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三维多孔盖拉平-辛伐他汀支架促进兔骨缺损愈合

Three-Dimensional Porous Gelapin-Simvastatin Scaffolds Promoted Bone Defect Healing in Rabbits.

作者信息

Moshiri Ali, Shahrezaee Mostafa, Shekarchi Babak, Oryan Ahmad, Azma Kamran

机构信息

Department of Orthopedic Surgery, School of Medicine, AJA University of Medical Science, Tehran, Iran.

出版信息

Calcif Tissue Int. 2015 Jun;96(6):552-64. doi: 10.1007/s00223-015-9981-9. Epub 2015 Mar 25.

Abstract

Treatment of large bone defects (LBDs) is technically demanding. Tissue engineering is an option. A bioactive graft may be produced by combining tissue scaffolds and healing promotive factors in order to accelerate bone repair. We investigated the role of Simvastatin (Sim)-embedded porous Gelapin (Gel) scaffold on experimental bone healing. At first, the effectiveness of different concentrations of Gel and Sim powders was investigated in an experimentally induced femoral hole model in rabbits (n = 6) for 30 days. Then bone bioactive grafts were produced by combination of the effective concentrations of Gel, Sim, and Genipin. The bioimplants were subcutaneously tested in a rabbit model (n = 9) to determine their biocompatibility and biodegradability for 10-30 days. Finally, a large radial bone defect model was produced in rabbits (n = 20), and the bioimplants were inserted in the defects. The untreated and autograft-treated bone defects were served as controls. The animals were euthanized after 30 and 60 days of bone injury. The bone samples were evaluated by radiography, three-dimensional CT scan, bone densitometry, histopathology, and nano-indentation. At a concentration of 5 mg/hole, Sim closed the femoral bone holes after 30 days, while in the defect, autograft, and Gel groups, the holes were open. Both the Gel and Gel-Sim scaffolds were biocompatible and biodegradable. Subcutaneously, the Gel-Sim scaffold was replaced with the newly regenerated ectopic bone after 30 days. After implantation of the Gel-Sim scaffold in the radial bone defects, the scaffold was completely replaced with new woven bone after 30 days which was then matured and remodeled into a cortical bone after 60 days. Sixty days after bone injury, the Gel-Sim-treated defects had significantly higher bone volume, matrix mineralization, elastic modulus, and contact hardness when compared to the controls. The Gel-Sim scaffold may be a suitable option in managing LBDs.

摘要

大型骨缺损(LBDs)的治疗在技术上具有挑战性。组织工程是一种选择。通过将组织支架和愈合促进因子相结合,可以制备生物活性移植物,以加速骨修复。我们研究了载有辛伐他汀(Sim)的多孔吉拉汀(Gel)支架在实验性骨愈合中的作用。首先,在兔实验性诱导股骨孔模型(n = 6)中研究了不同浓度的Gel和Sim粉末30天的有效性。然后,将有效浓度的Gel、Sim和京尼平组合制备骨生物活性移植物。在兔模型(n = 9)中对生物植入物进行皮下测试,以确定其10 - 30天的生物相容性和生物降解性。最后,在兔(n = 20)中制备大型桡骨骨缺损模型,并将生物植入物插入缺损处。未治疗和自体移植治疗的骨缺损作为对照。在骨损伤30天和60天后对动物实施安乐死。通过放射照相、三维CT扫描、骨密度测定、组织病理学和纳米压痕对骨样本进行评估。在浓度为5 mg/孔时,Sim在30天后封闭了股骨骨孔,而在缺损、自体移植和Gel组中,骨孔仍然开放。Gel和Gel - Sim支架均具有生物相容性和生物降解性。皮下注射后,30天后Gel - Sim支架被新再生的异位骨替代。在桡骨骨缺损中植入Gel - Sim支架后,30天后支架完全被新的编织骨替代,60天后新骨成熟并重塑为皮质骨。骨损伤60天后,与对照组相比,Gel - Sim治疗的缺损具有显著更高的骨体积、基质矿化、弹性模量和接触硬度。Gel - Sim支架可能是治疗大型骨缺损的合适选择。

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