A pH-Responsive Charge-Convertible Drug Delivery Nanocarrier for Precise Starvation and Chemo Synergistic Oncotherapy

被引:2
|
作者
Zhou, Yifei [1 ,2 ]
Gao, Xuan [1 ,2 ]
Lu, Yu [1 ,4 ]
Zhang, Ruohao [1 ,2 ]
Lv, Kehong [1 ,2 ]
Gong, Jitong [1 ,2 ]
Feng, Jing [1 ,2 ]
Zhang, Hongjie [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China
[2] Univ Sci & Technol China, Sch Appl Chem & Engn, Hefei 230026, Peoples R China
[3] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[4] Jilin Univ, Coll Chem, Changchun 130012, Peoples R China
来源
CHEMPLUSCHEM | 2023年 / 88卷 / 02期
基金
中国国家自然科学基金;
关键词
charge-convertible; glucose oxidase; pH-responsive; synergistic oncotherapy; tirapazamine; NANOPARTICLES; THERAPY; DESIGN;
D O I
10.1002/cplu.202200394
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A pH-responsive charge-convertible drug delivery nanocarrier (MSN-TPZ-GOx@ZnO@PAH-PEG-DMMA, abbreviated as MTGZ@PPD) was prepared, which could specifically release hypoxia-activated chemotherapeutic Tirapazamine (TPZ) and glucose oxidase (GOx) in the tumor site for precise starvation and chemo synergistic oncotherapy. Acid-responsive Schiff base structure modified mesoporous silica nanoparticles (MSN) co-load with GOx and TPZ, then link with ZnO quantum dots (QDs). PAH-PEG-DMMA (PPD) polymer makes MTGZ@PPD with biocompatibility and charge-convertible feature. MTGZ@PPD is negatively charged at physiological pH, and the charge reversal of PPD and acidolysis of the Schiff base structure under the acidic tumor microenvironment (TME) induce a positively charged surface, which could potentiate the cell internalization. ZnO QDs could decompose at acidic TME, achieving controllable drug release. GOx could starve the tumor cells and enhance hypoxia level, thus initiates the activation of TPZ to realize synergistic starvation therapy and chemotherapy. This intelligent MTGZ@PPD has shown great potential for starvation and chemo synergistic oncotherapy.
引用
收藏
页数:7
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