转移
癌症研究
壳聚糖
前列腺癌
聚吡咯
癌细胞
化疗
癌症
药物输送
纳米医学
靶向给药
医学
化学
纳米技术
材料科学
药理学
药品
内科学
纳米颗粒
聚合物
生物化学
有机化学
聚合
作者
Qiuyu Yu,Yue Gao,Waicong Dai,Danni Li,Lu Zhang,Meera Moydeen Abdulhameed,Rui Guo,Min Liu,Xiangyang Shi,Xueyan Cao
标识
DOI:10.1002/adhm.202400114
摘要
Abstract The development of functional nanoplatforms to improve the chemotherapy outcome and inhibit distal cancer cell metastasis remains an extreme challenge in cancer management. In this work, a human‐derived PC‐3 cancer cell membrane‐camouflaged chitosan‐polypyrrole nanogel (CH‐PPy NG) platform, which can be loaded with chemotherapeutic drug docetaxel (DTX) and RANK siRNA for targeted chemotherapy and gene silencing‐mediated metastasis inhibition of late‐stage prostate cancer in a mouse model, is reported. The prepared NGs with a size of 155.8 nm show good biocompatibility, pH‐responsive drug release profile, and homologous targeting specificity to cancer cells, allowing for efficient and precise drug/gene co‐delivery. Through in‐vivo antitumor treatment in a xenografted PC‐3 mouse tumor model, it is shown that such a CH‐PPy NG‐facilitated co‐delivery system allows for effective chemotherapy to slow down the tumor growth rate, and effectively inhibits the metastasis of prostate cancer to the bone via downregulation of the RANK/RANKL signaling pathway. The created CH‐Ppy NGs may be utilized as a promising platform for enhanced chemotherapy and anti‐metastasis treatment of prostate cancer.
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