Abstract:Red blood cells (RBCs) in microchannels has tendency to undergo axial migration due to the parabolic velocity profile, which results in a high shear stress around wall that forces the RBC to move towards the centre induced by the tank treading motion of the RBC membrane. As a result there is a formation of a cell free layer (CFL) with extremely low concentration of cells. Based on this phenomenon, several works have proposed microfluidic designs to separate the suspending physiological fluid from whole in vitr… Show more
“…These results corroborate qualitatively the blood flow studies performed by other authors. 8,9,12,22 The CFL thickness for the simple geometries M 1 and M T and for 20% of healthy RBCs (closer to in vivo microcirculation environments) is also in good agreement with the in vivo results of Kim et al 6 and Yamaguchi et al…”
Section: -15supporting
confidence: 83%
“…Moreover, at these small dimensions, the elasticity of the fluid can be assessed while limiting inertial effects. The microchannel M T has an abrupt contraction followed by a smooth triangular expansion and also has a high Henchy strain of 3 promoting the CFL formation downstream of the contraction, and as Rodrigues et al 9 conclude in their study, e H ! 3 has a strong impact on the CFL thickness.…”
Section: -6mentioning
confidence: 59%
“…9 Similar measurements were also carried out for the analogue fluid, i.e., PMMA microbeads at 1% (w/w) suspended in the viscoelastic base fluid. These latter results were compared with data obtained from the healthy and glucose-rich RBCs deformability tests.…”
Section: Deformability Analysismentioning
confidence: 85%
“…The orientation of the RBCs at high shear rates and their tendency to migrate to the center line of the microchannels (in vitro) [1][2][3] or microvessels (in vivo) 4,5 originate the formation of a cell depleted layer near the walls, known as the cell-free layer (CFL). The CFL is influenced by the formation of aggregates, cell interactions and deformability, hematocrit, flow rate, viscosity, and geometry 6,7 and is a microscopic level phenomenon that occurs in microfluidic devices 2,6,8,9 and in microvessels [10][11][12] with dimensions in the range of 300 lm down to 10 lm. Several studies have been performed both in vivo 11,13,14 and in vitro 2,9,[15][16][17][18] to better understand the CFL formation, which influences its thickness and the advantages and disadvantages of the presence of this layer in the human microcirculatory system 6 and in microchannels.…”
Section: Introductionmentioning
confidence: 99%
“…The CFL is influenced by the formation of aggregates, cell interactions and deformability, hematocrit, flow rate, viscosity, and geometry 6,7 and is a microscopic level phenomenon that occurs in microfluidic devices 2,6,8,9 and in microvessels [10][11][12] with dimensions in the range of 300 lm down to 10 lm. Several studies have been performed both in vivo 11,13,14 and in vitro 2,9,[15][16][17][18] to better understand the CFL formation, which influences its thickness and the advantages and disadvantages of the presence of this layer in the human microcirculatory system 6 and in microchannels. 8,16,19 It is also important to refer that in real blood, there is a migration of white blood cells from the core towards the wall region of the vessels, a phenomenon called margination, 20,21 but this issue is outside the scope of this work.…”
Suspensions of healthy and pathological red blood cells (RBC) flowing in microfluidic devices are frequently used to perform in vitro blood experiments for a better understanding of human microcirculation hemodynamic phenomena. This work reports the development of particulate viscoelastic analogue fluids able to mimic the rheological and hemorheological behavior of pathological RBC suspensions flowing in microfluidic systems. The pathological RBCs were obtained by an incubation of healthy RBCs at a high concentration of glucose, representing the pathological stage of hyperglycaemia in diabetic complications, and analyses of their deformability and aggregation were carried out. Overall, the developed in vitro analogue fluids were composed of a suspension of semi-rigid microbeads in a carrier viscoelastic fluid made of dextran 40 and xanthan gum. All suspensions of healthy and pathological RBCs, as well as their particulate analogue fluids, were extensively characterized in steady shear flow, as well as in small and large amplitude oscillatory shear flow. In addition, the well-known cell-free layer (CFL) phenomenon occurring in microchannels was investigated in detail to provide comparisons between healthy and pathological in vitro RBC suspensions and their corresponding analogue fluids at different volume concentrations (5% and 20%). The experimental results have shown a similar rheological behavior between the samples containing a suspension of pathological RBCs and the proposed analogue fluids. Moreover, this work shows that the particulate in vitro analogue fluids used have the ability to mimic well the CFL phenomenon occurring downstream of a microchannel contraction for pathological RBC suspensions. The proposed particulate fluids provide a more realistic behavior of the flow properties of suspended RBCs when compared with existing non-particulate blood analogues, and consequently, they are advantageous for detailed investigations of microcirculation.
