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Resolution-enhanced Fourier ptychographic microscopy based on high-numerical-aperture illuminations

High-resolution and wide field-of-view (FOV) microscopic imaging plays a central role in diverse applications such as high-throughput screening and digital pathology. However, conventional microscopes face inherent trade-offs between the spatial resolution and FOV, which are fundamental limited by t...

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Autores principales: Sun, Jiasong, Zuo, Chao, Zhang, Liang, 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/PMC5430655/
https://www.ncbi.nlm.nih.gov/pubmed/28446788
http://dx.doi.org/10.1038/s41598-017-01346-7
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author Sun, Jiasong
Zuo, Chao
Zhang, Liang
Chen, Qian
author_facet Sun, Jiasong
Zuo, Chao
Zhang, Liang
Chen, Qian
author_sort Sun, Jiasong
collection PubMed
description High-resolution and wide field-of-view (FOV) microscopic imaging plays a central role in diverse applications such as high-throughput screening and digital pathology. However, conventional microscopes face inherent trade-offs between the spatial resolution and FOV, which are fundamental limited by the space-bandwidth product (SBP) of the optical system. The resolution-FOV tradeoff can be effectively decoupled in Fourier ptychography microscopy (FPM), however, to date, the effective imaging NA achievable with a typical FPM system is still limited to the range of 0.4–0.7. Herein, we report, for the first time, a high-NA illumination based resolution-enhanced FPM (REFPM) platform, in which a LED-array-based digital oil-immersion condenser is used to create high-angle programmable plane-wave illuminations, endowing a 10×, 0.4 NA objective lens with final effective imaging performance of 1.6 NA. With REFPM, we present the highest-resolution results with a unprecedented half-pitch resolution of 154 nm at a wavelength of 435 nm across a wide FOV of 2.34 mm(2), corresponding to an SBP of 98.5 megapixels (~50 times higher than that of the conventional incoherent microscope with the same resolution). Our work provides an important step of FPM towards high-resolution large-NA imaging applications, generating comparable resolution performance but significantly broadening the FOV of conventional oil-immersion microscopes.
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spelling pubmed-54306552017-05-15 Resolution-enhanced Fourier ptychographic microscopy based on high-numerical-aperture illuminations Sun, Jiasong Zuo, Chao Zhang, Liang Chen, Qian Sci Rep Article High-resolution and wide field-of-view (FOV) microscopic imaging plays a central role in diverse applications such as high-throughput screening and digital pathology. However, conventional microscopes face inherent trade-offs between the spatial resolution and FOV, which are fundamental limited by the space-bandwidth product (SBP) of the optical system. The resolution-FOV tradeoff can be effectively decoupled in Fourier ptychography microscopy (FPM), however, to date, the effective imaging NA achievable with a typical FPM system is still limited to the range of 0.4–0.7. Herein, we report, for the first time, a high-NA illumination based resolution-enhanced FPM (REFPM) platform, in which a LED-array-based digital oil-immersion condenser is used to create high-angle programmable plane-wave illuminations, endowing a 10×, 0.4 NA objective lens with final effective imaging performance of 1.6 NA. With REFPM, we present the highest-resolution results with a unprecedented half-pitch resolution of 154 nm at a wavelength of 435 nm across a wide FOV of 2.34 mm(2), corresponding to an SBP of 98.5 megapixels (~50 times higher than that of the conventional incoherent microscope with the same resolution). Our work provides an important step of FPM towards high-resolution large-NA imaging applications, generating comparable resolution performance but significantly broadening the FOV of conventional oil-immersion microscopes. Nature Publishing Group UK 2017-04-26 /pmc/articles/PMC5430655/ /pubmed/28446788 http://dx.doi.org/10.1038/s41598-017-01346-7 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
Sun, Jiasong
Zuo, Chao
Zhang, Liang
Chen, Qian
Resolution-enhanced Fourier ptychographic microscopy based on high-numerical-aperture illuminations
title Resolution-enhanced Fourier ptychographic microscopy based on high-numerical-aperture illuminations
title_full Resolution-enhanced Fourier ptychographic microscopy based on high-numerical-aperture illuminations
title_fullStr Resolution-enhanced Fourier ptychographic microscopy based on high-numerical-aperture illuminations
title_full_unstemmed Resolution-enhanced Fourier ptychographic microscopy based on high-numerical-aperture illuminations
title_short Resolution-enhanced Fourier ptychographic microscopy based on high-numerical-aperture illuminations
title_sort resolution-enhanced fourier ptychographic microscopy based on high-numerical-aperture illuminations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430655/
https://www.ncbi.nlm.nih.gov/pubmed/28446788
http://dx.doi.org/10.1038/s41598-017-01346-7
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