Microfluidic devices for modeling cell-cell and particle-cell interactions in the microvasculature

被引:71
作者
Prabhakarpandian, Balabhaskar [1 ,2 ]
Shen, Ming-Che [2 ]
Pant, Kapil [2 ]
Kiani, Mohammad F. [1 ,3 ]
机构
[1] Temple Univ, Dept Mech Engn, Philadelphia, PA 19122 USA
[2] CFD Res Corp, Biomed Technol, Huntsville, AL 35805 USA
[3] Temple Univ, Dept Radiat Oncol, Philadelphia, PA 19122 USA
基金
美国国家卫生研究院;
关键词
Microvasculature; Drug delivery; Adhesion; Microfluidics; Cell-particle interaction; E-SELECTIN; IN-VITRO; ENDOTHELIAL-CELLS; P-SELECTIN; DRUG CARRIERS; BREAST-CANCER; STATE DIAGRAM; ADHESION; FLOW; TISSUE;
D O I
10.1016/j.mvr.2011.06.013
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Cell-fluid and cell-cell interactions are critical components of many physiological and pathological conditions in the microvasculature. Similarly, particle-cell interactions play an important role in targeted delivery of therapeutics to tissue. Development of in vitro fluidic devices to mimic these microcirculatory processes has been a critical step forward in our understanding of the inflammatory process, developing of nano-particulate drug carriers, and developing realistic in vitro models of the microvasculature and its surrounding tissue. However, widely used parallel plate flow based devices and assays have a number of important limitations for studying the physiological conditions in vivo. In addition, these devices are resource hungry and time consuming for performing various assays. Recently developed, more realistic, microfluidic based devices have been able to overcome many of these limitations. In this review, an overview of the fluidic devices and their use in studying the effects of shear forces on cell-cell and cell-particle interactions is presented. In addition, use of mathematical models and Computational Fluid Dynamics (CFD) based models for interpreting the complex flow patterns in the microvasculature is highlighted. Finally, the potential of 3D microfluidic devices and imaging for better representing in vivo conditions under which cell-cell and cell-particle interactions take place is discussed. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:210 / 220
页数:11
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