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Single-pixel phase and fluorescence microscope

delete2018-11-27
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OA
AI
刘
刘洋 (Yang Liu)
索
索津莉 (Jinli Suo) *
Y
Yuanlong Zhang
戴
戴琼海 (Qionghai Dai)
DOI:10.1364/OE.26.032451delete
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Abstract

Abstract

En 中文
Multimodal microscopes either use multiple cameras or a single camera to multiplex different modes spatially. The former needs expertise demanding alignment and the latter suffers from limited spatial resolution. Here, we report an alignment-free full-resolution simultaneous fluorescence and phase imaging approach using single-pixel detectors. By combining reference-free interferometry with single-pixel imaging scheme, we employ structured illumination to encode the phase and fluorescence of the sample into two single-pixel detection arms, and then conduct reconstruction computationally from the illumination patterns and recorded correlated measurements. The recovered fluorescence and phase images are inherently aligned thanks to single-pixel imaging scheme. To validate the proposed method, we built a proof-of-concept setup for first imaging the phase of an etched glass with given etching depth and then imaging the phase and fluorescence of the quantum dot sample. This method holds great potential for multispectral fluorescence microscopy with additional single-pixel detectors or a spectrometer. Besides, this cost-efficient multimodal system might find broad applications in biomedical science and material science. (C) 2018 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
Keywords:
QUANTITATIVE-PHASE
DIFFRACTION PHASE
HOLOGRAPHY

Journal

Optics Express cover
Optics Express
IF:
3.3
Papers:
6.1W
Citations:
14.3W

Organization

T
tsinghua university
Scholars:
11.9W
Papers: 10.0W
Citations: 137
Cited Papers

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