化学
小干扰RNA
基因敲除
脂质体
体外
纳米颗粒
RNA干扰
基因传递
生物相容性材料
胆固醇
生物物理学
生物化学
纳米技术
癌细胞
核糖核酸
体内
药物输送
转染
全身给药
输送系统
癌症治疗
肽
癌症研究
姜黄素
粒径
组合化学
固体脂质纳米粒
氨基酸
脂质代谢
毒品携带者
生物合成
作者
Suyoung Kang,Duc‐Toan Nguyen,Sangyong Jon
出处
期刊:ChemMedChem
[Wiley]
日期:2026-08-25
卷期号:21 (16): e70464-e70464
摘要
Lipid nanoparticles (LNPs) are clinically validated platform for the delivery of small interfering RNA (siRNA) therapeutics. However, conventional LNPs typically consist of multiple lipid components, which complicates formulation optimization and limits compositional flexibility. Furthermore, efficient delivery of siRNA to extrahepatic tissues, including solid tumors, remains a major challenge. To address these limitations, we developed a class of ionizable cholesterol derivatives by conjugating biocompatible dimethylated amino acids to cholesterol through a cleavable linker, thereby integrating the structural role of cholesterol and the pH-responsive ionization of ionizable lipids into a single molecule. Five i-Chol derivatives were synthesized and formulated into LNPs, which demonstrated efficient siRNA encapsulation and delivery in cancer cells. The resulting siRNA@i-Chol LNPs exhibited uniform particle size and near-neutral surface charge, indicating favorable physicochemical properties for systemic administration. Notably, phenylalanine-based cholesterol LNPs (Phe-Chol LNPs) loaded with siRNA targeting kinesin spindle protein (KIF11) achieved the most potent in vitro gene knockdown in PC3 prostate cancer cells and induced significant dose-dependent antitumor activity in a xenograft model without observable systemic toxicity. Collectively, this study establishes a simplified i-Chol LNP platform that maintains high siRNA delivery efficiency to solid tumors and provides a versatile framework for further LNP engineering and scalable manufacturing.
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