An initial investigation of photocurable three-dimensional lactic acid based scaffolds in a critical-sized cranial defect

被引:72
作者
Burdick, JA
Frankel, D
Dernell, WS
Anseth, KS
机构
[1] Univ Colorado, Ctr Engn, Dept Chem Engn, Boulder, CO 80309 USA
[2] Colorado State Univ, Coll Vet Med, Dept Clin Sci, VTH, Ft Collins, CO 80523 USA
[3] Univ Colorado, Ctr Engn, Howard Hughes Med Inst, Boulder, CO 80309 USA
关键词
bone tissue engineering; photopolymerization; cranial defect; degradable polymer; in situ forming; scaffolds;
D O I
10.1016/S0142-9612(02)00538-0
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Degradable polymer networks formed by the photoinitiated polymerization of multifunctional monomers have great potential as in situ forming materials, especially for bone tissue engineering. In this study, one specific chemistry was analyzed with respect to bone formation in a critical-sized defect model with and without adsorbed osteoinductive growth factors present. The scaffolds degraded in similar to8 months and possessed an elastic modulus similar to that of trabecular bone. A porous scaffold fabricated with similar to80% porosity and pore diameters ranging from 45 to 150mm was implanted in a critical-sized cranial defect in rats. When implanted alone, the scaffolds were filled primarily with fibrous tissue after 9 weeks with only mild inflammation at the defect site. When the scaffolds released osteoinductive growth factors, statistically more bone filled the scaffold. For instance, 65.8 +/- 9.4% (n = 5) of the defects were filled with radiopaque tissue in the osteoinductive releasing scaffolds, whereas only 24.2 +/- 7.4% (n = 5) of the defects were filled in the untreated defects 9 weeks after implantation. These results illustrate not only the benefits of delivering osteoinductive factors when developing synthetic bone grafts, but the potential of these materials for supporting the infiltration and development of bone in large defects. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1613 / 1620
页数:8
相关论文
共 25 条
  • [1] Agrawal CM, 2001, J BIOMED MATER RES, V55, P141, DOI 10.1002/1097-4636(200105)55:2<141::AID-JBM1000>3.0.CO
  • [2] 2-J
  • [3] Photopolymerizable degradable polyanhydrides with osteocompatibility
    Anseth, KS
    Shastri, VR
    Langer, R
    [J]. NATURE BIOTECHNOLOGY, 1999, 17 (02) : 156 - 159
  • [4] New directions in photopolymerizable biomaterials
    Anseth, KS
    Burdick, JA
    [J]. MRS BULLETIN, 2002, 27 (02) : 130 - 136
  • [5] Bauer TW., 2000, CLIN ORTHOP RELAT R, V371, P10, DOI DOI 10.1097/00003086-200002000-00003
  • [6] Delivery of osteoinductive growth factors from degradable PEG hydrogels influences osteoblast differentiation and mineralization
    Burdick, JA
    Mason, MN
    Hinman, AD
    Thorne, K
    Anseth, KS
    [J]. JOURNAL OF CONTROLLED RELEASE, 2002, 83 (01) : 53 - 63
  • [7] In situ forming lactic acid based orthopaedic biomaterials:: Influence of oligomer chemistry on osteoblast attachment and function
    Burdick, JA
    Mason, MN
    Anseth, KS
    [J]. JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2001, 12 (11) : 1253 - 1265
  • [8] An investigation of the cytotoxicity and histocompatibility of in situ forming lactic acid based orthopedic biomaterials
    Burdick, JA
    Padera, RF
    Huang, JV
    Anseth, KS
    [J]. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 63 (05): : 484 - 491
  • [9] Conversion and temperature profiles during the photoinitiated polymerization of thick orthopaedic biomaterials
    Burdick, JA
    Peterson, AJ
    Anseth, KS
    [J]. BIOMATERIALS, 2001, 22 (13) : 1779 - 1786
  • [10] Burdick JA, 2001, J POLYM SCI POL CHEM, V39, P683, DOI 10.1002/1099-0518(20010301)39:5<683::AID-POLA1040>3.0.CO