纳米毒理学
药物输送
白蛋白
纳米颗粒
材料科学
血液蛋白质类
纳米医学
纳米技术
体内
蛋白质吸附
涂层
毒品携带者
生物物理学
药品
化学
药理学
聚合物
医学
生物化学
生物技术
复合材料
生物
作者
Qiang Peng,Shu Zhang,Qin Yang,Ting Zhang,Xueqin Wei,Jiang Li,Chaoliang Zhang,Qianming Chen,Zhirong Zhang,Yunfeng Lin
出处
期刊:Biomaterials
[Elsevier]
日期:2013-08-06
卷期号:34 (33): 8521-8530
被引量:318
标识
DOI:10.1016/j.biomaterials.2013.07.102
摘要
The non-specific interaction between nanoparticles (NPs) and plasma proteins occurs immediately after NPs enter the blood, resulting in the formation of the protein corona that thereafter replaces the original NPs and becomes what the organs and cells really see. Consequently, the in vivo fate of NPs and the biological responses to the NPs are changed. This is one substantial reason for the two main problems of the NPs based drug delivery system, i.e. nanotoxicity and rapid clearance of NPs from the blood after intravenous injection. Here, we demonstrate the successful application of the preformed albumin corona in inhibiting the plasma proteins adsorption and decreasing the complement activation, and ultimately in prolonging the blood circulation time and reducing the toxicity of the polymeric PHBHHx NPs. Since the interaction of proteins with various nano-materials and/or -particles is ubiquitous, pre-forming albumin corona has a great potential to be a versatile strategy for optimizing the NPs based drug delivery system.
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