From the Hansjörg Wyss Department of Plastic Surgery, New York University Grossman School of Medicine.
Departments of Mechanical and Aerospace Engineering.
Plast Reconstr Surg. 2023 Aug 1;152(2):270e-280e. doi: 10.1097/PRS.0000000000010258. Epub 2023 Feb 1.
Three-dimensional printed bioceramic scaffolds composed of 100% β-tricalcium phosphate augmented with dipyridamole (3DPBC-DIPY) can regenerate bone across critically sized defects in skeletally mature and immature animal models. Before human application, safe and effective bone formation should be demonstrated in a large translational animal model. This study evaluated the ability of 3DPBC-DIPY scaffolds to restore critically sized calvarial defects in a skeletally immature, growing minipig.
Unilateral calvarial defects (~1.4 cm) were created in 6-week-old Göttingen minipigs ( n = 12). Four defects were filled with a 1000 μm 3DPBC-DIPY scaffold with a cap (a solid barrier on the ectocortical side of the scaffold to prevent soft-tissue infiltration), four defects were filled with a 1000 μm 3DPBC-DIPY scaffold without a cap, and four defects served as negative controls (no scaffold). Animals were euthanized 12 weeks postoperatively. Calvariae were subjected to micro-computed tomography, 3D reconstruction with volumetric analysis, qualitative histologic analysis, and nanoindentation.
Scaffold-induced bone growth was statistically greater than in negative controls ( P ≤ 0.001), and the scaffolds with caps produced significantly more bone generation compared with the scaffolds without caps ( P ≤ 0.001). Histologic analysis revealed woven and lamellar bone with haversian canals throughout the regenerated bone. Cranial sutures were observed to be patent, and there was no evidence of ectopic bone formation or excess inflammatory response. Reduced elastic modulus and hardness of scaffold-regenerated bone were found to be statistically equivalent to native bone ( P = 0.148 for reduced elastic modulus of scaffolds with and without caps and P = 0.228 and P = 0.902 for hardness of scaffolds with and without caps, respectively).
3DPBC-DIPY scaffolds have the capacity to regenerate bone across critically sized calvarial defects in a skeletally immature translational pig model.
This study assessed the bone generative capacity of 3D-printed bioceramic scaffolds composed of 100% β-tricalcium phosphate and augmented with dipyridamole placed within critical-sized calvarial defects in a growing porcine model.
由 100%β-磷酸三钙组成的三维打印生物陶瓷支架,加入双嘧达莫(3DPBC-DIPY),可以在骨骼成熟和未成熟的动物模型中再生临界大小的骨缺损。在应用于人体之前,应该在大型转化动物模型中证明安全有效的骨形成。本研究评估了 3DPBC-DIPY 支架在骨骼未成熟的生长小型猪中修复临界大小颅骨缺损的能力。
在 6 周龄的哥廷根小型猪(n=12)中创建单侧颅骨缺损(约 1.4cm)。四个缺损填充 1000μm 的 3DPBC-DIPY 支架(支架外皮质侧有一个实心帽,以防止软组织渗透),四个缺损填充 1000μm 的 3DPBC-DIPY 支架无帽,四个缺损作为阴性对照(无支架)。术后 12 周处死动物。颅骨进行微计算机断层扫描、三维重建和体积分析、定性组织学分析和纳米压痕分析。
支架诱导的骨生长明显大于阴性对照组(P≤0.001),有帽支架比无帽支架产生的骨生成量显著增加(P≤0.001)。组织学分析显示,再生骨中存在编织骨和板层骨,并有哈弗斯管。观察到头骨缝是开放的,没有异位骨形成或过度炎症反应的证据。发现支架再生骨的弹性模量和硬度降低,与正常骨统计学等效(有帽和无帽支架的弹性模量降低分别为 P=0.148,有帽和无帽支架的硬度分别为 P=0.228 和 P=0.902)。
3DPBC-DIPY 支架在骨骼未成熟的转化猪模型中具有跨越临界大小颅骨缺损再生骨的能力。
本研究评估了由 100%β-磷酸三钙组成的 3D 打印生物陶瓷支架在生长型猪模型中,在临界大小颅骨缺损中放置加入双嘧达莫后对骨生成的能力。