4.6 Article

In vitro blood flow visualizations and cell-free layer (CFL) measurements in a microchannel network

期刊

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.expthermflusci.2019.109847

关键词

Microchannel network; Cell-free layer; Blood flow; Microfluidics; Red blood cells

资金

  1. Fundacao para a Ciencia e a Tecnologia (FCT), Portugal [UID/EMS/04077/2019, UID/EEA/04436/2019, UID/EMS/00532/2019]
  2. FCT [POCI-01-0145-FEDER-016861, POCI-01-0145-FEDER-028159, NORTE-01-0145-FEDER-029394, NORTE-01-0145-FEDER-030171]
  3. COMPETE2020
  4. FEDER
  5. NORTE2020
  6. PORTUGAL2020
  7. PhD grant [SFRH/BD/91192/2012]
  8. Fundação para a Ciência e a Tecnologia [UID/EMS/00532/2019, UID/EMS/04077/2019] Funding Source: FCT

向作者/读者索取更多资源

Microvascular networks are not simple straight microchannels but rather complex geometries composed by successive asymmetric divergent and convergent bifurcations. Despite the extensive research work in this field, still lack of knowledge about the blood flow behavior in microvascular networks. The current study applies the most current advanced visualization and microfabrication techniques to provide further insights into to the blood flow in network geometries. Hence, by using a high-speed video microscopy system, blood flow measurements and visualizations of the cell-free layer (CFL) were performed along a microchannel network composed by several divergent and convergent bifurcations. The inlet flow rate was kept constant whereas the hematocrit (Hct) and the depth of the geometry was changed in order to evaluate their effects into the CFL thickness. The results, show clearly that the Hct has a significant impact on the CFL thickness whereas the effect of reducing the depth did not contribute to a noticeable change on the CFL. In addition, the in vitro blood flow results reported here provide for the first time that in microfluidic devices having several asymmetric confluences it is likely to have the formation of several CFLs not only around the walls but also in middle of the main channels just downstream of the last confluence apex. Although, to best of our knowledge there is no evidence that this kind of flow phenomenon also happens in vivo, we believe that for microvascular networks with similar geometries and under similar flow conditions tested in this work, this kind of phenomenon may also happen in vivo. Furthermore, the results from this study could be extremely helpful to validate current numerical microvascular network models and to develop more realistic multiphase numerical models of blood flow in microcirculation.

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