Literature DB >> 17013740

Accelerated repair of a bone defect with a synthetic biodegradable bone-inducing implant.

Naofumi Matsushita1, Hidetomi Terai, Takao Okada, Kazutoshi Nozaki, Hikaru Inoue, Shimpei Miyamoto, Kunio Takaoka.   

Abstract

BACKGROUND: Nothing has ever had osteoinductive capacity and degradability equivalent to that of autogenous bone, although many types of biomaterials have been developed. To address this issue, we constructed a new bone graft substitute with osteogenic potential and degradability by using porous beta-tricalcium phosphate (beta-TCP) granules, bone morphogenetic protein (BMP), and a synthetic block copolymer composed of poly-D: ,L: -lactic acid with randomly inserted p-dioxanone and polyethylene glycol (PLA-DX-PEG). In this experimental study, the bone-inducing capacity and degradation properties of the composite implant during the bone healing process were examined in vivo in a cortical and cancellous bone defect model in rabbits.
METHODS: The advantages of this type of implant have been examined in a cortical bone defect model created in the distal femur of rabbits. The defects (6.5 x 5 mm) were filled with 30 mg of various implants: BMP-H [rhBMP-2, 0.0025% (w/w)], BMP-L [rhBMP-2, 0.000625% (w/w)], control A (beta-TCP alone), and control B (no implant). The distal femurs were harvested at scheduled intervals after surgery and examined for the evaluation of the bony repair of the defects by three-dimensional computed tomography and histology.
RESULTS: The repair of both cortical and cancellous bone occurred predominantly in the BMP-H group, and only minor cortical bone repair and cancellous bone formation were noted in the BMP-L and control A groups. Most of the beta-TCP was resorbed in the BMP-H group at 6 weeks after surgery, whereas a significant amount of beta-TCP remained in the BMP-L and control A groups.
CONCLUSIONS: beta-TCP granules coated with a BMP-retaining synthetic polymer appear to be effective in enhancing the repair of both cancellous and cortical bone defects. The early disappearance of the implanted beta-TCP and restoration of the normal anatomy of bone tissue are two notable features of this approach.

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Year:  2006        PMID: 17013740     DOI: 10.1007/s00776-006-1048-3

Source DB:  PubMed          Journal:  J Orthop Sci        ISSN: 0949-2658            Impact factor:   1.601


  6 in total

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2.  Enhancement of bone formation with a synthetic matrix containing bone morphogenetic protein-2 by the addition of calcium citrate.

Authors:  Wei Wang; Qingyu Chen; Xiucui Li; Wei Zhang; Lei Peng; Liming Wang; Zhongqin Lin; Huazi Xu; Shifeng Song; Xiaolei Zhang; Shaowen Cheng; Dongquan Kou; Chuanzhu Lv; Ziming Yu
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3.  Protein conformation changes on block copolymer surfaces detected by antibody-functionalized atomic force microscope tips.

Authors:  Manuel L B Palacio; Scott R Schricker; Bharat Bhushan
Journal:  J Biomed Mater Res A       Date:  2011-10-04       Impact factor: 4.396

4.  Polycaprolactone coated porous tricalcium phosphate scaffolds for controlled release of protein for tissue engineering.

Authors:  Weichang Xue; Amit Bandyopadhyay; Susmita Bose
Journal:  J Biomed Mater Res B Appl Biomater       Date:  2009-11       Impact factor: 3.368

5.  Evaluation of a biodegradable graft substitute in rabbit bone defect model.

Authors:  Xiaobo Yang; Yong Li; Qiang Huang; Jing Yang; Bing Shen; Fuxing Pei
Journal:  Indian J Orthop       Date:  2012-05       Impact factor: 1.251

Review 6.  Bone Regeneration Using Bone Morphogenetic Proteins and Various Biomaterial Carriers.

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  6 in total

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