骨肉瘤
微泡
外体
间充质干细胞
阿霉素
骨髓
癌症研究
体内
药物输送
医学
纳米医学
干细胞
化疗
药理学
材料科学
免疫学
化学
生物
病理
小RNA
内科学
细胞生物学
生物技术
纳米技术
纳米颗粒
生物化学
基因
作者
Jinkui Wang,Mujie Li,Liming Jin,Peng Guo,Zhaoxia Zhang,Chenghao Zhanghuang,Xiaojun Tan,Tao Mi,Jiayan Liu,Xin Wu,Guanghui Wei,Dawei He
出处
期刊:Drug Delivery
[Taylor & Francis]
日期:2022-11-09
卷期号:29 (1): 3291-3303
被引量:46
标识
DOI:10.1080/10717544.2022.2141921
摘要
Osteosarcoma is a bone tumor with a high incidence in children and adolescents. Chemotherapy for osteosarcoma is limited, and effective targeted drugs are urgently needed to treat osteosarcoma. Exosomes as a natural nano drug delivery platform have been widely studied and proven to have good drug delivery performance. However, the low production of exosomes hinders its development as a carrier. Exosome mimetics (EMs) as an alternative product of exosomes solve the problem of low production of exosomes and maintain the good performance of exosomes as carriers. In this study, bone marrow mesenchymal stem cells (BMSCs) were sequentially extruded to generate EMs to encapsulate doxorubicin (EM-Dox) to treat osteosarcoma. The results showed that we successfully prepared EMs of BMSC, and EM-Dox was prepared using an active-loading approach. Our engineered EM-Dox demonstrated significantly more potent tumor inhibition activity and fewer side effects than free doxorubicin. This novel biological nanomedicine system provides a promising opportunity to develop novel precision medicine for osteosarcoma.
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