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双模 FeCuSe 和上转换纳米粒子组装用于细胞内 microRNA-21 的检测。

Dual-Modal FeCuSe and Upconversion Nanoparticle Assemblies for Intracellular MicroRNA-21 Detection.

出版信息

ACS Appl Mater Interfaces. 2021 Sep 8;13(35):41405-41413. doi: 10.1021/acsami.0c00434. Epub 2020 Mar 19.

Abstract

In situ quantification and imaging of low-level intracellular microRNAs (miRs) are important areas in biosensor research. Herein, DNA-driven FeCuSe@upconversion nanoparticle (UCNP) core@satellite nanostructures were developed to probe microRNA-21 (miR-21). FeCuSe@UCNP probes displayed dual signals: upconversion luminescence (UCL) and magnetic resonance imaging (MRI). In the presence of miR-21, the luminescence signal was restored and the value was significantly increased because of dissociation of UCNPs from the assemblies. There was a good linear relationship between the dual signals and the expression levels of miR-21 in the range of 0.035-31.824 amol/ng. The limit of detection (LOD) was 0.0058 amol/ng for the luminescence intensity and 0.0182 amol/ng for the MRI signal. This method opens a new avenue for intracellular miR-21 detection with high sensitivity and specificity.

摘要

在生物传感器研究中,对低水平细胞内 microRNA(miRs)进行原位定量和成像分析是一个重要的领域。本文构建了 DNA 驱动的 FeCuSe@上转换纳米粒子(UCNP)核@卫星纳米结构,用于探测 microRNA-21(miR-21)。FeCuSe@UCNP 探针表现出双信号:上转换发光(UCL)和磁共振成像(MRI)。在 miR-21 存在的情况下,由于 UCNPs 从组装体中解离,发光信号得到恢复, 值显著增加。双信号与 miR-21 的表达水平之间存在良好的线性关系,其范围为 0.035-31.824 amol/ng。发光强度的检测限(LOD)为 0.0058 amol/ng,MRI 信号的检测限为 0.0182 amol/ng。该方法为具有高灵敏度和特异性的细胞内 miR-21 检测开辟了新途径。

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