Influences of size and surface coating of gold nanoparticles on inflammatory activation of macrophages

被引:36
|
作者
Chen, Xinyi [1 ]
Gao, Changyou [1 ,2 ]
机构
[1] Zhejiang Univ, Dept Polymer Sci & Engn, Key Lab Macromol Synth & Functionalizat, MOE, Hangzhou 310027, Zhejiang, Peoples R China
[2] Zhejiang Univ, Dr Li Dak Sum & Yip Yio Chin Ctr Stem Cell & Regen, Hangzhou 310030, Zhejiang, Peoples R China
关键词
Gold nanoparticles; Size; Surface coating; Cytokine secretion; Inflammatory activation; CELLULAR UPTAKE; PARTICLE-SIZE; POLYELECTROLYTE CAPSULES; ENDOTHELIAL-CELLS; ANTIGEN DELIVERY; IMMUNE-RESPONSE; DRUG-DELIVERY; SHAPE; MICROPARTICLES; MICROCAPSULES;
D O I
10.1016/j.colsurfb.2017.09.046
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The widely used engineered nanoparticles have presented non-negligible immunotoxicity and specific patterns of inflammatory-activating behaviors, which remain to be revealed in a more systematic way. In this work, gold nanoparticles (GNPs) with 3 different diameters were prepared, and then were further modified with poly(ethylene glycol) (PEG) or chicken ovalbumin (OVA) to achieve different surface properties. Both types of GNPs had sizes of 12, 35, and 60 nm and possessed negatively charged surface, showing good colloidal stability in cell culture medium, respectively. The conjugated amount of OVA was around 110 ng/mm(2) regardless of the particle size. All the particles showed neglectable influence on viability of RAW246.7 macrophages when cocultured in vitro. The GNPs of larger size or conjugated with OVA were internalized with significantly larger amount. While the OVA-coated GNPs induced higher secretion of tumor necrosis factor-alpha, interleukin-6, and interleukin-1 beta the PEG coating did not induce significant inflammatory response especially when the size of NPs was larger than 35 nm. Comparatively, smaller GNPs induced stronger inflammatory responses regardless of their surface-conjugated molecules. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:372 / 380
页数:9
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