Smart self-assembled nanomedicine for ferroptotic tumor therapy

被引:0
作者
Liang, Chen [1 ,2 ,3 ,4 ,5 ]
Zhang, Tian [4 ,5 ]
Zhang, Qingming [6 ]
Mou, Xiaozhou [2 ,3 ]
机构
[1] Zhejiang Univ, Dept Polymer Sci & Engn, MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310027, Peoples R China
[2] Hangzhou Med Coll, Zhejiang Prov Peoples Hosp, Affiliated Peoples Hosp, Rehabil & Sports Med Res Inst Zhejiang Prov,Dept R, Hangzhou 310014, Peoples R China
[3] Hangzhou Med Coll, Zhejiang Prov Peoples Hosp, Affiliated Peoples Hosp, Clin Res Inst, Hangzhou 310014, Peoples R China
[4] Nanjing Tech Univ NanjingTech, Sch Flexible Elect Future Technol, State Key Lab Flexible Elect LoFE, Nanjing 211816, Peoples R China
[5] Nanjing Tech Univ NanjingTech, Inst Adv Mat IAM, Sch Flexible Elect Future Technol, Nanjing 211816, Peoples R China
[6] Jinling Hosp, Dept Pharm, 305 East Zhongshan Rd, Nanjing 210002, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Molecular self-assembly; Ferroptosis; Nanomedicine; Tumor therapy; CANCER-CELLS; MICROENVIRONMENT; DEATH;
D O I
10.1016/j.colcom.2025.100829
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Featured by iron-dependent lipid peroxidation, ferroptosis is increasingly recognized as a prominent route for programmed tumor therapy. However, the adaptivity, complexity, and heterogeneity of tumors hamper the performance of ferroptotic tumor therapies. Recent advances in molecularly self-assembled nanomedicine show promise in rejuvenating ferroptotic tumor therapies by leveraging the principles of molecular self-assembly (MSA). This review first sketches the basis of ferroptosis and MSA. Subsequently, representative nanoplatforms are discussed to elucidate how MSA can be devised, either in vitro or in vivo, to improve the precision, efficacy, and biosafety of ferroptotic tumor therapies. Finally, considerations and future perspectives toward clinical translation of molecularly self-assembled ferroptosis nanomedicine are addressed.
引用
收藏
页数:11
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