Polysaccharides screening for pulmonary mucus penetration by molecular dynamics simulation and in vitro verification

粘液 粘蛋白 渗透(战争) 纳米载体 化学 生物物理学 渗透 右旋糖酐 脂质体 药物输送 色谱法 生物化学 有机化学 生物 工程类 运筹学 生态学
作者
Jianqing Peng,Xiaobo Zhang,Ke Zhang,Qin Wang,Runbin Sun,Chen Yan,Yi Chen,Zipeng Gong
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:265: 130839-130839 被引量:1
标识
DOI:10.1016/j.ijbiomac.2024.130839
摘要

Mucus penetration is one of the physiologic barriers of inhalation and nanocarriers can effectively facilitate the permeation of drugs. The interactions between the nanocarriers and mucin are crucial for penetration across the mucus layer on the respiratory tract. In this study, we proposed a molecular dynamics (MD) simulation method for the screening of polysaccharides that acted as the surface modification materials for inhalable nano-preparations to facilitate mucus penetration. MD revealed all-atom interactions between the monomers of polysaccharides, including dextran (DEX)/hyaluronic acid (HA)/carboxymethyl chitosan (CMCS) and the human mucin protein MUC5AC (hMUC5AC). The obtained data showed that DEX formed stronger non-covalent bonds with hMUC5AC compared to HA and CMCS, which suggested that HA and CMCS had better mucus permeability than DEX. For the in vitro verification, HA/CMCS-coated liposomes and DEX/PEG-inserted liposomes were prepared. The results of mucin interactions and mucus penetration studies confirmed that HA and CMCS possessed the weakest interactions with mucin and facilitated the mucus penetration, which was in consistent with the data from MD simulation. This work may shed light on the MD simulation-based screening of surface modification materials for inhalable nano-preparations to facilitate mucus penetration.
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