Europium-doped amorphous calcium phosphate porous nanospheres: preparation and application as luminescent drug carriers

被引:70
作者
Chen, Feng [1 ]
Zhu, Ying-Jie [1 ]
Zhang, Kui-Hua [2 ]
Wu, Jin [1 ]
Wang, Ke-Wei [1 ]
Tang, Qi-Li [1 ]
Mo, Xiu-Mei [2 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine, Shanghai 200050, Peoples R China
[2] Donghua Univ, Coll Chem Chem Engn & Biotechnol, Shanghai 201620, Peoples R China
来源
NANOSCALE RESEARCH LETTERS | 2011年 / 6卷
基金
中国国家自然科学基金;
关键词
IRON-OXIDE NANOPARTICLES; IN-VIVO; MULTIFUNCTIONAL NANOPARTICLES; HYDROXYAPATITE NANOPARTICLES; GOLD NANOPARTICLES; HUMAN FIBROBLASTS; CARBON NANOTUBES; BIOLOGICAL PROBE; CONTRAST AGENT; BREAST-CANCER;
D O I
10.1186/1556-276X-6-67
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Calcium phosphate is the most important inorganic constituent of biological tissues, and synthetic calcium phosphate has been widely used as biomaterials. In this study, a facile method has been developed for the fabrication of amorphous calcium phosphate (ACP)/polylactide-block-monomethoxy(polyethyleneglycol) hybrid nanoparticles and ACP porous nanospheres. Europium-doping is performed to enable photoluminescence (PL) function of ACP porous nanospheres. A high specific surface area of the europium-doped ACP (Eu3+:ACP) porous nanospheres is achieved (126.7 m(/)(2)g). PL properties of Eu3+:ACP porous nanospheres are investigated, and the most intense peak at 612 nm is observed at 5 mol% Eu3+ doping. In vitro cytotoxicity experiments indicate that the as-prepared Eu3+:ACP porous nanospheres are biocompatible. In vitro drug release experiments indicate that the ibuprofen-loaded Eu3+:ACP porous nanospheres show a slow and sustained drug release in simulated body fluid. We have found that the cumulative amount of released drug has a linear relationship with the natural logarithm of release time (ln(t)). The Eu3+:ACP porous nanospheres are bioactive, and can transform to hydroxyapatite during drug release. The PL properties of drug-loaded nanocarriers before and after drug release are also investigated.
引用
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页数:9
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