期刊
BIOMATERIALS
卷 156, 期 -, 页码 204-216出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2017.11.047
关键词
Nanomedicine; Thrombolysis; Fucoidan; P-selectin; Drug delivery
资金
- INSERM
- Paris Diderot University
- Paris 13 University
- Fuco-Chem [ANR-13-LAB1-0005-01]
- EU project [FP7-NMP-2012-LARGE-6-309820]
- China Scholarship Council [201206180031]
Injection of recombinant tissue plasminogen activator (rt-PA) is the standard drug treatment for thrombolysis. However, rt-PA shows risk of hemorrhages and limited efficiency even at high doses. Polysaccharide-poly(isobutylcyanoacrylate) nanoparticles functionalized with fucoidan and loaded with rt-PA were designed to accumulate on the thrombus. Fucoidan has a nanomolar affinity for the P-selectin expressed by activated platelets in the thrombus. Solid spherical fluorescent nanoparticles with a hydrodynamic diameter of 136 +/- 4 nm were synthesized by redox radical emulsion polymerization. The clinical rt-PA formulation was successfully loaded by adsorption on aminated nanoparticles and able to be released in vitro. We validated the in vitro fibrinolytic activity and binding under flow to both recombinant P-selectin and activated platelet aggregates. The thrombolysis efficiency was demonstrated in a mouse model of venous thrombosis by monitoring the platelet density with intravital microscopy. This study supports the hypothesis that fucoidan-nanoparticles improve the rt-PA efficiency. This work establishes the proof-of-concept of fucoidan-based carriers for targeted thrombolysis. (C) 2017 Elsevier Ltd. All rights reserved.
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