An in vivo study of a growth-factor enhanced, cell free, two-layered collagen-tricalcium phosphate in deep osteochondral defects

被引:100
作者
Gotterbarm, T
Richter, W
Jung, M
Vilei, SB
Mainil-Varlet, P
Yamashita, T
Breusch, SJ
机构
[1] Heidelberg Univ, Dept Orthopaed, D-69118 Heidelberg, Germany
[2] Centerpulse Biol Inc, CH-8404 Winterthur, Switzerland
[3] Univ Bern, Inst Pathol, CH-3010 Bern, Switzerland
[4] Univ Edinburgh, New Royal Infirm, Dept Orthopaed, Edinburgh EH16 4SU, Midlothian, Scotland
关键词
osteochondral defect; two-layered implant; beta-TCP; collagen type I; growth factors; indentation test;
D O I
10.1016/j.biomaterials.2006.01.041
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Focal osteochondral defects are still a challenging problem in joint Surgery. We have developed a two-layered implant consisting of a basal porous beta-tricalcium phosphate (TCP) for bone reconstruction and a superficial fibrous collagen type I/III layer for cartilage regeneration. Fifty-four osteochondral defects in the trochlear groove of 27 Gottinger Minipigs were created and either left untreated, treated with the implant alone, or the implant augmented with an additional growth factor Mixture, which was assumed to Stimulate cell and tissue differentiation. Follow-up was 6, 12 and 52 weeks with n = 6 for each group. The repair tissue was evaluated for its gross appearance and biomechanical properties. Histological sections were semi-quantitatively scored for their histomorphological Structure. Treatment with the two-layered implant improved defect filling and subchondral bone repair at 6 and 12 weeks follow-up. The TCP was replaced by cancellous bone at 52 weeks. Cartilage repair tissue mainly consisted of fibrocartilage and showed a moderate cell density Lip to the joint surface. Growth factor treatment improved the mechanical and histomorphological properties of the cartilage repair tissue at 12, but not at 52 weeks postoperatively. In conclusion, the two-layered collagen-TCP implant augmented with chondroinductive growth factors seems a promising new option for the treatment of deep osteochondral defects in joint Surgery. (c)(c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3387 / 3395
页数:9
相关论文
共 42 条
[1]   Engineering of osteochondral tissue with bone marrow mesenchymal progenitor: Cells in a derivatized hyaluronan-gelatin composite sponge [J].
Angele, P ;
Kujat, R ;
Nerlich, M ;
Yoo, J ;
Goldberg, V ;
Johnstone, B .
TISSUE ENGINEERING, 1999, 5 (06) :545-553
[2]  
Atkinson BL, 1997, J CELL BIOCHEM, V65, P325, DOI 10.1002/(SICI)1097-4644(19970601)65:3<325::AID-JCB3>3.3.CO
[3]  
2-G
[4]   A prospective, randomised comparison of autologous chondrocyte implantation versus mosaicplasty for osteochondral defects in the knee [J].
Bentley, G ;
Biant, LC ;
Carrington, RWJ ;
Akmal, M ;
Goldberg, A ;
Williams, AM ;
Skinner, JA ;
Pringle, J .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 2003, 85B (02) :223-230
[5]   Ne-osteo bone growth factor for posterolateral lumbar spine fusion: Results from a nonhuman primate study and a prospective human clinical pilot study [J].
Boden, SD ;
Grob, D ;
Damien, C .
SPINE, 2004, 29 (05) :504-514
[6]  
ButnariuEphrat M, 1996, CLIN ORTHOP RELAT R, P234
[7]   Scaffold-based articular cartilage repair [J].
Capito, RM ;
Spector, M .
IEEE ENGINEERING IN MEDICINE AND BIOLOGY MAGAZINE, 2003, 22 (05) :42-50
[8]  
CONVERY FR, 1972, CLIN ORTHOP RELAT R, P253
[9]   Purified bovine BMP extract and collagen for spine arthrodesis - Preclinical safety and efficacy [J].
Damien, CJ ;
Grob, D ;
Boden, SD ;
Benedict, JJ .
SPINE, 2002, 27 (16) :S50-S58
[10]  
Draenert K, 1988, SANDORAMA, VIII-IV, P33