“…These results corroborate qualitatively the blood flow studies performed by other authors. 8,9,12,22 The CFL thickness for the simple geometries M 1 and M T and for 20% of healthy RBCs (closer to in vivo microcirculation environments) is also in good agreement with the in vivo results of Kim et al 6 and Yamaguchi et al…”
Section: -15supporting
confidence: 83%
“…Moreover, at these small dimensions, the elasticity of the fluid can be assessed while limiting inertial effects. The microchannel M T has an abrupt contraction followed by a smooth triangular expansion and also has a high Henchy strain of 3 promoting the CFL formation downstream of the contraction, and as Rodrigues et al 9 conclude in their study, e H ! 3 has a strong impact on the CFL thickness.…”
Section: -6mentioning
confidence: 59%
“…9 Similar measurements were also carried out for the analogue fluid, i.e., PMMA microbeads at 1% (w/w) suspended in the viscoelastic base fluid. These latter results were compared with data obtained from the healthy and glucose-rich RBCs deformability tests.…”
Section: Deformability Analysismentioning
confidence: 85%
“…The orientation of the RBCs at high shear rates and their tendency to migrate to the center line of the microchannels (in vitro) [1][2][3] or microvessels (in vivo) 4,5 originate the formation of a cell depleted layer near the walls, known as the cell-free layer (CFL). The CFL is influenced by the formation of aggregates, cell interactions and deformability, hematocrit, flow rate, viscosity, and geometry 6,7 and is a microscopic level phenomenon that occurs in microfluidic devices 2,6,8,9 and in microvessels [10][11][12] with dimensions in the range of 300 lm down to 10 lm. Several studies have been performed both in vivo 11,13,14 and in vitro 2,9,[15][16][17][18] to better understand the CFL formation, which influences its thickness and the advantages and disadvantages of the presence of this layer in the human microcirculatory system 6 and in microchannels.…”
Section: Introductionmentioning
confidence: 99%
“…The CFL is influenced by the formation of aggregates, cell interactions and deformability, hematocrit, flow rate, viscosity, and geometry 6,7 and is a microscopic level phenomenon that occurs in microfluidic devices 2,6,8,9 and in microvessels [10][11][12] with dimensions in the range of 300 lm down to 10 lm. Several studies have been performed both in vivo 11,13,14 and in vitro 2,9,[15][16][17][18] to better understand the CFL formation, which influences its thickness and the advantages and disadvantages of the presence of this layer in the human microcirculatory system 6 and in microchannels. 8,16,19 It is also important to refer that in real blood, there is a migration of white blood cells from the core towards the wall region of the vessels, a phenomenon called margination, 20,21 but this issue is outside the scope of this work.…”
Suspensions of healthy and pathological red blood cells (RBC) flowing in microfluidic devices are frequently used to perform in vitro blood experiments for a better understanding of human microcirculation hemodynamic phenomena. This work reports the development of particulate viscoelastic analogue fluids able to mimic the rheological and hemorheological behavior of pathological RBC suspensions flowing in microfluidic systems. The pathological RBCs were obtained by an incubation of healthy RBCs at a high concentration of glucose, representing the pathological stage of hyperglycaemia in diabetic complications, and analyses of their deformability and aggregation were carried out. Overall, the developed in vitro analogue fluids were composed of a suspension of semi-rigid microbeads in a carrier viscoelastic fluid made of dextran 40 and xanthan gum. All suspensions of healthy and pathological RBCs, as well as their particulate analogue fluids, were extensively characterized in steady shear flow, as well as in small and large amplitude oscillatory shear flow. In addition, the well-known cell-free layer (CFL) phenomenon occurring in microchannels was investigated in detail to provide comparisons between healthy and pathological in vitro RBC suspensions and their corresponding analogue fluids at different volume concentrations (5% and 20%). The experimental results have shown a similar rheological behavior between the samples containing a suspension of pathological RBCs and the proposed analogue fluids. Moreover, this work shows that the particulate in vitro analogue fluids used have the ability to mimic well the CFL phenomenon occurring downstream of a microchannel contraction for pathological RBC suspensions. The proposed particulate fluids provide a more realistic behavior of the flow properties of suspended RBCs when compared with existing non-particulate blood analogues, and consequently, they are advantageous for detailed investigations of microcirculation.
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