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Simultaneous Dual-Color Fluorescence Microscope: A Characterization Study

Background: High spatial resolution and geometric accuracy is crucial for chromosomal analysis of clinical cytogenetic applications. High resolution and rapid simultaneous acquisition of multiple fluorescent wavelengths can be achieved by utilizing concurrent imaging with multiple detectors. However...

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Autores principales: Li, Zheng, Chen, Xiaodong, Ren, Liqiang, Song, Jie, Li, Yuhua, Zheng, Bin, Liu, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4605718/
https://www.ncbi.nlm.nih.gov/pubmed/24844533
http://dx.doi.org/10.3233/ACP-140089
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author Li, Zheng
Chen, Xiaodong
Ren, Liqiang
Song, Jie
Li, Yuhua
Zheng, Bin
Liu, Hong
author_facet Li, Zheng
Chen, Xiaodong
Ren, Liqiang
Song, Jie
Li, Yuhua
Zheng, Bin
Liu, Hong
author_sort Li, Zheng
collection PubMed
description Background: High spatial resolution and geometric accuracy is crucial for chromosomal analysis of clinical cytogenetic applications. High resolution and rapid simultaneous acquisition of multiple fluorescent wavelengths can be achieved by utilizing concurrent imaging with multiple detectors. However, such class of microscopic systems functions differently from traditional fluorescence microscopes. Objective: To develop a practical characterization framework to assess and optimize the performance of a high resolution and dual-color fluorescence microscope designed for clinical chromosomal analysis. Methods: A dual-band microscopic imaging system utilizes a dichroic mirror, two sets of specially selected optical filters, and two detectors to simultaneously acquire two fluorescent wavelengths. The system’s geometric distortion, linearity, the modulation transfer function, and the dual detectors’ alignment were characterized. Results: Experiment results show that the geometric distortion at lens periphery is less than 1%. Both fluorescent channels show linear signal responses, but there exists discrepancy between the two due to the detectors’ non-uniform response ratio to different wavelengths. In terms of the spatial resolution, the two contrast transfer function curves trend agreeably with the spatial frequency. The alignment measurement allows quantitatively assessing the cameras' alignment. A result image of adjusted alignment is demonstrated to show the reduced discrepancy by using the alignment measurement method. Conclusions: In this paper, we present a system characterization study and its methods for a specially designed imaging system for clinical cytogenetic applications. The presented characterization methods are not only unique to this dual-color imaging system but also applicable to evaluation and optimization of other similar multi-color microscopic image systems for improving their clinical utilities for future cytogenetic applications.
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spelling pubmed-46057182015-12-13 Simultaneous Dual-Color Fluorescence Microscope: A Characterization Study Li, Zheng Chen, Xiaodong Ren, Liqiang Song, Jie Li, Yuhua Zheng, Bin Liu, Hong Anal Cell Pathol (Amst) Other Background: High spatial resolution and geometric accuracy is crucial for chromosomal analysis of clinical cytogenetic applications. High resolution and rapid simultaneous acquisition of multiple fluorescent wavelengths can be achieved by utilizing concurrent imaging with multiple detectors. However, such class of microscopic systems functions differently from traditional fluorescence microscopes. Objective: To develop a practical characterization framework to assess and optimize the performance of a high resolution and dual-color fluorescence microscope designed for clinical chromosomal analysis. Methods: A dual-band microscopic imaging system utilizes a dichroic mirror, two sets of specially selected optical filters, and two detectors to simultaneously acquire two fluorescent wavelengths. The system’s geometric distortion, linearity, the modulation transfer function, and the dual detectors’ alignment were characterized. Results: Experiment results show that the geometric distortion at lens periphery is less than 1%. Both fluorescent channels show linear signal responses, but there exists discrepancy between the two due to the detectors’ non-uniform response ratio to different wavelengths. In terms of the spatial resolution, the two contrast transfer function curves trend agreeably with the spatial frequency. The alignment measurement allows quantitatively assessing the cameras' alignment. A result image of adjusted alignment is demonstrated to show the reduced discrepancy by using the alignment measurement method. Conclusions: In this paper, we present a system characterization study and its methods for a specially designed imaging system for clinical cytogenetic applications. The presented characterization methods are not only unique to this dual-color imaging system but also applicable to evaluation and optimization of other similar multi-color microscopic image systems for improving their clinical utilities for future cytogenetic applications. IOS Press 2013 2014-05-20 /pmc/articles/PMC4605718/ /pubmed/24844533 http://dx.doi.org/10.3233/ACP-140089 Text en Copyright © 2013 Hindawi Publishing Corporation and the authors.
spellingShingle Other
Li, Zheng
Chen, Xiaodong
Ren, Liqiang
Song, Jie
Li, Yuhua
Zheng, Bin
Liu, Hong
Simultaneous Dual-Color Fluorescence Microscope: A Characterization Study
title Simultaneous Dual-Color Fluorescence Microscope: A Characterization Study
title_full Simultaneous Dual-Color Fluorescence Microscope: A Characterization Study
title_fullStr Simultaneous Dual-Color Fluorescence Microscope: A Characterization Study
title_full_unstemmed Simultaneous Dual-Color Fluorescence Microscope: A Characterization Study
title_short Simultaneous Dual-Color Fluorescence Microscope: A Characterization Study
title_sort simultaneous dual-color fluorescence microscope: a characterization study
topic Other
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4605718/
https://www.ncbi.nlm.nih.gov/pubmed/24844533
http://dx.doi.org/10.3233/ACP-140089
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