4.8 Article

The video-rate imaging of sub-10 nm plasmonic nanoparticles in a cellular medium free of background scattering

Journal

CHEMICAL SCIENCE
Volume 12, Issue 8, Pages 3017-3024

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0sc04764c

Keywords

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Funding

  1. National Natural Science Foundation of China [21675081, 22034003]
  2. Excellent Research Program of Nanjing University [ZYJH004]
  3. State Key Laboratory of Analytical Chemistry for Life Sciences [5431ZZXM2002]

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Plasmonic nanoparticles like gold and silver have potential as nanoprobes for biological sensing and imaging, with a demand for small gold nanoparticles (Au NPs) comparable in size to quantum dots and fluorescent proteins. Very small nanoparticles below the Rayleigh limit are difficult to visualize using light scattering with a dark-field microscope, and while a photothermal microscope can detect them, its imaging speed is too slow for live cell processes. The absorption modulated scattering microscopy (AMSM) method allows for imaging sub-10 nm Au NPs within a cellular medium, offering sensitivity similar to photothermal microscopy but with a much faster imaging speed suitable for dynamic tracking of small nanoparticles in living cells.
Plasmonic nanoparticles (e.g., gold, silver) have attracted much attention for biological sensing and imaging as promising nanoprobes. Practical biomedical applications demand small gold nanoparticles (Au NPs) with a comparable size to quantum dots and fluorescent proteins. Very small nanoparticles with a size below the Rayleigh limit (usually <30-40 nm) are hard to see by light scattering using a dark-field microscope, especially within a cellular medium. A photothermal microscope is able to detect very small nanoparticles, down to a few nanometers, but the imaging speed is usually too slow (minutes to hours) to image living cell processes. Here an absorption modulated scattering microscopy (AMSM) method is presented, which allows for the imaging of sub-10 nm Au NPs within a cellular medium. The unique physical mechanism of AMSM offers the remarkable ability to remove the light scattering background of the cellular component. In addition to having a sensitivity comparable to that of photothermal microscopy, AMSM has a much higher imaging speed, close to the video rate (20 fps), which allows for the dynamic tracking of small nanoparticles in living cells. This AMSM method might be a valuable tool for living cell imaging, using sub-10 nm Au NPs as biological probes, and thereby unlocking many new applications, such as single molecule labeling and the dynamic tracking of molecular interactions.

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