散乱媒質を透過する二光子顕微鏡におけるスペックル自己相関の活用
Abstract:
Two-photon (2P) microscopy is a powerful technique for deep-tissue fluorescence imaging; however, tissue scattering limits its effectiveness for depth imaging using conventional approaches. Despite typical strategies having been put forward to extend depth imaging capabilities based on wave-front shaping (WFS), computationally recovering images remains a significant challenge using the 2P signal. In this work, we demonstrate the successful reconstruction of fluorescent objects behind scattering layers using 2P microscopy, utilizing the optical memory effect (ME) along with the speckle autocorrelation technique and a phase retrieval algorithm. Our results highlight the effectiveness of this method, offering significant potential for improving depth imaging capabilities in 2P microscopy through scattering media.
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Confocal Fluorescence Microscopy
Super-resolution Fluorescence Microscopy
Phase Contrast and Differential Interference Contrast Microscopy
In-phase-contrast microscopes, interference between light directly passing through a cell and light refracted by cellular components is used to create high-contrast, high-resolution images without staining. It is the oldest and simplest type of microscope that creates an image by altering the wavelengths of light rays passing through the specimen. Altered wavelength paths are created using an annular stop in the condenser. The annular stop produces a hollow cone of...


