4.8 Article

Speeding Up the Line-Scan Raman Imaging of Living Cells by Deep Convolutional Neural Network

Journal

ANALYTICAL CHEMISTRY
Volume 91, Issue 11, Pages 7070-7077

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.8b05962

Keywords

-

Funding

  1. National Natural Science Foundation of China [21633005, 21373173, 21790354, 21711530704]
  2. Ministry of Science and Technology of China [2016YFA0200601]
  3. Collaborative Innovation Center of High-End Equipment Manufacturing in Fujian

Ask authors/readers for more resources

Raman imaging is a promising technique that allows the spatial distribution of different components in the sample to be obtained using the molecular fingerprint information on individual species. However, the imaging speed is the bottleneck for the current Raman imaging methods to monitor the dynamic process of living cells. In this paper, we developed an artificial intelligence assisted fast Raman imaging method over the already fast line scan Raman imaging method. The reduced imaging time is realized by widening the slit and laser beam, and scanning the sample with a large scan step. The imaging quality is improved by a data-driven approach to train a deep convolutional neural network, which statistically learns to transform low-resolution images acquired at a high speed into high-resolution ones that previously were only possible with a low imaging speed. Accompanied with the improvement of the image resolution, the deteriorated spectral resolution as a consequence of a wide slit is also restored, thereby the fidelity of the spectral information is retained. The imaging time can be reduced to within 1 min, which is about five times faster than the state-of-the-art line scan Raman imaging techniques without sacrificing spectral and spatial resolution. We then demonstrated the reliability of the current method using fixed cells. We finally used the method to monitor the dynamic evolution process of living cells. Such an imaging speed opens a door to the label-free observation of cellular events with conventional Raman microscopy.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available