4.8 Article

2D MOF Nanosensor-Integrated Digital Droplet Microfluidic Flow Cytometry for In Situ Detection of Multiple miRNAs in Single CTC Cells

期刊

SMALL
卷 18, 期 32, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202201779

关键词

droplet-based microfluidics; multiple miRNAs detection; nanosensor; single-cell analysis

资金

  1. Shenzhen-Hong Kong-Macao Science and Technology Plan Project [SGDX2020110309260000]
  2. Research Grants Council (RGC) of Hong Kong Collaborative Research Grant [C5011-19G]
  3. National Natural Science Foundation of China [61875221]
  4. Innovation and Technology Fund
  5. Guangdong-Hong Kong Cooperation Scheme [GHP-039-18GD, 2019A050503008]
  6. Research Grants Council (RGC) of Hong Kong General Research Grant [15217621, 15210818]
  7. Shenzhen Fundamental Research Program [JCYJ20200109115601720]

向作者/读者索取更多资源

Current strategies for detecting circulating tumor cells (CTCs) based on surface epithelial markers have low specificity in distinguishing between CTCs and epithelial cells in the hematopoietic cell population. As tumor-associated miRNAs are highly correlated with tumor development and progression, they are emerging as new biomarkers. However, simultaneous analysis of multiple miRNAs in a single CTC cell is still challenging. In this study, a digital droplet microfluidic flow cytometry platform based on biofunctionalized 2D metal-organic framework nanosensors (Nano-DMFC) was developed for in situ detection of dual miRNAs simultaneously in single living breast cancer cells. This platform successfully detected dual miRNAs at single-cell resolution and showed good reproducibility in the recovery experiment of spiked blood samples, demonstrating its high potential for CTC-based cancer early diagnosis and prognosis.
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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