Peptide-Decorated Gold Nanoparticles as Functional Nano-Capping Agent of Mesoporous Silica Container for Targeting Drug Delivery

被引:89
作者
Chen, Ganchao [1 ,4 ]
Xie, Yusheng [1 ,4 ]
Peltier, Raoul [1 ,4 ]
Lei, Haipeng [1 ,4 ]
Wang, Ping [1 ,4 ]
Chen, Jun [5 ]
Hu, Yi [5 ]
Wang, Feng [2 ]
Yao, Xi [3 ]
Sun, Hongyan [1 ,4 ]
机构
[1] City Univ Hong Kong, Dept Biol & Chem, 83 Tat Chee Ave, Kowloon, Hong Kong, Peoples R China
[2] City Univ Hong Kong, Dept Phys & Mat Sci, 83 Tat Chee Ave, Kowloon, Hong Kong, Peoples R China
[3] City Univ Hong Kong, Dept Biomed Sci, 83 Tat Chee Ave, Kowloon, Hong Kong, Peoples R China
[4] City Univ Hong Kong, Shenzhen Res Inst, Biotech & Hlth Ctr, Key Lab Biochip Technol, Shenzhen 518057, Peoples R China
[5] Chinese Acad Sci, Inst High Energy Phys, Multidisciplinary Res Div, Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
peptides; gold nanoparticles; charge reversal; targeted delivery; controlled release; CONTROLLED-RELEASE; MICELLES; PRODRUG; CELLS;
D O I
10.1021/acsami.6b02594
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A stimuli-responsive drug delivery system (DDS) with bioactive surface is constructed by end-capping mesoporous silica nanoparticles (MSNs) with functional peptide-coated gold nanoparticles (GNPs). MSNs are first functionalized with acid-labile alpha-amide-beta-carboxyl groups to carry negative charges, and then capped with positively charged GNPs that are decorated with oligo-lysine-containing peptide. The resulting hybrid delivery system exhibits endo/lysosomal pH triggered drug release, and the incorporation of RGD peptide facilitates targeting delivery to alpha(v)beta(3) integrin overexpressing cancer cells. The system can serve as a platform for preparing diversified multifunctional nanocomposites using various functional inorganic nanoparticles and bioactive peptides.
引用
收藏
页码:11204 / 11209
页数:6
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