Abstract

Optical imaging has played a crucial role in understanding the physiology of living specimens due to its high spatial resolution, molecular specificity, and minimal invasiveness. However, its working depth has been extremely shallow for tissue imaging, and many important reactions occurring deep inside living specimens have still been out of reach as a consequence. The main problem originates from multiple light scattering induced by inhomogeneous tissues, which severely obscures the image information.

© 2022 Japan Society of Applied Physics, Optica Publishing Group