脂质体
卵磷脂
幽门螺杆菌
磷脂
双层
胃
材料科学
脂质双层
螯合作用
粘液
炎症
生物化学
生物
纳米技术
医学
膜
免疫学
内科学
冶金
生态学
作者
Guiyun Deng,Yang Wu,Zhiyong Song,Shuojun Li,Moqing Du,Junliang Deng,Quan De Xu,You‐Nian Liu,Hagar Shendy Bahlol,Heyou Han
标识
DOI:10.1021/acsami.1c23342
摘要
Infection with Helicobacter pylori (Hp) is one of the leading causes of stomach cancer. The ability to treat Hp infection is hampered by a lack of stomach gastric acid environment. This work introduces a nanoliposome that can rapidly adjust the gastric acid environment to ensure a drug's optimal efficacy. We introduce CaCO3@Fe-TP@EggPC nanoliposomes (CTE NLs) that are composed of Fe3+ and tea polyphenols (TPs) forming complexes on the surface of internal CaCO3 and then with lecithin producing a phospholipid bilayer on the polyphenols' outer surface. Through the action of iron-TP chelate, the phospholipid layer can fuse with the bacterial membrane to eliminate Hp. Furthermore, CaCO3 can promptly consume the excessive gastric acid, ensuring an ideal operating environment for the chelate. TPs, on the other hand, can improve the inflammation and gut microbes in the body. The experimental results show that CTE NLs can quickly consume protons in the stomach and reduce the bacterial burden by 1.2 orders of magnitude while reducing the inflammatory factors in the body. The biosafety evaluation revealed that nanoliposomes have good biocompatibility and provide a new strategy for treating Hp infection.
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