Processing Pathway Dependence of Amorphous Silica Nanoparticle Toxicity: Colloidal vs Pyrolytic

被引:368
作者
Zhang, Haiyuan [2 ]
Dunphy, Darren R. [1 ]
Jiang, Xingmao [1 ,8 ]
Meng, Huan [3 ]
Sun, Bingbing [2 ]
Tarn, Derrick [4 ]
Xue, Min [4 ]
Wang, Xiang [2 ]
Lin, Sijie [2 ]
Ji, Zhaoxia [2 ]
Li, Ruibin [2 ]
Garcia, Fred L. [1 ]
Yang, Jing [5 ]
Kirk, Martin L. [5 ]
Xia, Tian [3 ]
Zink, Jeffrey I. [4 ]
Nel, Andre [2 ,3 ]
Brinker, C. Jeffrey [1 ,6 ,7 ]
机构
[1] Univ New Mexico, Dept Chem & Nucl Engn, Albuquerque, NM 87131 USA
[2] Univ Calif Los Angeles, Calif NanoSyst Inst, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Div NanoMed, Dept Med, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[5] Univ New Mexico, Dept Chem & Chem Biol, Albuquerque, NM 87131 USA
[6] Univ New Mexico, Dept Mol Genet & Microbiol, Albuquerque, NM 87131 USA
[7] Sandia Natl Labs, Self Assembled Mat Dept, Albuquerque, NM 87185 USA
[8] Changzhou Univ, Jiangsu Key Labs Adv Catalyt Mat & Technol & Fine, Changzhou 213164, Peoples R China
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
FREE-RADICAL GENERATION; MESOPOROUS SILICA; HUMAN ERYTHROCYTES; NALP3; INFLAMMASOME; HEMOLYTIC-ACTIVITY; HYDROXYL-GROUPS; IN-VITRO; SURFACE; PARTICLES; SIZE;
D O I
10.1021/ja304907c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have developed structure/toxicity relationships for amorphous silica nanoparticles (NPs) synthesized through low-temperature colloidal (e.g., Stober silica) or high-temperature pyrolysis (e.g., fumed silica) routes. Through combined spectroscopic and physical analyses, we have determined the state of aggregation, hydroxyl concentration, relative proportion of strained and unstrained siloxane rings, and potential to generate hydroxyl radicals for Stober and fumed silica NPs with comparable primary particle sizes (16 nm in diameter). On the basis of erythrocyte hemolytic assays and assessment of the viability and ATP levels in epithelial and macrophage cells, we discovered for fumed silica an important toxicity relationship to postsynthesis thermal annealing or environmental exposure, whereas colloidal silicas were essentially nontoxic under identical treatment conditions. Specifically, we find for fumed silica a positive correlation of toxicity with hydroxyl concentration and its potential to generate reactive oxygen species (ROS) and cause red blood cell hemolysis. We propose fumed silica toxicity stems from its intrinsic population of strained three-membered rings (3MRs) along with its chainlike aggregation and hydroxyl content. Hydrogen-bonding and electrostatic interactions of the silanol surfaces of fumed silica aggregates with the extracellular plasma membrane cause membrane perturbations sensed by the Nalp3 inflammasome, whose subsequent activation leads to secretion of the cytokine IL-1 beta. Hydroxyl radicals generated by the strained 3MRs in fumed silica, but largely absent in colloidal silicas, may contribute to the inflammasome activation. Formation of colloidal silica into aggregates mimicking those of fumed silica had no effect on cell viability or hemolysis. This study emphasizes that not all amorphous silicas are created equal and that the unusual toxicity of fumed silica compared to that of colloidal silica derives from its framework and surface chemistry along with its fused chainlike morphology established by high-temperature synthesis (> 1300 degrees C) and rapid thermal quenching.
引用
收藏
页码:15790 / 15804
页数:15
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