Deformability based sorting of stored red blood cells reveals donor-dependent aging curves

• Published in: Lab on a chip Vol. 2; no. 2; pp. 226 - 235
• Main Authors: Islamzada, Emel, Matthews, Kerryn, Guo, Quan, Santoso, Aline T, Duffy, Simon P, Scott, Mark D, Ma, Hongshen
• Format: Journal Article
• Language: English
• Published: England Royal Society of Chemistry 21.01.2020
• Subjects: Adolescent; Adult; Aged; Aging; Biomarkers; Blood Preservation; Blood transfusion; Cold storage; Deformation; Donations; Donors (electronic); Erythrocyte Count; Erythrocyte Deformability; Erythrocytes; Erythrocytes - cytology; Formability; Humans; Lab-On-A-Chip Devices; Microfluidics; Middle Aged; Organic chemistry; Rheological properties; Young Adult
• ISSN: 1473-0197; 1473-0189
• DOI: 10.1039/c9lc01058k

A fundamental challenge in the transfusion of red blood cells (RBCs) is that a subset of donated RBC units may not provide optimal benefit to transfusion recipients. This variability stems from the inherent ability of donor RBCs to withstand the physical and chemical insults of cold storage, which ultimately dictate their survival in circulation. The loss of RBC deformability during cold storage is well-established and has been identified as a potential biomarker for the quality of donated RBCs. While RBC deformability has traditionally been indirectly inferred from rheological characteristics of the bulk suspension, there has been considerable interest in directly measuring the deformation of RBCs. Microfluidic technologies have enabled single cell measurement of RBC deformation but have not been able to consistently distinguish differences between RBCs between healthy donors. Using the microfluidic ratchet mechanism, we developed a method to sensitively and consistently analyze RBC deformability. We found that the aging curve of RBC deformability varies significantly across donors, but is consistent for each donor over multiple donations. Specifically, certain donors seem capable of providing RBCs that maintain their deformability during two weeks of cold storage in standard test tubes. The ability to distinguish between RBC units with different storage potential could provide a valuable opportunity to identify donors capable of providing RBCs that maintain their integrity, in order to reserve these units for sensitive transfusion recipients. Cell sorting using microfluidic ratchets enables sensitive and consistent characterization of donor red blood cell deformability. Using this capability, we show the degradation of red blood cell deformability during cold storage is donor-dependent.