阿霉素
三阴性乳腺癌
脂质体
乳腺癌
癌症研究
巨噬细胞
癌症
免疫系统
药物输送
医学
癌细胞
化疗
材料科学
内科学
免疫学
化学
纳米技术
体外
生物化学
作者
Lan Yang,Yongshun Zhang,Yu Zhang,Yani Xu,Yuai Li,Zhiqiang Xie,Hairui Wang,Yunzhu Lin,Qing Lin,Tao Gong,Xun Sun,Zhirong Zhang,Ling Zhang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-06-09
卷期号:16 (6): 9799-9809
被引量:67
标识
DOI:10.1021/acsnano.2c03573
摘要
Triple-negative breast cancer is often aggressive and resistant to various cancer therapies, especially corresponding targeted drugs. It is shown that targeted delivery of chemotherapeutic drugs to tumor sites could enhance treatment outcome against triple-negative breast cancer. In this study, we exploited the active tumor-targeting capability of macrophages by loading doxorubicin-carrying liposomes on their surfaces via biotin–avidin interactions. Compared with conventional liposomes, this macrophage–liposome (MA-Lip) system further increased doxorubicin accumulation in tumor sites, penetrated deeper into tumor tissue, and enhanced antitumor immune response. As a result, the MA-Lip system significantly lengthened the survival rate of 4T1 cell-bearing mice with low toxicity. Besides, the MA-Lip system used highly biocompatible and widely approved materials, which ensured its long-term safety. This study provides a system for triple-negative breast cancer treatment and offers another macrophage-based strategy for tumor delivery.
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