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氨甲环酸基屏障膜引导骨再生在桡骨缺损模型中的应用。

Guided Bone Regeneration with Ammoniomethacrylate-Based Barrier Membranes in a Radial Defect Model.

机构信息

Department of Pharmaceutics, Institute for Drug Research, School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, 91120, Israel.

Goldyne Savad Institute of Gene Therapy, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel.

出版信息

Biomed Res Int. 2020 Oct 13;2020:5905740. doi: 10.1155/2020/5905740. eCollection 2020.

Abstract

Large bone defects pose an unsolved challenge for orthopedic surgeons. Our group has previously reported the construction of a barrier membrane made of ammoniomethacrylate copolymer USP (AMCA), which supports the adhesion, proliferation, and osteoblastic differentiation of human mesenchymal stem cells (hMSCs). In this study, we report the use of AMCA membranes to seclude critical segmental defect (~1.0 cm) created in the middle third of rabbit radius and test the efficiency of bone regeneration. Bone regeneration was assessed by radiography, biweekly for 8 weeks. The results were verified by histology and micro-CT at the end of the follow-up. The AMCA membranes were found superior to no treatment in terms of new bone formation in the defect, bone volume, callus surface area normalized to total volume, and the number of bone trabeculae, after eight weeks. Additional factors were then assessed, and these included the addition of simvastatin to the membrane, coating the membrane with human MSC, and a combination of those. The addition of simvastatin to the membranes demonstrated a stronger effect at a similar radiological follow-up. We conclude that AMCA barrier membranes and simvastatin delivered in a controlled manner improve bone regeneration outcome.

摘要

大骨缺损给矫形外科医生带来了一个尚未解决的挑战。我们的团队之前曾报道过一种由氨甲基丙烯酸酯共聚物 USP(AMCA)制成的屏障膜的构建,该膜支持人间充质干细胞(hMSCs)的黏附、增殖和成骨细胞分化。在这项研究中,我们报告了使用 AMCA 膜来隔离在兔桡骨中段造成的临界节段性缺损(约 1.0cm),并测试骨再生的效率。通过 X 射线每周两次进行 8 周的骨再生评估。在随访结束时,通过组织学和 micro-CT 进行验证。结果发现,在 8 周后,与无治疗相比,AMCA 膜在缺损处的新骨形成、骨体积、骨痂表面积与总体积的比值以及骨小梁数量方面更具优势。然后评估了其他因素,包括将辛伐他汀添加到膜中、将膜与人 MSC 涂层以及将两者结合。在类似的影像学随访中,发现将辛伐他汀添加到膜中具有更强的效果。我们得出结论,AMCA 屏障膜和以受控方式递送的辛伐他汀可改善骨再生效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/661c/7603551/7460e0572f2b/BMRI2020-5905740.sch.001.jpg

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