Alejo Andrew L, McDermott Scott, Khalil Yusuf, Ball Hope C, Robinson Gabrielle T, Solorzano Ernesto, Alejo Amanda M, Douglas Jacob, Samson Trinity K, Young Jesse W, Safadi Fayez F
College of Medicine, Northeast Ohio Medical University (NEOMED), Rootstown, OH, USA.
Musculoskeletal Research Group, NEOMED, Rootstown, OH, USA.
J Orthop Sports Med. 2022;4(3):224-240. doi: 10.26502/josm.511500060. Epub 2022 Sep 5.
The rat animal model is a cost effective and reliable model used in spinal pre-clinical research. Complications from various surgical procedures in humans often arise that were based on these pre-clinical animal models. Therefore safe and efficacious pre-clinical animal models are needed to establish continuity into clinical trials. A Standard Operating Procedure (SOP) is a validated method that allows researchers to safely and carefully replicate previously successful surgical techniques. Thus, the aim of this study is to describe in detail the procedures involved in a common rat bilateral posterolateral intertransverse spinal fusion SOP used to test the efficacy and safety different orthobiologics using a collagen-soaked sponge as an orthobiologic carrier. Only two orthobiologics are currently FDA approved for spinal fusion surgery which include recombinant bone morphogenetic protein 2 (rhBMP-2), and I-FACTOR. While there are many additional orthobiologics currently being tested, one way to show their safety profile and gain FDA approval, is to use well established pre-clinical animal models. A preoperative, intraoperative, and postoperative surgical setup including specific anesthesia and euthanasia protocols are outlined. Furthermore, we describe different postoperative methods used to validate the spinal fusion SOP, which include CT analysis, histopathology, biomechanical testing, and blood analysis. This SOP can help increase validity, transparency, efficacy, and reproducibly in future rat spinal fusion surgery procedures.
大鼠动物模型是一种用于脊柱临床前研究的经济高效且可靠的模型。基于这些临床前动物模型的人类各种外科手术常常会出现并发症。因此,需要安全有效的临床前动物模型来建立通向临床试验的连续性。标准操作规程(SOP)是一种经过验证的方法,它使研究人员能够安全、仔细地复制先前成功的手术技术。因此,本研究的目的是详细描述一种常见的大鼠双侧后外侧横突间脊柱融合SOP所涉及的程序,该SOP用于测试以胶原浸泡海绵作为骨科生物制剂载体的不同骨科生物制剂的疗效和安全性。目前美国食品药品监督管理局(FDA)仅批准了两种用于脊柱融合手术的骨科生物制剂,即重组骨形态发生蛋白2(rhBMP - 2)和I - FACTOR。虽然目前还有许多其他骨科生物制剂正在进行测试,但展示它们的安全性并获得FDA批准的一种方法是使用成熟的临床前动物模型。本文概述了术前、术中和术后的手术设置,包括特定的麻醉和安乐死方案。此外,我们描述了用于验证脊柱融合SOP的不同术后方法,包括CT分析、组织病理学、生物力学测试和血液分析。该SOP有助于提高未来大鼠脊柱融合手术程序的有效性、透明度、疗效和可重复性。