Hierarchically microporous/macroporous scaffold of magnesium-calcium phosphate for bone tissue regeneration

被引:183
作者
Wei, Jie [3 ,4 ]
Jia, Junfeng [3 ,4 ]
Wu, Fan [3 ,4 ]
Wei, Shicheng [1 ,2 ,6 ]
Zhou, Huanjun [3 ,4 ]
Zhang, Hongbo [3 ,4 ]
Shin, Jung-Woog [5 ]
Liu, Changsheng [3 ,4 ]
机构
[1] Peking Univ, Dept Oral & Maxillofacial Surg, Sch Stomatol, Beijing 100081, Peoples R China
[2] Peking Univ, Hosp Stomatol, Beijing 100081, Peoples R China
[3] E China Univ Sci & Technol, Engn Res Ctr Biomed Mat, Minist Educ, Shanghai 200237, Peoples R China
[4] E China Univ Sci & Technol, Key Lab Ultrafine Mat, Minist Educ, Shanghai 200237, Peoples R China
[5] Inje Univ, Dept Biomed Engn, Res Grp 1, BK 21, Gimhae 621749, South Korea
[6] Peking Univ, Ctr Biomed Mat & Tissue Engn, Acad Adv Interdisciplinary Studies, Beijing 100871, Peoples R China
关键词
Hierarchically porous scaffolds; Magnesium calcium phosphate; Biodegradability; Biocompatibility; Bone generation; IN-VITRO; CEMENT; CELLS; DIFFERENTIATION; INGROWTH; PROLIFERATION; IMPLANTATION; ADHESION; GLASS;
D O I
10.1016/j.biomaterials.2009.11.005
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Hierarchically 3D microporous/macroporous magnesium-calcium phosphate (micro/ma-MCP) scaffolds containing magnesium ammonium phosphate hexahydrate [NH4MgPO4 center dot 6H(2)O] and hydroxyapatite [Ca-10(PO4)(6)(CH)(2)] were fabricated from cement utilizing leaching method in the presence of sodium chloride (NaCl) particles and NaCl saturated water solution. NaCl particles produced macropororosity, and NaCl solution acted as both cement liquid and porogens, inducing the formation of microporosity. The micro/ma-MCP scaffolds with porosities varied from 52 to 78% showed well interconnected and open macropores with the sizes of 400-500 mu m, and degradation of the scaffolds was significantly enhanced in Tris-HCl solution compared with macroporous MCP (ma-MCP) and corresponding calcium phosphate cement (CPC) scaffolds. Cell attachment and proliferation of MG(63) on micro/ma-MCP were significantly better than ma-MCP and CPC scaffolds because of the presence of microporosity, which enhanced the surface area of the scaffolds. Moreover, the alkaline phosphatase (ALP) activity of the MG(63) cells on micro/ma-MCP was significantly higher than ma-MCP and CPC scaffolds at 7 days, and the MG(63) cells with normal phenotype spread well and formed confluent layers across the macroporous walls of the microlma-MCP scaffolds. Histological evaluation confirmed that the micro/ma-MCP scaffolds improved the efficiency of new bone regeneration, and exhibited excellent biocompatibility, biodegradability and faster and more effective osteogenesis in vivo. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1260 / 1269
页数:10
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