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Wide-field imaging and flow cytometric analysis of cancer cells in blood by fluorescent nanodiamond labeling and time gating
Nanodiamonds containing high density ensembles of negatively charged nitrogen-vacancy (NV(−)) centers are promising fluorescent biomarkers due to their excellent photostability and biocompatibility. The NV(−) centers in the particles have a fluorescence lifetime of up to 20 ns, which distinctly diff...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4081895/ https://www.ncbi.nlm.nih.gov/pubmed/24994610 http://dx.doi.org/10.1038/srep05574 |
Sumario: | Nanodiamonds containing high density ensembles of negatively charged nitrogen-vacancy (NV(−)) centers are promising fluorescent biomarkers due to their excellent photostability and biocompatibility. The NV(−) centers in the particles have a fluorescence lifetime of up to 20 ns, which distinctly differs from those (<10 ns) of cell and tissue autofluorescence, making it possible to achieve background-free detection in vivo by time gating. Here, we demonstrate the feasibility of using fluorescent nanodiamonds (FNDs) as optical labels for wide-field time-gated fluorescence imaging and flow cytometric analysis of cancer cells with a nanosecond intensified charge-coupled device (ICCD) as the detector. The combined technique has allowed us to acquire fluorescence images of FND-labeled HeLa cells in whole blood covered with a chicken breast of ~0.1-mm thickness at the single cell level, and to detect individual FND-labeled HeLa cells in blood flowing through a microfluidic device at a frame rate of 23 Hz, as well as to locate and trace FND-labeled lung cancer cells in the blood vessels of a mouse ear. It opens a new window for real-time imaging and tracking of transplanted cells (such as stem cells) in vivo. |
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