Determinants of Leukocyte Margination in Rectangular Microchannels

被引:76
作者
Jain, Abhishek
Munn, Lance L.
机构
[1] Steele Lab for Tumor Biology, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA
[2] Department of Biomedical Engineering, Boston University, Boston, MA
关键词
TOTAL ANALYSIS SYSTEMS; RED-CELL AGGREGATION; BLOOD-FLOW; WHOLE-BLOOD; SHEAR RATE; ADHESION; ERYTHROCYTES; MICROFLUIDICS; EMIGRATION; CAPILLARY;
D O I
10.1371/journal.pone.0007104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Microfabrication of polydimethylsiloxane (PDMS) devices has provided a new set of tools for studying fluid dynamics of blood at the scale of real microvessels. However, we are only starting to understand the power and limitations of this technology. To determine the applicability of PDMS microchannels for blood flow analysis, we studied white blood cell (WBC) margination in channels of various geometries and blood compositions. We found that WBCs prefer to marginate downstream of sudden expansions, and that red blood cell (RBC) aggregation facilitates the process. In contrast to tubes, WBC margination was restricted to the sidewalls in our low aspect ratio, pseudo-2D rectangular channels and consequently, margination efficiencies of more than 95% were achieved in a variety of channel geometries. In these pseudo-2D channels blood rheology and cell integrity were preserved over a range of flow rates, with the upper range limited by the shear in the vertical direction. We conclude that, with certain limitations, rectangular PDMS microfluidic channels are useful tools for quantitative studies of blood rheology.
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页数:8
相关论文
共 66 条
[1]   Rheological properties of the blood influencing selectin-mediated adhesion of flowing leukocytes [J].
Abbitt, KB ;
Nash, GB .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2003, 285 (01) :H229-H240
[2]   LIFETIME OF THE P-SELECTIN-CARBOHYDRATE BOND AND ITS RESPONSE TO TENSILE FORCE IN HYDRODYNAMIC FLOW [J].
ALON, R ;
HAMMER, DA ;
SPRINGER, TA .
NATURE, 1995, 374 (6522) :539-542
[3]   Microfluidic devices for cellomics: a review [J].
Andersson, H ;
van den Berg, A .
SENSORS AND ACTUATORS B-CHEMICAL, 2003, 92 (03) :315-325
[4]  
BAGGE U, 1983, INT J MICROCIRC, V2, P215
[5]   MAINTENANCE OF WHITE BLOOD-CELL MARGINATION AT THE PASSAGE THROUGH SMALL VENULAR JUNCTIONS [J].
BAGGE, U ;
KARLSSON, R .
MICROVASCULAR RESEARCH, 1980, 20 (01) :92-95
[6]   PREDICTION OF BLOOD FLOW IN TUBES WITH DIAMETERS AS SMALL AS 29-MU [J].
BARBEE, JH ;
COKELET, GR .
MICROVASCULAR RESEARCH, 1971, 3 (01) :17-&
[7]   FAHRAEUS EFFECT [J].
BARBEE, JH ;
COKELET, GR .
MICROVASCULAR RESEARCH, 1971, 3 (01) :6-&
[8]   ENDOTHELIAL-LEUKOCYTE ADHESION MOLECULES [J].
BEVILACQUA, MP .
ANNUAL REVIEW OF IMMUNOLOGY, 1993, 11 :767-804
[10]   Microfluidic chips for cell sorting [J].
Chen, Pu ;
Feng, Xiaojun ;
Du, Wei ;
Liu, Bi-Feng .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2008, 13 :2464-2483