Mapping nanoscale topographic features in thick tissues with speckle diffraction tomography

Resolving three-dimensional morphological features in thick specimens remains a significant challenge for label-free imaging. We report a new speckle diffraction tomography (SDT) approach that can image thick biological specimens with similar to 500 nm lateral resolution and similar to 1 mu m axial resolution in a reflection geometry. In SDT, multiple-scattering background is rejected through spatiotemporal gating provided by dynamic speckle-field interferometry, while depth-resolved refractive index maps are reconstructed by developing a comprehensive inverse-scattering model that also considers specimen-induced aberrations. Benefiting from the high-resolution and full-field quantitative imaging capabilities of SDT, we successfully imaged red blood cells and quantified their membrane fluctuations behind a turbid medium with a thickness of 2.8 scattering mean-free paths. Most importantly, we performed volumetric imaging of cornea inside an ex vivo rat eye and quantified its optical properties, including the mapping of nanoscale topographic features of Dua's and Descemet's membranes that had not been previously visualized.

Automated summary

Researchers report a new speckle diffraction tomography (SDT) approach that can image thick biological specimens with high resolution. By rejecting multiple-scattering background and considering specimen-induced aberrations, SDT achieves depth-resolved refractive index maps. Using SDT, they successfully imaged red blood cells and quantified their membrane fluctuations, as well as performed volumetric imaging of cornea inside an ex vivo rat eye.