纳米医学
微泡
药物输送
体内
细胞外小泡
癌症治疗
体外
血液循环
癌症研究
化学
药理学
医学
癌症
纳米技术
生物
细胞生物学
纳米颗粒
材料科学
内科学
生物化学
生物技术
小RNA
传统医学
基因
作者
Lei Gong,Li Tian,Kaisa Cui,Ying Chen,Bingxin Liu,Dan Li,Yuyang Feng,Surui Yao,Yuan Yin,Zhimeng Wu,Zhaohui Huang
标识
DOI:10.1016/j.jconrel.2023.11.013
摘要
Small extracellular vesicles (sEVs) have shown excellent prospects as drug delivery systems for cancer therapy. However, the inherent non-targeting and short blood circulation characteristics severely restrict their practical applications as a delivery system. In addition, post-encapsulating drugs into sEVs also remains challenging. Here, we constructed an engineered cell line that secreted multifunctional sEVs (termed NBsEV204) with 7D12 (an anti-EGFR nanobody) and hCD47 decorations on their surface, as well as high levels of miR-204-5p encapsulation. NBsEV204 exhibited extended blood circulation and improved macrophage-mediated phagocytosis of tumor cells by blocking CD47 signaling. Importantly, NBsEV204 specifically targeted EGFR+ tumor cells and showed robust tumor-suppressive effects both in vitro and in vivo. Overall, this study provides a convenient and feasible method to produce off-the-shelf anticancer sEV nanomedicine, which exhibits tremendous potential for clinical translation.
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