MOE Key Laboratory of Macromolecule Synthesis and Functionalization of Ministry of Education, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, 310027, PR China.
Nanoscale. 2021 Dec 13;13(47):19857-19863. doi: 10.1039/d1nr06756g.
Pandemics caused by viruses have resulted in incalculable losses to human beings, which are exacerbated due to the lack of antiviral drugs. Sulfonic group modified nanomedicine has been proved to possess a broad-spectrum antiviral ability. However, it is very challenging to maintain the antiviral activity in a high protein environment . To improve the tolerance to the complex biological environment, sulfonic mixed-charge modified gold nanoparticles (MC_AuNPs) were prepared in this research by introducing positively charged ligands into sulfonic ligand modified gold nanoparticles. The MC_AuNPs showed excellent non-fouling ability while retaining comparable antiviral ability to single sulfonic ligand modified gold nanoparticles (MDS_AuNPs). The MC_AuNPs maintained their antiviral ability in 10 mg mL protein solutions, but the MDS_AuNPs completely lost their antiviral capability in 1 mg mL protein medium. The mixed-charge modification strategy provides a practical avenue to maintain the antiviral capability of HSPG mimicking nanoparticles in high protein environments.
病毒引起的大流行给人类带来了无法估量的损失,而抗病毒药物的缺乏则使情况更加恶化。磺酸基修饰的纳米医学已被证明具有广谱抗病毒能力。然而,在高蛋白质环境中保持抗病毒活性是极具挑战性的。为了提高对复杂生物环境的耐受性,本研究通过向磺酸配体修饰的金纳米粒子中引入正电荷配体,制备了混合电荷修饰的金纳米粒子(MC_AuNPs)。MC_AuNPs 表现出优异的抗污能力,同时保持与单磺酸配体修饰的金纳米粒子(MDS_AuNPs)相当的抗病毒能力。MC_AuNPs 在 10 mg mL 蛋白质溶液中保持其抗病毒能力,而 MDS_AuNPs 在 1 mg mL 蛋白质介质中完全失去其抗病毒能力。混合电荷修饰策略为保持 HSPG 模拟纳米粒子在高蛋白环境中的抗病毒能力提供了一条实用途径。