Quantitative Phase Imaging During Cell Division Based on Dual-Channel Microscopic Interferometry System

Quantitative phase imaging (QPI) during cell division is implemented by ourhomemade dual-channel microscopic interferometry (DCMI) system. A pair of interferograms with a fixed phase shift of π/2 is simultaneously captured by the DCMI system, and two-step phase demodulation alg...

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Main Authors: Shengde Liu, Dejin Zheng, Jiaosheng Li, Jindong Tian, Liyun Zhong, Xiaoxu Lu
Format: Article
Language:English
Published: IEEE 2020-01-01
Series:IEEE Photonics Journal
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Online Access:https://ieeexplore.ieee.org/document/8924630/
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author Shengde Liu
Dejin Zheng
Jiaosheng Li
Jindong Tian
Liyun Zhong
Xiaoxu Lu
author_facet Shengde Liu
Dejin Zheng
Jiaosheng Li
Jindong Tian
Liyun Zhong
Xiaoxu Lu
author_sort Shengde Liu
collection DOAJ
description Quantitative phase imaging (QPI) during cell division is implemented by ourhomemade dual-channel microscopic interferometry (DCMI) system. A pair of interferograms with a fixed phase shift of π/2 is simultaneously captured by the DCMI system, and two-step phase demodulation algorithm is employed for phase retrieval. By capturing a sequence of paired-interferograms with the DCMI system, we achieve the dynamic QPI during cell division, and then the cellular surface area, volume and the ratio of surface area to volume (RSV) and their variations. Both the reliability and stability of the DCMI system are verified. In addition to maintaining the advantages of optical interferometry, this DCMI system is very suitable for dynamic QPI due to its rapid speed of phase retrieval. Importantly, this DCMI based QPI method will supply a powerful tool for studying the precise mechanism during cell division, differentiation, apoptosis and other dynamic processes.
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spelling doaj-art-4e8d6dc1a23e4c86a40040f8fe5c75a42025-07-01T23:46:10ZengIEEEIEEE Photonics Journal1943-06552020-01-0112111110.1109/JPHOT.2019.29557518924630Quantitative Phase Imaging During Cell Division Based on Dual-Channel Microscopic Interferometry SystemShengde Liu0https://orcid.org/0000-0002-1024-6843Dejin Zheng1Jiaosheng Li2https://orcid.org/0000-0001-7517-4177Jindong Tian3https://orcid.org/0000-0002-0334-1762Liyun Zhong4Xiaoxu Lu5https://orcid.org/0000-0001-6757-6061Guangdong Provincial Key Laboratory of Nanophotonic Functional Materials and Devices, South China Normal University, Guangzhou, ChinaGuangdong Provincial Key Laboratory of Nanophotonic Functional Materials and Devices, South China Normal University, Guangzhou, ChinaGuangdong Provincial Key Laboratory of Nanophotonic Functional Materials and Devices, South China Normal University, Guangzhou, ChinaShenzhen Key Laboratory of Micro-Nano Measuring and Imaging in Biomedical Optics, College of Optoelectronic Engineering, Shenzhen University, Shenzhen, ChinaGuangdong Provincial Key Laboratory of Nanophotonic Functional Materials and Devices, South China Normal University, Guangzhou, ChinaGuangdong Provincial Key Laboratory of Nanophotonic Functional Materials and Devices, South China Normal University, Guangzhou, ChinaQuantitative phase imaging (QPI) during cell division is implemented by ourhomemade dual-channel microscopic interferometry (DCMI) system. A pair of interferograms with a fixed phase shift of π/2 is simultaneously captured by the DCMI system, and two-step phase demodulation algorithm is employed for phase retrieval. By capturing a sequence of paired-interferograms with the DCMI system, we achieve the dynamic QPI during cell division, and then the cellular surface area, volume and the ratio of surface area to volume (RSV) and their variations. Both the reliability and stability of the DCMI system are verified. In addition to maintaining the advantages of optical interferometry, this DCMI system is very suitable for dynamic QPI due to its rapid speed of phase retrieval. Importantly, this DCMI based QPI method will supply a powerful tool for studying the precise mechanism during cell division, differentiation, apoptosis and other dynamic processes.https://ieeexplore.ieee.org/document/8924630/Quantitative phase imagingdual-channel microscopic interferometryphase shiftcell division.
spellingShingle Shengde Liu
Dejin Zheng
Jiaosheng Li
Jindong Tian
Liyun Zhong
Xiaoxu Lu
Quantitative Phase Imaging During Cell Division Based on Dual-Channel Microscopic Interferometry System
IEEE Photonics Journal
Quantitative phase imaging
dual-channel microscopic interferometry
phase shift
cell division.
title Quantitative Phase Imaging During Cell Division Based on Dual-Channel Microscopic Interferometry System
title_full Quantitative Phase Imaging During Cell Division Based on Dual-Channel Microscopic Interferometry System
title_fullStr Quantitative Phase Imaging During Cell Division Based on Dual-Channel Microscopic Interferometry System
title_full_unstemmed Quantitative Phase Imaging During Cell Division Based on Dual-Channel Microscopic Interferometry System
title_short Quantitative Phase Imaging During Cell Division Based on Dual-Channel Microscopic Interferometry System
title_sort quantitative phase imaging during cell division based on dual channel microscopic interferometry system
topic Quantitative phase imaging
dual-channel microscopic interferometry
phase shift
cell division.
url https://ieeexplore.ieee.org/document/8924630/
work_keys_str_mv AT shengdeliu quantitativephaseimagingduringcelldivisionbasedondualchannelmicroscopicinterferometrysystem
AT dejinzheng quantitativephaseimagingduringcelldivisionbasedondualchannelmicroscopicinterferometrysystem
AT jiaoshengli quantitativephaseimagingduringcelldivisionbasedondualchannelmicroscopicinterferometrysystem
AT jindongtian quantitativephaseimagingduringcelldivisionbasedondualchannelmicroscopicinterferometrysystem
AT liyunzhong quantitativephaseimagingduringcelldivisionbasedondualchannelmicroscopicinterferometrysystem
AT xiaoxulu quantitativephaseimagingduringcelldivisionbasedondualchannelmicroscopicinterferometrysystem