期刊
OPTICS LETTERS
卷 46, 期 19, 页码 4785-4788出版社
OPTICAL SOC AMER
DOI: 10.1364/OL.428731
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类别
资金
- Innovation and Technology Commission [ITS/394/17]
- Croucher Foundation [CM/CT/CF/CIA/0688/19ay]
This study introduces and demonstrates a high-speed FPM method based on laser illumination and digital micro-mirror devices for illumination angle scanning. With this method, quantitative phase imaging and intensity imaging can be achieved at over 42 frames per second with approximately 1 micron lateral resolution, enabling the visualization of membrane height fluctuations in red blood cells and subcellular features in stained cancer tissue slices.
Fourier ptychographic microscopy (FPM), as an emerging computational imaging method, has been applied to quantitative phase imaging with resolution bypassing the physical limit of the detection objective. Due to the weak illumination intensity and long image acquisition time, the achieved imaging speed in current FPM methods is still low, making them unsuitable for real-time imaging applications. We propose and demonstrate a high-speed FPM method based on using laser illumination and digital micro-mirror devices for illumination angle scanning. In this new, to the best of our knowledge, FPM method, we realized quantitative phase imaging and intensity imaging at over 42 frames per second (fps) with around 1 mu m lateral resolution. The quantitative phase images have revealed membrane height fluctuations of red blood cells with nanometer-scale sensitivity, while the intensity images have resolved subcellular features in stained cancer tissue slices. (C) 2021 Optical Society of America
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