Photoluminescent Silicon Nanocrystal-Based Multifunctional Carrier for pH-Regulated Drug Delivery

被引:45
|
作者
Xu, Zhigang [1 ]
Wang, Dongdong [1 ]
Guan, Min [1 ,4 ]
Liu, Xiaoyan [1 ]
Yang, Yanjie [1 ]
Wei, Dongfeng [2 ]
Zhao, Chunyan [3 ]
Zhang, Haixia [1 ]
机构
[1] Lanzhou Univ, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
[2] Lanzhou Univ, Sch Basic Med Sci, Lanzhou 730000, Peoples R China
[3] Lanzhou Univ, Sch Pharm, Lanzhou 730000, Peoples R China
[4] Sinopec Beijing Chem Ind Inst, Yanshan Branch, Beijing 102500, Peoples R China
基金
中国国家自然科学基金;
关键词
nanocrystalline silicon; cytotoxicity; controlled release; drug delivery; LUMINESCENT POROUS SILICON; QUANTUM DOTS; HYBRID NANOGELS; NANOPARTICLES; CYTOTOXICITY; SIZE; INTEGRATION; ACID);
D O I
10.1021/am300877v
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A core-shell structured multifunctional carrier with nanocrystalline silicon (ncSi) as the core and a water-soluble block copolymer as the shell based on a poly(methacrylic acid) (PMAA) inner shell and polyethylene glycol (MPEG) outer shell (ncSi-MPM) was synthesized for drug delivery. The morphology, composition, and properties of the resulting ncSi-MPM were determined by comprehensive multianalytical characterization, including H-1 NMR. spectroscopy, FTIR spectroscopy, XPS spectroscopy, TEM, DLS, and fluorescence spectroscopy analyses. The size of the resulting ncSi-MPM nanocarriers ranged from 40 to 110 nm under a simulated physiological environment. The loading efficiency of model drug doxorubicin (DOX) was approximately 6.1-74 wt % for ncSi-MPM and the drug release was pH controlled. Cytotoxicity studies demonstrated that DOX-loaded ncSi-MPM showed high anticancer activity against Hela cells. Hemolysis percentages (<2%) of ncSi-MPM were within the scope of safe values. Fluorescent imaging studies showed that the nanocarriers could be used as a tracker at the cellular level. Integration of the above functional components may result in ncSi-MPM becoming a promising multifunctional carrier for drug delivery and biomedical applications.
引用
收藏
页码:3424 / 3431
页数:8
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