Interplay of deformability and adhesion on localization of elastic micro-particles in blood flow

2018 ◽  
Vol 861 ◽  
pp. 55-87 ◽  
Author(s):  
Huilin Ye ◽  
Zhiqiang Shen ◽  
Ying Li
Keyword(s):  
Blood Flow ◽  
Fluid Flow ◽  
Adhesion Strength ◽  
Vessel Wall ◽  
Viscous Force ◽  
Cascade Process ◽  
Micro Particles ◽  
Region I ◽  
Region Ii ◽  
Near Wall

The margination and adhesion of micro-particles (MPs) have been extensively investigated separately, due to their important applications in the biomedical field. However, the cascade process from margination to adhesion should play an important role in the transport of MPs in blood flow. To the best of our knowledge, this has not been explored in the past. Here we numerically study the margination behaviour of elastic MPs to blood vessel walls under the interplay of their deformability and adhesion to the vessel wall. We use the lattice Boltzmann method and molecular dynamics to solve the fluid dynamics and particle dynamics (including red blood cells (RBCs) and elastic MPs) in blood flow, respectively. Additionally, a stochastic ligand–receptor binding model is employed to capture the adhesion behaviours of elastic MPs on the vessel wall. Margination probability is used to quantify the localization of elastic MPs at the wall. Two dimensionless numbers are considered to govern the whole process: the capillary number $Ca$, denoting the ratio of viscous force of fluid flow to elastic interfacial force of MP, and the adhesion number $Ad$, representing the ratio of adhesion strength to viscous force of fluid flow. We systematically vary them numerically and a margination probability contour is obtained. We find that there exist two optimal regimes favouring high margination probability on the plane $Ca{-}Ad$. The first regime, namely region I, is that with high adhesion strength and moderate particle stiffness; the other one, region II, has moderate adhesion strength and large particle stiffness. We conclude that the existence of optimal regimes is governed by the interplay of particle deformability and adhesion strength. The corresponding underlying mechanism is also discussed in detail. There are three major factors that contribute to the localization of MPs: (i) near-wall hydrodynamic collision between RBCs and MPs; (ii) deformation-induced migration due to the presence of the wall; and (iii) adhesive interaction between MPs and the wall. Mechanisms (i) and (iii) promote margination, while (ii) hampers margination. These three factors perform different roles and compete against each other when MPs are located in different regions of the flow channel, i.e. near-wall region. In optimal region I, adhesion outperforms deformation-induced migration; and in region II, the deformation-induced migration is small compared to the coupling of near-wall hydrodynamic collision and adhesion. The finding of optimal regimes can help the understanding of localization of elastic MPs at the wall under the adhesion effect in blood flow. More importantly, our results suggest that softer MP or stronger adhesion is not always the best choice for the localization of MPs.

Blood Flow Pattern and Anastomotic Compliance for Interrupted versus Continuous Coronary Bypass Grafts

2005 ◽  
Vol 6 (2) ◽  
pp. 65 ◽  
Author(s):  
Marc Gerdisch ◽  
Thomas Hinkamp ◽  
Stephen D. Ainsworth
Keyword(s):  
Blood Flow ◽  
Vessel Wall ◽  
Coronary Bypass ◽  
Bypass Grafts ◽  
Cross Sectional ◽  
Coronary Bypass Grafts ◽  
Geometric Consistency ◽  
Suturing Technique ◽  
Suturing Techniques ◽  
Key Indicators

<P>Background: Use of the interrupted coronary anastomosis has largely been abandoned in favor of the more rapid continuous suturing technique. The Coalescent U-CLIP anastomotic device allows the surgeon to create an interrupted distal anastomosis in the same amount of time that it would take to create a continuous anastomosis. This acute bovine study examined the effect of the anastomotic technique on blood flow and vessel wall function. </P><P>Methods: End-to-side coronary anastomoses were created in an open chest bovine model using the left and right internal thoracic arteries and the left anterior descending coronary artery. All other variables except suturing technique were carefully controlled. In each animal, one anastomosis was completed using a continuous suturing technique and the other was performed in an interrupted fashion using the Coalescent U-CLIP anastomotic device. Volumetric flow curves through each graft were analyzed using key indicators of anastomotic quality, and anastomotic compliance was evaluated using intravascular ultrasound. Luminal castings were created of each vessel to examine the interior surface of each anastomosis for constrictions and deformities. </P><P>Results: The interrupted anastomoses created with the Coalescent U-CLIP anastomotic device showed significant differences with respect to anastomotic compliance, pulsatility index, peak flow, and percentage of diastolic flow. The cross-sectional area and degree of luminal deformity were also different for the two suturing techniques. </P><P>Conclusions: In this acute bovine model, interrupted coronary anastomoses demonstrated superior geometric consistency and greater physiologic compliance than did continuously sutured anastomoses. The interrupted anastomosis also caused fewer disturbances to the flow waveform, behaving similarly to a normal vessel wall. The combination of these effects may influence both acute and long-term patency of the coronary bypass grafts.</P>

A Non-Newtonian Fluid Flow Model for the Slip Condition on Blood Flow through a Stenosed Artery using Power-law Fluid

