脂质体
广谱
脂质双层融合
融合
膜
材料科学
纳米技术
相(物质)
病毒学
化学
医学
组合化学
生物化学
语言学
哲学
有机化学
作者
Yutong Li,Yuhang Li,Li Xu,Fang Liu,Wenbin Dai,Min Chen,Jian Ji,Qiao Jin,Kaijun Wang
标识
DOI:10.1002/adhm.202501446
摘要
Abstract Viral infection is a significant threat to global public health. Available antiviral drugs are effective only for specific viruses. It is imperative to develop broad‐spectrum antiviral drugs. The heparin sulfate proteoglycan (HSPG) biomimetic strategy holds great promise to design broad‐spectrum antiviral materials. However, the reversible binding of HSPG‐mimicking nanoparticles with virions presents a potential risk of reinfection. Herein, a sulfonated liposome (SC_Lip) that can trigger phase transition below pH 6.5 is screened to combat viral infection at all stages. SC_Lip can realize pH‐induced phase transition, which triggers membrane fusion with viral envelope and subsequent viral inactivation. Therefore, SC_Lip exhibits virucidal activity via membrane fusion with viral envelope in both acidic viral infection microenvironment and intracellular acidic lysosomes. The broad‐spectrum virucidal activity of SC_Lip is confirmed by different types of viruses, including coronavirus (SARS‐CoV‐2), retrovirus (LV), and herpesvirus (HSV‐1). The in vivo antiviral effect of SC_Lip is further verified by a rat HSV‐1 anterior uveitis model. Overall, SC_Lip with broad‐spectrum virucidal ability holds great promise to fight against emerging viral pandemics in the future.
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