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本文引用的文献

1
Improved healing of large segmental defects in the rat femur by reverse dynamization in the presence of bone morphogenetic protein-2.骨形态发生蛋白-2 存在时反向动化促进大鼠股骨大节段缺损的愈合。
J Bone Joint Surg Am. 2012 Nov 21;94(22):2063-73. doi: 10.2106/JBJS.K.01604.
2
Design, characterisation and in vivo testing of a new, adjustable stiffness, external fixator for the rat femur.新型大鼠股骨可调刚度外固定器的设计、特性描述及体内试验
Eur Cell Mater. 2012 Apr 21;23:289-98; discussion 299. doi: 10.22203/ecm.v023a22.
3
Ability of recombinant human bone morphogenetic protein 2 to enhance bone healing in the presence of tobramycin: evaluation in a rat segmental defect model.重组人骨形态发生蛋白 2 在妥布霉素存在的情况下增强骨愈合的能力:在大鼠节段性缺损模型中的评估。
J Orthop Trauma. 2009 Nov-Dec;23(10):693-701. doi: 10.1097/BOT.0b013e3181b01b2f.
4
Mechanical characterization of external fixator stiffness for a rat femoral fracture model.大鼠股骨骨折模型中外固定器刚度的力学特性研究
J Orthop Res. 2009 May;27(5):687-93. doi: 10.1002/jor.20792.
5
Microcomputed tomography imaging in a rat model of delayed union/non-union fracture.大鼠骨折延迟愈合/不愈合模型中的微型计算机断层扫描成像
J Orthop Res. 2008 May;26(5):729-36. doi: 10.1002/jor.20540.
6
An easily reproducible and biomechanically standardized model to investigate bone healing in rats, using external fixation.一种易于复制且生物力学标准化的模型,用于通过外固定研究大鼠的骨愈合。
Biomed Tech (Berl). 2007 Dec;52(6):383-90. doi: 10.1515/BMT.2007.063.
7
Effect of osteoporosis on bone mineral density and fracture repair in a rat femoral fracture model.骨质疏松对大鼠股骨骨折模型骨密度及骨折修复的影响
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Healing of segmental bone defects by direct percutaneous gene delivery: effect of vector dose.经皮直接基因递送修复节段性骨缺损:载体剂量的影响
Hum Gene Ther. 2007 Oct;18(10):907-15. doi: 10.1089/hum.2007.077.
9
Direct percutaneous gene delivery to enhance healing of segmental bone defects.直接经皮基因递送以促进节段性骨缺损的愈合。
J Bone Joint Surg Am. 2006 Feb;88(2):355-65. doi: 10.2106/JBJS.E.00464.
10
Torsional stiffness in healing fractures: influence of ossification: an experimental study in rats.愈合骨折中的扭转刚度:骨化的影响:一项大鼠实验研究
Acta Orthop. 2005 Jun;76(3):428-33.

用于大鼠股骨截骨术和节段性骨缺损模型的可调刚度外固定器。

Adjustable stiffness, external fixator for the rat femur osteotomy and segmental bone defect models.

作者信息

Glatt Vaida, Matthys Romano

机构信息

Institute of Health and Biomedical Innovation, Queensland University of Technology;

RISystem AG.

出版信息

J Vis Exp. 2014 Oct 9(92):e51558. doi: 10.3791/51558.

DOI:10.3791/51558
PMID:25350129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4841304/
Abstract

The mechanical environment around the healing of broken bone is very important as it determines the way the fracture will heal. Over the past decade there has been great clinical interest in improving bone healing by altering the mechanical environment through the fixation stability around the lesion. One constraint of preclinical animal research in this area is the lack of experimental control over the local mechanical environment within a large segmental defect as well as osteotomies as they heal. In this paper we report on the design and use of an external fixator to study the healing of large segmental bone defects or osteotomies. This device not only allows for controlled axial stiffness on the bone lesion as it heals, but it also enables the change of stiffness during the healing process in vivo. The conducted experiments have shown that the fixators were able to maintain a 5 mm femoral defect gap in rats in vivo during unrestricted cage activity for at least 8 weeks. Likewise, we observed no distortion or infections, including pin infections during the entire healing period. These results demonstrate that our newly developed external fixator was able to achieve reproducible and standardized stabilization, and the alteration of the mechanical environment of in vivo rat large bone defects and various size osteotomies. This confirms that the external fixation device is well suited for preclinical research investigations using a rat model in the field of bone regeneration and repair.

摘要

骨折愈合周围的力学环境非常重要,因为它决定了骨折的愈合方式。在过去十年中,通过改变损伤周围的固定稳定性来改变力学环境以促进骨愈合,引起了临床的极大兴趣。该领域临床前动物研究的一个限制是,在大段骨缺损以及截骨愈合过程中,缺乏对局部力学环境的实验控制。在本文中,我们报告了一种用于研究大段骨缺损或截骨愈合的外固定器的设计和使用。该装置不仅在骨损伤愈合时能够控制轴向刚度,还能在体内愈合过程中改变刚度。进行的实验表明,在大鼠 unrestricted cage activity 期间,该固定器能够在体内维持至少 8 周的 5 毫米股骨缺损间隙。同样,在整个愈合期,我们未观察到变形或感染,包括针道感染。这些结果表明,我们新开发的外固定器能够实现可重复和标准化的稳定,并改变体内大鼠大骨缺损和不同尺寸截骨的力学环境。这证实了该外固定装置非常适合在骨再生和修复领域使用大鼠模型进行临床前研究调查。