scholarly journals Sorting same-size red blood cells in deep deterministic lateral displacement devices

2018 ◽  
Vol 859 ◽  
pp. 433-475 ◽  
Author(s):  
Gökberk Kabacaoğlu ◽  
George Biros

Microfluidic sorting of deformable particles finds many applications, for example, medical devices for cells. Deterministic lateral displacement (DLD) is one of them. Particle sorting via DLD relies only on hydrodynamic forces. For rigid spherical particles, this separation is to a great extent understood and can be attributed to size differences: large particles displace in the lateral direction with respect to the flow while small particles travel in the flow direction with negligible lateral displacement. However, the separation of non-spherical deformable particles such as red blood cells (RBCs) is more complicated than that of rigid particles. For example, is it possible to separate deformable particles that have the same size but different mechanical properties? We study deformability-based sorting of same-size RBCs via DLD using an in-house integral equation solver for vesicle flows in two dimensions. Our goal is to quantitatively characterize the physical mechanisms that enable the cell separation. To this end, we systematically investigate the effects of the interior fluid viscosity and membrane elasticity of a cell on its behaviour. In particular, we consider deep devices in which a cell can show rich dynamics such as taking a particular angular orientation depending on its mechanical properties. We have found out that cells moving with a sufficiently high positive inclination angle with respect to the flow direction displace laterally while those with smaller angles travel with the flow streamlines. Thereby, deformability-based cell sorting is possible. The underlying mechanism here is cell migration due to the cell’s positive inclination and the shear gradient. The higher the inclination is, the farther the cell can travel laterally. We also assess the efficiency of the technique for dense suspensions. It turns out that most of the cells in dense suspensions do not displace in the lateral direction no matter what their deformability is. As a result, separating cells using a DLD device becomes harder.

Micromachines ◽  
2019 ◽  
Vol 10 (6) ◽  
pp. 393 ◽  
Author(s):  
Yanying Jiao ◽  
Yongqing He ◽  
Feng Jiao

Deterministic lateral displacement (DLD) technology has great potential for the separation, enrichment, and sorting of red blood cells (RBCs). This paper presents a numerical simulation of the motion of RBCs using DLD devices with different pillar shapes and gap configurations. We studied the effect of the pillar shape, row shift, and pillar diameter on the performance of RBC separation. The numerical results show that the RBCs enter “displacement mode” under conditions of low row-shift (∆λ < 1.4 µm) and “zigzag mode” with large row shift (∆λ > 1.5 µm). RBCs can pass the pillar array when the size of the pillar (d > 6 µm) is larger than the cell size. We show that these conclusions can be helpful for the design of a reliable DLD microfluidic device for the separation of RBCs.


2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Ewa Guzniczak ◽  
Maryam Mohammad Zadeh ◽  
Fiona Dempsey ◽  
Melanie Jimenez ◽  
Henry Bock ◽  
...  

2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Frederik Barbarino ◽  
Lucas Wäschenbach ◽  
Virginia Cavalho-Lemos ◽  
Melissa Dillenberger ◽  
Katja Becker ◽  
...  

AbstractThe mechanical properties of red blood cells (RBCs) are fundamental for their physiological role as gas transporters. RBC flexibility and elasticity allow them to survive the hemodynamic changes in the different regions of the vascular tree, to dynamically contribute to the flow thereby decreasing vascular resistance, and to deform during the passage through narrower vessels. RBC mechanoproperties are conferred mainly by the structural characteristics of their cytoskeleton, which consists predominantly of a spectrin scaffold connected to the membrane via nodes of actin, ankyrin and adducin. Changes in redox state and treatment with thiol-targeting molecules decrease the deformability of RBCs and affect the structure and stability of the spectrin cytoskeleton, indicating that the spectrin cytoskeleton may contain redox switches. In this perspective review, we revise current knowledge about the structural and functional characterization of spectrin cysteine redox switches and discuss the current lines of research aiming to understand the role of redox regulation on RBC mechanical properties. These studies may provide novel functional targets to modulate RBC function, blood viscosity and flow, and tissue perfusion in disease conditions.


Blood ◽  
2017 ◽  
Vol 130 (Suppl_1) ◽  
pp. 964-964
Author(s):  
Erdem Kucukal ◽  
Jane A. Little ◽  
Umut A. Gurkan

