Transplanted Bone Morphogenetic Protein/Poly(lactic-co-glycolic Acid) Delayed-release Microcysts Combined with Rat Micromorselized Bone and Collagen for Bone Tissue Engineering

被引:5
作者
Ji, Y. [1 ]
Xu, G. P. [1 ]
Yan, J. L. [1 ]
Pan, S. H. [2 ]
机构
[1] Harbin Med Univ, Dept Orthopaed Surg, Affiliated Hosp 1, Harbin 150001, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Cent Lab, Affiliated Hosp 1, Harbin 150001, Heilongjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
BONE TRANSPLANTATION; BONE TISSUE ENGINEERING; BONE MORPHOGENETIC PROTEIN 2; GROWTH FACTORS; CONTROLLED-RELEASE TECHNOLOGY; MICROCYST; MORSELIZED ALLOGRAFT; IN-VITRO; MICROSPHERES; PROTEIN; DELIVERY; DEFECTS; FUSION;
D O I
10.1177/147323000903700412
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
This study was designed to optimize the preparation of delayed-release microcysts containing bone morphogenetic protein 2 (BMP-2) combined with poly(lactic-co-glycolic acid) (PLGA) and to investigate their osteogenic properties when combined with rat autologous micromorselized bone and collagen. Rat autologous micromorselized bone, collagen and BMP-2/PLGA delayed-release microcysts were implanted in various combinations into the rat gluteus maximus muscle sack model. The following post-operative measurements were made: general observations of the implant site, histological observations, osteogenesis measurements and alkaline phosphatase activity. Autologous micromorselized bone combined with collagen and BMP-2/PLGA delayed-release microcysts demonstrated significantly superior osteogenic properties than any of the other combinations of these three components. These findings suggest that micromorselized bone combined with collagen and BMP-2/PLGA delayed-release microcysts could reduce the quantity of BMP-2 and autologous bone required for these procedures, making their use feasible in human bone restoration.
引用
收藏
页码:1075 / 1087
页数:13
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