体内
纳米颗粒
纳米医学
胶体金
生物物理学
蛋白质吸附
纳米棒
日冕(行星地质学)
纳米材料
粒径
纳米技术
材料科学
化学
粒子(生态学)
血液蛋白质类
吸附
生物化学
生物
有机化学
生物技术
物理化学
天体生物学
生态学
维纳斯
作者
Rafaela García-Álvarez,Marilena Hadjidemetriou,Ana Sánchez‐Iglesias,Luis M. Liz‐Marzán,Kostas Kostarelos
出处
期刊:Nanoscale
[The Royal Society of Chemistry]
日期:2017-12-07
卷期号:10 (3): 1256-1264
被引量:312
摘要
The efficacy of drug delivery and other nanomedicine-related therapies largely relies on the ability of nanoparticles to reach the target organ. However, when nanoparticles are injected into the bloodstream, their surface is instantly modified upon interaction with blood components, principally with proteins. It is well known that a dynamic and multi-layered protein structure is formed spontaneously on the nanoparticle upon contact with physiological media, which has been termed protein corona. Although several determinant factors involved in protein corona formation have been identified from in vitro studies, specific relationships between the nanomaterial synthetic identity and its ensuing biological identity under realistic in vivo conditions remain elusive. We present here a detailed study of in vivo protein corona formation after blood circulation of anisotropic gold nanoparticles (nanorods and nanostars). Plasmonic gold nanoparticles of different shapes and sizes were coated with polyethyleneglycol, intravenously administered in CD-1 mice and subsequently recovered. The results from gel electrophoresis and mass spectrometry analysis revealed the formation of complex protein coronas, as early as 10 minutes post-injection. The total amount of protein adsorbed onto the particle surface and the protein corona composition were found to be affected by both the particle size and shape.
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