Synthetic aperture interference light (SAIL) microscopy for high-throughput label-free imaging

TL;DR

SAIL microscopy offers a novel high-resolution, wide field of view label-free imaging modality that directly measures phase delay using low-coherence interferometry, overcoming resolution and field of view trade-offs in traditional QPI systems.

Contribution

This paper introduces SAIL microscopy, a new method that provides high-resolution, large field of view quantitative phase imaging without complex computation or convergence issues.

Findings

Achieves a synthetic numerical aperture of 0.45.

Provides a field of view of 2.6 x 2.6 mm².

Successfully applied to biological samples and specimens.

Abstract

Quantitative phase imaging (QPI) is a valuable label-free modality that has gained significant interest due to its wide potentials, from basic biology to clinical applications. Most existing QPI systems measure microscopic objects via interferometry or nonlinear iterative phase reconstructions from intensity measurements. However, all imaging systems compromise spatial resolution for field of view and vice versa, i.e., suffer from a limited space bandwidth product. Current solutions to this problem involve computational phase retrieval algorithms, which are time-consuming and often suffer from convergence problems. In this article, we presented synthetic aperture interference light (SAIL) microscopy as a novel modality for high-resolution, wide field of view QPI. The proposed approach employs low-coherence interferometry to directly measure the optical phase delay under different illumination angles and produces large space-bandwidth product (SBP) label-free imaging. We validate the performance of SAIL on standard samples and illustrate the biomedical applications on various specimens: pathology slides, entire insects, and dynamic live cells in large cultures. The reconstructed images have a synthetic numeric aperture of 0.45, and a field of view of 2.6 x 2.6 mm2. Due to its direct measurement of the phase information, SAIL microscopy does not require long computational time, eliminates data redundancy, and always converges.