Abstract
Kinetics of optical tweezers (OT)-induced spontaneous aggregation and disaggregation of red blood cells (RBCs) were studied at the level of cell doublets to assess RBC interaction mechanics. Measurements were performed under in vitro conditions in plasma and fibrinogen and fibrinogen + albumin solutions. The RBC spontaneous aggregation kinetics was found to exhibit different behavior depending on the cell environment. In contrast, the RBC disaggregation kinetics was similar in all solutions qualitatively and quantitatively, demonstrating a significant contribution of the studied proteins to the process. The impact of the study on assessing RBC interaction mechanics and the protein contribution to the reversible RBC aggregation process is discussed.
Original language | English |
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Article number | 035001 |
Journal | Journal of Biomedical Optics |
Volume | 21 |
Issue number | 3 |
DOIs | |
Publication status | Published - 8 Mar 2016 |
Bibliographical note
© The Authors. Published by SPIE under a Creative Commons Attribution 3.0 Unported License. Distribution or reproduction of thiswork in whole or in part requires full attribution of the original publication, including its DOI. [DOI: 10.1117/1.JBO.21.3.035001]
Keywords
- aggregation
- albumin
- blood microcirculation
- cells interaction
- fibrinogen
- optical tweezers
- red blood cell