细胞内
凝聚
化学
药物输送
内体
胞浆
肽
纳米技术
细胞生物学
计算生物学
合理设计
细胞
电穿孔
生物物理学
细胞穿透肽
输送系统
生物相容性材料
细胞培养
细胞存活
光热治疗
作者
Lu Jiang,Qiantao Song,Zhixing Lin,Hai Liu,Jingqu Chen,Xi Zhang,Hui Li,Christina Cortez-Jugo,Jiajing Zhou,Lu Liu,Frank Caruso,Hejin Jiang
摘要
Precise intracellular delivery remains a critical barrier to the efficacy of therapeutic biomolecules. Coacervates, with their high loading capacity, have emerged as a transformative drug delivery platform that can facilitate the intracellular delivery of diverse therapeutic cargos but are limited by poor stability, nonspecific cellular internalization, and uncontrolled release. Herein, we report a simple and versatile surface-engineering strategy that improves the stability of coacervates and enables programmable cell targeting and precise intracellular delivery. Peptide coacervates (PCs) designed with programmable release were coated with polyphenol-peptide networks (PC@PPNs) to encapsulate diverse cargos, including fluorophores, toxic proteins, pro-apoptotic peptides, and plasmid DNA. The dual pH- and glutathione-responsive disassembly of PC@PPNs facilitates endosomal escape and enables controlled cytosolic release. Notably, the association of PC@PPNs with specific cells can be readily programmed by modulating the peptide sequence on PPNs. For example, incorporating HER2-targeting peptides increases the specific association of PC@PPNs with SKOV3 cells from 14% to 75%. The cell-specific targeting is further validated in vivo, as demonstrated by a pronounced size reduction in HER2-overexpressing tumors. This work establishes a rational framework for engineering functional coacervates, advancing their development as versatile and programmable platforms for intracellular delivery.
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