聚合物
点击化学
环加成
组合化学
生物相容性
叠氮化物
炔烃
乙二醇
连接器
化学
脂质体
材料科学
纳米技术
催化作用
有机化学
计算机科学
操作系统
作者
Florian T. Kaps,Anna‐Lena Ziegler,Paul Fritsche,Ekaterina Takmakova,Andrew Kerr,Susanne Boye,Albena Lederer,Robert Luxenhofer
标识
DOI:10.1002/anie.202501262
摘要
Polymer lipids (PLs) are essential components of liposomes and lipid nanoparticles (LNPs) for drug and gene delivery, providing colloidal stabilization and defining the biological interface. While poly(ethylene glycol) (PEG)‐based PLs are the current standard, they are suspected to be responsible for rare adverse reactions, e. g. to LNP‐based Covid‐19 vaccines. Therefore, PLs based on alternative stealth polymers are being intensively investigated for their use in LNPs. However, alternative PLs often lack comparability due to different synthesis protocols and are often not easily accessible. Herein we present a catalyst‐free, efficient and versatile coupling procedure for PL synthesis based on azide‐functionalized polymers and electron‐deficient acetylene dicarboxylate lipids. To highlight the versatility of this approach, we prepared PLs based on PEG and 4 alternative stealth polymers with quantitative coupling efficiencies. The linker structure showed appropriate pH stability and biocompatibility. All PLs enabled the preparation of well‐defined liposomes with excellent stability. Our facile and versatile approach yields comparable PLs with minimized linker size, making them promising candidates for future comparative studies and biomedical applications.
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