Fighting against Drug-Resistant Tumors using a Dual-Responsive Pt(IV)/Ru(II) Bimetallic Polymer

被引:113
作者
Zeng, Xiaolong [1 ,2 ]
Wang, Yufei [3 ,4 ]
Han, Jianxiong [1 ,2 ]
Sun, Wen [5 ]
Butt, Hans-Juergen [2 ]
Liang, Xing-Jie [3 ,4 ]
Wu, Si [1 ,2 ]
机构
[1] Univ Sci & Technol China, Dept Polymer Sci & Engn, Hefei Natl Lab Phys Sci Microscale, CAS Key Lab Soft Matter Chem, Hefei 230026, Peoples R China
[2] Max Planck Inst Polymer Res, Ackermannweg 10, D-55128 Mainz, Germany
[3] Natl Ctr Nanosci & Technol, CAS Ctr Excellence Nanosci, Key Lab Biomed Effects Nanomat & Nanosafety, Chinese Acad Sci CAS, Beijing 100190, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[5] Dalian Univ Technol, State Key Lab Fine Chem, 2 Linggong Rd, Dalian 116024, Peoples R China
基金
中国国家自然科学基金;
关键词
cisplatin; drug resistance; metallodrugs; phototherapy; polymers; CISPLATIN; COMPLEXES; NANOPARTICLES; DELIVERY; PRODRUG; LIGAND; REPAIR; LIGHT;
D O I
10.1002/adma.202004766
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Drug resistance is a major problem in cancer treatment. Herein, the design of a dual-responsive Pt(IV)/Ru(II) bimetallic polymer (PolyPt/Ru) to treat cisplatin-resistant tumors in a patient-derived xenograft (PDX) model is reported. PolyPt/Ru is an amphiphilic ABA-type triblock copolymer. The hydrophilic A blocks consist of biocompatible poly(ethylene glycol) (PEG). The hydrophobic B block contains reduction-responsive Pt(IV) and red-light-responsive Ru(II) moieties. PolyPt/Ru self-assembles into nanoparticles that are efficiently taken up by cisplatin-resistant cancer cells. Irradiation of cancer cells containing PolyPt/Ru nanoparticles with red light generates(1)O(2), induces polymer degradation, and triggers the release of the Ru(II) anticancer agent. Meanwhile, the anticancer drug, cisplatin, is released in the intracellular environment via reduction of the Pt(IV) moieties. The released Ru(II) anticancer agent, cisplatin, and the generated(1)O(2)have different anticancer mechanisms; their synergistic effects inhibit the growth of drug-resistant cancer cells. Furthermore, PolyPt/Ru nanoparticles inhibit tumor growth in a PDX mouse model because they circulate in the bloodstream, accumulate at tumor sites, exhibit good biocompatibility, and do not cause side effects. The results demonstrate that the development of stimuli-responsive multi-metallic polymers provides a new strategy to overcome drug resistance.
引用
收藏
页数:9
相关论文
共 41 条
[1]   Self-Assembled Peptide- and Protein-Based Nanomaterials for Antitumor Photodynamic and Photothermal Therapy [J].
Abbas, Manzar ;
Zou, Qianli ;
Li, Shukun ;
Yan, Xuehai .
ADVANCED MATERIALS, 2017, 29 (12)
[2]   New Ru(II) photocages operative with near-IR light: new platform for drug delivery in the PDT window [J].
Al-Afyouni, Malik H. ;
Rohrabaugh, Thomas N., Jr. ;
Al-Afyouni, Kathlyn F. ;
Turro, Claudia .
CHEMICAL SCIENCE, 2018, 9 (32) :6711-6720
[3]   Rational design of platinum(IV) compounds to overcome glutathione-S-transferase mediated drug resistance [J].
Ang, WH ;
Khalaila, I ;
Allardyce, CS ;
Juillerat-Jeanneret, L ;
Dyson, PJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (05) :1382-1383
[4]  
[Anonymous], 2017, ANGEW CHEM, V129, P11707
[5]   Overcoming tumor resistance to cisplatin by cationic lipid-assisted prodrug nanoparticles [J].
Cao, Zhi-Ting ;
Chen, Zhi-Yao ;
Sun, Chun Yang ;
Li, Hong-Jun ;
Wang, Hong-Xia ;
Cheng, Qin-Qin ;
Zuo, Zu-Qi ;
Wang, Ji-Long ;
Liu, Yang-Zhong ;
Wang, Yu-Cai ;
Wang, Jun .
BIOMATERIALS, 2016, 94 :9-19
[6]   Transient photocyclization in ruthenium(II) polypyridine complexes of indolamines [J].
Carrone, G. ;
Zayat, L. ;
Slep, L. D. ;
Etchenique, R. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2017, 19 (03) :2140-2147
[7]   Sequentially Responsive Shell-Stacked Nanoparticles for Deep Penetration into Solid Tumors [J].
Chen, Jinjin ;
Ding, Jianxun ;
Wang, Yucai ;
Cheng, Jianjun ;
Ji, Shengxiang ;
Zhuang, Xiuli ;
Chen, Xuesi .
ADVANCED MATERIALS, 2017, 29 (32)
[8]   Dual Drug Backboned Shattering Polymeric Theranostic Nanomedicine for Synergistic Eradication of Patient-Derived Lung Cancer [J].
Cong, Yuwei ;
Xiao, Haihua ;
Xiong, Hejian ;
Wang, Zigui ;
Ding, Jianxun ;
Li, Chan ;
Chen, Xuesi ;
Liang, Xing-Jie ;
Zhou, Dongfang ;
Huang, Yubin .
ADVANCED MATERIALS, 2018, 30 (11)
[9]  
del Pino P., 2016, Angew. Chem, V128, P5573, DOI DOI 10.1002/ANGE.201511733
[10]   Cisplatin binding to human serum albumin: a structural study [J].
Ferraro, Giarita ;
Massai, Lara ;
Messori, Luigi ;
Merlino, Antonello .
CHEMICAL COMMUNICATIONS, 2015, 51 (46) :9436-9439