The mechanical integrity of in vivo engineered heterotopic bone

被引:46
作者
Warnke, PH
Springer, IN
Acil, Y
Julga, G
Wiltfang, J
Ludwig, K
Russo, PAJ
Sherry, E
Sivananthan, S
Hedderich, J
Terheyden, H
机构
[1] Univ Kiel, Dept Oral & Maxillofacial Surg, D-24105 Kiel, Germany
[2] Univ Kiel, Dept Prosthodont & Mat Res, D-24105 Kiel, Germany
[3] Australian Natl Univ, Dept Rheumatol, Canberra, ACT, Australia
[4] Bond Univ, Dept Orthopaed Surg, Gold Coast, Australia
[5] Robert Jones & Agnes Hunt Orthopaed Hosp, Dept Orthopaed Surg, Oswestry SY10 7AG, Shrops, England
[6] Univ Kiel, Dept Med Informat & Stat, D-24105 Kiel, Germany
关键词
in vivo tissue engineering; BioOss; BMP; 7; Bone Morphogenetic Proteins; heterotopic bone; mechanical stability;
D O I
10.1016/j.biomaterials.2005.07.042
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Recent advances in tissue engineering have aroused interest in growth of heterotopic bone for the repair of skeletal defects. This study demonstrates an in vivo method in minipigs of engineering individual human-sized mandible replacements of heterotopic bone with a mechanical integrity similar to natural bone. Ten individualized mandible replacement scaffolds were created using computer-aided design (CAD) techniques. Five had a resorbable external scaffold made of polylactite mesh (test group 1) and five had had a non-resorbable external scaffold of titanium mesh (test group 2). The mesh scaffolds were loaded each with five BioOss (R) blocks serving as internal scaffolds and 3.5 mg recombinant human Bone Morphogenetic Protein-7. The loaded mesh scaffolds were implanted into the latissimus dorsi muscles of five infant minipigs. After 6 weeks the mandible replacements were harvested. Core biopsy cylinders were taken from the replacements of both test groups and from the natural pig mandibles (control 1). Also, core biopsies from plain BioOss Blocks were gained (control 2). The core biopsy cylinders were loaded axially into a compression test device to evaluate the mechanical compression resistance. Additional specimen underwent histological examination. Both test groups resulted in successful bone induction with degrees of compression resistance [Test 1: 1.62MPa (SD +/- 0.73); Test 2: 1.51 MPa (SD +/- 0.56)] statistically insignificant when compared to natural porcine mandibular bone [1.75MPa (SD +/- 0.69)]. This differed significantly from the much lower compression resistance seen in the unadulterated BioOss [0.92MPa (SD +/- 0.04)]. Following this. the in vivo engineered bone has a similar mechanical compression stability as natural bone. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1081 / 1087
页数:7
相关论文
共 24 条
[1]   Interspecies differences in bone composition, density, and quality:: Potential implications for in vivo bone research [J].
Aerssens, J ;
Boonen, S ;
Lowet, G ;
Dequeker, J .
ENDOCRINOLOGY, 1998, 139 (02) :663-670
[2]   Tissue-engineered osteochondral constructs in the shape of an articular condyle [J].
Alhadlaq, A ;
Mao, JJ .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2005, 87A (05) :936-944
[3]   Tissue-engineered neogenesis of human-shaped mandibular condyle from rat mesenchymal stem cells [J].
Alhadlaq, A ;
Mao, JJ .
JOURNAL OF DENTAL RESEARCH, 2003, 82 (12) :951-956
[4]   SKELETAL DEVELOPMENT AND BONE FUNCTIONAL ADAPTATION [J].
CARTER, DR ;
ORR, TE .
JOURNAL OF BONE AND MINERAL RESEARCH, 1992, 7 :S389-S395
[5]  
CHAMPY M, 1999, ATLAS CRANIOMAXILLOF, P5
[6]   EFFECT OF BONE DISTRIBUTION ON VERTEBRAL STRENGTH - ASSESSMENT WITH PATIENT-SPECIFIC NONLINEAR FINITE-ELEMENT ANALYSIS [J].
FAULKNER, KG ;
CANN, CE ;
HASEGAWA, BH .
RADIOLOGY, 1991, 179 (03) :669-674
[7]  
Friedlaender GE, 2001, J BONE JOINT SURG AM, V83A, pS151
[8]   Scaffolds in tissue engineering bone and cartilage [J].
Hutmacher, DW .
BIOMATERIALS, 2000, 21 (24) :2529-2543
[9]   TRABECULAR BONE STRENGTH PATTERNS AT THE PROXIMAL TIBIAL EPIPHYSIS [J].
HVID, I ;
HANSEN, SL .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1985, 3 (04) :464-472
[10]   Smooth muscle cell adhesion to tissue engineering scaffolds [J].
Nikolovski, J ;
Mooney, DJ .
BIOMATERIALS, 2000, 21 (20) :2025-2032