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Controlled Microfluidic Environment for Dynamic Investigation of Red Blood Cell Aggregation
Published on: June 4, 2015
Inversion of ultrasonic scattering data for red blood cell suspensions under different flow conditions
The Journal of the Acoustical Society of America
|September 1, 1987
Summary
Ultrasonic scattering from red blood cells reveals cell interactions. Lower correlation parameters suggest weaker repulsion and aggregative trends in cell suspensions under flow.
Area of Science:
- Biophysics
- Acoustics
- Fluid Dynamics
Background:
- Low-frequency scattering principles apply to complex particle distributions.
- Nonspherical particle scattering requires orientation averaging for accurate analysis.
- Ultrasonic data from red blood cell suspensions can reveal cellular behavior.
Purpose of the Study:
- To apply low-frequency scattering theory to invert ultrasonic data for red blood cell suspensions.
- To investigate red blood cell interactions and population dynamics under varying flow conditions.
- To determine correlation and cell population parameters from scattering data.
Main Methods:
- Utilizing recent advancements in low-frequency scattering by correlated random distributions of nonspherical particles.
- Applying orientation averaging techniques to scattering data.
- Inverting ultrasonic data using a generalized fluctuation function S(c;w)P.
Main Results:
- The inversion procedure successfully isolated a correlation parameter (c) and a cell population parameter (P).
- Peak scattering occurred at volume fractions (w) between 0.15 and 0.25, corresponding to c values from 0.4 to 2.1.
- These results contrast with hard spheres (w ≈ 0.13, c = 3), indicating weaker repulsion and potential aggregation in red blood cells.
Conclusions:
- Lower c values suggest weaker repulsion and possible interparticle attraction (aggregative trends) between deformable red blood cells.
- The correlation parameter c may also reflect flow alignment of discoid red blood cells.
- Ultrasonic scattering provides insights into the micro dynamics of red blood cell suspensions.

