Department of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, TN, 37235, USA.
Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, 37235, USA.
Biomaterials. 2018 Oct;179:29-45. doi: 10.1016/j.biomaterials.2018.06.032. Epub 2018 Jun 26.
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.
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。