Quantification of red blood cell deformation at high-hematocrit blood flow in microvessels

Journal of Biomechanics

Volumn 45, Issue 15, 2012, Pages 2684-2689

  Alizadehrad, Davod ^a   Imai, Yohsuke ^a   Nakaaki, Keita ^a   Ishikawa, Takuji ^a   Yamaguchi, Takami ^a  

^a TOHOKU UNIVERSITY   (Japan)

Author keywords

Dense suspension; Microcirculation; Numerical simulation; Red blood cell deformation

Indexed keywords

APPARENT VISCOSITY; BLOOD FLOW; CIRCULAR CHANNELS; DENSE SUSPENSION; MICROVESSELS; NEAR-WALL REGION; NUMERICAL RESULTS; RADIAL POSITION; RADIAL VARIATIONS; RED BLOOD CELL; SHAPE TRANSITIONS; VESSEL DIAMETER; WALL EFFECTS;

BLOOD VESSELS; CELLS; COMPUTER SIMULATION; MICROCIRCULATION; PARALLEL ARCHITECTURES; SHEAR DEFORMATION; SHEAR STRESS;

BLOOD;

ARTICLE; CELL MOTION; CONTROLLED STUDY; ERYTHROCYTE DEFORMABILITY; HEMATOCRIT; MATHEMATICAL COMPUTING; MATHEMATICAL MODEL; MICROCIRCULATION; MICROVASCULATURE; PREDICTION; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; SHEAR RATE; SHEAR STRESS; VALIDATION PROCESS; VEIN BLOOD FLOW; VEIN DIAMETER;

BLOOD VISCOSITY; COMPUTER SIMULATION; ERYTHROCYTE DEFORMABILITY; ERYTHROCYTES; HEMATOCRIT; MICROCIRCULATION; MICROVESSELS; MODELS, CARDIOVASCULAR; STRESS, MECHANICAL;

EID: 84866749285     PISSN: 00219290     EISSN: 18732380     Source Type: Journal    
DOI: 10.1016/j.jbiomech.2012.08.026     Document Type: Article

References (44)

