纳米囊
纳米颗粒
生物物理学
化学
补体系统
体内
体内分布
日冕(行星地质学)
纳米毒理学
乳状液
化学工程
肽
纳米技术
材料科学
体外
免疫系统
生物化学
免疫学
生物
生物技术
工程类
天体生物学
维纳斯
作者
Tengjisi,Yue Hui,Yuanyuan Fan,Da Zou,Gert Talbo,Guangze Yang,Chun‐Xia Zhao
标识
DOI:10.1016/j.jcis.2021.08.148
摘要
A protein corona forms around nanoparticles when they are intravenously injected into the bloodstream. The composition of the protein corona dictates the interactions between nanoparticles and the biological systems thus their immune evasion, blood circulation, and biodistribution. Here, we report for the first time the impact of nanoparticle stiffness on protein corona formation using a unique emulsion core silica shell nanocapsules library with a wide range of mechanical properties over four magnitudes (700 kPa to 10 GPa). The nanocapsules with different stiffness showed distinct proteomic fingerprints. The protein corona of the stiffest nanocapsules contained the highest amount of complement protein (Complement C3) and immunoglobulin proteins, which contributed to their high macrophage uptake, confirming the important role of nanocapsules stiffness in controlling the protein corona formation thus their in vitro and in vivo behaviors.
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