| Literature DB >> 28838798 |
Hagit Stauber1, Dan Waisman2, Netanel Korin1, Josué Sznitman3.
Abstract
Microfluidic-based assays have become increasingly popular to explore microcirculation in vitro. In these experiments, blood is resuspended to a desired haematocrit level in a buffer solution, where frequent choices for preparing RBC suspensions comprise notably Dextran and physiological buffer. Yet, the rational for selecting one buffer versus another is often ill-defined and lacks detailed quantification, including ensuing changes in RBC flow characteristics. Here, we revisit RBC suspensions in microflows and attempt to quantify systematically some of the differences emanating between buffers. We measure bulk flow rate (Q) of RBC suspensions, using PBS- and Dextran-40, as a function of the applied pressure drop (ΔP) for two hematocrits (∼0% and 23%). Two distinct microfluidic designs of varying dimensions are employed: a straight channel larger than and a network array similar to the size of individual RBCs. Using the resulting pressure-flow curves, we extract the equivalent hydrodynamic resistances and estimate the relative viscosities. These efforts are a first step in rigorously quantifying the influence of the 'background' buffer on RBC flows within microfluidic devices and thereby underline the importance of purposefully selecting buffer suspensions for microfluidic in vitro assays.Entities:
Keywords: Hydrodynamic resistance; In vitro models; Microfluidics; Pressure-flow measurements; Red blood cells (RBCs); Suspensions
Mesh:
Substances:
Year: 2017 PMID: 28838798 PMCID: PMC5610902 DOI: 10.1016/j.medengphy.2017.08.006
Source DB: PubMed Journal: Med Eng Phys ISSN: 1350-4533 Impact factor: 2.242