Growth factor-loaded scaffolds for bone engineering

被引:147
作者
Jansen, JA
Vehof, JWM
Ruhé, PQ
Kroeze-Deutman, H
Kuboki, Y
Takita, H
Hedberg, EL
Mikos, AG
机构
[1] Univ Nijmegen, Med Ctr, Dept Periodontol & Biomat, NL-6500 HB Nijmegen, Netherlands
[2] Hokkaido Univ, Dept Biochem, Sapporo, Hokkaido 060, Japan
[3] Rice Univ, Dept Bioengn, Houston, TX 77251 USA
关键词
calcium phosphate cement; transforming growth factor beta-1; recombinant human BMP-2; titanium fiber mesh; osteoinduction; bone engineering;
D O I
10.1016/j.jconrel.2004.07.005
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The objective of the study presented here was to investigate the bone inductive properties as well as release kinetics of rhTGF-beta 1- and rhBMP-2-loaded Ti-fiber mesh and Cap cement scaffolds. Therefore, Ti-fiber mesh and porous Cap cement scaffolds were provided with these growth factors and inserted in subcutaneous and cranial implant locations in rats and rabbits. In vitro, a rapid release of rhTGF-beta(1) was observed during the first 2 h of the Ti-fiber mesh scaffolds. During this time, more than 50% of the total dose of rhTGF-beta(1) was released. Following this initial peak, a decline in the level of rhTGF-beta(1) Occurred. After 1 week, the entire theoretical initial dose was observed to have been released. This in contrast to the rhTGF-beta(1), and rhBMP-2 release of the porous Cap cement scaffolds. Here, no substantial initial burst release was observed. The scaffolds showed an initial release of about 1% after 1 day, followed by an additional marginal release after 1 week. Histological analysis revealed excellent osteoconductive properties of non-loaded Ca-P material. Inside non-loaded Ti-mesh fiber scaffolds, also bone ingrowth occurred. Quantification of the bone ingrowth showed that bone formation was increased significantly in all scaffold materials by administration of rhTGF-beta(1) and rhBMP-2. Consequently, we conclude that the release kinetics of growth factors from porous Cap cement differs from other scaffold materials. like metals and polymers. Nevertheless, orthotopic bone formation in a rabbit cranial defect model was stimulated in rhTGF-beta(1)- and rhBMP-2-loaded Cap cement and Ti-fiber mesh scaffolds compared with non-loaded implants. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 136
页数:10
相关论文
共 47 条
[31]   EFFECT OF POLY DL-LACTIDE-CO-GLYCOLIDE IMPLANTS AND XENOGENEIC BONE MATRIX-DERIVED GROWTH-FACTORS ON CALVARIAL BONE REPAIR IN THE RABBIT [J].
MEIKLE, MC ;
PAPAIOANNOU, S ;
RATLEDGE, TJ ;
SPEIGHT, PM ;
WATTSMITH, SR ;
HILL, PA ;
REYNOLDS, JJ .
BIOMATERIALS, 1994, 15 (07) :513-521
[32]   Promotion of the osteogenetic activity of recombinant human bone morphogenetic protein by prostaglandin E(1) [J].
Ono, I ;
Inoue, M ;
Kuboki, Y .
BONE, 1996, 19 (06) :581-588
[33]  
Ono I, 1999, J BIOMED MATER RES, V45, P337
[34]   Trabecular bone response to injectable calcium phosphate (Ca-P) cement [J].
Ooms, EM ;
Wolke, JGC ;
van der Waerden, JPCM ;
Jansen, JA .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 61 (01) :9-18
[35]   Corrosion behaviour of metal fibre web structures [J].
Paquay, YCGJ ;
DeBlieckHogervorst, JMA ;
Jansen, JA .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 1996, 7 (10) :585-589
[36]  
Puleo DA, 1997, J CELL PHYSIOL, V173, P93, DOI 10.1002/(SICI)1097-4652(199710)173:1<93::AID-JCP11>3.0.CO
[37]  
2-O
[38]  
REDDI AH, 1993, J BONE MINER RES, V8, pS499
[39]   Bone morphogenetic protein-2: Biology and applications [J].
Riley, EH ;
Lane, JM ;
Urist, MR ;
Lyons, KM ;
Lieberman, JR .
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 1996, (324) :39-46
[40]  
Ripamonti U, 1996, J BONE MINER RES, V11, P938