Therapeutic Polymersome Nanoreactors with Tumor-Specific Activable Cascade Reactions for Cooperative Cancer Therapy

被引:260
作者
Ke, Wendong [1 ]
Li, Junjie [2 ]
Mohammed, Fathelrahman [1 ]
Wang, Yuheng [1 ]
Tou, Kazuko [2 ]
Liu, Xueying [2 ]
Wen, Panyue [2 ]
Kinoh, Hiroaki [2 ]
Anraku, Yasutaka [5 ]
Chen, Huabing [3 ]
Kataoka, Kazunori [2 ,4 ]
Ge, Zhishen [1 ]
机构
[1] Univ Sci & Technol China, Dept Polymer Sci & Engn, CAS Key Lab Soft Matter Chem, Hefei 230026, Anhui, Peoples R China
[2] Kawasaki Inst Ind Promot, Innovat Ctr NanoMed iCONM, Kawasaki Ku, 3-25-14 Tonomachi, Kawasaki, Kanagawa 2100821, Japan
[3] Soochow Univ, Coll Pharmaceut Sci, State Key Lab Radiat Med & Protect, Jiangsu Key Lab Neuropsychiat Dis, Suzhou 215123, Peoples R China
[4] Univ Tokyo, Policy Alternat Res Inst, Tokyo 1130033, Japan
[5] Univ Tokyo, Grad Sch Engn, Tokyo 1138656, Japan
基金
中国国家自然科学基金; 日本科学技术振兴机构;
关键词
nanoreactor; polyprodrug; cancer therapy; Fenton reaction; reactive oxygen species responsive; NANOPARTICLES; ACTIVATION; CAPSULES; MICELLES; VESICLES; OXIDE;
D O I
10.1021/acsnano.8b09082
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Therapeutic nanoreactors are of increasing interest in precise cancer therapy, which have been explored to in situ produce therapeutic compounds from inert prodrugs or intrinsic molecules at the target sites. However, engineering a nanoreactor with tumor activable cascade reactions for efficient cooperative cancer therapy remains a great challenge. Herein, we demonstrate a polymersome nanoreactor with tumor acidity-responsive membrane permeability to activate cascade reactions for orchestrated cooperative cancer treatment. The nanoreactors are constructed from responsive polyprodrug polymersomes incorporating ultrasmall iron oxide nanoparticles and glucose oxidase in the membranes and inner aqueous cavities, respectively. The cascade reactions including glucose consumption to generate H2O2, accelerated iron ion release, Fenton reaction between H2O2 and iron ion to produce hydroxyl radicals (center dot OH), and center dot OH-triggered rapid release of parent drugs can be specifically activated by the tumor acidity-responsive membrane permeability. During this process, the orchestrated cooperative cancer therapy including starving therapy, chemodynamic therapy, and chemotherapy is realized for high-efficiency tumor suppression by the in situ consumed and produced compounds. The nanoreactor design with tumor-activable cascade reactions represents an insightful paradigm for precise cooperative cancer therapy.
引用
收藏
页码:2357 / 2369
页数:13
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