2018 ◽  
Vol 9 (7) ◽  
pp. 871-879
Author(s):  
Rajesh Shrivastava ◽  
R. S. Chandel ◽  
Ajay Kumar ◽  
Keerty Shrivastava and Sanjeet Kumar
Keyword(s):  
Blood Flow ◽  
Fluid Flow ◽  
Newtonian Fluid ◽  
Power Law ◽  
Flow Model ◽  
Slip Condition ◽  
Power Law Fluid ◽  
Stenosed Artery ◽  
Flow Through

Effect of Blood Viscosity on Thrombosis Potential Near a Step Wall Transition

2009 ◽  
Author(s):  
Scott C. Corbett ◽  
Amin Ajdari ◽  
Ahmet U. Coskun ◽  
Hamid N.-Hashemi
Keyword(s):  
Blood Flow ◽  
Vessel Wall ◽  
Coagulation Factors ◽  
Artificial Organs ◽  
Physical Factors ◽  
Local Geometry ◽  
Induce Platelet Aggregation ◽  
Shear Rates ◽  
Chemical Factors ◽  
Low Shear

Thrombosis and hemolysis are two problems encountered when processing blood in artificial organs. Physical factors of blood flow alone can influence the interaction of proteins and cells with the vessel wall, induce platelet aggregation and influence coagulation factors responsible for the formation of thrombus, even in the absence of chemical factors in the blood. These physical factors are related to the magnitude of the shear rate/stress, the duration of the applied force and the local geometry. Specifically, high blood shear rates (or stress) lead to damage (hemolysis, platelet activation), while low shear rates lead to stagnation and thrombosis [1].

Interactions of Flow Structure With Nano- and Micro-Particles in Turbulent Channel Flows

2018 ◽  
Author(s):  
Amir A. Mofakham ◽  
Goodarz Ahmadi ◽  
John McLaughlin
Keyword(s):  
Relaxation Time ◽  
Coherent Structures ◽  
Concentration Distribution ◽  
Channel Flows ◽  
Small Scale ◽  
Turbulence Structure ◽  
Micro Particles ◽  
Turbulent Channel Flows ◽  
Wide Range ◽  
Near Wall

This study is concerned with the effects of the flow structures including the near-wall coherent eddies in turbulent channel flows on the dispersion and deposition of nano- and micro-particles. A pseudo-spectral computational code was used for direct numerical simulations (DNS) of the Navier-Stokes equations and the corresponding time histories of the instantaneous fluid velocities were evaluated. Under the oneway coupling assumption, the trajectories of a wide range of particle sizes from 10 nm to 80 μm with dimensionless relaxation time of 2.2e−6 to 142 were obtained by solving the particle equation of motion including Stokes drag and Brownian excitations. Dispersion and deposition of particles in the turbulent flow were evaluated and the effects of turbulence structure on different size particles were studied. The simulation results showed that the concentration distribution of small particles that behave like fluid tracer particles were quite random. However, the preferential concentrations appeared as the dimensionless relaxation time increased to 2–20. In particular, the influence of coherent structures in the near-wall regions was clearly detectable on the concentration distribution of particles, as well as, in their deposition pattern. For τ+ = 20 particles due to the increase of relaxation time and inertia of particles, the small-scale turbulent features were filtered out and only the effect of large-scale turbulent eddies could be identified. For τ+ = 2–20 particles, the ensemble/time average of the position of the deposited particles showed specific spacing which was comparable to the size of the near-wall coherent structures.

Plasmodium falciparum EBA-175 kDa protein peptides which bind to human red blood cells

Parasitology ◽  
2000 ◽  
Vol 120 (3) ◽  
pp. 225-235 ◽  
Author(s):  
L. E. RODRIGUEZ ◽  
M. URQUIZA ◽  
M. OCAMPO ◽  
J. SUAREZ ◽  
H. CURTIDOR ◽  
...  
Keyword(s):  
Plasmodium Falciparum ◽  
Binding Activity ◽  
Ligand Interaction ◽  
Merozoite Invasion ◽  
Human Red Blood Cells ◽  
Affinity Constants ◽  
Region I ◽  
Binding Peptides ◽  
V Region ◽  
Region Ii

Solid experimental evidence indicates that EBA-175 is used as a ligand by the Plasmodium falciparum merozoite to bind to human RBC, via different binding processing fragments. Using synthetic peptides and specific receptor-ligand interaction methodology, we have identified 6 high-activity binding sequences from the EBA-175 CAMP strain; peptide 1758 (KSYGTPDNIDKNMSLIHKHN), located in the so-called region I for which no binding activity has been reported before, peptides 1779 (NIDRIYDKNLLMIKEHILAI) and 1783 (HRNKKNDKLYRDEWWKVIKK), located in region II, in a sub-region known as 5′ Cys F2, previously reported as being a binding region, and peptides 1814 (DRNSNTLHLKDYRNEENERH), 1815 (YTNQNINISQERDLQKHGFH) and 1818 (NNNFNNIPSRYNLYDKKLDL), in region III–V where antibodies inhibit merozoite invasion of erythrocytes. The affinity constants were between 60 and 180 nM and the critical amino acids involved in the binding were identified. The binding of these peptides to enzyme-treated RBC was analysed; binding of peptide 1814, located in the III–V region, was found to be sialic acid dependent. Some of these high binding peptides were able to inhibit in vitro merozoite invasion and to block the binding of recombinant RII-EBA to RBC. Several of these peptides are located in regions recognized by protective immune clusters of merozoites (ICMs) eluted antibodies.

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