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环形照明的高分辨率强度传输定量相显微镜。

High-resolution transport-of-intensity quantitative phase microscopy with annular illumination.

机构信息

Smart Computational Imaging (SCI) Laboratory, Nanjing University of Science and Technology, Nanjing, Jiangsu Province, 210094, China.

Jiangsu Key Laboratory of Spectral Imaging & Intelligent Sense, Nanjing University of Science and Technology, Nanjing, Jiangsu Province, 210094, China.

出版信息

Sci Rep. 2017 Aug 9;7(1):7654. doi: 10.1038/s41598-017-06837-1.

DOI:10.1038/s41598-017-06837-1
PMID:28794472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5550517/
Abstract

For quantitative phase imaging (QPI) based on transport-of-intensity equation (TIE), partially coherent illumination provides speckle-free imaging, compatibility with brightfield microscopy, and transverse resolution beyond coherent diffraction limit. Unfortunately, in a conventional microscope with circular illumination aperture, partial coherence tends to diminish the phase contrast, exacerbating the inherent noise-to-resolution tradeoff in TIE imaging, resulting in strong low-frequency artifacts and compromised imaging resolution. Here, we demonstrate how these issues can be effectively addressed by replacing the conventional circular illumination aperture with an annular one. The matched annular illumination not only strongly boosts the phase contrast for low spatial frequencies, but significantly improves the practical imaging resolution to near the incoherent diffraction limit. By incorporating high-numerical aperture (NA) illumination as well as high-NA objective, it is shown, for the first time, that TIE phase imaging can achieve a transverse resolution up to 208 nm, corresponding to an effective NA of 2.66. Time-lapse imaging of in vitro Hela cells revealing cellular morphology and subcellular dynamics during cells mitosis and apoptosis is exemplified. Given its capability for high-resolution QPI as well as the compatibility with widely available brightfield microscopy hardware, the proposed approach is expected to be adopted by the wider biology and medicine community.

摘要

用于基于强度传输方程(TIE)的定量相位成像(QPI),部分相干照明提供无散斑成像、与明场显微镜兼容以及超越相干衍射极限的横向分辨率。不幸的是,在具有圆形照明孔径的传统显微镜中,部分相干往往会降低相位对比度,从而加剧 TIE 成像中固有噪声与分辨率的权衡取舍,导致强烈的低频伪影和成像分辨率受损。在这里,我们通过用环形照明孔径代替传统的圆形照明孔径来展示如何有效解决这些问题。匹配的环形照明不仅强烈增强了低空间频率的相位对比度,而且显著提高了实际成像分辨率,接近非相干衍射极限。通过结合高数值孔径(NA)照明和高 NA 物镜,首次表明 TIE 相位成像可以实现高达 208nm 的横向分辨率,对应于 2.66 的有效 NA。通过体外 HeLa 细胞的延时成像,展示了细胞有丝分裂和细胞凋亡过程中细胞形态和亚细胞动力学的变化。鉴于其高分辨率 QPI 的能力以及与广泛可用的明场显微镜硬件的兼容性,预计该方法将被更广泛的生物学和医学领域所采用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca1/5550517/2a1263d00986/41598_2017_6837_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca1/5550517/687139d28051/41598_2017_6837_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca1/5550517/b3e166049f2e/41598_2017_6837_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca1/5550517/274a02da5b7d/41598_2017_6837_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca1/5550517/8e260cd967aa/41598_2017_6837_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca1/5550517/b36a77329560/41598_2017_6837_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca1/5550517/d5a39f8b5a66/41598_2017_6837_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca1/5550517/2a1263d00986/41598_2017_6837_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca1/5550517/687139d28051/41598_2017_6837_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca1/5550517/b3e166049f2e/41598_2017_6837_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca1/5550517/274a02da5b7d/41598_2017_6837_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca1/5550517/8e260cd967aa/41598_2017_6837_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca1/5550517/b36a77329560/41598_2017_6837_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca1/5550517/d5a39f8b5a66/41598_2017_6837_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ca1/5550517/2a1263d00986/41598_2017_6837_Fig8_HTML.jpg

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