共 51 条
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
收藏
页数:9
相关论文