Rational design of non-toxic GOx-based biocatalytic nanoreactor for multimodal synergistic therapy and tumor metastasis suppression

被引:24
|
作者
Hang, Lifeng [1 ]
Zhang, Tao [2 ]
Wen, Hua [1 ]
Li, Meng [1 ]
Liang, Lianbao [1 ]
Tang, Xinfeng [3 ]
Zhou, Chunze [4 ]
Tian, JunZhang [1 ]
Ma, Xiaofen [1 ]
Jiang, Guihua [1 ]
机构
[1] Guangdong Second Prov Gen Hosp, Dept Med Imaging, Guangzhou 518037, Peoples R China
[2] Chinese Acad Sci, Inst Solid State Phys, Key Lab Mat Phys, HFIPS, Hefei 230031, Peoples R China
[3] Univ Sci & Technol China, Sch Life Sci, Div Mol Med, Hefei Natl Lab Phys Sci Microscale, Hefei 230001, Peoples R China
[4] Univ Sci & Technol China, Affiliated Hosp USTC 1, Intervent Radiol Dept, Div Life Sci & Med, Hefei 230001, Peoples R China
来源
THERANOSTICS | 2021年 / 11卷 / 20期
基金
中国国家自然科学基金;
关键词
Glucose oxidase; tirapazamine; metal-organic framework; biocatalytic nanoreactor; starvation therapy; METAL-ORGANIC-FRAMEWORKS; ONE-POT SYNTHESIS; GLUCOSE-OXIDASE; CANCER STARVATION; STRATEGY; ENZYMES;
D O I
10.7150/thno.65399
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Rationale: Glucose oxidase (GOx)-based biocatalytic nanoreactors can cut off the energy supply of tumors for starvation therapy and deoxygenation-activated chemotherapy. However, these nanoreactors, including mesoporous silica, calcium phosphate, metal-organic framework, or polymer nanocarriers, cannot completely block the reaction of GOx with glucose in the blood, inducing systemic toxicity from hydrogen peroxide (H2O2) and anoxia. The low enzyme loading capacity can reduce systemic toxicity but limits its therapeutic effect. Here, we describe a real 'ON/OFF' intelligent nanoreactor with a core-shell structure (GOx + tirazapamine (TPZ))/ZIF-8@ZIF-8 modified with the red cell membrane (GTZ@Z-RBM) for cargo delivery. Methods: GTZ@Z-RBM nanoparticles (NPs) were prepared by the co-precipitation and epitaxial growth process under mild conditions. The core-shell structure loaded with GOx and TPZ was characterized for hydrate particle size and surface charge. The GTZ@Z-RBM NPs morphology, drug, and GOx loading/releasing abilities, system toxicity, multimodal synergistic therapy, and tumor metastasis suppression were investigated. The in vitro and in vivo outcomes of GTZ@Z-RBM NPs were assessed in 4T1 breast cancer cells. Results: GTZ@Z-RBM NPs could spatially isolate the enzyme from glucose in a physiological environment, reducing systemic toxicity. The fabricated nanoreactor with high enzyme loading capacity and good biocompatibility could deliver GOx and TPZ to the tumors, thereby exhausting glucose, generating H2O2, and aggravating hypoxic microenvironment for starvation therapy, DNA damage, and deoxygenation-activated chemotherapy. Significantly, the synergistic therapy effectively suppressed the breast cancer metastasis in mice and prolonged life without systemic toxicity. The in vitro and in vivo results provided evidence that our biomimetic nanoreactor had a powerful synergistic cascade effect in treating breast cancer. Conclusion: GTZ@Z-RBM NPs can be used as an 'ON/OFF' intelligent nanoreactor to deliver GOx and TPZ for multimodal synergistic therapy and tumor metastasis suppression.
引用
收藏
页码:10001 / 10011
页数:11
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