An evaluation of human demineralized bone matrices in a rat femoral defect model

被引:48
作者
Oakes, DA
Lee, CC
Lieberman, JR
机构
[1] Univ Calif Los Angeles, Med Ctr, Dept Orthopaed Surg, David Geffen Sch Med, Los Angeles, CA 90095 USA
[2] Albany Med Coll, Dept Orthopaed Surg, Albany, NY 12208 USA
关键词
D O I
10.1097/01.blo.0000073347.50837.16
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
The osteoconductive and osteoinductive potential of two human allogeneic demineralized bone matrix putties were compared in a critical-sized athymic rat femoral defect model. Defects were treated with (1) a demineralized bone matrix in a hyaluronic acid carrier, (2) a demineralized bone matrix in a glycerol carrier, (3) a hyaluronic acid carrier alone, or (4) with no implant. Radiographic examinations and histologic analyses were done at 4, 8, and 16 weeks postoperatively. Eight of the 48 defects treated with a demineralized bone matrix and none of the 36 surgical controls showed complete radiographic healing by 16 weeks and no statistically significant difference between the radiographic scores for the two demineralized bone matrix preparations was found. On histologic review, both preparations of demineralized bone matrix had passive remineralization. The largest foci of endochondral ossification were seen in limbs treated with a demineralized bone matrix in a hyaluronic acid carrier. The 8-mm rat femoral defect allows for stringent assessment of the osteoinductive potential of bone graft substitutes. Hyaluronic acid and glycerol are viable carriers for demineralized bone matrices. As both demineralized bone matrices tested provided an adequate osteoconductive matrix and showed some, although limited, osteoinductive capacity, these materials should be used in clinical practice only as bone graft extenders or enhancers.
引用
收藏
页码:281 / 290
页数:10
相关论文
共 25 条
[1]   COMPARISON BETWEEN ALLOGRAFT PLUS DEMINERALIZED BONE-MATRIX VERSUS AUTOGRAFT IN ANTERIOR CERVICAL FUSION - A PROSPECTIVE MULTICENTER STUDY [J].
AN, HS ;
SIMPSON, JM ;
GLOVER, JM ;
STEPHANY, J .
SPINE, 1995, 20 (20) :2211-2216
[2]  
BROSTROM MPG, 1999, ORTHOP CLIN N AM, V30, P647
[3]   The cylindrical titanium mesh cage for treatment of a long bone segmental defect: Description of a new technique and report of two cases [J].
Cobos, JA ;
Lindsey, RW ;
Gugala, Z .
JOURNAL OF ORTHOPAEDIC TRAUMA, 2000, 14 (01) :54-59
[4]   Osteoinduction of human demineralized bone: Characterization in a rat model [J].
Edwards, JT ;
Diegmann, MH ;
Scarborough, NL .
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 1998, (357) :219-228
[5]  
EINHORN TA, 1984, J BONE JOINT SURG AM, V66A, P274, DOI 10.2106/00004623-198466020-00015
[6]   Induction of bone by a demineralized bone matrix gel: A study in a rat femoral defect model [J].
Feighan, JE ;
Davy, D ;
Prewett, IB ;
Stevenson, S .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1995, 13 (06) :881-891
[7]  
GOULET JA, 1997, CLIN ORTHOP RELAT R, V339, P76, DOI DOI 10.1097/00003086-199706000-00011
[8]  
Lane JM, 1998, AAOS INSTR COURS LEC, V47, P525
[9]   Regional gene therapy with a BMP-2-producing murine stromal cell line induces heterotopic and orthotopic bone formation in rodents [J].
Lieberman, JR ;
Le, LQ ;
Wu, L ;
Finerman, GAM ;
Berk, A ;
Witte, ON ;
Stevenson, O .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1998, 16 (03) :330-339
[10]   The effect of regional gene therapy with bone morphogenetic protein-2-producing bone-marrow cells on the repair of segmental femoral defects in rats [J].
Lieberman, JR ;
Daluiski, A ;
Stevenson, S ;
Wu, L ;
McAllister, P ;
Lee, YP ;
Kabo, JM ;
Finerman, GAM ;
Berk, AJ ;
Witte, ON .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1999, 81A (07) :905-917