凝聚
原细胞
化学
生物物理学
膜
药剂学
戊二醛
棘细胞
生物相容性
纳米技术
生物化学
材料科学
色谱法
生物
药理学
有机化学
作者
Qian Hu,Hongbing Lan,Yinmei Tian,Xiao‐Nan Li,Mengmeng Wang,Jianyu Zhang,Yulin Yu,Wei Chen,Li Kong,Yuanyuan Guo,Zhiping Zhang
标识
DOI:10.1016/j.jconrel.2023.11.030
摘要
Coacervate droplets formed by liquid-liquid phase separation have attracted considerable attention due to their ability to enrich biomacromolecules while preserving their bioactivities. However, there are challenges to develop coacervate droplets as delivery vesicles for therapeutics resulting from the lack of physiological stability and inherent lack of membranes in coacervate droplets. Herein, polylysine-polynucleotide complex coacervate droplets with favorable physiological stability are formulated to efficiently and facilely concentrate small molecules, biomacromolecules and nanoparticles without organic solvents. To improve the biocompatibility, the PEGylated phospholipid membrane is further coated on the surface of the coacervate droplets to prepare coacervate-based artificial protocells (ArtPC) with membrane-like and cytoplasm-like structures. The ArtPC can confine the cyclic catalytic system of uricase and catalase inside to degrade uric acid and deplete the toxicity of H2O2. This biofunctional ArtPC effectively reduces blood uric acid levels and prevents renal injuries in mice with persistent hyperuricemia. The ArtPC-based therapy can bridge the disciplines of synthetic biology, pharmaceutics and therapeutics.
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