Microfluidics and Coagulation Biology

被引:107
作者
Colace, Thomas V. [1 ]
Tormoen, Garth W. [2 ]
McCarty, Owen J. T. [2 ]
Diamond, Scott L. [1 ]
机构
[1] Univ Penn, Inst Med & Engn, Dept Chem & Biomol Engn, Philadelphia, PA 19104 USA
[2] Oregon Hlth & Sci Univ, Dept Biomed Engn, Portland, OR 97239 USA
来源
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, VOL 15 | 2013年 / 15卷
关键词
thrombosis; hemostasis; platelet function; von Willebrand factor; collagen; fibrin; VON-WILLEBRAND-FACTOR; VIII-VONWILLEBRAND FACTOR; HUMAN-BLOOD PLATELETS; FACTOR-XI ACTIVATION; TISSUE FACTOR; BINDING-SITE; ARTERY SUBENDOTHELIUM; SUBSTRATE-SPECIFICITY; THROMBUS FORMATION; FIBRIN FORMATION;
D O I
10.1146/annurev-bioeng-071812-152406
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The study of blood ex vivo can occur in closed or open systems, with or without flow. Microfluidic devices, which constrain fluids to a small (typically submillimeter) scale, facilitate analysis of platelet function, coagulation biology, cellular biorheology, adhesion dynamics, and pharmacology and, as a result, can be an invaluable tool for clinical diagnostics. An experimental session can accommodate hundreds to thousands of unique clotting, or thrombotic, events. Using microfluidics, thrombotic events can be studied on defined surfaces of biopolymers, matrix proteins, and tissue factor, under constant flow rate or constant pressure drop conditions. Distinct shear rates can be generated on a device using a single perfusion pump. Microfluidics facilitated both the determination of intraluminal thrombus permeability and the discovery that platelet contractility can be activated by a sudden decrease in flow. Microfluidic devices are ideal for multicolor imaging of platelets, fibrin, and phosphatidylserine and provide a human blood analog to mouse injury models. Overall, microfluidic advances offer many opportunities for research, drug testing under relevant hemodynamic conditions, and clinical diagnostics.
引用
收藏
页码:283 / 303
页数:21
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