促炎细胞因子
2019年冠状病毒病(COVID-19)
炎症
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
冠状病毒
2019-20冠状病毒爆发
细胞因子
药理学
体外
大流行
病毒学
医学
生物
免疫学
生物化学
传染病(医学专业)
内科学
爆发
疾病
作者
Zhaoyan Zhao,Yuchen Xiao,Lingqing Xu,Ye Liu,Guanmin Jiang,Wei Wang,Bin Li,Tianchuan Zhu,Qingqin Tan,Lantian Tang,Haibo Zhou,Xi Huang,Hong Shan
标识
DOI:10.1021/acsami.1c02755
摘要
COVID-19 has been diffusely pandemic around the world, characterized by massive morbidity and mortality. One of the remarkable threats associated with mortality may be the uncontrolled inflammatory processes, which were induced by SARS-CoV-2 in infected patients. As there are no specific drugs, exploiting safe and effective treatment strategies is an instant requirement to dwindle viral damage and relieve extreme inflammation simultaneously. Here, highly biocompatible glycyrrhizic acid (GA) nanoparticles (GANPs) were synthesized based on GA. In vitro investigations revealed that GANPs inhibit the proliferation of the murine coronavirus MHV-A59 and reduce proinflammatory cytokine production caused by MHV-A59 or the N protein of SARS-CoV-2. In an MHV-A59-induced surrogate mouse model of COVID-19, GANPs specifically target areas with severe inflammation, such as the lungs, which appeared to improve the accumulation of GANPs and enhance the effectiveness of the treatment. Further, GANPs also exert antiviral and anti-inflammatory effects, relieving organ damage and conferring a significant survival advantage to infected mice. Such a novel therapeutic agent can be readily manufactured into feasible treatment for COVID-19.
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