S-亚硝基谷胱甘肽
一氧化氮
纳米颗粒
X射线光电子能谱
催化作用
激进的
纳米技术
表面改性
组合化学
化学
氧化物
材料科学
化学工程
谷胱甘肽
有机化学
酶
物理化学
工程类
作者
Zijie Luo,Yingzhu Zhou,Tao Yang,Yuan Gao,Priyank V. Kumar,Rona Chandrawati
出处
期刊:Small
[Wiley]
日期:2022-01-20
卷期号:18 (11)
被引量:20
标识
DOI:10.1002/smll.202105762
摘要
Ceria nanoparticles (NPs) are widely reported to scavenge nitric oxide (NO) radicals. This study reveals evidence that an opposite effect of ceria NPs exists, that is, to induce NO generation. Herein, S-nitrosoglutathione (GSNO), one of the most biologically abundant NO donors, is catalytically decomposed by ceria NPs to produce NO. Ceria NPs maintain a high NO release recovery rate and retain their crystalline structure for at least 4 weeks. Importantly, the mechanism of this newly discovered NO generation capability of ceria NPs from GSNO is deciphered to be attributed to the oxidation of Ce3+ to Ce4+ on their surface, which is supported by X-ray photoelectron spectroscopy and density functional theory analysis. The prospective therapeutic effect of NO-generating ceria NPs is evaluated by the suppression of cancer cells, displaying a significant reduction of 93% in cell viability. Overall, this report is, to the authors' knowledge, the first study to identify the capability of ceria NPs to induce NO generation from GSNO, which overturns the conventional concept of them acting solely as a NO-scavenging agent. This study will deepen our knowledge about the therapeutic effects of ceria NPs and open a new route toward the NO-generating systems for biomedical applications.
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