Title
Estimation of polydispersity in aggregating red blood cells by quantitative ultrasound backscatter analysis
Date Issued
01 April 2018
Access level
open access
Resource Type
journal article
Author(s)
De Monchy R.
Destrempes F.
Chayer B.
Cloutier G.
Franceschini E.
Aix-Marseille Université
Publisher(s)
Acoustical Society of America
Abstract
Quantitative ultrasound techniques based on the backscatter coefficient (BSC) have been commonly used to characterize red blood cell (RBC) aggregation. Specifically, a scattering model is fitted to measured BSC and estimated parameters can provide a meaningful description of the RBC aggregates' structure (i.e., aggregate size and compactness). In most cases, scattering models assumed monodisperse RBC aggregates. This study proposes the Effective Medium Theory combined with the polydisperse Structure Factor Model (EMTSFM) to incorporate the polydispersity of aggregate size. From the measured BSC, this model allows estimating three structural parameters: the mean radius of the aggregate size distribution, the width of the distribution, and the compactness of the aggregates. Two successive experiments were conducted: a first experiment on blood sheared in a Couette flow device coupled with an ultrasonic probe, and a second experiment, on the same blood sample, sheared in a plane-plane rheometer coupled to a light microscope. Results demonstrated that the polydisperse EMTSFM provided the best fit to the BSC data when compared to the classical monodisperse models for the higher levels of aggregation at hematocrits between 10% and 40%. Fitting the polydisperse model yielded aggregate size distributions that were consistent with direct light microscope observations at low hematocrits.
Start page
2207
End page
2216
Volume
143
Issue
4
Language
English
OCDE Knowledge area
Patología Radiología, Medicina nuclear, Imágenes médicas
Scopus EID
2-s2.0-85045928794
PubMed ID
Source
Journal of the Acoustical Society of America
ISSN of the container
00014966
Sponsor(s)
Agence Nationale de la Recherche - ANR-15-CE19-0017 This research was supported by the French National Research Agency (Grant No. ANR-15-CE19-0017), and the Labex MEC (Grant No. ANR-10-LABX-0092) and the A*MIDEX project (Grant No. ANR-11-IDEX-0001-02) funded by the Investissements Avenir French Government program. Support was also obtained from the Canadian Institutes of Health Research (Grant No. MOP-84358).
Sources of information: Directorio de Producción Científica Scopus