循环肿瘤细胞
流式细胞术
纳米传感器
原位
微流控
单细胞分析
细胞
纳米技术
材料科学
费斯特共振能量转移
癌细胞
小RNA
化学
荧光
癌症
分子生物学
生物
基因
生物化学
转移
有机化学
物理
量子力学
遗传学
作者
Junyue Chen,Gerile Oudeng,Hongtao Feng,Sixi Liu,Hung‐Wing Li,Yi‐Ping Ho,Yan Chen,Ying Tan,Mo Yang
出处
期刊:Small
[Wiley]
日期:2022-07-14
卷期号:18 (32)
被引量:32
标识
DOI:10.1002/smll.202201779
摘要
Abstract Current circulating tumor cells (CTCs) detection strategies based on surface epithelial markers suffer from low specificity in distinguishing between CTCs and epithelial cells in hematopoietic cell population. Tumor‐associated miRNAs within CTCs are emerging as new biomarkers due to their high correlation with tumor development and progress. However, in‐situ simultaneous analysis of multiple miRNAs in single CTC cell is still challenging. To overcome this limitation, a digital droplet microfluidic flow cytometry based on biofunctionalized 2D metal‐organic framework nanosensor (Nano‐DMFC) is developed for in situ detection of dual miRNAs simultaneously in single living breast cancer cells. Here, 2D MOF‐based fluorescent resonance energy transfer (FRET) nanosensors are established by conjugating dual‐color fluorescence dye‐labeled DNA probes on MOF nanosheet surface. In the Nano‐DMFC, 2D MOF‐based nanoprobes are precisely microinjected into each single‐cell encapsulated droplets to achieve dual miRNA characterization in single cancer cell. This Nano‐DMFC platform successfully detects dual miRNAs at single‐cell resolution in 10 mixed positive MCF‐7 cells out of 10 000 negative epithelial cells in serum biomimic samples. Moreover, this Nano‐DMFC platform shows good reproductivity in the recovery experiment of spiked blood samples, which demonstrate the high potential for CTC‐based cancer early diagnosis and prognosis.
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