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

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...

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Autores principales: Zuo, Chao, Sun, Jiasong, Li, Jiaji, Zhang, Jialin, Asundi, Anand, Chen, Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550517/
https://www.ncbi.nlm.nih.gov/pubmed/28794472
http://dx.doi.org/10.1038/s41598-017-06837-1
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author Zuo, Chao
Sun, Jiasong
Li, Jiaji
Zhang, Jialin
Asundi, Anand
Chen, Qian
author_facet Zuo, Chao
Sun, Jiasong
Li, Jiaji
Zhang, Jialin
Asundi, Anand
Chen, Qian
author_sort Zuo, Chao
collection PubMed
description 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.
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spelling pubmed-55505172017-08-11 High-resolution transport-of-intensity quantitative phase microscopy with annular illumination Zuo, Chao Sun, Jiasong Li, Jiaji Zhang, Jialin Asundi, Anand Chen, Qian Sci Rep Article 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. Nature Publishing Group UK 2017-08-09 /pmc/articles/PMC5550517/ /pubmed/28794472 http://dx.doi.org/10.1038/s41598-017-06837-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zuo, Chao
Sun, Jiasong
Li, Jiaji
Zhang, Jialin
Asundi, Anand
Chen, Qian
High-resolution transport-of-intensity quantitative phase microscopy with annular illumination
title High-resolution transport-of-intensity quantitative phase microscopy with annular illumination
title_full High-resolution transport-of-intensity quantitative phase microscopy with annular illumination
title_fullStr High-resolution transport-of-intensity quantitative phase microscopy with annular illumination
title_full_unstemmed High-resolution transport-of-intensity quantitative phase microscopy with annular illumination
title_short High-resolution transport-of-intensity quantitative phase microscopy with annular illumination
title_sort high-resolution transport-of-intensity quantitative phase microscopy with annular illumination
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550517/
https://www.ncbi.nlm.nih.gov/pubmed/28794472
http://dx.doi.org/10.1038/s41598-017-06837-1
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