A chemo/chemodynamic nanoparticle based on hyaluronic acid induces ferroptosis and apoptosis for triple-negative breast cancer therapy

被引:18
|
作者
Wang, Ning [1 ]
Zhang, Qiyu [1 ]
Wang, Zhuoya [1 ]
Liu, Yichao [1 ]
Yang, Sen [1 ]
Zhao, Xuerong [1 ]
Peng, Jinyong [1 ,2 ,3 ]
机构
[1] Dalian Med Univ, Coll Pharm, Dalian 116044, Peoples R China
[2] Anhui Univ Chinese Med, Coll Pharm, Hefei 230012, Peoples R China
[3] Hubei Univ Chinese Med, Coll Pharm, Wuhan 430065, Peoples R China
关键词
Chemo/chemodynamic therapy; Ferroptosis/apoptosis; Hyaluronic acid; Controlled drugs release; TNBC; DRUG-DELIVERY SYSTEM;
D O I
10.1016/j.carbpol.2024.121795
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Triple-negative breast cancer (TNBC) poses a serious threat to women's life and health due to its high malignancy, strong invasiveness, and propensity for early recurrence and metastasis. Therefore, there is an urgent need to develop a highly effective and low-toxic TNBC treatment scheme to enhance the anti-cancer efficacy and prolong the survival of patients. In this work, we designed and synthesized a chemodynamic therapy (CDT) agent (HA-Fc-Mal). The chemo/chemodynamic (CT/CDT) nanoparticle (HCM@DOX) based on hyaluronic acid induces ferroptosis and apoptotic for TNBC therapy was constructed via self-assembled of HA-Fc-Mal and doxorubicin (DOX). HCM@DOX orderly realized the TNBC targeting, controlled DOX release, GSH depletion and induce ROS erupt. In vivo and in vitro experiments confirmed that HCM@DOX inhibited the growth of 4 T1 tumors through ferroptosis and apoptosis, and the tumor inhibition rate was as high as 81.87 %. In addition, HCM@DOX significantly inhibited lung metastasis and exhibited excellent biosafety. Overall, our findings offer a new strategy for TNBC therapy using a CT/CDT nanoparticle that induces ferroptosis and apoptosis.
引用
收藏
页数:16
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