Multifunctional envelope-type mesoporous silica nanoparticles for pH-responsive drug delivery and magnetic resonance imaging

被引:165
作者
Chen, Yan [1 ,2 ]
Ai, Kelong [1 ]
Liu, Jianhua [3 ]
Sun, Guoying [4 ]
Yin, Qi [4 ]
Lu, Lehui [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
[3] Jilin Univ, Hosp 2, Dept Radiol, Changchun 130022, Peoples R China
[4] Changchun Univ Technol, Chem & Life Sci Sch, Changchun 130022, Peoples R China
关键词
pH-responsiveness; Drug delivery; Magnetic resonance imaging; EPR effect; UP-CONVERSION NANOPARTICLES; CONTROLLED-RELEASE; CANCER-THERAPY; THERAPEUTICS; LUMINESCENCE; NANOSPHERES; MODALITY;
D O I
10.1016/j.biomaterials.2015.05.003
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A novel multifunctional envelope-type mesoporous silica nanoparticle (MEMSN) system combining the merits of pH-responsiveness, non-toxicity and biological specificity, is demonstrated for drug delivery and magnetic resonance imaging (MRI). This system is constructed by immobilizing acetals on the surface of mesoporous silica, and then coupling to ultra small lanthanide doped upconverting nanoparticle, which act as a gate keeper. The anticancer drug DOX is thus locked in the pores, and its burst release can be achieved under acidic environment on account of the hydrolyzation reactions of acetals. The nanogated drug release system is highly efficacious for cancer therapy both in vitro and in vivo. Importantly, the nanocomposite could be harmlessly metabolized and degraded into apparently nontoxic products within a few days. The nanoscale effect of the system allows for passive tumor targeting and increased tumor accumulation of the probes via the enhanced permeation and retention (EPR) effect, which is visualized by MRI in vivo. Therefore, such nanosystem should be of great significance in the future development of highly efficient and tumor targeted drug delivery vehicles for cancer chemotherapy. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:111 / 120
页数:10
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