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Using Fourier ptychography microscopy to achieve high-resolution chromosome imaging: an initial evaluation
SIGNIFICANCE: Searching analyzable metaphase chromosomes is a critical step for the diagnosis and treatment of leukemia patients, and the searching efficiency is limited by the difficulty that the conventional microscopic systems have in simultaneously achieving high resolution and a large field of...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society of Photo-Optical Instrumentation Engineers
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802907/ https://www.ncbi.nlm.nih.gov/pubmed/35102727 http://dx.doi.org/10.1117/1.JBO.27.1.016504 |
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author | Zhang, Ke Lu, Xianglan Chen, Xuxin Zhang, Roy Fung, Kar-Ming Liu, Hong Zheng, Bin Li, Shibo Qiu, Yuchen |
author_facet | Zhang, Ke Lu, Xianglan Chen, Xuxin Zhang, Roy Fung, Kar-Ming Liu, Hong Zheng, Bin Li, Shibo Qiu, Yuchen |
author_sort | Zhang, Ke |
collection | PubMed |
description | SIGNIFICANCE: Searching analyzable metaphase chromosomes is a critical step for the diagnosis and treatment of leukemia patients, and the searching efficiency is limited by the difficulty that the conventional microscopic systems have in simultaneously achieving high resolution and a large field of view (FOV). However, this challenge can be addressed by Fourier ptychography microscopy (FPM) technology. AIM: The purpose of this study is to investigate the feasibility of utilizing FPM to reconstruct high-resolution chromosome images. APPROACH: An experimental FPM prototype, which was equipped with [Formula: see text] or [Formula: see text] objective lenses to achieve a theoretical equivalent NA of 0.48 and 0.63, respectively, was developed. Under these configurations, we first generated the system modulation transfer function (MTF) curves to assess the resolving power. Next, a group of analyzable metaphase chromosomes were imaged by the FPM system, which were acquired from the peripheral blood samples of the leukemia patients. The chromosome feature qualities were evaluated and compared with the results accomplished by the corresponding conventional microscopes. RESULTS: The MTF curve results indicate that the resolving power of the [Formula: see text] FPM system is equivalent and comparable to the [Formula: see text] conventional microscope, whereas the performance of the [Formula: see text] FPM system is close to the [Formula: see text] conventional microscope. When imaging the chromosomes, the feature qualities of the [Formula: see text] FPM system are comparable to the results under the conventional [Formula: see text] lens, whereas the feature qualities of the [Formula: see text] FPM system are better than the conventional [Formula: see text] lens and comparable to the conventional [Formula: see text] lens. CONCLUSIONS: This study initially verified that it is feasible to utilize FPM to develop a high-resolution and wide-field chromosome sample scanner. |
format | Online Article Text |
id | pubmed-8802907 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Society of Photo-Optical Instrumentation Engineers |
record_format | MEDLINE/PubMed |
spelling | pubmed-88029072022-02-02 Using Fourier ptychography microscopy to achieve high-resolution chromosome imaging: an initial evaluation Zhang, Ke Lu, Xianglan Chen, Xuxin Zhang, Roy Fung, Kar-Ming Liu, Hong Zheng, Bin Li, Shibo Qiu, Yuchen J Biomed Opt Microscopy SIGNIFICANCE: Searching analyzable metaphase chromosomes is a critical step for the diagnosis and treatment of leukemia patients, and the searching efficiency is limited by the difficulty that the conventional microscopic systems have in simultaneously achieving high resolution and a large field of view (FOV). However, this challenge can be addressed by Fourier ptychography microscopy (FPM) technology. AIM: The purpose of this study is to investigate the feasibility of utilizing FPM to reconstruct high-resolution chromosome images. APPROACH: An experimental FPM prototype, which was equipped with [Formula: see text] or [Formula: see text] objective lenses to achieve a theoretical equivalent NA of 0.48 and 0.63, respectively, was developed. Under these configurations, we first generated the system modulation transfer function (MTF) curves to assess the resolving power. Next, a group of analyzable metaphase chromosomes were imaged by the FPM system, which were acquired from the peripheral blood samples of the leukemia patients. The chromosome feature qualities were evaluated and compared with the results accomplished by the corresponding conventional microscopes. RESULTS: The MTF curve results indicate that the resolving power of the [Formula: see text] FPM system is equivalent and comparable to the [Formula: see text] conventional microscope, whereas the performance of the [Formula: see text] FPM system is close to the [Formula: see text] conventional microscope. When imaging the chromosomes, the feature qualities of the [Formula: see text] FPM system are comparable to the results under the conventional [Formula: see text] lens, whereas the feature qualities of the [Formula: see text] FPM system are better than the conventional [Formula: see text] lens and comparable to the conventional [Formula: see text] lens. CONCLUSIONS: This study initially verified that it is feasible to utilize FPM to develop a high-resolution and wide-field chromosome sample scanner. Society of Photo-Optical Instrumentation Engineers 2022-01-31 2022-01 /pmc/articles/PMC8802907/ /pubmed/35102727 http://dx.doi.org/10.1117/1.JBO.27.1.016504 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/Published by SPIE under a Creative Commons Attribution 4.0 International License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI. |
spellingShingle | Microscopy Zhang, Ke Lu, Xianglan Chen, Xuxin Zhang, Roy Fung, Kar-Ming Liu, Hong Zheng, Bin Li, Shibo Qiu, Yuchen Using Fourier ptychography microscopy to achieve high-resolution chromosome imaging: an initial evaluation |
title | Using Fourier ptychography microscopy to achieve high-resolution chromosome imaging: an initial evaluation |
title_full | Using Fourier ptychography microscopy to achieve high-resolution chromosome imaging: an initial evaluation |
title_fullStr | Using Fourier ptychography microscopy to achieve high-resolution chromosome imaging: an initial evaluation |
title_full_unstemmed | Using Fourier ptychography microscopy to achieve high-resolution chromosome imaging: an initial evaluation |
title_short | Using Fourier ptychography microscopy to achieve high-resolution chromosome imaging: an initial evaluation |
title_sort | using fourier ptychography microscopy to achieve high-resolution chromosome imaging: an initial evaluation |
topic | Microscopy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802907/ https://www.ncbi.nlm.nih.gov/pubmed/35102727 http://dx.doi.org/10.1117/1.JBO.27.1.016504 |
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