Negatively charged nanoparticles of multiple materials inhibit shear-induced platelet accumulation

被引:5
|
作者
Griffin, Michael T. [1 ,2 ]
Ashworth, Katrina [3 ,4 ]
Hill, Nathaniel [1 ,2 ]
von Behren, Jaydra [1 ,2 ]
Di Paola, Jorge [4 ]
Ku, David N. [1 ,2 ]
机构
[1] Georgia Inst Technol, GW Woodruff Sch Mech Engn, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, Parker H Petit Inst Bioengn & Biosci, Atlanta, GA 30332 USA
[3] Univ Colorado, Pediat Hematol, Oncol, Anschutz Med Campus, Aurora, CO USA
[4] Washington Univ, Sch Med, St Louis, MO USA
基金
美国国家科学基金会;
关键词
VON-WILLEBRAND-FACTOR; PROTEIN CORONA; THROMBOSIS; EPTIFIBATIDE; ASPIRIN; SIZE;
D O I
10.1016/j.nano.2021.102405
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Platelet accumulation by VWF under high shear rates at the site of atherosclerotic plaque rupture leads to myocardial infarction and stroke. Current anti-platelet therapies remain ineffective for a large percentage of the population, while presenting significant risks for bleeding. We explore a novel way to inhibit arterial thrombus formation. Theoretically, a negative charge may influence the tertiary structure of VWF to favor the globular configuration by biophysical means without the use of platelet inactivating drugs. We tested this hypothesis experimentally for charged nanoparticles (CNPs) to inhibit thrombus formation in a microfluidic thrombosis assay (MTA). Several different CNPs demonstrated the ability to retard thrombotic occlusion in the MTA. A preliminary study in mice shows that thrombus stability is weaker with CNP administration and bleeding times are not markedly prolonged. The CNPs tested here show promise as a new class of antithrombotic therapies that act by biophysical means rather than biochemical pathways. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页数:10
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