Potentiation of the activity of bone morphogenetic protein-2 in bone regeneration by a PLA-PEG/hydroxyapatite composite

被引:146
作者
Kaito, T
Myoui, A
Takaoka, K
Saito, N
Nishikawa, M
Tamai, N
Ohgushi, H
Yoshikawa, H
机构
[1] Osaka Univ, Grad Sch Med, Dept Orthopaed Surg, Suita, Osaka 5650871, Japan
[2] Shinshu Univ, Sch Med, Dept Orthopaed Surg, Matsumoto, Nagano 3908621, Japan
[3] Osaka City Univ, Grad Sch Med, Dept Orthopaed Surg, Abeno Ku, Osaka 5450051, Japan
[4] Natl Inst AIST, TERC, Amagasaki, Hyogo 6610974, Japan
关键词
BMP (bone morphogenetic protein); hydroxyapatite; drug delivery; polylactic acid; bone tissue engineering;
D O I
10.1016/j.biomaterials.2004.02.010
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Bone morphogenetic proteins (BMPs) are biologically active molecules capable of inducing new bone formation, and show potential for clinical use in bone defect repair. However, an ideal system for delivering BMPs that can potentiate their bone-inducing ability and provide initial mechanical strength and scaffold for bone ingrowth has not yet been developed. In this study, to construct a carrier/scaffold system for BMPs, we combined two biomaterials: interconnected-porous calcium hydroxyapatite ceramics (IPCHA), and the synthetic biodegradable polymer Poly D,L,-lactic acid-polyethyleneglycol block co-polymer (PLA-PEG). We used a rabbit radii model to evaluate the bone-regenerating efficacy of rhBMP-2/PLA PEG/IP-CHA composite. At 8 weeks after implantation, all bone defects in groups treated with 5 or 20 mug of BMP were completely repaired with sufficient strength. Furthermore, using this carrier scaffold system, we reduced the amount of BMP necessary for such results to about a tenth of the amount needed in previous studies, probably due to the superior osteoconduction ability of IP-CHA and the optimal drug delivery system provided by PLA-PEG, inducing new bone formation in the interconnected pores. The present findings indicate that the synthetic biodegradable polymer/IP-CHA composite is an excellent combination carrier/scaffold delivery system for rhBMP-2, and that it strongly promotes the clinical effects of rhBMP-2 in bone tissue regeneration. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:73 / 79
页数:7
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