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Controlled Microfluidic Environment for Dynamic Investigation of Red Blood Cell Aggregation
Published on: June 4, 2015
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RBC aggregation in dextran solutions can be measured by flow cytometry
Lian Zhao1, Waraporn Kaewprayoon2, Hong Zhou1
1Institute of Transfusion Medicine, Academy of Military Medical Sciences, Beijing, China.
Clinical Hemorheology and Microcirculation
|October 8, 2016
Summary
Flow cytometry offers a novel method to quantify red blood cell (RBC) aggregation in dextran solutions. This technique accurately measures RBC aggregates, providing advantages over traditional methods.
Area of Science:
- Biophysics
- Hematology
- Analytical Chemistry
Background:
- Red blood cell (RBC) aggregation is crucial in microcirculation, but current measurement techniques have limitations.
- Understanding macromolecule-induced RBC aggregation is vital for various physiological and pathological conditions.
Purpose of the Study:
- To develop and validate a flow cytometry-based method for quantifying RBC aggregation.
- To assess the impact of dextran T500 concentration on RBC aggregation.
Main Methods:
- Red blood cells were suspended in dextran T500 solutions and fixed in their aggregated state using glutaraldehyde.
- Flow cytometry was used to detect RBC auto-fluorescence, correlating fluorescence intensity with the number of RBCs per event.
- Quantitative analysis distinguished between single cells and various sizes of RBC aggregates.
Main Results:
- RBC aggregation, including larger aggregates, increased with dextran T500 concentrations up to 6% and then decreased at 8% and 10%.
- The highest percentage of larger aggregates was observed at a 4% dextran T500 concentration.
- Flow cytometry data were validated by microscopic observations and aligned with existing literature.
Conclusions:
- Flow cytometry provides a rapid, quantitative, and sensitive method for measuring RBC aggregation.
- This technique offers advantages in terms of sample volume and detailed aggregate distribution analysis compared to conventional methods.

