Single-pixel phase and fluorescence microscope

被引:61
作者
Liu, Yang [1 ]
Suo, Jinli [1 ]
Zhang, Yuanlong [1 ]
Dai, Qionghai [1 ]
机构
[1] Tsinghua Univ, Dept Automat, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
QUANTITATIVE-PHASE; DIFFRACTION PHASE; HOLOGRAPHY;
D O I
10.1364/OE.26.032451
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
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
引用
收藏
页码:32451 / 32462
页数:12
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