Jinan 250022, China.

Central Laboratory, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, China.

出版信息

Biosens Bioelectron. 2016 Nov 15;85:142-150. doi: 10.1016/j.bios.2016.04.099. Epub 2016 Apr 30.

Abstract

An ultrasensitive photoelectrochemical (PEC) aptasensor based on a novel signal amplification strategy was developed for the quantitative determination of microRNA (miR)-155. CH3NH3PbI3 quantum dots (QDs) functionalized ZnO nanosheets (NSs) were employed as the light harvester. Owing to the synergetic effect between CH3NH3PbI3 QDs and ZnO NSs, ZnO@CH3NH3PbI3 can provide an obviously increasing PEC signal by forming the heterojunction. Due to the larger steric hindrance, the sensitive decrease of the PEC signal can be achieved by the specific recognition between the primers and ssDNA of miR-155. In this sense, this developed aptasensor can achieve a high sensitivity (especially in the presence of the low concentrations of miR-155) and a wide detection range (0.01fmol/L to 20,000pmol/L). Under the optimal conditions, the proposed aptasensor offered an ultrasensitive and specific determination of miR-155 down to 0.005fmol/L. This aptassay method would open up a new promising platform at ultralow levels for early diagnose of different miRNA.

摘要

基于一种新颖的信号放大策略,开发了一种超灵敏光电化学(PEC)适体传感器,用于定量测定 microRNA(miR)-155。CH3NH3PbI3 量子点(QDs)功能化的 ZnO 纳米片(NSs)被用作光收集器。由于 CH3NH3PbI3 QDs 和 ZnO NSs 之间的协同效应,ZnO@CH3NH3PbI3 可以通过形成异质结提供明显增加的 PEC 信号。由于较大的空间位阻,引物和 miR-155 的 ssDNA 之间的特异性识别可以实现 PEC 信号的灵敏降低。从这个意义上说,这种开发的适体传感器可以实现高灵敏度(特别是在低浓度 miR-155 的存在下)和宽检测范围(0.01fmol/L 至 20,000pmol/L)。在最佳条件下,该适体传感器提供了对 miR-155 的超灵敏和特异性检测,低至 0.005fmol/L。这种适体分析方法将为不同 miRNA 的早期诊断开辟一个用于超低水平的新的有前途的平台。

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