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

被引:13
作者
Jiang, Xiaoqian [1 ,2 ]
Hao, Changlong [1 ,2 ]
Zhang, Hongyu [1 ,2 ]
Wu, Xiaoling [1 ,2 ]
Xu, Liguang [1 ,2 ]
Sun, Maozhong [1 ,2 ]
Xu, Chuanlai [1 ,2 ]
Kuang, Hua [1 ,2 ]
机构
[1] Jiangnan Univ, State Key Lab Food Sci & Technol, Int Joint Res Lab Biointerface & Biodetect, Wuxi 214122, Jiangsu, Peoples R China
[2] Jiangnan Univ, Sch Food Sci & Technol, Wuxi 214122, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
FexCuySe; upconversion nanoparticles; assemblies; intracellular; nicroRNA-21; detection; MAGNETIC-RESONANCE; LUMINESCENCE; FLUORESCENCE; NANOPLATFORM; NANOPROBES;
D O I
10.1021/acsami.0c00434
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In situ quantification and imaging of low-level intracellular microRNAs (miRs) are important areas in biosensor research. Herein, DNA-driven FexCuySe@ upconversion nanoparticle (UCNP) core@satellite nanostructures were developed to probe microRNA-21 (miR-21). FexCuySe@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 T-2 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(RNA). The limit of detection (LOD) was 0.0058 amol/ng(RNA) for the luminescence intensity and 0.0182 amol/ng(RNA) for the MRI signal. This method opens a new avenue for intracellular miR-21 detection with high sensitivity and specificity.
引用
收藏
页码:41405 / 41413
页数:9
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