In vivo study of magnesium plate and screw degradation and bone fracture healing

被引:299
作者
Chaya, Amy [1 ,2 ,4 ]
Yoshizawa, Sayuri [1 ,3 ]
Verdelis, Kostas [1 ,3 ,4 ]
Myers, Nicole [1 ,3 ]
Costello, Bernard J. [1 ,4 ,5 ]
Chou, Da-Tren [1 ,2 ,4 ]
Pal, Siladitya [2 ]
Maiti, Spandan [2 ]
Kumta, Prashant N. [1 ,2 ,3 ,4 ]
Sfeir, Charles [1 ,2 ,3 ,4 ]
机构
[1] Univ Pittsburgh, Ctr Craniofacial Regenerat, Pittsburgh, PA USA
[2] Univ Pittsburgh, Dept Bioengn, Pittsburgh, PA USA
[3] Univ Pittsburgh, Dept Oral Biol, Pittsburgh, PA USA
[4] Univ Pittsburgh, McGowan Inst Regenerat Med, Pittsburgh, PA USA
[5] Univ Pittsburgh, Dept Oral & Maxillofacial Surg, Pittsburgh, PA USA
基金
美国国家科学基金会;
关键词
Magnesium; Fixation devices; Fracture fixation; MicroCT; ALLOY; CORROSION; IMPLANTS; BEHAVIOR; FIXATION; BIOCOMPATIBILITY; REMOVAL; VITRO;
D O I
10.1016/j.actbio.2015.02.010
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Each year, millions of Americans suffer bone fractures, often requiring internal fixation. Current devices, like plates and screws, are made with permanent metals or resorbable polymers. Permanent metals provide strength and biocompatibility, but cause long-term complications and may require removal. Resorbable polymers reduce long-term complications, but are unsuitable for many load-bearing applications. To mitigate complications, degradable magnesium (Mg) alloys are being developed for craniofacial and orthopedic applications. Their combination of strength and degradation make them ideal for bone fixation. Previously, we conducted a pilot study comparing Mg and titanium devices with a rabbit ulna fracture model. We observed Mg device degradation, with uninhibited healing. Interestingly, we observed bone formation around degrading Mg, but not titanium, devices. These results highlighted the potential for these fixation devices. To better assess their efficacy, we conducted a more thorough study assessing 99.9% Mg devices in a similar rabbit ulna fracture model. Device degradation, fracture healing, and bone formation were evaluated using microcomputed tomography, histology and biomechanical tests. We observed device degradation throughout, and calculated a corrosion rate of 0.40 +/- 0.04 mm/year after 8 weeks. In addition, we observed fracture healing by 8 weeks, and maturation after 16 weeks. In accordance with our pilot study, we observed bone formation surrounding Mg devices, with complete over-growth by 16 weeks. Bend tests revealed no difference in flexural load of healed ulnae with Mg devices compared to intact ulnae. These data suggest that Mg devices provide stabilization to facilitate healing, while degrading and stimulating new bone formation. (C) 2015 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:262 / 269
页数:8
相关论文
共 42 条
[11]   Surgeons' beliefs and perceptions about removal of orthopaedic implants [J].
Hanson, Beate ;
van der Werken, Chris ;
Stengel, Dirk .
BMC MUSCULOSKELETAL DISORDERS, 2008, 9 (1)
[12]   In vitro degradation and cytotoxicity response of Mg-4% Zn-0.5% Zr (ZK40) alloy as a potential biodegradable material [J].
Hong, Daeho ;
Saha, Partha ;
Chou, Da-Tren ;
Lee, Boeun ;
Collins, Boyce E. ;
Tan, Zongqing ;
Dong, Zhongyun ;
Kumta, Prashant N. .
ACTA BIOMATERIALIA, 2013, 9 (10) :8534-8547
[13]   Corrosion of metal orthopaedic implants [J].
Jacobs, JJ ;
Gilbert, JL ;
Urban, RM .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1998, 80A (02) :268-282
[14]   Magnesium hydroxide temporarily enhancing osteoblast activity and decreasing the osteoclast number in peri-implant bone remodelling [J].
Janning, C. ;
Willbold, E. ;
Vogt, C. ;
Nellesen, J. ;
Meyer-Lindenberg, A. ;
Windhagen, H. ;
Thorey, F. ;
Witte, F. .
ACTA BIOMATERIALIA, 2010, 6 (05) :1861-1868
[15]   Magnesium alloys for temporary implants in osteosynthesis: In vivo studies of their degradation and interaction with bone [J].
Kraus, Tanja ;
Fischerauer, Stefan F. ;
Haenzi, Anja C. ;
Uggowitzer, Peter J. ;
Loeffler, Joerg F. ;
Weinberg, Annelie M. .
ACTA BIOMATERIALIA, 2012, 8 (03) :1230-1238
[16]   Recombinant human bone morphogenetic protein-2 enhances osteotomy healing in glucocorticoid-treated rabbits [J].
Luppen, CA ;
Blake, CA ;
Ammirati, KM ;
Stevens, ML ;
Seeherman, HJ ;
Wozney, L ;
Bouxsein, ML .
JOURNAL OF BONE AND MINERAL RESEARCH, 2002, 17 (02) :301-310
[17]   The heating potential of the periosteum Molecular aspects [J].
Malizos, KN ;
Papatheodorou, LK .
INJURY-INTERNATIONAL JOURNAL OF THE CARE OF THE INJURED, 2005, 36 :13-19
[18]   In vivo models of bone repair [J].
Mills, L. A. ;
Simpson, A. H. R. W. .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 2012, 94B (07) :865-874
[19]   Bone-like matrix formation on magnesium and magnesium alloys [J].
Pietak, Alexis ;
Mahoney, Patricia ;
Dias, George J. ;
Staiger, Mark P. .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2008, 19 (01) :407-415
[20]   ACUTE TOXICITY OF METAL-IONS IN CULTURES OF OSTEOGENIC CELLS DERIVED FROM BONE-MARROW STROMAL CELLS [J].
PULEO, DA ;
HUH, WW .
JOURNAL OF APPLIED BIOMATERIALS, 1995, 6 (02) :109-116