Biomineralization inspired surface engineering of nanocarriers for pH-responsive, targeted drug delivery

被引:99
作者
Chen, Zhaowei [1 ,2 ,3 ]
Li, Zhenhua [1 ,2 ,3 ]
Lin, Youhui [1 ,2 ,3 ]
Yin, Meili [1 ,2 ]
Ren, Jinsong [1 ,2 ]
Qu, Xiaogang [1 ,2 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resources Utilizat, Changchun 130022, Jilin, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, Biol Chem Lab, Changchun 130022, Jilin, Peoples R China
[3] Chinese Acad Sci, Grad Sch, Beijing 1000039, Peoples R China
基金
中国国家自然科学基金;
关键词
Biomineralization; Hyaluronic acid; pH-responsive; Targeted drug delivery; Cancer therapy; Mesoporous nanomaterials; PHOSPHATE NANOCOMPOSITE PARTICLES; CALCIUM-PHOSPHATE; HYALURONIC-ACID; CONTROLLED-RELEASE; GUEST MOLECULES; NANOPARTICLES; CD44; DNA; BONE; CARRIERS;
D O I
10.1016/j.biomaterials.2012.10.060
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Recent insight into the molecular mechanisms of natural biomineralization has enabled biomimetic synthesis of functional organic-inorganic hybrid materials under mild reaction conditions. Here, we describe a novel method to construct organic-inorganic hybrid on mesoporous silica nanoparticles by utilizing electrostatically absorbed hyaluronic acid (HA) as a reaction site for deposition of calcium phosphate (Cap) minerals. The addition of another layer of HA on the CaP surfaces not only stabilizes the nanocomposites but also confers target ability toward CD44 overexpressed cancer cells. The nanomaterials enable controlled release of loaded anticancer drugs in acidic subcellular environments after receptor mediated endocytosis. More importantly, our study demonstrated that the cancer targeting nanomaterials dramatically enhanced cellular uptake and cytotoxicity toward breast carcinoma cells. These results thus open new opportunities for biomineralization guided nanostructure assemblies with great potential for biomedical applications. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1364 / 1371
页数:8
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