Evaluation of Bone Regeneration of Simvastatin Loaded Chitosan Nanofiber Membranes in Rodent Calvarial Defects

Najib Ghadri, K. M. Anderson, Pradeep Adatrow, S. Stein, H. Su, F. García-Godoy, A. Karydis, J. Bumgardner
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引用次数: 20

Abstract

Chitosan nanofiber membranes have been known to have a high degree of biocompatibility and support new bone formation with controllable biodegradation. The surface area of these membranes may allow them to serve as local delivery carriers for different biologic mediators. Simvastatin, a drug commonly used for lowering cholesterol, has demonstrated promising bone regenerative capability. The aim of this study was to evaluate simvastatin loaded chitosan nanofiber membranes for guided bone regeneration (GBR) applications and their ability to enhance bone formation in rat calvarial defects. Nanofibrous chitosan membranes with random fiber orientation were fabricated by electrospinning technique and loaded with 0.25 mg of simvastatin under sterile conditions. One membrane was implanted subperiosteally to cover an 8 mm diameter critical size calvarial defect. Two groups: 1) Control: non-loaded chitosan membranes; 2) Experimental: chitosan membranes loaded with 0.25 mg of simvastatin were evaluated histologically and via micro-computed tomography (micro-CT) for bone formation at 4 and 8 weeks time points (n = 5/group per time point). Both groups exhibited good biocompatibility with only mild or moderate inflammatory response during the healing process. Histologic and micro-CT evaluations confirmed bone formation in calvarial defects as early as 4 weeks using control and experimental membranes. In addition, newly-formed bony bridges consolidating calvarial defects histologically along with partial radiographic defect coverage were observed at 8 weeks in both groups. Although control and experimental groups demonstrated no significant statistical differences in results of bone formation, biodegradable chitosan nanofiber membranes loaded with simvastatin showed a promising regenerative potential as a barrier material for guided bone regeneration applications.
辛伐他汀负载壳聚糖纳米纤维膜修复鼠脑颅骨缺损骨再生的研究
壳聚糖纳米纤维膜具有高度的生物相容性,支持新骨形成,生物降解可控。这些膜的表面积可能允许它们作为不同生物介质的局部递送载体。辛伐他汀,一种通常用于降低胆固醇的药物,已被证明具有良好的骨再生能力。本研究的目的是评估辛伐他汀负载壳聚糖纳米纤维膜在引导骨再生(GBR)中的应用及其促进大鼠颅骨缺损骨形成的能力。在无菌条件下,采用静电纺丝技术制备了具有随机纤维取向的壳聚糖纳米纤维膜,并负载0.25 mg辛伐他汀。在骨膜下植入一层膜以覆盖直径8毫米的临界尺寸颅骨缺损。两组:1)对照组:无负载壳聚糖膜;2)实验:在4周和8周时间点(每个时间点n = 5/组),通过组织学和显微计算机断层扫描(micro-CT)评估负载0.25 mg辛伐他汀的壳聚糖膜对骨形成的影响。两组均表现出良好的生物相容性,在愈合过程中仅出现轻度或中度炎症反应。使用对照膜和实验膜,组织学和显微ct评估证实早在4周颅骨缺损骨形成。此外,在8周时,两组均观察到新形成的骨桥在组织学上巩固颅骨缺损,同时影像学上缺损部分覆盖。尽管对照组和实验组在骨形成结果上没有显着的统计学差异,但负载辛伐他汀的可生物降解壳聚糖纳米纤维膜作为引导骨再生的屏障材料显示出有希望的再生潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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