PLGA公司
壳聚糖
纳米颗粒
血小板
致电离效应
化学
血小板活化
微粒
药理学
纳米技术
受体
材料科学
化学工程
生物化学
免疫学
医学
工程类
NMDA受体
作者
Xue Li,Anna Radomski,Owen I. Corrigan,Lidia Tajber,Fábio de Sousa Menezes,Sibylle Endter,Carlos Medina,Marek W. Radomski
出处
期刊:Nanomedicine
[Future Medicine]
日期:2009-10-01
卷期号:4 (7): 735-746
被引量:43
摘要
Aim: The increasing interest in biodegradable nanoparticles containing biomaterials such as poly(D,L-lactide-co-glycolide) (PLGA) and chitosan for drug delivery raises issues regarding the blood compatibility of these nanoparticles, since some nanoparticles, including carbon nanoparticles, can affect human platelet aggregation and cause vascular thrombosis. Therefore, the aim of this work was to investigate the effect of polymeric nanoparticles on human platelet function by measuring aggregation and receptor expression in vitro. Materials & method: PLGA, chitosan–PLGA and a series of chitosan nanoparticles were prepared by the single emulsion technique and ionotropic gelation method. The effects of these nanoparticles (0.01–100 µg/ml) on resting platelets, as well as on platelet aggregation and expression of receptors (GPIIb/IIIa and P-selectin) induced by agonists in platelet-rich plasma were examined using light aggregometry and flow cytometry. Results & conclusion: All tested nanoparticles at concentrations below 10 µg/ml did not modify platelet aggregation, showing that they may be used for the delivery of active molecules to the bloodstream.
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