Initial non-invasive in vivo sensing of the lung using time domain diffuse optics

Non-invasive in vivo sensing of the lung with light would help diagnose and monitor pulmonary disorders (caused by e.g. COVID-19, emphysema, immature lung tissue in infants). We investigated the possibility to probe the lung with time domain diffuse optics, taking advantage of the increased depth (few cm) reached by photons detected after a long (few ns) propagation time. An initial study on 5 healthy volunteers included time-resolved broadband diffuse optical spectroscopy measurements at 3 cm source-detector distance over the 600-1100 nm range, and long-distance (6-9 cm) measurements at 820 nm performed during a breathing protocol. The interpretation of the in vivo data with a simplified homogeneous model yielded a maximum probing depth of 2.6-3.9 cm, suitable to reach the lung. Also, signal changes related to the inspiration act were observed, especially at high photon propagation times. Yet, intra- and inter-subject variability and inconsistencies, possibly alluring to competing scattering and absorption effects, prevented a simple interpretation. Aspects to be further investigated to gain a deeper insight are discussed.

Beyond multi-view deconvolution for inherently-aligned fluorescence tomography

In multi-view fluorescence microscopy, each angular acquisition needs to be aligned with care to obtain an optimal volumetric reconstruction. Here, instead, we propose a neat protocol based on auto-correlation inversion, that leads directly to the formation of inherently aligned tomographies. Our method generates sharp reconstructions, with the same accuracy reachable after sub-pixel alignment but with improved point-spread-function. The procedure can be performed simultaneously with deconvolution further increasing the reconstruction resolution.