材料科学
水泡性口炎病毒
光敏剂
药品
药物输送
纳米技术
分泌物
胞外囊泡
脂质双层融合
细胞培养
癌症研究
微泡
化学
药理学
生物
生物化学
小RNA
膜
有机化学
遗传学
基因
作者
Min Gao,Qiuting Sun,Rui-Jie Zhang,Guisong Shan,Huiru Zhang,Rui Peng,Mengyu Liu,Gengyun Sun,Lei Qiao,Li Yang,Xiaoyan He
出处
期刊:Biomaterials
[Elsevier]
日期:2024-09-10
卷期号:314: 122829-122829
标识
DOI:10.1016/j.biomaterials.2024.122829
摘要
Developing drug delivery systems capable of achieving deep tumor penetration is a challenging task, yet there is a significant demand for such systems in cancer treatment. Hitchhiking on tumor-derived extracellular vesicles (EVs) represents a promising strategy for enhancing drug penetration into tumors. However, the limited drug assembly on EVs restricts its further application. Here, we present a novel approach to efficiently attach antitumor drugs to EVs using an engineered cell membrane-based vector. This vector includes the AS1411 aptamer for tumor-specific targeting, the vesicular stomatitis virus glycoprotein (VSV-G) for tumor cell membrane fusion, and a photosensitizer as the therapeutic agent while ensuring optimal drug encapsulation and stability. Upon injection, photosensitizers are firstly transferred to the tumor cell membrane and subsequently piggybacked onto EVs with the inherent secretion process. By hitchhiking with EVs, photosensitizers can be transferred layer by layer deep into the solid tumors. The results suggest that this EVs-hitchhiking strategy enables photosensitizers to penetrate deeply into tumor tissue, thereby enhancing the efficacy of phototherapy. This study offers broad application prospects for delivering drugs deeply into tumor tissues.
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