聚磷酸盐
动态光散射
化学
生物物理学
脂质体
纳米颗粒
凝血时间
化学工程
血小板
色谱法
材料科学
纳米技术
生物化学
免疫学
磷酸盐
生物
工程类
作者
Alexander J. Donovan,Joseph Kalkowski,Magdalena Szymusiak,Canhui Wang,Stephanie A. Smith,Robert F. Klie,James H. Morrissey,Ying Liu
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2016-07-13
卷期号:17 (8): 2572-2581
被引量:26
标识
DOI:10.1021/acs.biomac.6b00577
摘要
Granular platelet-sized polyphosphate nanoparticles (polyP NPs) were encapsulated in sterically stabilized liposomes, forming a potential, targeted procoagulant nanotherapy resembling human platelet dense granules in both structure and functionality. Dynamic light scattering (DLS) measurements reveal that artificial dense granules (ADGs) are colloidally stable and that the granular polyP NPs are encapsulated at high efficiencies. High-resolution scanning transmission electron microscopy (HR-STEM) indicates that the ADGs are monodisperse particles with a 150 nm diameter dense core consisting of P, Ca, and O surrounded by a corrugated 25 nm thick shell containing P, C, and O. Further, the ADGs manifest promising procoagulant activity: Detergent solubilization by Tween 20 or digestion of the lipid envelope by phospholipase C (PLC) allows for ADGs to trigger autoactivation of Factor XII (FXII), the first proteolytic step in the activation of the contact pathway of clotting. Moreover, ADGs' ability to reduce the clotting time of human plasma in the presence of PLC further demonstrate the feasibility to develop ADGs into a potential procoagulant nanomedicine.
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