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用于评估无需自体移植物即可治疗临界骨缺损的合成植入物的临床前诱导膜模型。

Preclinical induced membrane model to evaluate synthetic implants for healing critical bone defects without autograft.

机构信息

Departiment of Orthopaedic Surgery, Stanford University, Stanford, California.

Departiment of Chemistry, Stanford University, Stanford, California.

出版信息

J Orthop Res. 2019 Jan;37(1):60-68. doi: 10.1002/jor.24153. Epub 2018 Oct 29.

Abstract

Critical bone defects pose a formidable orthopaedic problem in patients with bone loss. We developed a preclinical model based on the induced membrane technique using a synthetic graft to replace autograft for healing critical bone defects. Additionally, we used a novel osteoconductive scaffold coupled with a synthetic membrane to evaluate the potential for single-stage bone regeneration. Three experimental conditions were investigated in critical femoral defects in rats. Group A underwent a two-stage procedure with insertion of a polymethylmethacrylate (PMMA) spacer followed by replacement with a 3D printed polycaprolactone(PCL)/β-tricalcium phosphate (β-TCP) osteoconductive scaffold after 4 weeks. Group B received a single-stage PCL/β-TCP scaffold wrapped in a PCL-based microporous polymer film creating a synthetic membrane. Group C received a single-stage bare PCL/β-TCP scaffold. All groups were examined by serial radiographs for callus formation. After 12 weeks, the femurs were explanted and analyzed with micro-CT and histology. Mean callus scores tended to be higher in Group A. Group A showed statistically significant greater bone formation on micro-CT compared with other groups, although bone volume fraction was similar between groups. Histology results suggested extensive bone ingrowth and new bone formation within the macroporous scaffolds in all groups and cell infiltration into the microporous synthetic membrane. This study supports the use of a critical size femoral defect in rats as a suitable model for investigating modifications to the induced membrane technique without autograft harvest. Future investigations should focus on bioactive synthetic membranes coupled with growth factors for single-stage bone healing. © 2018 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res.

摘要

在患有骨质流失的患者中,临界骨缺损构成了一个严峻的骨科问题。我们开发了一种基于诱导膜技术的临床前模型,使用合成移植物代替自体移植物来治疗临界骨缺损。此外,我们使用了一种新型的骨传导支架,结合合成膜,评估了单阶段骨再生的潜力。在大鼠的临界股骨缺损中研究了三种实验条件。A 组接受两阶段手术,先插入聚甲基丙烯酸甲酯(PMMA)间隔物,4 周后再更换 3D 打印的聚己内酯(PCL)/β-磷酸三钙(β-TCP)骨传导支架。B 组接受包裹在聚己内酯基微孔聚合物膜中的单阶段 PCL/β-TCP 支架,形成合成膜。C 组接受单阶段裸 PCL/β-TCP 支架。所有组均通过连续射线照相术检查骨痂形成情况。12 周后,取出股骨并进行微 CT 和组织学分析。平均骨痂评分在 A 组中趋于更高。与其他组相比,A 组的微 CT 显示出统计学上显著更高的骨形成,尽管各组的骨体积分数相似。组织学结果表明,所有组的大孔支架内均有广泛的骨内生长和新骨形成,并且微孔合成膜内有细胞浸润。这项研究支持在大鼠中使用临界尺寸股骨缺损作为研究诱导膜技术改良而无需自体移植物采集的合适模型。未来的研究应集中在具有生长因子的生物活性合成膜上,以实现单阶段骨愈合。

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