3.8 Editorial Material

Computational optical phase imaging: From digital holographic interferometry to intensity diffraction tomography

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Summary: Optical diffraction tomography (ODT) is a powerful tool for studying unlabeled biological cells by quantitatively and noninvasively measuring the three-dimensional refractive index distribution of samples. However, conventional transmission ODT has poor axial resolution due to limited angular coverage of the incident beam. In this Letter, a new type of ODT method called opposite illumination Fourier ptychographic diffraction tomography (OI-FPDT) is proposed, which combines transmissive angle-scanning and reflective wavelength-scanning to achieve almost isotropic resolution.

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Summary: We propose a new label-free 3D microscopy technique that can retrieve the 3D refractive index distribution of biological samples through 3D intensity measurements. This technique allows for incoherent 3D phase-contrast imaging without the need for interferometric detection. It provides strong defocus phase contrast and better optical sectioning capabilities, making it suitable for high-resolution tomography of thick biological samples. The technique was validated on various unlabeled fixed and live samples, demonstrating its potential for widespread biological and medical applications.

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Summary: Optical diffraction tomography (ODT) is a promising label-free three-dimensional microscopic method for measuring the refractive index distribution of optically transparent samples. Non-interferometric ODT techniques have gained attention, but suffer from low-frequency missing problems in high numerical aperture systems. Researchers have proposed transport-of-intensity Fourier ptychographic diffraction tomography (TI-FPDT) to address this issue. TI-FPDT combines ptychographic angular diversity with transport of intensity measurements to overcome reconstruction quality deterioration and refractive index underestimation in conventional FPDT.

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Summary: Quantitative phase imaging (QPI) is a valuable tool in biomedical research for quantifying optical thickness variation in living cells and tissues. Fourier ptychographic microscopy (FPM) is a high-resolution QPI method that allows long-term label-free observation and quantitative analysis of large cell populations. However, achieving high spatial and temporal resolution over a long-time scale remains a challenge. This study presents an adaptive optical QPI method based on annular illumination FPM, which utilizes low-resolution images and real-time aberration correction to recover high-resolution phase images and achieve diffraction-limited performance across a wide field of view.

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