4.7 Article

Time-domain diffuse correlation spectroscopy (TD-DCS) for noninvasive, depth-dependent blood flow quantification in human tissue in vivo

Journal

SCIENTIFIC REPORTS
Volume 11, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41598-021-81448-5

Keywords

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Funding

  1. Horizon 2020: Marie Sklodowska-Curie Innovative Training Networks [675332]
  2. Horizon 2020: research and innovation program [666295]
  3. Narodowe Centrum Nauki (NCN) [2016/22/A/ST2/00313, 2019/33/N/ST7/03024]

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Time-domain diffuse correlation spectroscopy (TD-DCS) allows for noninvasive blood flow measurement and accurate quantification of TOF-resolved blood flow in human tissues. The new approach detects depth-dependent reactive hyperemia and separates superficial from deep blood flow, showing potential benefits for neuroimaging sensing applications.
Monitoring of human tissue hemodynamics is invaluable in clinics as the proper blood flow regulates cellular-level metabolism. Time-domain diffuse correlation spectroscopy (TD-DCS) enables noninvasive blood flow measurements by analyzing temporal intensity fluctuations of the scattered light. With time-of-flight (TOF) resolution, TD-DCS should decompose the blood flow at different sample depths. For example, in the human head, it allows us to distinguish blood flows in the scalp, skull, or cortex. However, the tissues are typically polydisperse. So photons with a similar TOF can be scattered from structures that move at different speeds. Here, we introduce a novel approach that takes this problem into account and allows us to quantify the TOF-resolved blood flow of human tissue accurately. We apply this approach to monitor the blood flow index in the human forearm in vivo during the cuff occlusion challenge. We detect depth-dependent reactive hyperemia. Finally, we applied a controllable pressure to the human forehead in vivo to demonstrate that our approach can separate superficial from the deep blood flow. Our results can be beneficial for neuroimaging sensing applications that require short interoptode separation.

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