Single-shot refractive index slice imaging using spectrally multiplexed optical transfer function reshaping

被引:1
|
作者
Lee, Chungha [1 ,2 ]
Hugonnet, Herve [1 ,2 ]
Park, Juyeon [1 ,2 ]
Lee, Mahn Jae [2 ,3 ]
Park, Weisun [1 ,2 ]
Park, Yongkeun [1 ,2 ,4 ]
机构
[1] Korea Adv Inst Sci & Technol KAIST, Dept Phys, Daejeon, South Korea
[2] Korea Adv Inst Sci & Technol, KAIST Inst Hlth Sci & Technol, Daejeon, South Korea
[3] Korea Adv Inst Sci & Technol, Grad Sch Med Sci & Engn, Daejeon, South Korea
[4] Tomocube Inc, Daejeon, South Korea
基金
新加坡国家研究基金会;
关键词
DIFFRACTION TOMOGRAPHY; CONTRAST; MICROSCOPY; CELLS; QUANTIFICATION; ILLUMINATION; RESOLUTION;
D O I
10.1364/OE.485559
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
The refractive index (RI) of cells and tissues is crucial in pathophysiology as a noninvasive and quantitative imaging contrast. Although its measurements have been demon-strated using three-dimensional quantitative phase imaging methods, these methods often require bulky interferometric setups or multiple measurements, which limits the measurement sensitivity and speed. Here, we present a single-shot RI imaging method that visualizes the RI of the in-focus region of a sample. By exploiting spectral multiplexing and optical transfer function engineering, three color-coded intensity images of a sample with three optimized illuminations were simultaneously obtained in a single-shot measurement. The measured intensity images were then deconvoluted to obtain the RI image of the in-focus slice of the sample. As a proof of concept, a setup was built using Fresnel lenses and a liquid-crystal display. For validation purposes, we measured microspheres of known RI and cross-validated the results with simulated results. Various static and highly dynamic biological cells were imaged to demonstrate that the proposed method can conduct single-shot RI slice imaging of biological samples with subcellular resolution.
引用
收藏
页码:13806 / 13816
页数:11
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