化学
糖脂
免疫原性
体内
还原胺化
生物化学
PEG比率
药物输送
体外
组合化学
肺表面活性物质
纳米颗粒
甘油
抗原性
重组DNA
脂质代谢
连接器
化学合成
抗体
脂质积聚
作者
Jiahui Jin,Zhifen Liang,Ziqian Wang,Xiaoyi Liu,Xingwu Liu,Feng-Chen An,Tao Jiang,Xingyue Gao,Xingyun Wang,Cong Liu,Shangxi Zhang,Hanchao Cheng,Peng George Wang,Chen Zeng
摘要
Lipid nanoparticles (LNPs) have become a pivotal platform for mRNA drug delivery, yet the immunogenicity of poly(ethylene glycol) (PEG) lipids compromises efficacy upon repeated administration, making it necessary to develop PEG-free LNP formulations. Carbohydrates share the highly hydrophilic properties of PEG, making them good alternatives. Here we report a chemically driven strategy to replace PEG lipids with rationally designed glycolipids synthesized via a one-pot Borch reductive amination reaction. This method enabled conjugation of maltoheptaose (G7) to alkyl diamines, forming glycolipids that self-assemble into stable LNPs. Structural optimization revealed that G7-based glycolipids with C14 tails (G7B2) exhibited favorable physicochemical properties. Crucially, in vivo studies revealed that G7B2 LNPs significantly enhanced splenic accumulation, while minimizing anti-PEG antibody production. Furthermore, G7B2 LNPs maintained a consistent delivery efficiency over repeated administrations, a notable advantage over conventional PEGylated LNPs. As a proof of concept, G7B2-OVA mRNA achieved robust antitumor efficacy in a B16F10-OVA melanoma model. These results establish glycolipids as chemically tunable and immunogenically inert alternatives to the PEG lipids, offering a promising strategy for next-generation LNP formulations.
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