1. Alizadehrad D., Imai Y., Nakaaki K., Ishikawa T., Yamaguchi T. Parallel simulation of cellular flow in microvessels using a particle method. Journal of Biomechanical Science and Engineering 2012, 7:57-71.
2. Clausen J.R., Reasor D.A., Aidun C.K. Parallel performance of a lattice-Boltzmann/finite element cellular blood flow solver on the IBM Blue Gene/P architecture. Computer Physics Communications 2010, 181:1013-1020.
3. Cooke B.M., Mohandas N., Coppel R.L. The malaria-infected red blood cell: structural and functional changes. Advances in Parasitology 2001, 50:1-86.
4. Cranston H.A., Boylan C.W., Carroll G.L., Sutera S.P., Williamson J.R., Gluzman I.Y., Krogstad D.J. Plasmodium falciparum maturation abolishes physiologic red cell deformability. Science 1984, 223:400-403.
5. Dondorp A.M., Vreeken K.J., White N.J. Abnormal blood fl{ligature}ow and red blood cell deformability in severe malaria. Parasitology Today 2000, 16:228-232.
6. Dupin M.M., Halliday I., Care C.M., Alboul L., Munn L.L. Modeling the flow of dense suspensions of deformable particles in three dimensions. Physical Review E 2007, 75:066707.
7. Evans E.A. Bending elastic modulus of red blood cell membrane derived from buckling instability in micropipette aspiration tests. Biophysical Journal 1983, 43:27-30.
8. Evans E.A. Structure and deformation properties of red blood cells: concepts and quantitative methods. Methods in Enzymology 1989, 173:3-35.
9. Fåhræus R. The suspension stability of the blood. Physiological Reviews 1929, 9:241-274.
10. Fåhræus R., Lindqvist T. The viscosity of the blood in narrow capillary tubes. American Journal of Physiology 1931, 96:562-568.
11. Fedosov D.A., Caswell B., Popel A.S., Karniadakis G.E. Blood flow and cell-free layer in microvessels. Microcirculation 2010, 17:615-628.
12. Fedosov D.A., Pan W., Caswell B., Gompper G., Karniadakis G.E. Predicting human blood viscosity in silico. Proceedings of the National Academy of Sciences of the United States of America 2011, 108:11772-11777.
13. Fedosov D.A., Caswell B., Suresh S., Karniadakis G.E. Quantifying the biophysical characteristics of Plasmodium-falciparum-parasitized red blood cells in microcirculation. Proceedings of the National Academy of Sciences of the United States of America 2011, 108:35-39.
14. Fischer D.J., Torrence N.J., Sprung R.J., Spence D.M. Determination of erythrocyte deformability and its correlation to cellular ATP release using microbore tubing with diameters that approximate resistance vessels in vivo. Analyst 2003, 128:v1163-v1168.
15. Forsyth A.M., Wan J., Owrutsky P.D., Abkarian M., Stone H.A. Multiscale approach to link red blood cell dynamics, shear viscosity, and ATP release. Proceedings of the National Academy of Sciences of the United States of America 2011, 108:10986-10991.
16. Freund J.B., Orescanin M.M. Cellular fl{ligature}ow in a small blood vessel. Journal of Fluid Mechanics 2011, 671:466-490.
17. Goldsmith H.L. Red cell motions and wall interactions in tube flow. Federation Proceedings 1971, 30:1578-1590.
18. Higgins J.M., Eddington D.T., Bhatia S.N., Mahadevan L. Sickle cell vasoocclusion and rescue in a microfl{ligature}uidic device. Proceedings of the National Academy of Sciences of the United States of America 2007, 104:20496-20500.
19. Imai Y., Kondo H., Ishikawa T., Yamaguchi T. Modeling of hemodynamics arising from malaria infection. Journal of Biomechanics 2010, 43:1386-1393.
20. Imai Y., Nakaaki K., Kondo H., Ishikawa T., Lim C.T., Yamaguchi T. Margination of red blood cells infected by Plasmodium falciparum in a microvessel. Journal of Biomechanics 2011, 44:1553-1558.
21. Kamada, H., Imai, Y., Nakamura, M., Ishikawa, T., Yamaguchi, T. Computational analysis on the mechanical interaction between a thrombus and red blood cells: possible causes of membrane damage of red blood cells at microvessels. Medical Engineering and Physics, , in press. http://dx.doi.org/10.1016/j.medengphy.2012.01.003.
22. Kim S., Kong R.L., Popel A.S., Intaglietta M., Johnson P.C. Temporal and spatial variations of cell-free layer width in arterioles. American Journal of Physiology Heart and Circulatory Physiology 2007, 293:H1526-H1535.
23. Kondo H., Imai Y., Ishikawa T., Tsubota K., Yamaguchi T. Hemodynamic analysis of microcirculation in malaria infection. Annals of Biomedical Engineering 2009, 37:702-709.
24. Koshizuka S., Oka Y. Moving-particle semi-implicit method for fragmentation of incompressible fl{ligature}uid. Nuclear Science and Engineering 1996, 123:421-434.
25. Lima R., Ishikawa T., Imai Y., Takeda M., Wada S., Yamaguchi T. Measurement of individual red blood cell motions under high hematocrit conditions using a confocal micro-PTV system. Annals of Biomedical Engineering 2009, 37:1546-1559.
26. Lima R., Wada S., Takeda M., Tsubota K., Yamaguchi T. In vitro confocal micro-PIV measurements of blood fl{ligature}ow in a square microchannel: the effect of the haematocrit on instantaneous velocity profi{ligature}les. Journal of Biomechanics 2007, 40:2752-2757.
27. Lipowsky H.H., Kovalcheck S., Zweifach B.W. The distribution of blood rheological parameters in the microvasculature of cat mesentery. Circulation Research 1978, 43:738-749.
28. Lipowsky H.H., Usami S., Chien S. In vivo measurements of "apparent viscosity" and microvessel hematocrit in the mesentery of the cat. Microvascular Research 1980, 19:297-319.
29. McWhirter J.L., Noguchi H., Gompper G. Flow-induced clustering and alignment of vesicles and red blood cells in microcapillaries. Proceedings of the National Academy of Sciences of the United States of America 2009, 106:6039-6043.
30. Moehlenbrock M.J., Price A.K., Martin R.S. Use of microchip-based hydrodynamic focusing to measure the deformation-induced release of ATP from erythrocytes. Analyst 2006, 131:930-937.
31. Mohandas N., Evans E. Mechanical properties of the red cell membrane in relation to molecular structure and genetic defects. Annual Review of Biophysics and Biomolecular Structure 1994, 23:787-818.
32. Noguchi H., Gompper G. Shape transitions of fluid vesicles and red blood cells in capillary flows. Proceedings of the National Academy of Sciences of the United States of America 2005, 102:14159-14164.
33. Pan W., Caswell B., Karniadakis G.E. A low-dimensional model for the red blood cell. Soft Matter 2010, 6:4366-4376.
34. Pfafferott C., Nash G.B., Meiselman H.J. Red blood cell deformation in shear flow. Effects of internal and external phase viscosity and of in vivo aging. Biophysical Journal 1985, 47:695-704.
35. Pries A.R., Neuhaus D., Gaehtgens P. Blood viscosity in tube fl{ligature}ow: dependence on diameter and hematocrit. American Journal of Physiology Heart and Circulatory Physiology 1992, 263:H1770-H1778.
36. Reinke W., Gaehtgens P., Johnson P.C. Blood viscosity in small tubes: effect of shear rate, aggregation, and sedimentation. American Journal of Physiology Heart and Circulatory Physiology 1987, 253:H540-H547.
37. Saadatmand M., Ishikawa T., Matsuki N., Abdekhodaie M.J., Imai Y., Ueno H., Yamaguchi T. Fluid particle diffusion through high-hematocrit blood flow within a capillary tube. Journal of Biomechanics 2011, 44:170-175.
38. Suresh S., Spatz J., Mills J.P., Micoulet A., Dao M., Lim C.T., Beil M., Seufferlein T. Connection between single-cell biomechanics and human disease states: gastrointestinal cancer and malaria. Acta Biomaterialia 2005, 1:15-30.
39. Suresh S. Mechanical response of human red blood cells in health and disease: some structure-property-function relationships. Journal of Materials Research 2006, 21:1871-1877.
40. Tateishi N., Suzuki Y., Soutani M., Maeda N. Flow dynamics of erythrocytes in microvessels of isolated rabbit mesentery: cell-free layer and flow resistance. Journal of Biomechanics 1994, 27:1119-1125.
41. Tsukada K., Sekizuka E., Oshio C., Minamitani H. Direct measurement of erythrocyte deformability in diabetes mellitus with a transparent microchannel capillary model and high-speed video camera system. Microvascular Research 2001, 61:231-239.
42. Wan J., Ristenpart W.D., Stone H.A. Dynamics of shear-induced ATP release from red blood cells. Proceedings of the National Academy of Sciences of the United States of America 2008, 105:16432-16437.
43. Wells R.E.J., Merrill E.W. Shear rate dependence of the viscosity of whole blood and plasma. Science 1961, 133:763-764.
44. Zhao H., Isfahani A.H.G., Olson L.N., Freund J.B. A spectral boundary integral method for fl{ligature}owing blood cells. Journal of Computational Physics 2010, 229:3726-3744.