Abstract
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.
Highlights
The blood flow is responsible for distributing nutrients and removing metabolic waste products
In Time-domain diffuse correlation spectroscopy (TD-diffuse correlation spectroscopy (DCS)), the light from a pulsed laser is injected into the sample through the multi-mode fiber (MMF), and the diffusively reflected light is collected with the single-mode fiber (SMF), and detected with a single-photon avalanche detector (SPAD) (Fig. 1)
To validate the feasibility of separating different flows in turbid media, we performed TD-DCS measurements in liquid phantoms
Summary
The blood flow is responsible for distributing nutrients and removing metabolic waste products. The desired, cortical signal is confounded by photons traversing the skull and scalp without reaching the cortex This problem is compensated for by increasing source-detector distance (SDS) to 2–3 cm. Interferometric near-infrared spectroscopy (iNIRS) quantifies TOF-resolved dynamics in the turbid media[12], rodent brain in vivo[13], and humans in vivo[14] through Fourier-domain interferometric detection. Another promising approach is the time-domain (TD-) D CS9,15–18.
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