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J Mater Chem B. 2017 Jun 14;5(22):4198-4206. doi: 10.1039/c7tb00657h. Epub 2017 May 11.
2
Ex vivo replication of phenotypic functions of osteocytes through biomimetic 3D bone tissue construction.通过仿生 3D 骨组织构建实现破骨细胞表型功能的体外复制。
Bone. 2018 Jan;106:148-155. doi: 10.1016/j.bone.2017.10.019. Epub 2017 Oct 21.
3
Oxidatively Degradable Poly(thioketal urethane)/Ceramic Composite Bone Cements with Bone-Like Strength.具有类骨强度的可氧化降解聚(硫缩酮聚氨酯)/陶瓷复合骨水泥
RSC Adv. 2016;6(111):109414-109424. doi: 10.1039/c6ra24642g. Epub 2016 Nov 8.
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Bonekey Rep. 2016 Aug 24;5:829. doi: 10.1038/bonekey.2016.60. eCollection 2016.
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Substrate Modulus Regulates Osteogenic Differentiation of Rat Mesenchymal Stem Cells through Integrin β1 and BMP Receptor Type IA.底物模量通过整合素β1和IA型骨形态发生蛋白受体调节大鼠间充质干细胞的成骨分化。
J Mater Chem B. 2016 May 28;4(20):3584-3593. doi: 10.1039/C5TB02747K. Epub 2016 Apr 1.
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Remodeling of injectable, low-viscosity polymer/ceramic bone grafts in a sheep femoral defect model.可注射低粘度聚合物/陶瓷骨移植物在绵羊股骨缺损模型中的重塑。
J Biomed Mater Res B Appl Biomater. 2017 Nov;105(8):2333-2343. doi: 10.1002/jbm.b.33767. Epub 2016 Aug 10.
7
In Vivo Bone Formation Within Engineered Hydroxyapatite Scaffolds in a Sheep Model.羊模型中工程化羟基磷灰石支架内的体内骨形成
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Establishment of a preclinical ovine screening model for the investigation of bone tissue engineering strategies in cancellous and cortical bone defects.建立用于研究松质骨和皮质骨缺损骨组织工程策略的临床前绵羊筛选模型。
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Effects of Recombinant Human Bone Morphogenetic Protein-2 Dose and Ceramic Composition on New Bone Formation and Space Maintenance in a Canine Mandibular Ridge Saddle Defect Model.重组人骨形态发生蛋白-2剂量和陶瓷成分对犬下颌牙槽嵴鞍形缺损模型新骨形成和空间维持的影响
Tissue Eng Part A. 2016 Mar;22(5-6):469-79. doi: 10.1089/ten.TEA.2015.0355. Epub 2016 Mar 14.
10
Compressive fatigue and fracture toughness behavior of injectable, settable bone cements.可注射、可固化骨水泥的压缩疲劳和断裂韧性行为
J Mech Behav Biomed Mater. 2015 Nov;51:345-55. doi: 10.1016/j.jmbbm.2015.07.027. Epub 2015 Aug 1.

可固定聚合物/陶瓷复合骨移植物稳定负重胫骨平台槽状缺损,并在羊模型中与宿主骨整合。

Settable polymer/ceramic composite bone grafts stabilize weight-bearing tibial plateau slot defects and integrate with host bone in an ovine model.

机构信息

Department of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, TN, 37235, USA.

Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37235, USA.

出版信息

Biomaterials. 2018 Oct;179:29-45. doi: 10.1016/j.biomaterials.2018.06.032. Epub 2018 Jun 26.

DOI:10.1016/j.biomaterials.2018.06.032
PMID:29960822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6065109/
Abstract

Bone fractures at weight-bearing sites are challenging to treat due to the difficulty in maintaining articular congruency. An ideal biomaterial for fracture repair near articulating joints sets rapidly after implantation, stabilizes the fracture with minimal rigid implants, stimulates new bone formation, and remodels at a rate that maintains osseous integrity. Consequently, the design of biomaterials that mechanically stabilize fractures while remodeling to form new bone is an unmet challenge in bone tissue engineering. In this study, we investigated remodeling of resorbable bone cements in a stringent model of mechanically loaded tibial plateau defects in sheep. Nanocrystalline hydroxyapatite-poly(ester urethane) (nHA-PEUR) hybrid polymers were augmented with either ceramic granules (85% β-tricalcium phosphate/15% hydroxyapatite, CG) or a blend of CG and bioactive glass (BG) particles to form a settable bone cement. The initial compressive strength and fatigue properties of the cements were comparable to those of non-resorbable poly(methyl methacrylate) bone cement. In animals that tolerated the initial few weeks of early weight-bearing, CG/nHA-PEUR cements mechanically stabilized the tibial plateau defects and remodeled to form new bone at 16 weeks. In contrast, cements incorporating BG particles resorbed with fibrous tissue filling the defect. Furthermore, CG/nHA-PEUR cements remodeled significantly faster at the full weight-bearing tibial plateau site compared to the mechanically protected femoral condyle site in the same animal. These findings are the first to report a settable bone cement that remodels to form new bone while providing mechanical stability in a stringent large animal model of weight-bearing bone defects near an articulating joint.

摘要

承重部位的骨折很难治疗,因为难以维持关节的一致性。一种理想的用于关节附近骨折修复的生物材料,在植入后能迅速凝固,用最小的刚性植入物稳定骨折,刺激新骨形成,并以保持骨质完整性的速度进行重塑。因此,设计能够在重塑以形成新骨的同时机械稳定骨折的生物材料,是骨组织工程中尚未满足的挑战。在这项研究中,我们研究了可吸收骨水泥在绵羊承重胫骨平台缺损严格模型中的重塑。纳米晶羟基磷灰石-聚酯尿烷(nHA-PEUR)杂化聚合物与陶瓷颗粒(85%β-磷酸三钙/15%羟基磷灰石,CG)或 CG 和生物活性玻璃(BG)颗粒的混合物一起形成可凝固的骨水泥。水泥的初始抗压强度和疲劳性能与不可吸收的聚甲基丙烯酸甲酯骨水泥相当。在能够耐受最初几周早期负重的动物中,CG/nHA-PEUR 水泥能够机械稳定胫骨平台缺损,并在 16 周时重塑形成新骨。相比之下,含有 BG 颗粒的水泥则被纤维组织吸收,填充了缺损。此外,CG/nHA-PEUR 水泥在负重的胫骨平台部位的重塑速度明显快于同一动物中机械保护的股骨髁部位。这些发现首次报道了一种可凝固的骨水泥,它在关节附近承重骨缺损的严格大动物模型中既能提供机械稳定性,又能重塑形成新骨。