A salt-assisted acid etching strategy for hollow mesoporous silica/organosilica for pH-responsive drug and gene co-delivery

被引:67
作者
Wu, Meiying [1 ]
Chen, Yu [1 ]
Zhang, Lingxia [1 ]
Li, Xiaoyu [1 ]
Cai, Xiaojun [1 ]
Du, Yanyan [1 ]
Zhang, Linlin [1 ]
Shi, Jianlin [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine, Shanghai 200050, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
SILICA NANOPARTICLES; MULTIDRUG-RESISTANCE; TEMPLATE SYNTHESIS; CARBON NANOTUBES; ANTICANCER DRUG; CANCER; DOXORUBICIN; TUMOR; CHEMISTRY; THERAPY;
D O I
10.1039/c4tb01581a
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
A salt-assisted acid etching (SAAE) strategy has been developed to construct rattle/hollow mesoporous silica/organosilica nanovehicles (R/HMSVs or R/HMOVs), which settles the drawbacks of traditional silica etching approaches, such as undesirable by-products, by alkaline etching and strong corrosion of the HF etching process. The hollow structure and phenylene-bridged framework of HMOVs were found to be responsible for the high cargo-loading capacity and pH-responsive drug releasing behavior, respectively, based on the special cargo-framework interaction. Especially, the molecularly organic-inorganic hybrid HMOVs have been, for the first time, successfully engineered to concurrently deliver anticancer drugs and P-gp-associated shRNA molecules for enhancing the intracellular drug concentrations and reversing the multidrug resistance (MDR) of cancer cells. On the basis of this special SAAE strategy, a wide range of mesoporous silica-based hollow nanostructures are anticipated to be synthesized to satisfy the strict requirements in various nano-catalytic and biomedical applications.
引用
收藏
页码:766 / 775
页数:10
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