Long-wavelength oblique back-illumination microscopy for deep <i>in vivo</i> imaging

Oblique back-illumination microscopy (OBM) is a label-free imaging technique that captures differential forward scattering in reflection mode to generate high-contrast pseudo-transmission images of cells and microvessels. While OBM benefits from multiple light scattering to detect forward-scattered signals, its imaging depth is constrained by tissue scattering between the objective lens and the imaging plane. In this study, we introduce a long-wavelength OBM system operating at 1650 nm-significantly longer than previous implementations-to mitigate scattering effects and extend imaging depth. Compared to a similar system using an 800 nm light source, our 1650 nm OBM achieves markedly deeper <i>in vivo</i> imaging of the mouse brain. This advancement in high-contrast, deep-tissue imaging holds promise for more detailed investigations into the pathophysiology of living biological systems.

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Publication Details

Journal
Biomedical Optics Express
Published
2025-11-28
DOI
https://doi.org/10.1364/boe.579269
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
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article

Long-wavelength oblique back-illumination microscopy for deep in vivo imaging

Sungsam Kang, Wonjun Choi, Wonshik Choi, Yookyung Jung et al.
Biomedical Optics Express
Advanced Fluorescence Microscopy Techniques
article

Long-wavelength oblique back-illumination microscopy for deep in vivo imaging

Sungsam Kang, Wonjun Choi, Wonshik Choi, Yookyung Jung, Jin Hee Hong, Cho Ye-Chan
article en

Abstract

Oblique back-illumination microscopy (OBM) is a label-free imaging technique that captures differential forward scattering in reflection mode to generate high-contrast pseudo-transmission images of cells and microvessels. While OBM benefits from multiple light scattering to detect forward-scattered signals, its imaging depth is constrained by tissue scattering between the objective lens and the imaging plane. In this study, we introduce a long-wavelength OBM system operating at 1650 nm-significantly longer than previous implementations-to mitigate scattering effects and extend imaging depth. Compared to a similar system using an 800 nm light source, our 1650 nm OBM achieves markedly deeper <i>in vivo</i> imaging of the mouse brain. This advancement in high-contrast, deep-tissue imaging holds promise for more detailed investigations into the pathophysiology of living biological systems.

Biomedical Optics ExpressVol. 17(1)
Albert Einstein College of Medicine (US), Korea University (KR), National University College (PR)
Openalex Percentile: Top 74%
Advanced Fluorescence Microscopy Techniques
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