Controlled free radical generation against tumor cells by pH-responsive mesoporous silica nanocomposite

被引:45
作者
Fu, Jingke [1 ]
Zhu, Yingchun [1 ]
Zhao, Yang [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, Key Lab Inorgan Coating Mat, Shanghai 200050, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
DRUG-DELIVERY; BENZOYL PEROXIDE; CONTROLLED-RELEASE; OXIDATIVE STRESS; CRYSTAL-STRUCTURE; ANTICANCER DRUG; ELECTRIC-FIELD; CANCER-CELLS; NANOPARTICLES; CHITOSAN;
D O I
10.1039/c4tb00387j
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
082905 [生物质能源与材料]; 100103 [病原生物学];
摘要
Free radicals are toxic entities known to cause cellular damage and to mediate cell death. We herein develop a controlled free radical generation strategy for cancer therapy via pH-responsive release of benzoyl peroxide (BPO) in tumor cells and producing free radicals to mediate cell death. BPO as the free radical resource was encapsulated into a chitosan (Cs)-coated mesoporous silica nanocomposite (BPO@HMSNs-Cs). The mesoporous silica carrier improved the BPO solubility by preventing its crystallization and promoted its stability by inclusion. Chitosan imparted the nanocomposite pH-responsive BPO release capacity with enhanced BP release in simulated acidic tumor media (pH 6.5) and minor release in simulated normal tissue media (pH 7.4). The enhanced free radical generation in tumor media further led to significantly higher cytotoxicity in the tumor at acidic pH 6.5 than at physiological pH 7.4. The free radical-mediated cytotoxicity of BPO@HMSNs-Cs was verified by the observation of free radical-induced green fluorescence in cells. This pH-responsive free radical generation nanocomposite may provide new opportunities for controlled drug delivery and cancer therapy.
引用
收藏
页码:3538 / 3548
页数:11
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