共 15 条
Porous calcium phosphate granules containing drug-loaded polymeric nanoparticles for bone regeneration
被引:14
作者:
Son, Jun Sik
[1
]
Lee, Kyu-Bok
[2
]
Kim, Su-Gwan
[3
]
Kwon, Tae-Yub
[1
,4
]
Kim, Kyo-Han
[1
,4
]
机构:
[1] Kyungpook Natl Univ, Inst Biomat Res & Dev, Taegu, South Korea
[2] Kyungpook Natl Univ, Dept Prosthodont, Sch Dent, Taegu, South Korea
[3] Chosun Univ, Dept Oral & Maxillofacial Surg, Sch Dentistry, Kwangju, South Korea
[4] Kyungpook Natl Univ, Dept Dent Biomat, Sch Dent, Taegu, South Korea
来源:
关键词:
Calcium phosphate granule;
PLGA;
Nanoparticle;
Drug delivery;
HYDROXYAPATITE GRANULES;
DEXAMETHASONE;
SCAFFOLD;
RELEASE;
SYSTEM;
D O I:
10.1016/j.matlet.2012.02.114
中图分类号:
T [工业技术];
学科分类号:
08 ;
摘要:
A simple and highly efficient method for fabrication of drug-loaded porous calcium phosphate (CP) granules using biodegradable nanoparticles was developed in this study. Porous CP granules were used as a bone graft substitute with a localized drug delivery structure. Spherical CP granules with open micro-channels and PLGA nanoparticles loaded with dexamethasone (DEX) as a model drug were fabricated by a liquid nitrogen method and a single emulsion method, respectively. The produced nanoparticles were pre-coated with positively charged poly(ethyleneimmine) (PEI) molecules and then immobilized via electrical interaction in the microchannels on the surfaces of CP granules, which have a negative charge. The results indicated that the PEI-coated PLGA nanoparticles loaded with DEX were successfully incorporated and well-dispersed in the micro-channels of the CP granules. The nanoparticles were not released from the CP granules and allowed a sustained release of DEX from the nanoparticle-based CP granules over the course of 1 month. (C) 2012 Elsevier B.V. All rights reserved.
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页码:243 / 246
页数:4
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