Kienle Annette, Graf Nicolas, Krais Carina, Wilke Hans-Joachim
SpineServ GmbH & Co. KG, Ulm 89077, Germany.
Institute of Orthopaedic Research and Biomechanics, Ulm University Medical Centre, Ulm 89081, Germany.
Med Devices (Auckl). 2020 Sep 25;13:315-324. doi: 10.2147/MDER.S270789. eCollection 2020.
There are various cervical disc prostheses on the market today. They can be subdivided into implants with a ball-and-socket design and implants with a flexible core, which is captured between the implant endplates and sealed using various sheaths. Implants with an articulating surface are mostly metal-on-metal or metal-on-UHMWPE designs and, thus, do not allow for axial damping. The aim of this study is to provide mechanical safety and performance data of the MOVE-C cervical disc prosthesis which combines both an articulating surface and a flexible core.
MOVE-C consists of a cranial and caudal metal plate made of TiAl6V4. The cranial plate is TiNbN coated on its articulating surface. The caudal plate has a fixed polycarbonate-urethane (PCU) core. The TiNbN coating is meant to optimize the wear behavior of the titanium endplate, whereas the PCU core is meant to allow for a reversible axial deformation, a pre-defined neutral zone and a progressive load-deformation curve in all planes.
Various standard testing procedures (for example, ISO 18192-1 and ASTM F2364) and non-standard mechanical tests were carried out to prove the implant's mechanical safety. Due to the new implant design, wear and creep testing was deemed most important. The wear rate for the PCU was in maximum 1.54 mg per million cycles. This value was within the range of the UHMWPE wear rates reported for other cervical disc prostheses (0.53 to 2.59 mg/million cycles). Also in the creep-relaxation test, a qualitatively physiological behavior was shown with a certain amount of remaining deformation but no failure.
The mechanical safety of the MOVE-C cervical disc prosthesis was shown to be comparable to other cervical disc prostheses. Since PCU wear particles were elsewhere shown to be less bioactive than cross-linked UHMWPE particles, wear-related failure in vivo may be less frequent compared to other prostheses. This, however, will have to be shown in further studies.
如今市场上有多种颈椎间盘假体。它们可细分为球窝设计的植入物和具有柔性核心的植入物,柔性核心夹在植入物终板之间,并使用各种护套进行密封。具有关节表面的植入物大多是金属对金属或金属对超高分子量聚乙烯(UHMWPE)设计,因此不具备轴向阻尼功能。本研究的目的是提供兼具关节表面和柔性核心的MOVE-C颈椎间盘假体的机械安全性和性能数据。
MOVE-C由两块由TiAl6V4制成的颅骨和尾骨金属板组成。颅骨板在其关节表面涂有TiNbN涂层。尾骨板有一个固定的聚碳酸酯聚氨酯(PCU)核心。TiNbN涂层旨在优化钛终板的磨损行为,而PCU核心旨在允许可逆的轴向变形、预定义的中性区以及在所有平面上呈现渐进的载荷-变形曲线。
进行了各种标准测试程序(例如ISO 18192-1和ASTM F2364)以及非标准机械测试,以证明植入物的机械安全性。由于采用了新的植入物设计,磨损和蠕变测试被认为最为重要。PCU的磨损率最高为每百万次循环1.54毫克。该值在其他颈椎间盘假体报道的UHMWPE磨损率范围内(0.53至2.59毫克/百万次循环)。同样在蠕变松弛测试中,呈现出定性的生理行为,有一定量的残余变形但未失效。
MOVE-C颈椎间盘假体的机械安全性与其他颈椎间盘假体相当。由于其他地方已表明PCU磨损颗粒的生物活性低于交联UHMWPE颗粒,与其他假体相比,体内与磨损相关的失效可能不太频繁。然而,这还有待进一步研究证实。