光敏剂
脂质体
嵌合抗原受体
光动力疗法
癌细胞
化学
药物输送
细胞穿透肽
癌症研究
小泡
细胞生物学
生物物理学
材料科学
细胞
纳米技术
癌症
生物化学
生物
免疫疗法
膜
免疫学
免疫系统
有机化学
遗传学
作者
Ha Eun Shin,Seung Wook Oh,Wooram Park
标识
DOI:10.1016/j.jiec.2023.02.015
摘要
Effective cancer therapeutics based on extracellular vesicles (EVs) require high-efficiency cancer-targeting and drug-encapsulation technology. Here, we demonstrate hybrid nanovesicles by fusing anti-epidermal growth factor receptor-chimeric antigen receptor-expressing cell-derived vesicles (anti-EGFR-CAR-CDVs) with drug-encapsulated liposomes for effective cancer treatment. HEK293 cells were genetically engineered with the anti-EGFR-CAR plasmid, and CAR-CDVs were produced by serial extrusion of the engineered cells. CAR-CDVs and drug-encapsulated liposomes were then efficiently fused to generate hybrid nanovesicles in 30% EtOH. This study employed a photosensitizer as a model drug for photodynamic therapy (PDT). The hybrid nanovesicles retained the CAR-CDV membrane proteins with a size of ∼ 170 nm. Indeed, photosensitizer-encapsulated hybrid nanovesicles could effectively target tumor cells and inhibit tumor growth upon laser irradiation. We believe that the proposed technology for the successful fusion of CDVs and liposomes can be used as a drug delivery platform with high tumor targeting and encapsulation efficiency.
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