Volume 11, Issue 8 e201700364
FULL ARTICLE

Isotropic differential phase contrast microscopy for quantitative phase bio-imaging

Hsi-Hsun Chen

Hsi-Hsun Chen

Department of Electrical Engineering and Graduate Institute of Photonics and Optoelectronics, National Taiwan University, Taipei, Taiwan

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Yu-Zi Lin

Yu-Zi Lin

Department of Mechanical Engineering, National Taiwan University, Taipei, Taiwan

Institute of Medical Device and Imaging, National Taiwan University, Taipei, Taiwan

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Yuan Luo

Corresponding Author

Yuan Luo

Institute of Medical Device and Imaging, National Taiwan University, Taipei, Taiwan

Molecular Imaging Center, National Taiwan University, Taipei, Taiwan

YongLin Institute of Health, National Taiwan University, Taipei, Taiwan

Correspondence

Yuan Luo, Institute of Medical Device and Imaging, National Taiwan University, Taipei 10051, Taiwan.

Email: [email protected]

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First published: 16 May 2018
Citations: 31
Funding information Ministry of Science and Technology, Taiwan, Grant/Award Numbers: 105-2628-E-002-008-MY3, 106-2221-E-002-157-MY3; National Taiwan University, Grant/Award Numbers: NTU-106M103, NTU-106R7807

Abstract

Quantitative phase imaging (QPI) has been investigated to retrieve optical phase information of an object and applied to biological microscopy and related medical studies. In recent examples, differential phase contrast (DPC) microscopy can recover phase image of thin sample under multi-axis intensity measurements in wide-field scheme. Unlike conventional DPC, based on theoretical approach under partially coherent condition, we propose a new method to achieve isotropic differential phase contrast (iDPC) with high accuracy and stability for phase recovery in simple and high-speed fashion. The iDPC is simply implemented with a partially coherent microscopy and a programmable thin-film transistor (TFT) shield to digitally modulate structured illumination patterns for QPI. In this article, simulation results show consistency of our theoretical approach for iDPC under partial coherence. In addition, we further demonstrate experiments of quantitative phase images of a standard micro-lens array, as well as label-free live human cell samples.

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