Fabrication and characterization of poly-D-L-lactide/nano-hydroxyapatite composite scaffolds with poly (ethylene glycol) coating and dexamethasone releasing

被引:39
作者
Chen, L. [1 ]
Tang, C. Y. [1 ]
Chen, D. Z. [2 ]
Wong, C. T. [1 ]
Tsui, C. P. [1 ]
机构
[1] Hong Kong Polytech Univ, Dept Ind & Syst Engn, Kowloon, Hong Kong, Peoples R China
[2] Shenzhen Univ, Coll Mat Sci & Engn, Shenzhen, Guangdong, Peoples R China
关键词
Porosity/Voids; Surface treatments; Casting; CONTROLLED DRUG-DELIVERY; MESENCHYMAL STEM-CELLS; BONE; PROLIFERATION; NANOCOMPOSITE; CULTURE; DESIGN;
D O I
10.1016/j.compscitech.2011.08.015
中图分类号
TB33 [复合材料];
学科分类号
080505 [复合材料];
摘要
The control of pore size and structure, drug release capacity, and biodegradation of scaffolds is of importance for bone tissue engineering. In this study, a technique combining polymer coagulation, cold compression molding, salt particulate leaching and drug coating method was developed to fabricate poly (ethylene glycol)/dexamethasone coated porous poly-D-L-lactide/nano-hydroxyapatite (PDLLA/nano-HAp) scaffolds. These scaffolds possess homogenous pore networks with high porosity (66-82%) and controllable pore size (200-300 mu m). The compressive moduli and strength of the scaffolds after incorporation of nano-HAp were improved by 50% and 20%, respectively. The surface hydrophilicity of the scaffold was significantly improved by poly (ethylene glycol)/dexamethasone coating and nano-HAp addition, leading to a higher initial drug loading amount. The results showed that the drug release behavior of the scaffolds after 35-day immersion in water could be adjusted by varying the porosity level and by incorporation of 20 wt.% of nano-HAp. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1842 / 1849
页数:8
相关论文
共 29 条
[1]
Controlled drug delivery in tissue engineering [J].
Biondi, Marco ;
Ungaro, Francesca ;
Quaglia, Fabiana ;
Netti, Paolo Antonio .
ADVANCED DRUG DELIVERY REVIEWS, 2008, 60 (02) :229-242
[2]
Dynamic mechanical properties and in vitro bioactivity of PHBHV/HA nanocomposite [J].
Chen, D. Z. ;
Tang, C. Y. ;
Chan, K. C. ;
Tsui, C. P. ;
Yu, Peter H. F. ;
Leung, Mason C. P. ;
Uskokovic, P. S. .
COMPOSITES SCIENCE AND TECHNOLOGY, 2007, 67 (7-8) :1617-1626
[3]
Porous polymer/hydroxyapatite scaffolds: characterization and biocompatibility investigations [J].
Douglas, Timothy ;
Pamula, Elzbieta ;
Hauk, Dominik ;
Wiltfang, Joerg ;
Sivananthan, Sureshan ;
Sherry, Eugene ;
Warnke, Patrick H. .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2009, 20 (09) :1909-1915
[4]
Dexamethasone-loaded scaffolds prepared by supercritical-assisted phase inversion [J].
Duarte, Ana Rita C. ;
Mano, Joao F. ;
Reis, Rui L. .
ACTA BIOMATERIALIA, 2009, 5 (06) :2054-2062
[5]
Design and manufacture of microporous polymeric materials with hierarchal complex structure for biomedical application [J].
Guarino, V. ;
Causa, F. ;
Salerno, A. ;
Ambrosio, L. ;
Netti, P. A. .
MATERIALS SCIENCE AND TECHNOLOGY, 2008, 24 (09) :1111-1117
[6]
Porous polymeric structures for tissue engineering prepared by a coagulation, compression moulding and salt leaching technique [J].
Hou, QP ;
Grijpma, DW ;
Feijen, J .
BIOMATERIALS, 2003, 24 (11) :1937-1947
[7]
Scaffolds in tissue engineering bone and cartilage [J].
Hutmacher, DW .
BIOMATERIALS, 2000, 21 (24) :2529-2543
[8]
Evaluation of hot-pressed hydroxyapatite/poly-L-lactide composite biomaterial characteristics [J].
Ignjatovic, N ;
Suijovrujic, E ;
Budinski-Simendic, J ;
Krakovsky, I ;
Uskokovic, D .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS, 2004, 71B (02) :284-294
[9]
Porosity of 3D biomaterial scaffolds and osteogenesis [J].
Karageorgiou, V ;
Kaplan, D .
BIOMATERIALS, 2005, 26 (27) :5474-5491
[10]
Sustained release of ascorbate-2-phosphate and dexamethasone from porous PLGA scaffolds for bone tissue engineering using mesenchymal stem cells [J].
Kim, H ;
Kim, HW ;
Suh, H .
BIOMATERIALS, 2003, 24 (25) :4671-4679