Revascularization study of the hollow hydroxyapatite composite rhBMP-2 in repairing the bone defect

  • LUO Feng-Gang ,
  • XIONG Long ,
  • CENG Jian-Hua ,
  • XIONG Gao ,
  • TUN Ceng-Zhi ,
  • LING Hua-Jun ,
  • JIA Xiong-Chao
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  • 1.Second Department of Orthopaedics,GaoMing People’s Hospital Affiliated to Guangdong Medical College,Foshan 528500,China; 2.Department of Orthopaedics, Jiangxi Province People’s Hospital, Nanchang 330006, China

Received date: 2013-10-28

  Online published: 2014-04-21

Abstract

Objective To study and observe the revascularization process of the hollow hydroxyapatite composite rhBMP-2 in repairing the bone defect. Methods 48 adult male New Zealand rabbits with artificially-established radius defect were randomly divided into 3 groups, each group were implanted with the following materials: hollow HA/ rhBMP-2 composite artificial bone(A groups), hollow HA(B groups),rhBMP-2(C groups). After implantation in 4、8、12、16 weeks, the process was  observed using radionuclide bone imaging, X ray, histological observation. Results Different time after the operation, X-ray and histological score, bone radionuclide-gathering strength of the rabbits in the hollow HA/ rhBMP-2 composite artificial bone group in the were higher than that of hollow HA artificial bone (P<0.05). In the control group, synostosis and bone sclerosis were observed in bone defect area bone defect failed to heal. Conclusion Hollow HA/ rhBMP-2 composite artificial bone has good ability in revascularization and repairing segmental bone defect and is expected to be an ideal material for bone defect repair.  

Cite this article

LUO Feng-Gang , XIONG Long , CENG Jian-Hua , XIONG Gao , TUN Ceng-Zhi , LING Hua-Jun , JIA Xiong-Chao . Revascularization study of the hollow hydroxyapatite composite rhBMP-2 in repairing the bone defect[J]. Chinese Journal of Clinical Anatomy, 2014 , 32(2) : 196 -200 . DOI: 10.13418/j.issn.1001-165x.2014

References


[1]  易诚青, 姚爱华, 马春辉, 等. 装载趋化因子CXCLl3的中空羟基磷灰石微球对间充质干细胞的趋化效应研究
[J].上海交通大学学报(医学版), 2012, 32(12):1532-1535.

[2]  姚爱华, 徐为, 艾凡荣, 等 .中空羟基磷灰石微球作为 rhBMP-2 缓释载体的研究
[J]. 无机材料学报, 2011, 26(9):975-978.

[3]  江捍平, 王大平, 朱伟民, 等. 放射性核素骨显像在骨缺损修复实验中的研究
[J]. 中国临床解剖学杂志, 2006, 24(4): 437-440.

[4]  Lane JM, Sandhu HS. Current approaches to experimental bone grafting
[J]. Orthop Clin North Am, 1987,18(2):213-225.

[5] Rohanizadeh R, Chung K. Hydroxyapatite as a Carrier for Bone Morphogenetic Protein
[J]. J Oral Implantol, 2011, 37(6):659-672.

[6]  Xie G, Sun J, Zhong G, et al. Hydroxyapatite nanoparticles as a controlled-release carrier of BMP-2: absorption and release kinetics in vitro
[J]. J Mater Sci Mater Med, 2010, 21(6):1875-1880.

[7]  Kim M, Choe S. BMPs and their clinical potentials
[J]. BMB Rep,  2011,44(10): 619-634.

[8]  Gottfried On, Dailey AT. Mesenchayma stem cell and gene therapies for spinal fusion
[J]. Neurosurgery, 2008, 63(3):380-391.

[9]  Fu H, Rahaman MN, Day DE,et al.Hollow hydroxyapatite microspheres as a device for controlled delivery of proteins
[J]. J Mater Sci Mater Med, 2011, 22(3): 579-591.

[10]Gross TP, Cox QG, Jinnah RH. History and current application of bone transplantation
[J]. Orthopedics, 1993,16(8):895-900.

[11]赵俊华, 孟纯阳, 蒋电明, 等. 纳米羟基磷灰石/聚酰胺66/成骨细胞/血管内皮生长因子165组织工程骨修复骨缺损再血管化与成骨活性
[J]. 中华创伤杂志, 2011,27(9):852-857.

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