ROS scavenging Manganese-loaded mesoporous silica nanozymes for catalytic anti-inflammatory therapy

被引:9
作者
Xiong, Yi [1 ]
Zhang, Yi [1 ]
Zhou, Changren [1 ]
Yu, Tao [1 ]
机构
[1] Jinan Univ, Coll Chem & Mat Sci, Guangzhou 510632, Peoples R China
基金
中国国家自然科学基金;
关键词
Reactive oxygen species; Mesoporous silica; Manganese; Catalyze anti-inflammatory; NANOPARTICLES; INFLAMMATION; PERFORMANCE; GENERATION; RADICALS; OXYGEN;
D O I
10.1016/j.apt.2022.103886
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Reactive oxygen species (ROS) are reactive substances closely related to the inflammatory response, and previous studies have shown that anti-inflammatory therapy can achieve significant effects by scavenging ROS. Nanozymes are synthetic mimics of natural enzymes that are more stable, customizable, inexpensive, and catalytic for ROS. Therefore, we prepared a novel manganese-loaded mesoporous silica nanozyme (MnMSN) by template method and KMnO4 oxidation surfactant templates. The physicochemical properties of the nanomaterials were investigated by XRD, TEM, SEM, size, Zeta potential and BET, etc. The results showed that MnMSN contains MnO2 (Mn4+) and MnSiO3 (Mn2+), and the particle size of MnMSN is smaller with the increase of KMnO4 oxidation surfactant templates time, and the in vitro scavenging of ROS (H2O2, OH and O2-) is more effective. MnMSN has good cytocompatibility, scavenging intracellular ROS and inducing a shift from M1 to anti-inflammatory M2 phenotype. Furthermore, the intrinsic mechanism of MnMSN regulation of macrophage polarization was investigated by ELISA and qPCR, and the results showed that MnMSN is through scavenging ROS, leading to the down-regulation of NF-KB, which further leads to the down-regulation of TNF-a and IL-Ib. The results of this work highlight the potential of MnMSN in catalyzing anti-inflammatory therapy. CO 2022 Published by Elsevier B.V. on behalf of The Society of Powder Technology Japan.
引用
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页数:11
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