Abstract
Continuous monitoring of cerebral blood flow (CBF) with high spatiotemporal resolution and depth sensitivity is essential for accurate diagnosis and effective management of neurological disorders. Although conventional laser speckle contrast imaging (LSCI) enables widefield, high-resolution CBF mapping, its limited penetration depth and signal integration across all tissue layers hinder depth-resolved imaging. To address these limitations, we developed an advanced time-resolved LSCI (TR-LSCI) system that employs picosecond-pulsed laser illumination and a customized SPAD5122 camera operating in gated mode, enabling noncontact, widefield, and depth-sensitive CBF imaging. However, photon scattering and diffusive noise still degrade image quality, particularly at greater depths. To overcome this challenge, we incorporated a multiscale latent diffusion model (LTDiff++) into the TR-LSCI analysis pipeline to suppress photon diffusion noise. Trained and validated using overlapping image patches from head-simulating phantoms and neonatal rat CBF images with high-quality ground truth references, LTDiff++ effectively suppressed photon diffusion noise while preserving structural and vascular features at greater imaging depths. Moreover, in vivo studies demonstrated that LTDiff++ maintained image quality using only 5-frame averaging, reducing acquisition time by a factor of 20 compared to the conventional 100-frame averaging approach without deep learning enhancement. The integrated TR-LSCI and LTDiff++ framework thus enables robust, high-speed, and depth-resolved imaging of cerebral hemodynamics, offering a promising platform for preclinical research and future clinical applications in bedside neuroimaging and patient monitoring.
| Original language | English |
|---|---|
| Pages (from-to) | 3895-3911 |
| Number of pages | 17 |
| Journal | Biomedical Optics Express |
| Volume | 16 |
| Issue number | 10 |
| DOIs | |
| State | Published - Oct 1 2025 |
Bibliographical note
Publisher Copyright:© 2025 Optica Publishing Group (formerly OSA). All rights reserved.
Funding
Acknowledgements. We acknowledge partial financial support from the National Institutes of Health (NIH) #R01 EB028792, #R01-HD101508, #R21-HD091118, #R21-NS114771, #R41-NS122722, #R42-MH135825, #R56-NS117587 (G.Y.) and the Halcomb Fellowship in Medicine and Engineering at the University of Kentucky (F.F.). This work was also supported, in part, by the Swiss National Science Foundation (grants 20QT21_187716 Qu3D “Quantum 3D Imaging at high speed and high resolution” and 200021_166289). National Institutes of Health (R01 EB028792, R01-HD101508, R21-HD091118, R21-NS114771, R41-NS122722, R42-MH135825, R56-NS117587); University of Kentucky (F.F.) Halcomb Fellowship in Medicine and Engineering; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (20QT21_187716 Qu3D, 200021_166289). We acknowledge partial financial support from the National Institutes of Health (NIH) #R01 EB028792, #R01-HD101508, #R21-HD091118, #R21-NS114771, #R41-NS122722, #R42-MH135825, #R56-NS117587 (G.Y.) and the Halcomb Fellowship in Medicine and Engineering at the University of Kentucky (F.F.). This work was also supported, in part, by the Swiss National Science Foundation (grants 20QT21_187716 Qu3D “Quantum 3D Imaging at high speed and high resolution” and 200021_166289).
| Funders | Funder number |
|---|---|
| University of Kentucky | |
| Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung | 20QT21_187716 Qu3D, HD091118, 20QT21_187716, 200021_166289, EB028792 |
| National Institutes of Health (NIH) | HD101508, MH135825, HD091118, NS117587, EB028792, NS114771, NS122722 |
ASJC Scopus subject areas
- Biotechnology
- Atomic and Molecular Physics, and Optics
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