Abstract The pathophysiology of sickle cell disease (SCD) involves altered biophysical properties of red blood cells (RBCs) and increased cellular adhesion, which can synergistically trigger recurrent and painful vaso-occlusive events in the microcirculatory network. RBC adhesion to the endothelial wall is heterogeneous and may initiate such occlusions by disrupting the local flow thus activating platelets and promoting subsequent cell-cell interactions. Moreover, these episodic events take place within a wide range of dynamically changing shear rates at the microscale. In order to better understand the role of shear rate on this process, we quantified shear-dependent RBC adhesion to endothelial proteins fibronectin (FN) and laminin (LN) utilizing a microfluidic system that can simulate physiologically relevant shear gradients of microcirculatory blood flow at a single flow rate. Whole blood samples were collected from 20 patients (10 males and 10 females) with homozygous SCD (HbSS). Samples were perfused through FN and LN immobilized shear-gradient microchannels (Fig. 1A) in which the shear rate continuously changes along flow direction. Computational simulations characterized the flow dynamics near the adherent RBCs (Fig. 1B). Based on the numerical results, a rectangular "field of interest (FOI)", along which the shear rate dropped approximately three-fold, was chosen for quantification of shear-dependent RBC adhesion. We observed changes in RBC adhesion to LN and FN in the shear gradient flow. Figure 1C and 1D show typical adhesion curves of surface adherent RBCs for an individual SCD sample within the FOI. To assess patient specific shear-dependent adhesion, we defined a parameter, "shear dependent adhesion rate (SDAR)", which is the slope of the adhesion curves based on normalized RBC adhesion numbers. A higher SDAR value was indicative of marked numbers of adherent RBCs that detach at higher shear rates whereas the effect of shear rate on RBC detachment was less for a lower SDAR. We observed an inverse relationship between SDAR and number of persistently adherent RBCs at high shear rates. Shear-dependent RBC adhesion to LN was heterogeneous among SCD patients. Patients with higher WBC counts constituted the low SDAR population with a threshold SDAR value of 60 (Fig. 1E, p=0.005, ANOVA). WBCs from patients with higher SDARs (and fewer persistently adhered cells) were all within the normal range. Patients in the low SDAR group also had significantly elevated absolute neutrophil counts (Fig. 1F, p=0.006, ANOVA), and ferritin levels (Fig. 1G, p=0.007, ANOVA). The mean ferritin level of those with low SDAR was nearly ten times greater than normal (mean= [3272.3 ± 791.9] μg/L vs. [784.5±219.6] μg/L). No white blood cell (WBC) adhesion was observed in the experiments. Here, we report a novel shear dependent adhesion ratio of sickle RBCs utilizing LN and FN functionalized microchannels. The approach presented here enabled us to create a shear gradient throughout the channel which may simulate the physiological flow conditions in the post-capillary venules. We further analyzed shear-dependent RBC adhesion in a patient specific manner and identified patient groups with low and high SDAR. The findings also suggested a link between lower shear dependent sickle RBC adhesion to LN and patient clinical phenotypes including inflammation and iron overload. Acknowledgments: This work was supported by grant #2013126 from the Doris Duke Charitable Foundation, National Heart Lung and Blood Institute R01HL133574, and National Science Foundation CAREER Award 1552782. Figure 1: Shear-dependent sickle RBC adhesion in microscale flow. (A) Macroscopic image of the shear-gradient microchannel with the arrow indicating flow direction. (B) Velocity and shear rate contours on a 2D plane above the bottom surface. The dashed rectangular area indicates the field of interest (FOI) where the experimental data were obtained. (C, D) Typical distribution of adherent deformable and non-deformable RBCs in LN and FN functionalized microchannels with the shear gradient. Dashed lines represent the adhesion curves and the corresponding equations were used to quantify shear dependent adhesion data. Shear-dependent RBC adhesion was lower (nSDAR&lt;60) in patients with elevated white blood cell counts (E), absolute neutrophil counts (F), and serum ferritin levels (G). The dashed rectangles indicate the normal clinical values. Figure 1 Figure 1. Disclosures Little: Hemex Health: Equity Ownership. Gurkan: Hemex Health: Employment, Equity Ownership.


Parasitology ◽  
1979 ◽  
Vol 78 (3) ◽  
pp. 263-270 ◽  
Author(s):  
R. J. Howard ◽  
F. L. Battye

SUMMARYA cell-sorting method is described for the analysis and separation of red blood cells in Plasmodium berghei-infected mouse blood based on their DNA content. This method involves a selective uptake of the bis-benzimidazole dye 33258 Hoechst, a DNA-binding dye, by red blood cells containing parasites. Infected blood is incubated at 37 °C with the dye then washed at 4 °C to remove unbound dye. Uninfected cells are then non-fluorescent at the characteristic wavelengths for 33258 Hoechst excitation and emission, whereas parasitized cells display fluorescence intensities in approximately direct proportion to the number of parasite nuclei (i.e. amount of parasite DNA) within the cell and can be sorted accordingly. Providing cells were incubated in a complex nutrient medium during dye uptake at 37°C, the sorted parasite cells produced lethal P. berghei infections when injected into BALB/c mice. The dyelabelling technique is simple and sufficient red blood cells at various stages of infection can be collected for biochemical or immunochemical studies by cell sorting.


Blood ◽  
1998 ◽  
Vol 92 (8) ◽  
pp. 2975-2977 ◽  
Author(s):  
R.R. Huruta ◽  
M.L. Barjas-Castro ◽  
S.T.O. Saad ◽  
F.F. Costa ◽  
A. Fontes ◽  
...  

2020 ◽  
Vol 26 (S1) ◽  
pp. 47-48
Author(s):  
Georges Minatchy ◽  
Laurence Romana ◽  
Grégory Francius ◽  
Marc Romana

2005 ◽  
Author(s):  
Adriana Fontes ◽  
Andre Alexandre de Thomaz ◽  
Liliana de Ysasa Pozzo ◽  
Maria de Lourdes Barjas-Castro ◽  
Marcelo M. Brandao ◽  
...  

2008 ◽  
Vol 13 (1) ◽  
pp. 014001 ◽  
Author(s):  
Adriana Fontes ◽  
Heloise P. Fernandes ◽  
André A. de Thomaz ◽  
Luiz C. Barbosa ◽  
Maria L. Barjas-Castro ◽  
...  

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