“…By applying the method to in vivo measurements for healthy subjects, the estimated sizes were close to 8 μm corresponding to the diameter of a single RBC under normal blood flow, and they increased by approximately 14 μm under the low shear rate condition by avascularization. 31) In our previous study, 30) there were differences in the shape between the power spectra measured from the microparticles simulating RBCs and the reference scattering power spectra corresponding to the microparticle diameters. In this study, we calculated the reference scattering power spectra by simulating a condition in which only a single scatterer existed at the focus of the ultrasound beam.…”
Section: Introductionmentioning
confidence: 86%
“…We have studied a noninvasive and quantitative method for measuring the RBC aggregate size using a high-frequency focused ultrasound transducer. [26][27][28][29][30][31] Fukushima et al assumed that aggregated RBCs are single-sphere scatterers and estimated their size from the scattering characteristics by normalizing the power spectrum measured from the vessel lumen by that from the posterior wall of the blood vessel as a reflector. [26][27][28][29] However, the vessel wall could have exhibited a slope to the probe surface and roughness on the surface.…”
We have studied a noninvasive and quantitative method for measuring the aggregate size of red blood cells (RBCs). In our previous study, the scattering power spectrum obtained from the vascular lumen was fitted to the reference scattering spectra calculated from the scattering spectrum of a single-sphere scatterer. In this paper, we propose a method for calculating the reference scattering spectra by summing the scattering spectra for numerous scatterers in the ultrasound focal region. By applying this method to the size estimation of microparticles simulating RBC aggregates, the estimated sizes are found to be close to the true values. In in vivo measurements, the estimated sizes at rest are equivalent to the size of a single sphere with the same volume as an RBC, and those during avascularization are larger than those at rest, which is reasonable. The proposed method has the potential to accurately estimate the size of RBC aggregates.
“…By applying the method to in vivo measurements for healthy subjects, the estimated sizes were close to 8 μm corresponding to the diameter of a single RBC under normal blood flow, and they increased by approximately 14 μm under the low shear rate condition by avascularization. 31) In our previous study, 30) there were differences in the shape between the power spectra measured from the microparticles simulating RBCs and the reference scattering power spectra corresponding to the microparticle diameters. In this study, we calculated the reference scattering power spectra by simulating a condition in which only a single scatterer existed at the focus of the ultrasound beam.…”
Section: Introductionmentioning
confidence: 86%
“…We have studied a noninvasive and quantitative method for measuring the RBC aggregate size using a high-frequency focused ultrasound transducer. [26][27][28][29][30][31] Fukushima et al assumed that aggregated RBCs are single-sphere scatterers and estimated their size from the scattering characteristics by normalizing the power spectrum measured from the vessel lumen by that from the posterior wall of the blood vessel as a reflector. [26][27][28][29] However, the vessel wall could have exhibited a slope to the probe surface and roughness on the surface.…”
We have studied a noninvasive and quantitative method for measuring the aggregate size of red blood cells (RBCs). In our previous study, the scattering power spectrum obtained from the vascular lumen was fitted to the reference scattering spectra calculated from the scattering spectrum of a single-sphere scatterer. In this paper, we propose a method for calculating the reference scattering spectra by summing the scattering spectra for numerous scatterers in the ultrasound focal region. By applying this method to the size estimation of microparticles simulating RBC aggregates, the estimated sizes are found to be close to the true values. In in vivo measurements, the estimated sizes at rest are equivalent to the size of a single sphere with the same volume as an RBC, and those during avascularization are larger than those at rest, which is reasonable. The proposed method has the potential to accurately estimate the size of RBC aggregates.
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