Artificial anaerobic cell dormancy for tumor gaseous microenvironment regulation therapy

被引:10
|
作者
Chen, Chen [1 ,2 ,3 ]
Su, Weiwei [4 ]
Liu, Yanyan [3 ]
Zhang, Jiawen [5 ]
Zuo, Changjing [4 ]
Yao, Zhenwei [5 ]
Bu, Wenbo [1 ,3 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine, Shanghai 200050, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] East China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R China
[4] Second Mil Med Univ, Changhai Hosp, Dept Nucl Med, Shanghai 200433, Peoples R China
[5] Fudan Univ, Huashan Hosp, Dept Radiol, Shanghai 200040, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Gaseous microenvironment regulation; Cell dormancy; Hypoxia; Anaerobic; Controlled drug release; CANCER; HYPOXIA; TIRAPAZAMINE;
D O I
10.1016/j.biomaterials.2019.02.007
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Oxygen is known as an irreplaceable gas in the lives of most eukaryotic cells, yet researchers underestimate its importance, as in the case in many studies of tumors. The variable oxygen content of malignant solid tumors increases the difficulty of treatment. Thus, it could be reasonably inferred that the tumor oxygen micro environment, if efficiently and completely regulated, could bring certain changes to existing therapies. Based on this speculation, an acid-responsive, oxygen-scavenging and anaerobic-sensitizing nanoparticle was designed to regulate the oxygen level of solid tumor by creating an artificial anaerobic environment in our study. The Mg2Si core, which acted as a deoxygenating agent, was able to consume tumor oxygen and cause cell dormancy, while the incorporated hydrophobic tirapazamin (TPZ) helped to kill the now-dormant tumor cells. This simple and nontoxic nanoparticle achieved controllable factitious anaerobic circumstance in solid tumor for the first time, displaying the considerable potential and promising application of tumor gaseous microenvironment regulation therapy.
引用
收藏
页码:48 / 55
页数:8
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