Affiliations: [a] Charité-Universitätsmedizin Berlin, Institute of Transfusion Medicine, Berlin, Germany
| [b]
Institute of Transfusion Medicine, Academy of Military Medical Sciences, Beijing, China
Correspondence:
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Corresponding author: Lian Zhao, Institute of Transfusion Medicine, Academy of Military Medical Sciences, Beijing, China. Tel.: +86 1066931969; E-mail: [email protected] and Hans Bäumler, Charité-Universitätsmedizin Berlin, Institute of Transfusion Medicine, 10117 Berlin, Germany. Tel.: +49 30450525131; E-mail: [email protected].
Abstract: The impact of macromolecules on RBC aggregation continues to be of interest, nevertheless present measurements still have limitations and need improvement. We applied flow cytometry to measure RBC aggregation in dextran T500 (Dx500) solution. The samples were fixed in the aggregated state by glutaraldehyde. Fixed RBC exhibit auto fluorescence, which can be detected by flow cytometry. Single cells, doublets, triplets and larger aggregates can be distinguished quantitatively and quickly due to the correlation between auto fluorescence intensity and number of RBC per measured event. With the increase in concentration of Dx500, percentages of all aggregates and bigger aggregates increased significantly at concentration of 2%, 4% and 6%, while decreased when the concentration reached 8% and 10%. The percentage of bigger aggregates in concentration of 4% was higher than that in 2% and 6%. The data of flow cytometry was confirmed by microscopic observation and are in good agreement with the literature. The method provide additional advantages to the conventional measurement of RBC aggregation. It gets the distribution of single cells and aggregates as derived from the microscopic observation with hematocrit of physiological level. It uses sample volume as 1/5∼1/10 as needed in sendimentation and photometricmethods.
