Abstract
While optical coherence tomography (OCT) provides a resolution down to 1 µm it has difficulties to visualize cellular structures due to a lack of scattering contrast. By evaluating signal fluctuations, a significant contrast enhancement was demonstrated using time-domain full-field OCT (FF-OCT), which makes cellular and subcellular structures visible. The putative cause of the dynamic OCT signal is ATP-dependent motion of cellular structures in a sub-micrometer range, which provides histology-like contrast. Here we demonstrate dynamic contrast with a scanning frequency-domain OCT (FD-OCT). Given the inherent sectional imaging geometry, scanning FD-OCT provides depth-resolved images across tissue layers, a perspective known from histopathology, much faster and more efficiently than FF-OCT. Both, shorter acquisition times and tomographic depth-sectioning reduce the sensitivity of dynamic contrast for bulk tissue motion artifacts and simplify their correction in post-processing. The implementation of dynamic contrast makes microscopic FD-OCT a promising tool for histological analysis of unstained tissues.
| Original language | English |
|---|---|
| Journal | Optics Letters |
| Volume | 45 |
| Issue number | 17 |
| Pages (from-to) | 4766-4769 |
| Number of pages | 4 |
| ISSN | 0146-9592 |
| DOIs | |
| Publication status | Published - 28.02.2020 |
Funding
Funding. European Union project within Interreg Deutschland-Denmark from the European Regional Development Fund (ERDF) (CELLTOM); German Ministry of Research, Innovation and Science, Helmholtz Center Munich of Health and Environment DZL-ARCN (82DZL001A2); Deutsche Forschungsgemeinschaft (RA 1771/4-1, EXC 2167).
Research Areas and Centers
- Academic Focus: Biomedical Engineering