首页> 外文学位 >Etude de l'implant chitosane glycerol-phosphate/sang avec/sans facteurs de coagulation sur la reparation du cartilage articulaire et de l'os sous-chondral.
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Etude de l'implant chitosane glycerol-phosphate/sang avec/sans facteurs de coagulation sur la reparation du cartilage articulaire et de l'os sous-chondral.

机译:含/不含凝血因子的磷酸甘油/血液壳聚糖植入物对关节软骨和软骨下骨修复的研究。

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摘要

The first part of this study investigated the solidification mechanisms of chitosan-GP/blood implant in vitro with and without added clotting factors, and investigated different methods for adding the factors into the implants in an in vivo cartilage repair model. Using thromboelastography, in vitro studies found that chitosan-GP/blood implants solidify through coagulation mechanisms which lead to a dual fibrin-polysaccharide clot scaffold that resists enzymatic lysis and is physically more stable than normal blood clots. Clotting factors, especially thrombin and the combo rhFVIIa + TF, significantly reduced in vitro and in vivo clotting times of the implants, which demonstrated the potential of clotting factors for enhancing the practical clinical use, the implant residency, and the therapeutic activity of chitosan-GP/blood implants for repairing cartilage.;Finally, the long-term (6.5 months) cartilage and bone repair of microdrilled defects treated with chitosan-GP/blood implants with thrombin was investigated in bilateral, full-thickness, trochlear defects in skeletally mature rabbit knees. This study showed that thrombin-solidified implants enhanced cartilage repair tissue integration, promoted a higher structural integrity, elicited a more hyaline-like tissue and promoted a more complete bone repair of the drill holes, compared to defects treated by microdrilling and thrombin-alone. Microdrill hole diameter had no specific effect on cartilage repair. The subchondral bone plate was regenerated in all defects, but it was significantly more porous and incompletely mineralized compared to intact knees. All repaired defects showed subchondral bone plate thickening outside the defect area. Bone below control defect bone contained more residual drill holes and thicker trabeculae. Low osteoclast numbers suggested that bone was no longer remodeling at 6.5 months post-drilling. In summary, thrombin-solidified chitosan-GP/blood implants generated a more hyaline and structurally integrated osteochondral unit, features needed for long-term durability. Furthermore, we observed that debridement and drilling can also lead to long-term subchondral bone changes outside a cartilage defect.;The innovation of this research project lies in the original idea of adding blood clotting factors to the hybrid implant to accelerate its solidification and reduce surgical waiting time. The improved clinical ease-of-use through better control of the in situ solidification further supports the concept of a liquid implant for cartilage repair, as it can easily adapt itself to most osteochondral defect shapes, which is a considerable advantage with regards to other pre-formed implants. Furthermore, the initial liquid state of the implant allows it to be delivered by arthroscopy, a minimally invasive surgical procedure compared to an arthrotomy. The completion of this thesis project contributed not only to the technological development of a chitosan-GP/blood implant with clotting factors but in several other ways to the advancement of knowledge within the field of biomedical engineering. (Abstract shortened by UMI.);In the second part of this study, micro-computed tomography (micro-CT) was used to characterize the subchondral bone structure of intact trochlea and acute, microdrilled, trochlear defects. As current methods were lacking to analyze three-dimensional (3D) volumes of interest (VOI) in bone with curved articular bone surfaces, 2 novel VOI models with adapted surfaces were developed. These VOIs were shown to be better than previously used simple geometric VOI shapes for quantifying structural features of subchondral bone below a curved articular surface because simple geometric shapes failed to include 17% of subchondral bone structure. Depthdependent bone structural differences were best captured when using a smaller 250 mum deep "curved-rectangular adapted surface" (C-RAS) VOI model than a 1 mm deep "rectangular adapted surface" (RAS) VOI model.
机译:本研究的第一部分研究了在有或没有添加凝血因子的条件下,壳聚糖-GP /血液植入物的体外固化机制,并研究了在体内软骨修复模型中将这些因素添加到植入物中的不同方法。使用血栓弹力图,体外研究发现,壳聚糖-GP /血液植入物通过凝血机制固化,这导致了双纤维蛋白-多糖凝块支架能够抵抗酶解,并且在物理上比正常的血凝块更稳定。凝血因子,尤其是凝血酶和组合的rhFVIIa + TF,显着减少了植入物的体外和体内凝血时间,这表明了凝血因子具有增强临床实际应用,植入物驻留性以及壳聚糖-壳聚糖的治疗活性的潜力。 GP /血液植入物修复软骨。最后,研究了用壳聚糖-GP /凝血酶处理的微钻孔缺损的长期(6.5个月)软骨和骨修复,研究了骨骼成熟的双侧,全层,滑车缺损兔子的膝盖。这项研究表明,与仅通过微钻孔和单独使用凝血酶治疗的缺陷相比,凝血酶固化的植入物增强了软骨修复组织的整合,促进了更高的结构完整性,引发了更透明的组织,并促进了钻孔的更彻底的骨修复。微孔直径对软骨修复没有特殊影响。软骨下骨板在所有缺损中均得以再生,但与完整的膝盖相比,它的多孔性和矿化程度均不明显。所有修复的缺损均在缺损区域外显示软骨下骨板增厚。对照缺损骨下方的骨包含更多的残留钻孔和较厚的小梁。低的破骨细胞数量表明,钻孔后6.5个月骨骼不再重塑。总之,凝血酶固化的壳聚糖-GP /血液植入物产生了更多的透明质酸和结构整合的骨软骨单元,这是长期耐用性所必需的。此外,我们观察到清创术和钻孔术还可导致软骨缺损以外的长期软骨下骨改变。;本研究项目的创新之处在于最初的想法是向杂交植入物添加凝血因子以加速其凝固并减少手术等待时间。通过更好地控制原位凝固,改善的临床易用性进一步支持了用于软骨修复的液体植入物的概念,因为它可以轻松地适应大多数骨软骨缺损的形状,相对于其他前体而言,这是一个相当大的优势形成的植入物。此外,植入物的初始液体状态允许通过关节镜检查将其植入,这是与关节切开术相比微创的外科手术。该论文项目的完成,不仅促进了具有凝血因子的壳聚糖-GP /血液植入物的技术发展,而且还以其他几种方式促进了生物医学工程领域知识的发展。 (本文由UMI缩短。);在本研究的第二部分中,使用微型计算机断层扫描(micro-CT)来表征完整小车的软骨下骨结构以及急性,微钻孔的小车的股骨缺损。由于当前的方法缺乏分析具有弯曲关节骨表面的骨骼中感兴趣的三维(3D)体积(VOI)的能力,因此开发了2种具有适应性表面的新型VOI模型。这些VOI表现出比以前使用的简单几何VOI形状更好的量化弯曲关节表面下方的软骨下骨的结构特征,因为简单的几何形状无法包括17%的软骨下骨结构。当使用比1毫米深的“矩形适应表面”(RAS)VOI模型小的250毫米深的“弯曲矩形适应表面”(C-RAS)VOI模型时,可以最好地捕获深度依赖性的骨结构差异。

著录项

  • 作者

    Marchand, Catherine.;

  • 作者单位

    Ecole Polytechnique, Montreal (Canada).;

  • 授予单位 Ecole Polytechnique, Montreal (Canada).;
  • 学科 Engineering Biomedical.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 188 p.
  • 总页数 188
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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